JP2014040411A - Pyrazole derivative and pest controlling agent - Google Patents
Pyrazole derivative and pest controlling agent Download PDFInfo
- Publication number
- JP2014040411A JP2014040411A JP2013153740A JP2013153740A JP2014040411A JP 2014040411 A JP2014040411 A JP 2014040411A JP 2013153740 A JP2013153740 A JP 2013153740A JP 2013153740 A JP2013153740 A JP 2013153740A JP 2014040411 A JP2014040411 A JP 2014040411A
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- Prior art keywords
- sme
- ome
- scf
- sch
- alkyl
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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- 241000607479 Yersinia pestis Species 0.000 title claims abstract description 26
- 150000003217 pyrazoles Chemical class 0.000 title claims abstract description 22
- 125000005843 halogen group Chemical group 0.000 claims abstract description 32
- 150000003839 salts Chemical class 0.000 claims abstract description 27
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 17
- 125000004093 cyano group Chemical group *C#N 0.000 claims abstract description 11
- 239000002917 insecticide Substances 0.000 claims abstract description 8
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims abstract description 7
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- 239000000642 acaricide Substances 0.000 claims abstract description 5
- 230000000895 acaricidal effect Effects 0.000 claims abstract description 4
- 125000004390 alkyl sulfonyl group Chemical group 0.000 claims abstract description 4
- 125000003226 pyrazolyl group Chemical group 0.000 claims abstract description 4
- -1 C 1 -C 6 alkyl Chemical group 0.000 claims description 99
- 125000004432 carbon atom Chemical group C* 0.000 claims description 37
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 28
- 238000000034 method Methods 0.000 claims description 26
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims description 16
- 125000000217 alkyl group Chemical group 0.000 claims description 15
- 239000004480 active ingredient Substances 0.000 claims description 11
- 229910052799 carbon Inorganic materials 0.000 claims description 10
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims description 8
- 239000002689 soil Substances 0.000 claims description 8
- 125000004738 (C1-C6) alkyl sulfinyl group Chemical group 0.000 claims description 6
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- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 1
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- 229910052788 barium Inorganic materials 0.000 description 1
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
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- 239000010949 copper Substances 0.000 description 1
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- GBRBMTNGQBKBQE-UHFFFAOYSA-L copper;diiodide Chemical compound I[Cu]I GBRBMTNGQBKBQE-UHFFFAOYSA-L 0.000 description 1
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- 125000004772 dichloromethyl group Chemical group [H]C(Cl)(Cl)* 0.000 description 1
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- 230000007613 environmental effect Effects 0.000 description 1
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- 238000005194 fractionation Methods 0.000 description 1
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- 125000006343 heptafluoro propyl group Chemical group 0.000 description 1
- 125000000268 heptanoyl group Chemical group O=C([*])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000003187 heptyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 230000002363 herbicidal effect Effects 0.000 description 1
- 239000004009 herbicide Substances 0.000 description 1
- 125000000623 heterocyclic group Chemical group 0.000 description 1
- 125000003104 hexanoyl group Chemical group O=C([*])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
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- 229910052744 lithium Inorganic materials 0.000 description 1
- YNESATAKKCNGOF-UHFFFAOYSA-N lithium bis(trimethylsilyl)amide Chemical compound [Li+].C[Si](C)(C)[N-][Si](C)(C)C YNESATAKKCNGOF-UHFFFAOYSA-N 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 231100000053 low toxicity Toxicity 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
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- 235000011090 malic acid Nutrition 0.000 description 1
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- UKVIEHSSVKSQBA-UHFFFAOYSA-N methane;palladium Chemical compound C.[Pd] UKVIEHSSVKSQBA-UHFFFAOYSA-N 0.000 description 1
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- 125000001160 methoxycarbonyl group Chemical group [H]C([H])([H])OC(*)=O 0.000 description 1
- 125000002816 methylsulfanyl group Chemical group [H]C([H])([H])S[*] 0.000 description 1
- 125000006216 methylsulfinyl group Chemical group [H]C([H])([H])S(*)=O 0.000 description 1
- 125000004170 methylsulfonyl group Chemical group [H]C([H])([H])S(*)(=O)=O 0.000 description 1
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- 125000002950 monocyclic group Chemical group 0.000 description 1
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- 125000006095 n-butyl sulfinyl group Chemical group 0.000 description 1
- 125000006126 n-butyl sulfonyl group Chemical group 0.000 description 1
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- 125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 description 1
- 125000006093 n-propyl sulfinyl group Chemical group 0.000 description 1
- 125000006256 n-propyloxycarbonyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])OC(*)=O 0.000 description 1
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- 239000005645 nematicide Substances 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 125000005246 nonafluorobutyl group Chemical group FC(F)(F)C(F)(F)C(F)(F)C(F)(F)* 0.000 description 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 235000020636 oyster Nutrition 0.000 description 1
- PIBWKRNGBLPSSY-UHFFFAOYSA-L palladium(II) chloride Chemical compound Cl[Pd]Cl PIBWKRNGBLPSSY-UHFFFAOYSA-L 0.000 description 1
- YJVFFLUZDVXJQI-UHFFFAOYSA-L palladium(ii) acetate Chemical compound [Pd+2].CC([O-])=O.CC([O-])=O YJVFFLUZDVXJQI-UHFFFAOYSA-L 0.000 description 1
- 125000006340 pentafluoro ethyl group Chemical group FC(F)(F)C(F)(F)* 0.000 description 1
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229960003975 potassium Drugs 0.000 description 1
- 244000144977 poultry Species 0.000 description 1
- 125000001844 prenyl group Chemical group [H]C([*])([H])C([H])=C(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- 125000001501 propionyl group Chemical group O=C([*])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
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- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 150000003460 sulfonic acids Chemical class 0.000 description 1
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- 238000003786 synthesis reaction Methods 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 125000005931 tert-butyloxycarbonyl group Chemical group [H]C([H])([H])C(OC(*)=O)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 125000001973 tert-pentyl group Chemical group [H]C([H])([H])C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 229910052723 transition metal Inorganic materials 0.000 description 1
- 150000003624 transition metals Chemical class 0.000 description 1
- 125000003866 trichloromethyl group Chemical group ClC(Cl)(Cl)* 0.000 description 1
- ITMCEJHCFYSIIV-UHFFFAOYSA-N triflic acid Chemical compound OS(=O)(=O)C(F)(F)F ITMCEJHCFYSIIV-UHFFFAOYSA-N 0.000 description 1
- 125000005034 trifluormethylthio group Chemical group FC(S*)(F)F 0.000 description 1
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 description 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 1
- 125000001889 triflyl group Chemical group FC(F)(F)S(*)(=O)=O 0.000 description 1
- 125000003774 valeryl group Chemical group O=C([*])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Landscapes
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
Description
本発明は、新規なピラゾール誘導体及びそれらの塩、並びに該化合物を有効成分として含有することを特徴とする有害生物防除剤に関するものである。本発明における有害生物防除剤とは、農園芸分野又は畜産・衛生分野(家畜や愛玩動物としての哺乳動物又は鳥類に対する内部寄生虫・外部寄生虫や家庭用及び業務用の衛生害虫・不快害虫)等における有害な節足動物を対象とした害虫防除剤を意味する。また、本発明における農薬とは、農園芸分野における殺虫・殺ダニ剤、殺線虫剤、除草剤及び殺菌剤等を意味する。 The present invention relates to a novel pyrazole derivative and a salt thereof, and a pest control agent containing the compound as an active ingredient. The pest control agent in the present invention is the field of agriculture and horticulture or the field of livestock and hygiene (internal parasites / external parasites for domestic animals and pets, hygiene pests and unpleasant pests for domestic and commercial use) It means a pest control agent for harmful arthropods such as The agrochemical in the present invention means an insecticide / acaricide, nematicide, herbicide, fungicide, etc. in the field of agriculture and horticulture.
特許文献3〜17及び非特許文献1及び2には、ある種のピラゾール誘導体が開示されているが、殺虫活性を有することは示唆も開示もされていない。 Patent Documents 3 to 17 and Non-Patent Documents 1 and 2 disclose certain pyrazole derivatives, but neither suggest nor disclose that they have insecticidal activity.
また特許文献1及び特許文献2には、ピラゾール誘導体が殺虫剤として有用であることが開示されているが、本発明に係るピラゾール化合物については何ら開示されていない。 Patent Documents 1 and 2 disclose that pyrazole derivatives are useful as insecticides, but do not disclose any pyrazole compounds according to the present invention.
農園芸病害虫、森林病害虫、或いは衛生病害虫等、各種病害虫の防除を目的とする有害生物防除剤の開発が進み、多種多様な薬剤が今日まで実用に供されてきた。 The development of pest control agents for the purpose of controlling various pests such as agricultural and horticultural pests, forest pests, and hygiene pests has progressed, and a wide variety of drugs have been put to practical use to date.
しかしながら、こうした薬剤の長年にわたる使用により、近年、病害虫が薬剤抵抗性を獲得し、従来用いられてきた既存の殺虫剤や殺菌剤による防除が困難となる場面が増えてきている。また、既存の有害生物防除剤の一部のものは毒性が高く、或いはあるものは環境中に長期間残留することにより、生態系を攪乱するという問題も顕在化しつつある。このような状況下、高度な有害生物防除活性を有するのみならず、低毒性且つ低残留性の新規な有害生物防除剤の開発が常に期待されている。 However, due to the long-term use of such drugs, in recent years, pests have acquired drug resistance, making it difficult to control with existing insecticides and fungicides that have been used. In addition, some existing pest control agents are highly toxic, or some of them remain in the environment for a long time, and the problem of disturbing the ecosystem is becoming apparent. Under such circumstances, development of a novel pest control agent having not only high pest control activity but also low toxicity and low persistence is always expected.
本発明者らは、上記の課題解決を目標に鋭意研究を重ねた結果、本発明に係る下記式(1)で表される新規なピラゾール誘導体が優れた有害生物防除活性、特に殺虫・殺ダニ活性を示し、且つ、ホ乳動物、魚類及び益虫等の非標的生物に対してほとんど悪影響の無い、極めて有用な化合物であることを見い出し、本発明を完成した。 As a result of intensive studies aimed at solving the above problems, the present inventors have found that the novel pyrazole derivative represented by the following formula (1) according to the present invention has excellent pest control activity, particularly insecticide / miticide. The present invention has been completed by finding it to be an extremely useful compound that exhibits activity and has almost no adverse effects on non-target organisms such as mammals, fish and beneficial insects.
すなわち、本発明は下記〔1〕〜〔9〕に関するものである。 That is, the present invention relates to the following [1] to [9].
〔1〕
式(1):
[1]
Formula (1):
[式中、Bは、下記の構造式で表されるピラゾール環を表し、 [In the formula, B represents a pyrazole ring represented by the following structural formula;
A1は、−N(−O)m2又は−CR1を表し、
A2はD1−8、D1−15、D1−17、D1−22、D1−52又はD1−106を表し、
R1は、水素原子、ハロゲン原子、シアノ、ニトロ、C1〜C6アルキル、C1〜C6ハロアルキル、C1〜C6アルコキシ、C1〜C6ハロアルコキシ、C1〜C6アルキルチオ、C1〜C6アルキルスルフィニル、C1〜C6アルキルスルホニル、C1〜C6ハロアルキルチオ、C1〜C6ハロアルキルスルフィニル又はC1〜C6ハロアルキルスルホニルを表し、
R2は、ハロゲン原子、シアノ、ニトロ、C1〜C6アルキル、C1〜C6ハロアルキル、C1〜C6アルコキシ、C1〜C6ハロアルコキシ、C1〜C6アルキルチオ、C1〜C6アルキルスルフィニル、C1〜C6アルキルスルホニル、C1〜C6ハロアルキルチオ、C1〜C6ハロアルキルスルフィニル又はC1〜C6ハロアルキルスルホニルを表し、n1が2以上の整数を表すとき、各々のR2は互いに同一であっても又は互いに相異なってもよく、
R4は、水素原子、ハロゲン原子、C1〜C6アルキル、C3〜C6シクロアルキル、C2〜C6アルケニル、C2〜C6アルキニル、C1〜C6ハロアルキル、C1〜C6アルコキシ、C1〜C6ハロアルコキシ、C1〜C6アルキルチオ、C1〜C6アルキルスルフィニル、C1〜C6アルキルスルホニル、C1〜C6ハロアルキルチオ、C1〜C6ハロアルキルスルフィニル、C1〜C6ハロアルキルスルホニル、シアノ、C1〜C6アルコキシカルボニル、C1〜C6アルキルカルボニル、C1〜C6アルキルアミノカルボニル又はジ(C1〜C6アルキル)アミノカルボニルを表し、
D1−8、D1−15、D1−17、D1−22、D1−52及びD1−106は、それぞれ下記の構造式で表される環を表し、
A 1 represents —N (—O) m 2 or —CR 1 ,
A 2 represents D1-8, D1-15, D1-17, D1-22, D1-52 or D1-106,
R 1 is a hydrogen atom, a halogen atom, cyano, nitro, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 alkoxy, C 1 -C 6 haloalkoxy, C 1 -C 6 alkylthio, C 1 -C 6 alkylsulfinyl, C 1 -C 6 represent alkylsulfonyl, C 1 -C 6 haloalkylthio, a C 1 -C 6 haloalkylsulfinyl or C 1 -C 6 haloalkylsulfonyl,
R 2 is a halogen atom, cyano, nitro, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 alkoxy, C 1 -C 6 haloalkoxy, C 1 -C 6 alkylthio, C 1- C 6 alkylsulfinyl, C 1 -C 6 alkylsulfonyl, C 1 -C 6 haloalkylthio, represents C 1 -C 6 haloalkylsulfinyl or C 1 -C 6 haloalkylsulfonyl, when n1 represents an integer of 2 or more, each R 2 may be the same as or different from each other.
R 4 is a hydrogen atom, a halogen atom, C 1 -C 6 alkyl, C 3 -C 6 cycloalkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 1 -C 6 haloalkyl, C 1 -C 6 alkoxy, C 1 -C 6 haloalkoxy, C 1 -C 6 alkylthio, C 1 -C 6 alkylsulfinyl, C 1 -C 6 alkylsulfonyl, C 1 -C 6 haloalkylthio, C 1 -C 6 haloalkylsulfinyl, C 1 -C 6 haloalkylsulfonyl, represents cyano, C 1 -C 6 alkoxycarbonyl, C 1 -C 6 alkylcarbonyl, a C 1 -C 6 alkylaminocarbonyl or di (C 1 -C 6 alkyl) aminocarbonyl,
D1-8, D1-15, D1-17, D1-22, D1-52 and D1-106 each represent a ring represented by the following structural formula;
X及びR3は、一緒になってC2〜C4アルキレン鎖又はC2〜C4アルケニレン鎖を形成することにより、Xの結合する炭素原子とR3の結合する炭素原子及びA2の結合する炭素原子と共に6〜8員環を形成し、このときアルキレン鎖又はアルケニレン鎖は、酸素原子又は硫黄原子を含んでもよく、
X1は、C1〜C12アルキル、R5によって任意に置換された(C1〜C12)アルキル、−OH、−OR6、−SH、−S(O)rR6、−N(R8)R9、−C(O)R7、−C(O)OH、−C(O)OR6、−C(O)N(R8)R9、−C(S)N(R8)R9、D2−32、D2−33、D2−34、D2−36、D2−37又はD2−38を表し、p2又はp3が2以上の整数を表すとき、各々のX1は互いに同一であっても又は互いに相異なってもよく、
X1aは、水素原子、C1〜C12アルキル、R5aによって任意に置換された(C1〜C12)アルキル又は−C(O)R7aを表し、
D2−32、D2−33、D2−34、D2−36、D2−37及びD2−38は、それぞれ下記の構造式で表される環を表し、
X and R 3 together form a C 2 to C 4 alkylene chain or a C 2 to C 4 alkenylene chain, whereby the carbon atom to which X is bonded to the carbon atom to which R 3 is bonded and the bond of A 2 Together with the carbon atom to form a 6-8 membered ring, wherein the alkylene chain or alkenylene chain may contain an oxygen atom or a sulfur atom,
X 1 is C 1 -C 12 alkyl, (C 1 -C 12 ) alkyl optionally substituted with R 5 , —OH, —OR 6 , —SH, —S (O) r R 6 , —N ( R 8) R 9, -C ( O) R 7, -C (O) OH, -C (O) OR 6, -C (O) N (R 8) R 9, -C (S) N (R 8 ) R 9 , D2-32, D2-33, D2-34, D2-36, D2-37 or D2-38, and when p2 or p3 represents an integer of 2 or more, each X 1 is the same as each other Or may be different from each other,
X 1a represents a hydrogen atom, C 1 -C 12 alkyl, (C 1 -C 12 ) alkyl optionally substituted with R 5a or —C (O) R 7a ,
D2-32, D2-33, D2-34, D2-36, D2-37 and D2-38 each represent a ring represented by the following structural formula;
R5は、ハロゲン原子、−OH、−OR11、−SH、−S(O)rR11を表し、
R5aは、ハロゲン原子、シアノ、−OH,−OR11a、−SH又は−S(O)rR11aを表し、
R6は、C1〜C6アルキル又はC1〜C6ハロアルキルを表し、
R7は、水素原子、C1〜C6アルキル又はR14によって任意に置換された(C1〜C6)アルキルを表し、
R7aは、水素原子、C1〜C6アルキル、−C(R12a)=NOH又は−C(R12a)=NOR11aを表し、
R8及びR9は、各々独立して水素原子、C1〜C6アルキル又は−C(O)R12を表し、
R11は、C1〜C6アルキル又はR14によって任意に置換された(C1〜C6)アルキルを表し、
R11aは、C1〜C6アルキル又はR14aによって任意に置換された(C1〜C6)アルキルを表し、
R12は、水素原子又はC1〜C6アルキルを表し、
R12aは、水素原子、C1〜C6アルキル又はR14aによって任意に置換された(C1〜C6)アルキルを表し、
R14は、ハロゲン原子、C3〜C6シクロアルキル、−OH,−OR15、−SH又は−S(O)rR15
R14aは、ハロゲン原子、C3〜C6シクロアルキル、−OH,−OR15a、−SH又は−S(O)rR15aを表し、
R15及びR15aは、各々独立してC1〜C6アルキルを表し、
X2は、ハロゲン原子、シアノ、ニトロ、−OH、−SH、−NH2、C1〜C6アルキル、C2〜C6アルケニル、C2〜C6アルキニル、C3〜C8シクロアルキルを表し、
n1、p3及びt1は、各々独立して0〜3の整数を表し、
p1は、0〜1の整数を表し、
p2は、0〜2の整数を表し、
t4は、0〜4の整数を表し、
m1及びm2は、各々独立して0又は1の整数を表し、
rは、0〜2の整数を表す。]で表されるピラゾール誘導体又はその塩。
R 5 represents a halogen atom, —OH, —OR 11 , —SH, —S (O) r R 11 ,
R 5a represents a halogen atom, cyano, —OH, —OR 11a , —SH or —S (O) r R 11a ,
R 6 represents C 1 -C 6 alkyl or C 1 -C 6 haloalkyl,
R 7 represents a hydrogen atom, C 1 -C 6 alkyl or (C 1 -C 6 ) alkyl optionally substituted with R 14 ,
R 7a represents a hydrogen atom, C 1 -C 6 alkyl, —C (R 12a ) ═NOH or —C (R 12a ) = NOR 11a ,
R 8 and R 9 each independently represents a hydrogen atom, C 1 -C 6 alkyl or —C (O) R 12 ;
R 11 represents C 1 -C 6 alkyl or (C 1 -C 6 ) alkyl optionally substituted by R 14 ,
R 11a represents C 1 -C 6 alkyl or (C 1 -C 6 ) alkyl optionally substituted with R 14a ,
R 12 represents a hydrogen atom or C 1 -C 6 alkyl;
R 12a represents a hydrogen atom, C 1 -C 6 alkyl or (C 1 -C 6 ) alkyl optionally substituted with R 14a ,
R 14 is a halogen atom, C 3 -C 6 cycloalkyl, —OH, —OR 15 , —SH or —S (O) r R 15.
R 14a represents a halogen atom, C 3 -C 6 cycloalkyl, —OH, —OR 15a , —SH or —S (O) r R 15a ,
R 15 and R 15a each independently represent C 1 -C 6 alkyl;
X 2 represents a halogen atom, cyano, nitro, —OH, —SH, —NH 2 , C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 3 -C 8 cycloalkyl. Represent,
n1, p3 and t1 each independently represents an integer of 0 to 3,
p1 represents an integer of 0 to 1,
p2 represents an integer of 0 to 2,
t4 represents an integer of 0 to 4,
m1 and m2 each independently represent an integer of 0 or 1,
r represents an integer of 0-2. ] The pyrazole derivative represented by these, or its salt.
〔2〕
A1は、−CR1を表し、
R1及びR4は、各々独立して水素原子、ハロゲン原子又はC1〜C6アルキルを表し、
R2は、ハロゲン原子又はC1〜C6アルキルを表す上記〔1〕記載のピラゾール誘導体又はその塩。
[2]
A 1 represents -CR 1
R 1 and R 4 each independently represent a hydrogen atom, a halogen atom or C 1 -C 6 alkyl;
R 2 represents a pyrazole derivative or a salt thereof according to the above [1], wherein R 2 represents a halogen atom or C 1 -C 6 alkyl.
〔3〕
R1及びR4は、水素原子を表し、
Bは、B−1a、B−2a、B−3a、B−4a、B−5a乃至B−6aのいずれかで表される環を表し、
[3]
R 1 and R 4 represent a hydrogen atom,
B represents a ring represented by any of B-1a, B-2a, B-3a, B-4a, B-5a to B-6a,
X1は、C1〜C6アルキル、R5によって任意に置換された(C1〜C6)アルキル、−S(O)rR6、−N(R8)R9、−C(O)OH、−C(O)OR6又はD2−33を表し、p3が2の整数を表すとき、各々のX1は互いに同一であっても又は互いに相異なってもよく、
X1aは、水素原子、R5aによって任意に置換された(C1〜C6)アルキル又は−C(O)R7aを表し、
R5は、−S(O)rR11を表し、
R5aは、ハロゲン原子、又は−S(O)rR11aを表し、
R6は、C1〜C6アルキルを表し、
R7aは、−C(R12a)=NOR11aを表し、
R8は、水素原子を表し、
R9は、−C(O)R12を表し、
R11、R11a及びR12は、各々独立してC1〜C6アルキルを表し、
R12aは、R14aによって任意に置換された(C1〜C6)アルキルを表し、
R14aは、−S(O)rR15aを表し、
R15aは、C1〜C6アルキルを表し、
n1及びt4は、0を表し、
p1は、0〜1の整数を表し、
p2は、1の整数を表し、
p3は、2の整数を表し、
rは、0〜2の整数を表す上記〔2〕記載のピラゾール誘導体又はその塩。
X 1 is C 1 -C 6 alkyl, (C 1 -C 6 ) alkyl optionally substituted by R 5 , —S (O) r R 6 , —N (R 8 ) R 9 , —C (O ) Represents OH, —C (O) OR 6 or D2-33, and p3 represents an integer of 2, each X 1 may be the same as or different from each other;
X 1a represents a hydrogen atom, (C 1 -C 6 ) alkyl or —C (O) R 7a optionally substituted with R 5a ,
R 5 represents —S (O) r R 11 ,
R 5a represents a halogen atom or —S (O) r R 11a ,
R 6 represents C 1 -C 6 alkyl,
R 7a represents -C (R 12a ) = NOR 11a ,
R 8 represents a hydrogen atom,
R 9 represents —C (O) R 12 ,
R 11 , R 11a and R 12 each independently represent C 1 -C 6 alkyl;
R 12a represents (C 1 -C 6 ) alkyl optionally substituted with R 14a ,
R 14a represents -S (O) r R 15a ;
R 15a represents C 1 -C 6 alkyl;
n1 and t4 represent 0;
p1 represents an integer of 0 to 1,
p2 represents an integer of 1,
p3 represents an integer of 2,
r is a pyrazole derivative according to the above [2] or a salt thereof, wherein r represents an integer of 0 to 2;
〔4〕
上記〔1〕〜〔3〕記載のピラゾール誘導体及びそれらの塩から選ばれる1種又は2種以上を有効成分として含有する有害生物防除剤。
[4]
A pest control agent containing one or more selected from the pyrazole derivatives described in the above [1] to [3] and salts thereof as an active ingredient.
〔5〕
上記〔1〕〜〔3〕記載のピラゾール誘導体及びそれらの塩から選ばれる1種又は2種以上を有効成分として含有する農薬。
[5]
An agrochemical containing, as an active ingredient, one or more selected from the pyrazole derivatives described in the above [1] to [3] and salts thereof.
〔6〕
上記〔1〕〜〔3〕記載のピラゾール誘導体及びそれらの塩から選ばれる1種又は2種以上を有効成分として含有する哺乳動物又は鳥類の内部もしくは外部寄生虫防除剤。
[6]
A mammal or bird internal or ectoparasite control agent comprising one or more selected from the pyrazole derivatives described in [1] to [3] above and salts thereof as an active ingredient.
〔7〕
上記〔1〕〜〔3〕記載のピラゾール誘導体及びそれらの塩から選ばれる1種又は2種以上を有効成分として含有する殺虫剤又は殺ダニ剤。
[7]
An insecticide or acaricide containing as an active ingredient one or more selected from the pyrazole derivatives described in [1] to [3] above and salts thereof.
〔8〕
上記〔1〕〜〔3〕記載のピラゾール誘導体及びそれらの塩から選ばれる1種又は2種以上を有効成分として含有する土壌処理剤。
[8]
The soil treatment agent which contains the 1 type (s) or 2 or more types chosen from the pyrazole derivative and their salts as described in said [1]-[3] as an active ingredient.
〔9〕
土壌処理方法が土壌潅注処理である上記〔8〕記載の土壌処理剤。
[9]
The soil treatment agent according to the above [8], wherein the soil treatment method is soil irrigation treatment.
本発明化合物は多くの農業害虫、ハダニ類、哺乳動物又は鳥類の内部もしくは外部寄生虫に対して優れた殺虫・殺ダニ活性を有し、既存の殺虫剤に対して抵抗性を獲得した害虫に対しても十分な防除効果を発揮する。さらに、ホ乳類、魚類及び益虫に対してほとんど悪影響を及ぼさず、低残留性で環境に対する負荷も軽い。 The compound of the present invention has excellent insecticidal / miticidal activity against many agricultural pests, spider mites, mammals or birds, or against insects that have acquired resistance to existing insecticides. Even against this, it exhibits a sufficient control effect. Furthermore, it has little adverse effect on mammals, fish and beneficial insects, has low persistence, and has a light environmental impact.
従って、本発明は有用な新規有害生物防除剤を提供することができる。 Therefore, the present invention can provide a useful novel pest control agent.
本発明に包含される化合物には、置換基の種類によってはE−体及びZ−体の幾何異性体が存在する場合があるが、本発明はこれらE−体、Z−体又はE−体及びZ−体を任意の割合で含む混合物を包含するものである。また、本発明に包含される化合物は、1個又は2個以上の不斉炭素原子の存在に起因する光学活性体が存在するが、本発明は全ての光学活性体又はラセミ体を包含する。 The compounds included in the present invention may have geometrical isomers of E-form and Z-form depending on the type of substituent, and the present invention is not limited to these E-form, Z-form or E-form. And a mixture containing the Z-form in an arbitrary ratio. In addition, the compounds included in the present invention include optically active substances resulting from the presence of one or more asymmetric carbon atoms, but the present invention includes all optically active substances or racemates.
本発明に包含される化合物のうちで、常法に従って酸付加塩にすることができるものは、例えば、フッ化水素酸、塩酸、臭化水素酸、ヨウ化水素酸等のハロゲン化水素酸の塩、硝酸、硫酸、燐酸、塩素酸、過塩素酸等の無機酸の塩、メタンスルホン酸、エタンスルホン酸、トリフルオロメタンスルホン酸、ベンゼンスルホン酸、p−トルエンスルホン酸等のスルホン酸の塩、ギ酸、酢酸、プロピオン酸、トリフルオロ酢酸、フマール酸、酒石酸、蓚酸、マレイン酸、リンゴ酸、コハク酸、安息香酸、マンデル酸、アスコルビン酸、乳酸、グルコン酸、クエン酸等のカルボン酸の塩又はグルタミン酸、アスパラギン酸等のアミノ酸の塩とすることができる。 Among the compounds included in the present invention, those that can be converted into acid addition salts according to a conventional method include, for example, hydrohalic acids such as hydrofluoric acid, hydrochloric acid, hydrobromic acid, hydroiodic acid, and the like. Salts of inorganic acids such as salts, nitric acid, sulfuric acid, phosphoric acid, chloric acid, perchloric acid, salts of sulfonic acids such as methanesulfonic acid, ethanesulfonic acid, trifluoromethanesulfonic acid, benzenesulfonic acid, p-toluenesulfonic acid, Salts of carboxylic acids such as formic acid, acetic acid, propionic acid, trifluoroacetic acid, fumaric acid, tartaric acid, succinic acid, maleic acid, malic acid, succinic acid, benzoic acid, mandelic acid, ascorbic acid, lactic acid, gluconic acid, citric acid, etc. A salt of an amino acid such as glutamic acid or aspartic acid can be used.
或いは、本発明に包含される化合物のうちで、常法に従って金属塩にすることができるものは、例えば、リチウム、ナトリウム、カリウムといったアルカリ金属の塩、カルシウム、バリウム、マグネシウムといったアルカリ土類金属の塩又はアルミニウムの塩とすることができる。 Alternatively, among the compounds included in the present invention, those that can be converted into a metal salt according to a conventional method include, for example, alkali metal salts such as lithium, sodium, and potassium, and alkaline earth metals such as calcium, barium, and magnesium. It can be a salt or a salt of aluminum.
次に、本明細書において示した各置換基の具体例を以下に示す。ここで、n−はノルマル、i−はイソ、s−はセカンダリー及びtert−はターシャリーを各々意味し、Phはフェニルを意味する。 Next, specific examples of each substituent shown in the present specification are shown below. Here, n- represents normal, i- represents iso, s- represents secondary, and tert- represents tertiary, and Ph represents phenyl.
本明細書におけるハロゲン原子としては、フッ素原子、塩素原子、臭素原子及びヨウ素原子が挙げられる。尚、本明細書中「ハロ」の表記もこれらのハロゲン原子を表す。 Examples of the halogen atom in the present specification include a fluorine atom, a chlorine atom, a bromine atom and an iodine atom. In the present specification, the notation “halo” also represents these halogen atoms.
本明細書におけるCa〜Cbアルキルの表記は、炭素原子数がa〜b個よりなる直鎖状又は分岐鎖状の炭化水素基を表し、例えばメチル基、エチル基、n−プロピル基、i−プロピル基、n−ブチル基、i−ブチル基、s−ブチル基、tert−ブチル基、n−ペンチル基、1,1−ジメチルプロピル基、n−ヘキシル基等が具体例として挙げられ、各々の指定の炭素原子数の範囲で選択される。 The notation of C a -C b alkyl in the present specification represents a linear or branched hydrocarbon group having a carbon number of a to b , for example, methyl group, ethyl group, n-propyl group, Specific examples include i-propyl group, n-butyl group, i-butyl group, s-butyl group, tert-butyl group, n-pentyl group, 1,1-dimethylpropyl group, n-hexyl group, and the like. Each selected range of carbon atoms is selected.
本明細書におけるCa〜Cbハロアルキルの表記は、炭素原子に結合した水素原子が、ハロゲン原子によって任意に置換された、炭素原子数がa〜b個よりなる直鎖状又は分岐鎖状の炭化水素基を表し、このとき、2個以上のハロゲン原子によって置換されている場合、それらのハロゲン原子は互いに同一でも、又は互いに相異なっていてもよい。例えばフルオロメチル基、クロロメチル基、ブロモメチル基、ヨードメチル基、ジフルオロメチル基、ジクロロメチル基、トリフルオロメチル基、クロロジフルオロメチル基、トリクロロメチル基、ブロモジフルオロメチル基、2−フルオロエチル基、2−クロロエチル基、2−ブロモエチル基、2,2−ジフルオロエチル基、2,2,2−トリフルオロエチル基、2−クロロ−2,2−ジフルオロエチル基、2,2,2−トリクロロエチル基、1,1,2,2−テトラフルオロエチル基、2−クロロ−1,1,2−トリフルオロエチル基、ペンタフルオロエチル基、3,3,3−トリフルオロプロピル基、2,2,3,3,3−ペンタフルオロプロピル基、1,1,2,3,3,3−ヘキサフルオロプロピル基、ヘプタフルオロプロピル基、2,2,2−トリフルオロ−1−(トリフルオロメチル)エチル基、1,2,2,2−テトラフルオロ−1−(トリフルオロメチル)エチル基、2,2,3,3,4,4,4−ヘプタフルオロブチル基、ノナフルオロブチル基等が具体例として挙げられ、各々の指定の炭素原子数の範囲で選択される。 In the present specification, C a -C b haloalkyl is represented by a linear or branched chain having a to b carbon atoms in which a hydrogen atom bonded to a carbon atom is optionally substituted with a halogen atom. Represents a hydrocarbon group, and when substituted by two or more halogen atoms, the halogen atoms may be the same as or different from each other. For example, fluoromethyl group, chloromethyl group, bromomethyl group, iodomethyl group, difluoromethyl group, dichloromethyl group, trifluoromethyl group, chlorodifluoromethyl group, trichloromethyl group, bromodifluoromethyl group, 2-fluoroethyl group, 2- Chloroethyl group, 2-bromoethyl group, 2,2-difluoroethyl group, 2,2,2-trifluoroethyl group, 2-chloro-2,2-difluoroethyl group, 2,2,2-trichloroethyl group, 1 , 1,2,2-tetrafluoroethyl group, 2-chloro-1,1,2-trifluoroethyl group, pentafluoroethyl group, 3,3,3-trifluoropropyl group, 2,2,3,3 , 3-pentafluoropropyl group, 1,1,2,3,3,3-hexafluoropropyl group, heptafluoropropyl group 2,2,2-trifluoro-1- (trifluoromethyl) ethyl group, 1,2,2,2-tetrafluoro-1- (trifluoromethyl) ethyl group, 2,2,3,3,4, Specific examples include 4,4-heptafluorobutyl group, nonafluorobutyl group and the like, and each is selected within the range of the number of carbon atoms designated.
本明細書におけるCa〜Cbシクロアルキルの表記は、炭素原子数がa〜b個よりなる環状の炭化水素基を表し、3員環から6員環までの単環又は複合環構造を形成することが出来る。また、各々の環は指定の炭素原子数の範囲でアルキル基によって任意に置換されていてもよい。例えばシクロプロピル基、1−メチルシクロプロピル基、2−メチルシクロプロピル基、2,2−ジメチルシクロプロピル基、シクロブチル基、シクロペンチル基、シクロヘキシル基等が具体例として挙げられ、各々の指定の炭素原子数の範囲で選択される。 In the present specification, C a -C b cycloalkyl represents a cyclic hydrocarbon group having a carbon number of a to b , and forms a monocyclic or complex ring structure having 3 to 6 members. I can do it. Each ring may be optionally substituted with an alkyl group within the range of the specified number of carbon atoms. Specific examples include, for example, cyclopropyl group, 1-methylcyclopropyl group, 2-methylcyclopropyl group, 2,2-dimethylcyclopropyl group, cyclobutyl group, cyclopentyl group, cyclohexyl group and the like. Selected in a range of numbers.
本明細書におけるCa〜Cbアルケニルの表記は、炭素原子数がa〜b個よりなる直鎖状又は分岐鎖状で、且つ分子内に1個又は2個以上の二重結合を有する不飽和炭化水素基を表し、例えばビニル基、1−プロペニル基、2−プロペニル基、1−メチルエテニル基、2−ブテニル基、2−メチル−2−プロペニル基、3−メチル−2−ブテニル基、1,1−ジメチル−2−プロペニル基等が具体例として挙げられ、各々の指定の炭素原子数の範囲で選択される。 In the present specification, C a -C b alkenyl is a linear or branched chain composed of a to b carbon atoms and has one or more double bonds in the molecule. Represents a saturated hydrocarbon group, for example, vinyl group, 1-propenyl group, 2-propenyl group, 1-methylethenyl group, 2-butenyl group, 2-methyl-2-propenyl group, 3-methyl-2-butenyl group, 1 , 1-dimethyl-2-propenyl group and the like are listed as specific examples, and each is selected within the range of the designated number of carbon atoms.
本明細書におけるCa〜Cbアルキニルの表記は、炭素原子数がa〜b個よりなる直鎖状又は分岐鎖状で、且つ分子内に1個又は2個以上の三重結合を有する不飽和炭化水素基を表し、例えばエチニル基、1−プロピニル基、2−プロピニル基、1−ブチニル基、2−ブチニル基、3−ブチニル基、1,1−ジメチル−2−プロピニル基等が具体例として挙げられ、各々の指定の炭素原子数の範囲で選択される。 In the present specification, C a -C b alkynyl is a linear or branched chain composed of a to b carbon atoms and has one or more triple bonds in the molecule. Represents a hydrocarbon group, for example, ethynyl group, 1-propynyl group, 2-propynyl group, 1-butynyl group, 2-butynyl group, 3-butynyl group, 1,1-dimethyl-2-propynyl group, etc. Each of which is selected for each specified number of carbon atoms.
本明細書におけるCa〜Cbアルコキシの表記は、炭素原子数がa〜b個よりなる前記の意味であるアルキル−O−基を表し、例えばメトキシ基、エトキシ基、n−プロピルオキシ基、i−プロピルオキシ基、n−ブチルオキシ基、i−ブチルオキシ基、s−ブチルオキシ基、tert−ブチルオキシ基等が具体例として挙げられ、各々の指定の炭素原子数の範囲で選択される。 The notation of C a -C b alkoxy in the present specification represents an alkyl-O— group having the above-mentioned meaning consisting of a to b carbon atoms, for example, methoxy group, ethoxy group, n-propyloxy group, Specific examples include an i-propyloxy group, an n-butyloxy group, an i-butyloxy group, an s-butyloxy group, a tert-butyloxy group, and the like, and each is selected within the range of the designated number of carbon atoms.
本明細書におけるCa〜Cbハロアルコキシの表記は、炭素原子数がa〜b個よりなる前記の意味であるハロアルキル−O−基を表し、例えばジフルオロメトキシ基、トリフルオロメトキシ基、クロロジフルオロメトキシ基、ブロモジフルオロメトキシ基、2−フルオロエトキシ基、2−クロロエトキシ基、2,2,2−トリフルオロエトキシ基、1,1,2,2,−テトラフルオロエトキシ基、2−クロロ−1,1,2−トリフルオロエトキシ基、1,1,2,3,3,3−ヘキサフルオロプロピルオキシ基等が具体例として挙げられ、各々の指定の炭素原子数の範囲で選択される。 The notation of C a -C b haloalkoxy in the present specification represents a haloalkyl-O— group having the above-mentioned meaning consisting of a to b carbon atoms, for example, difluoromethoxy group, trifluoromethoxy group, chlorodifluoro Methoxy group, bromodifluoromethoxy group, 2-fluoroethoxy group, 2-chloroethoxy group, 2,2,2-trifluoroethoxy group, 1,1,2,2, -tetrafluoroethoxy group, 2-chloro-1 Specific examples include 1,2,2-trifluoroethoxy group, 1,1,2,3,3,3-hexafluoropropyloxy group and the like, and each is selected within the range of the designated number of carbon atoms.
本明細書におけるCa〜Cbアルキルチオの表記は、炭素原子数がa〜b個よりなる前記の意味であるアルキル−S−基を表し、例えばメチルチオ基、エチルチオ基、n−プロピルチオ基、i−プロピルチオ基、n−ブチルチオ基、i−ブチルチオ基、s−ブチルチオ基、tert−ブチルチオ基等が具体例として挙げられ、各々の指定の炭素原子数の範囲で選択される。 The notation of C a -C b alkylthio in the present specification represents an alkyl-S-group having the above-mentioned meaning consisting of a to b carbon atoms, for example, methylthio group, ethylthio group, n-propylthio group, i Specific examples include -propylthio group, n-butylthio group, i-butylthio group, s-butylthio group, tert-butylthio group and the like, which are selected within the range of the number of carbon atoms specified.
本明細書におけるCa〜Cbハロアルキルチオの表記は、炭素原子数がa〜b個よりなる前記の意味であるハロアルキル−S−基を表し、例えばジフルオロメチルチオ基、トリフルオロメチルチオ基、クロロジフルオロメチルチオ基、ブロモジフルオロメチルチオ基、2,2,2−トリフルオロエチルチオ基、1,1,2,2−テトラフルオロエチルチオ基、2−クロロ−1,1,2−トリフルオロエチルチオ基、ペンタフルオロエチルチオ基、1,1,2,3,3,3−ヘキサフルオロプロピルチオ基、ヘプタフルオロプロピルチオ基、1,2,2,2−テトラフルオロ−1−(トリフルオロメチル)エチルチオ基、ノナフルオロブチルチオ基等が具体例として挙げられ、各々の指定の炭素原子数の範囲で選択される。 The notation of C a -C b haloalkylthio in the present specification represents a haloalkyl-S-group having the above-mentioned meaning consisting of a to b carbon atoms, for example, difluoromethylthio group, trifluoromethylthio group, chlorodifluoro Methylthio group, bromodifluoromethylthio group, 2,2,2-trifluoroethylthio group, 1,1,2,2-tetrafluoroethylthio group, 2-chloro-1,1,2-trifluoroethylthio group, Pentafluoroethylthio group, 1,1,2,3,3,3-hexafluoropropylthio group, heptafluoropropylthio group, 1,2,2,2-tetrafluoro-1- (trifluoromethyl) ethylthio group , Nonafluorobutylthio group and the like are given as specific examples, and each is selected within the range of the designated number of carbon atoms.
本明細書におけるCa〜Cbアルキルスルフィニルの表記は、炭素原子数がa〜b個よりなる前記の意味であるアルキル−S(O)−基を表し、例えばメチルスルフィニル基、エチルスルフィニル基、n−プロピルスルフィニル基、i−プロピルスルフィニル基、n−ブチルスルフィニル基、i−ブチルスルフィニル基、s−ブチルスルフィニル基、tert−ブチルスルフィニル基等が具体例として挙げられ、各々の指定の炭素原子数の範囲で選択される。 The notation of C a -C b alkylsulfinyl in the present specification represents an alkyl-S (O) -group having the above-mentioned meaning consisting of a to b carbon atoms, for example, methylsulfinyl group, ethylsulfinyl group, Specific examples include n-propylsulfinyl group, i-propylsulfinyl group, n-butylsulfinyl group, i-butylsulfinyl group, s-butylsulfinyl group, tert-butylsulfinyl group and the like. The range is selected.
本明細書におけるCa〜Cbハロアルキルスルフィニルの表記は、炭素原子数がa〜b個よりなる前記の意味であるハロアルキル−S(O)−基を表し、例えばジフルオロメチルスルフィニル基、トリフルオロメチルスルフィニル基、クロロジフルオロメチルスルフィニル基、ブロモジフルオロメチルスルフィニル基、2,2,2−トリフルオロエチルスルフィニル基、1,2,2,2−テトラフルオロ−1−(トリフルオロメチル)エチルスルフィニル基、ノナフルオロブチルスルフィニル基等が具体例として挙げられ、各々の指定の炭素原子数の範囲で選択される。 The notation of C a -C b haloalkylsulfinyl in the present specification represents a haloalkyl-S (O) -group having the above-mentioned meaning consisting of a to b carbon atoms, for example, difluoromethylsulfinyl group, trifluoromethyl Sulfinyl group, chlorodifluoromethylsulfinyl group, bromodifluoromethylsulfinyl group, 2,2,2-trifluoroethylsulfinyl group, 1,2,2,2-tetrafluoro-1- (trifluoromethyl) ethylsulfinyl group, nona Specific examples include a fluorobutylsulfinyl group and the like, and each is selected within the range of the designated number of carbon atoms.
本明細書におけるCa〜Cbアルキルスルホニルの表記は、炭素原子数がa〜b個よりなる前記の意味であるアルキル−SO2−基を表し、例えばメチルスルホニル基、エチルスルホニル基、n−プロピルスルホニル基、i−プロピルスルホニル基、n−ブチルスルホニル基、i−ブチルスルホニル基、s−ブチルスルホニル基、tert−ブチルスルホニル基等が具体例として挙げられ、各々の指定の炭素原子数の範囲で選択される。 The notation of C a -C b alkylsulfonyl in the present specification represents an alkyl-SO 2 -group having the above-mentioned meaning consisting of a to b carbon atoms, for example, methylsulfonyl group, ethylsulfonyl group, n- Specific examples include a propylsulfonyl group, an i-propylsulfonyl group, an n-butylsulfonyl group, an i-butylsulfonyl group, an s-butylsulfonyl group, a tert-butylsulfonyl group, and the range of each designated number of carbon atoms. Selected.
本明細書におけるCa〜Cbハロアルキルスルホニルの表記は、炭素原子数がa〜b個よりなる前記の意味であるハロアルキル−SO2−基を表し、例えばジフルオロメチルスルホニル基、トリフルオロメチルスルホニル基、クロロジフルオロメチルスルホニル基、ブロモジフルオロメチルスルホニル基、2,2,2−トリフルオロエチルスルホニル基、1,1,2,2−テトラフルオロエチルスルホニル基、2−クロロ−1,1,2−トリフルオロエチルスルホニル基等が具体例として挙げられ、各々の指定の炭素原子数の範囲で選択される。 The notation of C a -C b haloalkylsulfonyl in the present specification represents a haloalkyl-SO 2 -group having the above-mentioned meaning consisting of a to b carbon atoms, such as a difluoromethylsulfonyl group or a trifluoromethylsulfonyl group. Chlorodifluoromethylsulfonyl group, bromodifluoromethylsulfonyl group, 2,2,2-trifluoroethylsulfonyl group, 1,1,2,2-tetrafluoroethylsulfonyl group, 2-chloro-1,1,2-trimethyl Specific examples include a fluoroethylsulfonyl group and the like, and each is selected within the range of the designated number of carbon atoms.
本明細書におけるCa〜Cbアルキルカルボニルの表記は、炭素原子数がa〜b個よりなる前記の意味であるアルキル−C(O)−基を表し、例えばアセチル基、プロピオニル基、ブチリル基、イソブチリル基、バレリル基、イソバレリル基、2−メチルブタノイル基、ピバロイル基、ヘキサノイル基、ヘプタノイル基等が具体例として挙げられ、各々の指定の炭素原子数の範囲で選択される。 The notation of C a -C b alkylcarbonyl in the present specification represents an alkyl-C (O) -group having the above-mentioned meaning consisting of a to b carbon atoms, for example, acetyl group, propionyl group, butyryl group. , Isobutyryl group, valeryl group, isovaleryl group, 2-methylbutanoyl group, pivaloyl group, hexanoyl group, heptanoyl group, and the like, and specific examples thereof are selected within the range of the number of carbon atoms designated.
本明細書におけるCa〜Cbアルコキシカルボニルの表記は、炭素原子数がa〜b個よりなる前記の意味であるアルキル−O−C(O)−基を表し、例えばメトキシカルボニル基、エトキシカルボニル基、 n−プロピルオキシカルボニル基、i−プロピルオキシカルボニル基、n−ブトキシカルボニル基、i−ブトキシカルボニル基、tert−ブトキシカルボニル基等が具体例として挙げられ、各々の指定の炭素原子数の範囲で選択される。 The notation of C a -C b alkoxycarbonyl in the present specification represents an alkyl-O—C (O) — group having the above-mentioned meaning consisting of a to b carbon atoms, for example, methoxycarbonyl group, ethoxycarbonyl Group, n-propyloxycarbonyl group, i-propyloxycarbonyl group, n-butoxycarbonyl group, i-butoxycarbonyl group, tert-butoxycarbonyl group and the like, and specific ranges of the number of carbon atoms are designated. Selected.
本明細書におけるCa〜Cbアルキルアミノカルボニルの表記は、水素原子の一方が炭素原子数がa〜b個よりなる前記の意味であるアルキル基によって置換されたカルバモイル基を表し、例えばメチルカルバモイル基、エチルカルバモイル基、n−プロピルカルバモイル基、i−プロピルカルバモイル基、n−ブチルカルバモイル基、i−ブチルカルバモイル基、s−ブチルカルバモイル基、tert−ブチルカルバモイル基等が具体例として挙げられ、各々の指定の炭素原子数の範囲で選択される。 The notation of C a -C b alkylaminocarbonyl in the present specification represents a carbamoyl group in which one of the hydrogen atoms is substituted with an alkyl group having the above-mentioned meaning consisting of a to b carbon atoms, for example, methylcarbamoyl Group, ethylcarbamoyl group, n-propylcarbamoyl group, i-propylcarbamoyl group, n-butylcarbamoyl group, i-butylcarbamoyl group, s-butylcarbamoyl group, tert-butylcarbamoyl group, etc. Is selected within the range of the specified number of carbon atoms.
本明細書におけるジ(Ca〜Cbアルキル)アミノカルボニルの表記は、水素原子が両方とも、それぞれ同一でも又は互いに相異なっていてもよい炭素原子数がa〜b個よりなる前記の意味であるアルキル基によって置換されたカルバモイル基を表し、例えばN,N−ジメチルカルバモイル基、N−エチル−N−メチルカルバモイル基、N,N−ジエチルカルバモイル基、N,N−ジ(n−プロピル)カルバモイル基、N,N−ジ(n−ブチル)カルバモイル基等が具体例として挙げられ、各々の指定の炭素原子数の範囲で選択される。 In the present specification, the notation of di (C a -C b alkyl) aminocarbonyl means in the above meaning that the number of carbon atoms which may be the same or different from each other is a to b. Represents a carbamoyl group substituted by an alkyl group, such as N, N-dimethylcarbamoyl group, N-ethyl-N-methylcarbamoyl group, N, N-diethylcarbamoyl group, N, N-di (n-propyl) carbamoyl Specific examples include a group, an N, N-di (n-butyl) carbamoyl group, and the like, and each is selected within the range of the designated number of carbon atoms.
本明細書におけるR5によって任意に置換された(Ca〜Cb)アルキル、R5aによって任意に置換された(Ca〜Cb)アルキル、R14によって任意に置換された(Ca〜Cb)アルキル又はR14aによって任意に置換された(Ca〜Cb)アルキル等の表記は、任意のR5、R5a、R14又はR14aによって、炭素原子に結合した水素原子が任意に置換された炭素原子数がa〜b個よりなる前記の意味であるアルキル基を表し、各々の指定の炭素原子数の範囲で選択される。このとき、それぞれの(Ca〜Cb)アルキル基上の置換基R5、R5a、R14又はR14aが2個以上存在するとき、それぞれのR5、R5a、R14又はR14aは互いに同一でも異なってもよい。 Optionally substituted by R 5 in this specification (C a ~C b) alkyl, optionally substituted by R 5a (C a ~C b) alkyl, optionally substituted by R 14 (C a ~ The notation such as C b ) alkyl or (C a -C b ) alkyl optionally substituted by R 14a is any R 5 , R 5a , R 14 or R 14a , and a hydrogen atom bonded to a carbon atom is arbitrary Represents an alkyl group having the above meaning consisting of a to b carbon atoms, and is selected within the range of the respective designated number of carbon atoms. At this time, when two or more substituents R 5 , R 5a , R 14 or R 14a on each (C a -C b ) alkyl group are present, each R 5 , R 5a , R 14 or R 14a is present. May be the same as or different from each other.
本発明化合物は、以下の方法で製造することができる。 The compound of the present invention can be produced by the following method.
製造法A Manufacturing method A
式(20)[式中A1、R2、R4及びn1は前記と同じ意味を表し、A3は酸素原子、硫黄原子、−C(R51a)R51−を表し、R51及びR51aは各々独立して水素原子又はC1〜C6アルキルを表し、nは0〜3の整数を表す。]で表される化合物と、NH2NH2を反応させることにより、式(21)[式中A1、A3、R2、R4、n及びn1は前記と同じ意味を表す。]で表される本発明化合物を合成することができる。 Equation (20) [is wherein A 1, R 2, R 4 and n1 represent the same meanings as defined above, A 3 represents an oxygen atom, a sulfur atom, -C (R 51a) R 51 - represents, R 51 and R 51a represents a hydrogen atom or a C 1 -C 6 alkyl each independently, n is an integer of 0 to 3. A compound represented by, by reacting NH 2 NH 2, formula (21) [wherein A 1, A 3, R 2 , R 4, n and n1 are as defined above. This invention compound represented by this can be synthesize | combined.
本反応では,NH2NH2は、式(20)で表される化合物1当量に対して0.5〜50当量の範囲で用いることができる。 In this reaction, NH 2 NH 2 can be used in a range of 0.5 to 50 equivalents relative to 1 equivalent of the compound represented by Formula (20).
必要ならば塩酸、硫酸、p−トルエンスルホン酸等の酸又は、炭酸カリウム、トリエチルアミン、ピリジン、4−(ジメチルアミノ)ピリジン等の塩基を使用することができる。 If necessary, an acid such as hydrochloric acid, sulfuric acid or p-toluenesulfonic acid, or a base such as potassium carbonate, triethylamine, pyridine or 4- (dimethylamino) pyridine can be used.
本反応は、無溶媒でも実施することができるが、溶媒を用いてもよい。例えば、N,N−ジメチルホルムアミド、N,N−ジメチルアセトアミド、アセトニトリル、ジメチルスルホキシド、1,3−ジメチル−2−イミダゾリノン、水等の極性溶媒、メタノール、エタノール、プロパノール、2−プロパノール、エチレングリコール等のアルコール類、ジエチルエーテル、テトラヒドロフラン、ジフェニルエーテル等のエーテル類、ベンゼン、トルエン、キシレン等の芳香族炭化水素類、塩化メチレン、クロロホルム、四塩化炭素等のハロゲン化炭化水素類、ペンタン、n−ヘキサン等の脂肪族炭化水素類が挙げられる。これらの溶媒は単独で用いても、これらの内の2種類以上を混合して用いてもよい。 This reaction can be carried out without solvent, but a solvent may be used. For example, polar solvent such as N, N-dimethylformamide, N, N-dimethylacetamide, acetonitrile, dimethyl sulfoxide, 1,3-dimethyl-2-imidazolinone, water, methanol, ethanol, propanol, 2-propanol, ethylene glycol Alcohols such as diethyl ether, tetrahydrofuran and diphenyl ether, aromatic hydrocarbons such as benzene, toluene and xylene, halogenated hydrocarbons such as methylene chloride, chloroform and carbon tetrachloride, pentane and n-hexane And aliphatic hydrocarbons. These solvents may be used alone or as a mixture of two or more thereof.
反応温度は、−60℃から反応混合物の還流温度までの任意の温度を設定することができ、反応時間は、反応基質の濃度、反応温度によって変化するが、通常5分から100時間の範囲で任意に設定できる。 The reaction temperature can be set to any temperature from −60 ° C. to the reflux temperature of the reaction mixture, and the reaction time varies depending on the concentration of the reaction substrate and the reaction temperature, but is usually arbitrary in the range of 5 minutes to 100 hours. Can be set.
こうして得られた式(21)で表される化合物と、式(8)[式中X1aは前記と同じ意味を表し、Jaはハロゲン原子、−OH、−OSO2CH3、−OSO2CF3等の脱離基を表す。]で表される化合物を反応させることにより、式(22)[式中A1、A3、R2、R4、X1a、n及びn1は前記と同じ意味を表す。]及び式(23)[式中A1、A3、R2、R4、X1a、n及びn1は前記と同じ意味を表す。]で表される本発明化合物を得ることができる。 The compound represented by formula (21) thus obtained and formula (8) [wherein X 1a represents the same meaning as described above, J a represents a halogen atom, —OH, —OSO 2 CH 3 , —OSO 2 Represents a leaving group such as CF 3 . By reacting the compound represented by formula (22), A 1 , A 3 , R 2 , R 4 , X 1a , n and n1 have the same meaning as described above. ] And formula (23) [wherein A 1 , A 3 , R 2 , R 4 , X 1a , n and n1 represent the same meaning as described above.] This invention compound represented by this can be obtained.
本反応は、無溶媒でも実施することができるが、溶媒を用いてもよい。例えば、N,N−ジメチルホルムアミド、N,N−ジメチルアセトアミド、アセトニトリル、ジメチルスルホキシド、1,3−ジメチル−2−イミダゾリノン、水等の極性溶媒、メタノール、エタノール、プロパノール、2−プロパノール、エチレングリコール等のアルコール類、ジエチルエーテル、テトラヒドロフラン、ジフェニルエーテル等のエーテル類、ベンゼン、トルエン、キシレン等の芳香族炭化水素類、塩化メチレン、クロロホルム、四塩化炭素等のハロゲン化炭化水素類、ペンタン、n−ヘキサン等の脂肪族炭化水素類が挙げられる。これらの溶媒は単独で用いても、これらの内の2種類以上を混合して用いてもよい。 This reaction can be carried out without solvent, but a solvent may be used. For example, polar solvent such as N, N-dimethylformamide, N, N-dimethylacetamide, acetonitrile, dimethyl sulfoxide, 1,3-dimethyl-2-imidazolinone, water, methanol, ethanol, propanol, 2-propanol, ethylene glycol Alcohols such as diethyl ether, tetrahydrofuran and diphenyl ether, aromatic hydrocarbons such as benzene, toluene and xylene, halogenated hydrocarbons such as methylene chloride, chloroform and carbon tetrachloride, pentane and n-hexane And aliphatic hydrocarbons. These solvents may be used alone or as a mixture of two or more thereof.
反応温度は、−60℃から反応混合物の還流温度までの任意の温度を設定することができ、反応時間は、反応基質の濃度、反応温度によって変化するが、通常5分から100時間の範囲で任意に設定できる。 The reaction temperature can be set to any temperature from −60 ° C. to the reflux temperature of the reaction mixture, and the reaction time varies depending on the concentration of the reaction substrate and the reaction temperature, but is usually arbitrary in the range of 5 minutes to 100 hours. Can be set.
また、必要ならば塩酸、硫酸、p−トルエンスルホン酸等の酸、炭酸カリウム、トリエチルアミン、ピリジン、4−(ジメチルアミノ)ピリジン、水素化ナトリウム、水酸化ナトリウム、水酸化カリウム等の塩基を又は、ジエチルアゾジカルボキシレートとトリフェニルホスフィン等を使用する光延反応を使用することができる。 Further, if necessary, a base such as hydrochloric acid, sulfuric acid, p-toluenesulfonic acid, etc., potassium carbonate, triethylamine, pyridine, 4- (dimethylamino) pyridine, sodium hydride, sodium hydroxide, potassium hydroxide, or Mitsunobu reaction using diethyl azodicarboxylate and triphenylphosphine or the like can be used.
また式(20)で表される化合物と、公知の式(6)で表される化合物とを反応させることにより、式(22)及び式(23)で表される本発明化合物を合成することもできる。 Further, the compound of the present invention represented by the formula (22) and the formula (23) is synthesized by reacting the compound represented by the formula (20) with the compound represented by the known formula (6). You can also.
本反応では式(20)で表される化合物1当量に対して、式(6)で表される化合物を、0.5〜50当量の範囲で用いることができる。 In this reaction, the compound represented by formula (6) can be used in the range of 0.5 to 50 equivalents with respect to 1 equivalent of the compound represented by formula (20).
必要ならば塩酸、硫酸、p−トルエンスルホン酸等の酸又は、炭酸カリウム、トリエチルアミン、ピリジン、4−(ジメチルアミノ)ピリジン等の塩基を使用することができる。 If necessary, an acid such as hydrochloric acid, sulfuric acid or p-toluenesulfonic acid, or a base such as potassium carbonate, triethylamine, pyridine or 4- (dimethylamino) pyridine can be used.
本反応は、無溶媒でも実施することができるが、溶媒を用いてもよい。例えば、N,N−ジメチルホルムアミド、N,N−ジメチルアセトアミド、アセトニトリル、ジメチルスルホキシド、1,3−ジメチル−2−イミダゾリノン、水等の極性溶媒、メタノール、エタノール、プロパノール、2−プロパノール、エチレングリコール等のアルコール類、ジエチルエーテル、テトラヒドロフラン、ジフェニルエーテル等のエーテル類、ベンゼン、トルエン、キシレン等の芳香族炭化水素類、塩化メチレン、クロロホルム、四塩化炭素等のハロゲン化炭化水素類、ペンタン、n−ヘキサン等の脂肪族炭化水素類が挙げられる。これらの溶媒は単独で用いても、これらの内の2種類以上を混合して用いてもよい。 This reaction can be carried out without solvent, but a solvent may be used. For example, polar solvent such as N, N-dimethylformamide, N, N-dimethylacetamide, acetonitrile, dimethyl sulfoxide, 1,3-dimethyl-2-imidazolinone, water, methanol, ethanol, propanol, 2-propanol, ethylene glycol Alcohols such as diethyl ether, tetrahydrofuran and diphenyl ether, aromatic hydrocarbons such as benzene, toluene and xylene, halogenated hydrocarbons such as methylene chloride, chloroform and carbon tetrachloride, pentane and n-hexane And aliphatic hydrocarbons. These solvents may be used alone or as a mixture of two or more thereof.
反応温度は、−60℃から反応混合物の還流温度までの任意の温度を設定することができ、反応時間は、反応基質の濃度、反応温度によって変化するが、通常5分から100時間の範囲で任意に設定できる。 The reaction temperature can be set to any temperature from −60 ° C. to the reflux temperature of the reaction mixture, and the reaction time varies depending on the concentration of the reaction substrate and the reaction temperature, but is usually arbitrary in the range of 5 minutes to 100 hours. Can be set.
また式(20)で表される化合物と、公知の式(7)で表される化合物とを反応させることにより、式(24)[式中A1、A3、R2、R4、X1、n及びn1は前記と同じ意味を表す。]で表される本発明化合物を合成することができる。 Further, by reacting the compound represented by the formula (20) with a known compound represented by the formula (7), the compound represented by the formula (24) [wherein A 1 , A 3 , R 2 , R 4 , X 1 , n and n1 represent the same meaning as described above. This invention compound represented by this can be synthesize | combined.
本反応では式(20)で表される化合物1当量に対し、式(7)で表される化合物は、0.5〜50当量の範囲で用いることができる。 In this reaction, the compound represented by the formula (7) can be used in the range of 0.5 to 50 equivalents with respect to 1 equivalent of the compound represented by the formula (20).
必要ならば塩酸、硫酸、p−トルエンスルホン酸等の酸又は、炭酸カリウム、トリエチルアミン、ピリジン、4−(ジメチルアミノ)ピリジン等の塩基を使用することができる。 If necessary, an acid such as hydrochloric acid, sulfuric acid or p-toluenesulfonic acid, or a base such as potassium carbonate, triethylamine, pyridine or 4- (dimethylamino) pyridine can be used.
本反応は、無溶媒でも実施することができる、溶媒を用いてもよい。例えば、N,N−ジメチルホルムアミド、N,N−ジメチルアセトアミド、アセトニトリル、ジメチルスルホキシド、1,3−ジメチル−2−イミダゾリノン、水等の極性溶媒、メタノール、エタノール、プロパノール、2−プロパノール、エチレングリコール等のアルコール類、ジエチルエーテル、テトラヒドロフラン、ジフェニルエーテル等のエーテル類、ベンゼン、トルエン、キシレン等の芳香族炭化水素類、塩化メチレン、クロロホルム、四塩化炭素等のハロゲン化炭化水素類、ペンタン、n−ヘキサン等の脂肪族炭化水素類が挙げられる。これらの溶媒は単独で用いても、これらの内の2種類以上を混合して用いても良い。 This reaction can be carried out without solvent, and a solvent may be used. For example, polar solvent such as N, N-dimethylformamide, N, N-dimethylacetamide, acetonitrile, dimethyl sulfoxide, 1,3-dimethyl-2-imidazolinone, water, methanol, ethanol, propanol, 2-propanol, ethylene glycol Alcohols such as diethyl ether, tetrahydrofuran and diphenyl ether, aromatic hydrocarbons such as benzene, toluene and xylene, halogenated hydrocarbons such as methylene chloride, chloroform and carbon tetrachloride, pentane and n-hexane And aliphatic hydrocarbons. These solvents may be used alone or in combination of two or more of them.
反応温度は、−60℃から反応混合物の還流温度までの任意の温度を設定することができ、反応時間は、反応基質の濃度、反応温度によって変化するが、通常5分から100時間の範囲で任意に設定できる。 The reaction temperature can be set to any temperature from −60 ° C. to the reflux temperature of the reaction mixture, and the reaction time varies depending on the concentration of the reaction substrate and the reaction temperature, but is usually arbitrary in the range of 5 minutes to 100 hours. Can be set.
製造法B Manufacturing method B
式(39)[式中A3、R4、X1a及びnは前記と同じ意味を表す。]で表される化合物と、式(16)[式中A1、R2及びn1は前記と同じ意味を表し、L1はフッ素原子、塩素原子、臭素原子、ヨウ素原子、−B(OH)2基又は−B(OR50)2基(式中R50は、同一又は異なってもよいC1〜C6アルキルを表し、或いは、2つのGが一緒になって−CH2CH2−又は−C(CH3)2C(CH3)2−を形成してもよい)を表す。]で表される化合物を、反応させることにより、式(22)で表される本発明化合物を合成することができる。 Formula (39) [wherein A 3 , R 4 , X 1a and n represent the same meaning as described above. And a compound represented by formula (16) [wherein A 1 , R 2 and n1 represent the same meaning as described above, and L 1 represents a fluorine atom, a chlorine atom, a bromine atom, an iodine atom, —B (OH) 2 groups or —B (OR 50 ) 2 groups (wherein R 50 represents C 1 to C 6 alkyl which may be the same or different, or two G together represent —CH 2 CH 2 — or It represents a may be formed) - -C (CH 3) 2 C (CH 3) 2. The compound of the present invention represented by the formula (22) can be synthesized by reacting the compound represented by the formula:
式(16)で表される化合物の量は、式(39)で表される化合物1当量に対して0.8〜5当量の範囲で、用いることができる。 The amount of the compound represented by formula (16) can be used in the range of 0.8 to 5 equivalents relative to 1 equivalent of the compound represented by formula (39).
ここで用いられる式(16)で表される化合物の或るものは公知化合物であり、一部は市販品として入手できる。また、それ以外のものも文献記載の方法に準じて合成することができる。 Some of the compounds represented by the formula (16) used here are known compounds, and some of them are available as commercial products. Others can be synthesized according to the methods described in the literature.
本反応で使用できる触媒としては、例えば、パラジウム−炭素、塩化パラジウム、酢酸パラジウム、ビス(トリフェニルホスフィン)パラジウムジクロリド、テトラキス(トリフェニルホスフィン)パラジウム等のパラジウム触媒又は金属銅、酢酸銅(1価)、酢酸銅(2価)、酸化銅(1価)、酸化銅(2価)、ヨウ化銅等の銅触媒が挙げられる。触媒の使用量は、式(30)で表される化合物1当量に対して0.001〜1.0当量、好ましくは、0.01〜0.5当量、さらに好ましくは0.05〜0.2当量の範囲で、用いることができる。 Examples of the catalyst that can be used in this reaction include palladium catalysts such as palladium-carbon, palladium chloride, palladium acetate, bis (triphenylphosphine) palladium dichloride, tetrakis (triphenylphosphine) palladium, copper metal, copper acetate (monovalent). ), Copper acetate (divalent), copper oxide (monovalent), copper oxide (divalent), copper iodide and the like. The usage-amount of a catalyst is 0.001-1.0 equivalent with respect to 1 equivalent of compounds represented by Formula (30), Preferably, it is 0.01-0.5 equivalent, More preferably, it is 0.05-0. It can be used in the range of 2 equivalents.
使用する塩基としては、例えば、ピリジン、ジイソプロピルエチルアミン、トリエチルアミン等の三級アミン化合物、例えば水酸化ナトリウム、水酸化カリウム、炭酸ナトリウム、炭酸カリウム、炭酸セシウム、炭酸水素ナトリウム等の無機塩基等が挙げられる。塩基の使用量は、式(39)で表される化合物1当量に対して0.1〜10.0当量の範囲で用いることができる。 Examples of the base used include tertiary amine compounds such as pyridine, diisopropylethylamine, and triethylamine, and inorganic bases such as sodium hydroxide, potassium hydroxide, sodium carbonate, potassium carbonate, cesium carbonate, and sodium bicarbonate. . The usage-amount of a base can be used in 0.1-10.0 equivalent with respect to 1 equivalent of compounds represented by Formula (39).
本反応は、無溶媒も実施することができるが、溶媒を用いてもよい。例えば、N,N−ジメチルホルムアミド、N,N−ジメチルアセトアミド、アセトニトリル、ジメチルスルホキシド、1,3−ジメチル−2−イミダゾリノン、水等の極性溶媒、メタノール、エタノール、プロパノール、2−プロパノール、エチレングリコール等のアルコール類、ジエチルエーテル、テトラヒドロフラン、ジフェニルエーテル等のエーテル類、ベンゼン、トルエン、キシレン等の芳香族炭化水素類、塩化メチレン、クロロホルム、四塩化炭素等のハロゲン化炭化水素類、ペンタン、n−ヘキサン等の脂肪族炭化水素類が挙げられる。これらの溶媒は単独で用いても、これらの内の2種類以上を混合して用いてもよい。 This reaction can be carried out without a solvent, but a solvent may be used. For example, polar solvent such as N, N-dimethylformamide, N, N-dimethylacetamide, acetonitrile, dimethyl sulfoxide, 1,3-dimethyl-2-imidazolinone, water, methanol, ethanol, propanol, 2-propanol, ethylene glycol Alcohols such as diethyl ether, tetrahydrofuran and diphenyl ether, aromatic hydrocarbons such as benzene, toluene and xylene, halogenated hydrocarbons such as methylene chloride, chloroform and carbon tetrachloride, pentane and n-hexane And aliphatic hydrocarbons. These solvents may be used alone or as a mixture of two or more thereof.
反応温度は、−60℃から反応混合物の還流温度までの任意の温度を設定することができ、反応時間は、反応基質の濃度、反応温度によって変化するが、通常5分から100時間の範囲で任意に設定できる。 The reaction temperature can be set to any temperature from −60 ° C. to the reflux temperature of the reaction mixture, and the reaction time varies depending on the concentration of the reaction substrate and the reaction temperature, but is usually arbitrary in the range of 5 minutes to 100 hours. Can be set.
製造法C Manufacturing method C
式(41)[式中A3、R4、X1及びnは前記と同じ意味を表す。]で表される化合物と、式(16)で表される化合物とを、製造法Bと同様の方法で反応させることにより、式(24)で表される本発明化合物を合成することができる。 Formula (41) [wherein A 3 , R 4 , X 1 and n represent the same meaning as described above. The compound of the present invention represented by formula (24) can be synthesized by reacting the compound represented by formula (16) with the compound represented by formula (16) in the same manner as in Production Method B. .
製造法D Manufacturing method D
式(42)[式中A1、A3、R2、R4、n及びn1は前記と同じ意味を表し、Jbはハロゲン原子を表す。]で表される化合物と、式(43)[式中X1は前記と同じ意味を表す。]で表される化合物を反応させることにより、式(44)[式中A1、A3、R2、R4、X1、n及びn1は前記と同じ意味を表す。]で表される本発明化合物を合成することができる。 Equation (42) [wherein A 1, A 3, R 2 , R 4, n , and n1 are as defined above, J b represents a halogen atom. And a compound represented by formula (43), wherein X 1 represents the same meaning as described above. By reacting the compound represented by formula (44), wherein A 1 , A 3 , R 2 , R 4 , X 1 , n and n1 have the same meaning as described above. This invention compound represented by this can be synthesize | combined.
本反応では式(42)で表される化合物1当量に対して、式(43)で表される化合物を、0.8〜5当量の範囲で、用いることができる。 In this reaction, the compound represented by the formula (43) can be used in the range of 0.8 to 5 equivalents with respect to 1 equivalent of the compound represented by the formula (42).
必要ならば塩酸、硫酸、p−トルエンスルホン酸等の酸又は、炭酸カリウム、トリエチルアミン、ピリジン、4−(ジメチルアミノ)ピリジン等の塩基を使用することができる。 If necessary, an acid such as hydrochloric acid, sulfuric acid or p-toluenesulfonic acid, or a base such as potassium carbonate, triethylamine, pyridine or 4- (dimethylamino) pyridine can be used.
本反応は、無溶媒でも実施することができるが、溶媒を用いてもよい。例えば、N,N−ジメチルホルムアミド、N,N−ジメチルアセトアミド、アセトニトリル、ジメチルスルホキシド、1,3−ジメチル−2−イミダゾリノン、水等の極性溶媒、メタノール、エタノール、プロパノール、2−プロパノール、エチレングリコール等のアルコール類、ジエチルエーテル、テトラヒドロフラン、ジフェニルエーテル等のエーテル類、ベンゼン、トルエン、キシレン等の芳香族炭化水素類、塩化メチレン、クロロホルム、四塩化炭素等のハロゲン化炭化水素類、ペンタン、n−ヘキサン等の脂肪族炭化水素類が挙げられる。これらの溶媒は単独で用いても、これらの内の2種類以上を混合して用いてもよい。 This reaction can be carried out without solvent, but a solvent may be used. For example, polar solvent such as N, N-dimethylformamide, N, N-dimethylacetamide, acetonitrile, dimethyl sulfoxide, 1,3-dimethyl-2-imidazolinone, water, methanol, ethanol, propanol, 2-propanol, ethylene glycol Alcohols such as diethyl ether, tetrahydrofuran and diphenyl ether, aromatic hydrocarbons such as benzene, toluene and xylene, halogenated hydrocarbons such as methylene chloride, chloroform and carbon tetrachloride, pentane and n-hexane And aliphatic hydrocarbons. These solvents may be used alone or as a mixture of two or more thereof.
反応温度は、−60℃から反応混合物の還流温度までの任意の温度を設定することができ、反応時間は、反応基質の濃度、反応温度によって変化するが、通常5分から100時間の範囲で任意に設定できる。 The reaction temperature can be set to any temperature from −60 ° C. to the reflux temperature of the reaction mixture, and the reaction time varies depending on the concentration of the reaction substrate and the reaction temperature, but is usually arbitrary in the range of 5 minutes to 100 hours. Can be set.
ここで用いられる式(43)で表される化合物の或るものは公知化合物であり、一部は市販品として入手できる。また、それ以外のものも文献記載の方法に準じて合成することができる。 Some of the compounds represented by formula (43) used here are known compounds, and some of them are available as commercial products. Others can be synthesized according to the methods described in the literature.
製造法E Manufacturing method E
式(20)で表される化合物と、式(45)[式中X1は前記と同じ意味を表す。]で表される化合物及び酢酸アンモニウムを反応させることにより、式(46)[式中A1、A3、R2、R4、n及びn1は前記と同じ意味を表し、X1−1及びX1−2は、各々独立してX1を表し、X1は前記と同じ意味を表す。]で表される本発明化合物を合成することができる。 The compound represented by formula (20) and formula (45) [wherein X 1 represents the same meaning as described above. The compound represented by formula (46) [wherein A 1 , A 3 , R 2 , R 4 , n and n1 represent the same meaning as described above, and X 1-1 and X 1-2 represents X 1 each independently, X 1 are as defined above. This invention compound represented by this can be synthesize | combined.
本反応では式(20)で表される化合物1当量に対して、式(45)で表される化合物を、0.8〜5当量の範囲で、用いることができる。また、酢酸アンモニウムは式(20)で表される化合物1当量に対して、0.5〜50当量の範囲で用いることができる。 In this reaction, the compound represented by the formula (45) can be used in the range of 0.8 to 5 equivalents with respect to 1 equivalent of the compound represented by the formula (20). Moreover, ammonium acetate can be used in 0.5-50 equivalent with respect to 1 equivalent of compounds represented by Formula (20).
必要ならば塩酸、硫酸、p−トルエンスルホン酸等の酸又は、炭酸カリウム、トリエチルアミン、ピリジン、4−(ジメチルアミノ)ピリジン等の塩基を使用することができる。 If necessary, an acid such as hydrochloric acid, sulfuric acid or p-toluenesulfonic acid, or a base such as potassium carbonate, triethylamine, pyridine or 4- (dimethylamino) pyridine can be used.
本反応は、無溶媒でも実施することができるが、溶媒を用いてもよい。例えば、N,N−ジメチルホルムアミド、N,N−ジメチルアセトアミド、アセトニトリル、ジメチルスルホキシド、1,3−ジメチル−2−イミダゾリノン、水等の極性溶媒、メタノール、エタノール、プロパノール、2−プロパノール、エチレングリコール等のアルコール類、ジエチルエーテル、テトラヒドロフラン、ジフェニルエーテル等のエーテル類、ベンゼン、トルエン、キシレン等の芳香族炭化水素類、塩化メチレン、クロロホルム、四塩化炭素等のハロゲン化炭化水素類、ペンタン、n−ヘキサン等の脂肪族炭化水素類が挙げられる。これらの溶媒は単独で用いても、これらの内の2種類以上を混合して用いてもよい。 This reaction can be carried out without solvent, but a solvent may be used. For example, polar solvent such as N, N-dimethylformamide, N, N-dimethylacetamide, acetonitrile, dimethyl sulfoxide, 1,3-dimethyl-2-imidazolinone, water, methanol, ethanol, propanol, 2-propanol, ethylene glycol Alcohols such as diethyl ether, tetrahydrofuran and diphenyl ether, aromatic hydrocarbons such as benzene, toluene and xylene, halogenated hydrocarbons such as methylene chloride, chloroform and carbon tetrachloride, pentane and n-hexane And aliphatic hydrocarbons. These solvents may be used alone or as a mixture of two or more thereof.
反応温度は、−60℃から反応混合物の還流温度までの任意の温度を設定することができ、反応時間は、反応基質の濃度、反応温度によって変化するが、通常5分から100時間の範囲で任意に設定できる。 The reaction temperature can be set to any temperature from −60 ° C. to the reflux temperature of the reaction mixture, and the reaction time varies depending on the concentration of the reaction substrate and the reaction temperature, but is usually arbitrary in the range of 5 minutes to 100 hours. Can be set.
ここで用いられる式(45)で表される化合物の或るものは公知化合物であり、一部は市販品として入手できる。また、それ以外のものも文献記載の方法に準じて合成することができる。 Some of the compounds represented by the formula (45) used here are known compounds, and some of them are available as commercial products. Others can be synthesized according to the methods described in the literature.
製造法F Manufacturing method F
式(47)[式中A1、A3、R2、R4、X1、n及びn1は前記と同じ意味を表す。]で表される化合物と、NH2NH2を、製造法Aと同様の方法を用いて反応させることにより、式(48)[式中A1、A3、R2、R4、X1、n及びn1は前記と同じ意味を表す。]で表される本発明化合物を合成することができる。 Formula (47) [wherein A 1 , A 3 , R 2 , R 4 , X 1 , n and n1 represent the same meaning as described above. The compound represented by formula (48) [wherein A 1 , A 3 , R 2 , R 4 , X 1 is reacted with NH 2 NH 2 using a method similar to Production Method A]. , N and n1 represent the same meaning as described above. This invention compound represented by this can be synthesize | combined.
更に、式(48)で表される化合物と、式(8)で表される化合物を製造法Aと同様の方法を用いて反応させることにより、式(49)[式中A1、A3、R2、R4、X1、n及びn1は前記と同じ意味を表す。]で表される本発明化合物及び式(52)[式中A1、A3、R2、R4、X1、n及びn1は前記と同じ意味を表す。]で表される本発明化合物を合成することができる。 Furthermore, by reacting the compound represented by the formula (48) and the compound represented by the formula (8) by the same method as in the production method A, the compound represented by the formula (49) [in the formula, A 1 , A 3 , R 2 , R 4 , X 1 , n and n1 represent the same meaning as described above. The compound of the present invention represented by the formula (52): wherein A 1 , A 3 , R 2 , R 4 , X 1 , n and n1 have the same meaning as described above. This invention compound represented by this can be synthesize | combined.
製造法A乃至製造法Fの反応は必要であれば窒素、アルゴン等の不活性ガス雰囲気下で実施しても良い。 The reaction of production method A to production method F may be carried out in an inert gas atmosphere such as nitrogen or argon if necessary.
製造法A乃至製造法Fの反応において、反応終了後の反応混合物は、直接濃縮、又は有機溶媒に溶解し、水洗後濃縮、又は氷水に投入、有機溶媒抽出後濃縮といった通常の後処理を行ない、目的の本発明化合物を得ることができる。また、精製の必要が生じたときには、再結晶、カラムクロマトグラフ、薄層クロマトグラフ、液体クロマトグラフ分取等の任意の精製方法によって分離、精製することができる。 In the reaction of production method A to production method F, the reaction mixture after completion of the reaction is directly concentrated or dissolved in an organic solvent, concentrated after washing with water, or poured into ice water and concentrated after extraction with an organic solvent, followed by normal post-treatment. The objective compound of the present invention can be obtained. Moreover, when the necessity for purification arises, it can be separated and purified by any purification method such as recrystallization, column chromatograph, thin layer chromatograph, liquid chromatographic fractionation and the like.
製造法Aで用いられる式(20)で表される化合物は、例えば以下のようにして合成することが出来る。 The compound represented by the formula (20) used in the production method A can be synthesized, for example, as follows.
反応式1 Reaction formula 1
式(18)[式中A3及びR4は前記と同じ意味を表し、nは0〜3の整数を表す。]で表される化合物は、テトラへドロン 2006年,62巻,11704頁等の公知の方法により合成することができる。 Equation (18) [wherein A 3 and R 4 are as defined above, n represents an integer of 0 to 3. ] Can be synthesized by known methods such as tetrahedron 2006, 62, 11704.
すなわち、式(18)で表される化合物を、上記製造法Bと同様に公知の式(16)で表される化合物と、パラジウムなどの遷移金属触媒及び塩基の存在下で反応させることにより、式(19)[式中A1、A3、R2、R4、n及びn1は前記と同じ意味を表す。]の化合物を容易に製造することができる。 That is, by reacting the compound represented by the formula (18) with a known compound represented by the formula (16) in the same manner as the production method B in the presence of a transition metal catalyst such as palladium and a base, equation (19) [wherein a 1, a 3, R 2 , R 4, n and n1 are as defined above. ] Can be easily produced.
さらに式(19)で表される化合物を、文献既知の公知の方法に準じてN、N−ジメチルホルムアミドジメチルアセタール(DMFDMA)と反応させることにより、式(20)[式中A1、A3、R2、R4、n及びn1は前記と同じ意味を表す。]で表される化合物を容易に製造することができる。 Further, the compound represented by the formula (19) is reacted with N, N-dimethylformamide dimethyl acetal (DMFDMA) according to a known method known in the literature, whereby the compound represented by the formula (20) [wherein A 1 , A 3 , R 2 , R 4 , n and n1 have the same meaning as described above. ] Can be easily produced.
また、式(19)で表される化合物は以下の方法でも合成することが出来る。
すなわち、ジャーナル オブ メディシナル ケミストリー 2002年,45巻,5397頁等の公知の方法により合成することができる式(53)[式中A1、R2及びn1は前記と同じ意味を表す。]で表される化合物と式(54)で表される化合物を、シンセシス 2009年,721頁等の公知の方法により、式(55)[式中A1、A3、R2、n及びn1は前記と同じ意味を表す。]で表される化合物を合成することができる。
Moreover, the compound represented by Formula (19) is compoundable also with the following method.
That is, formula (53) which can be synthesized by a known method such as Journal of Medicinal Chemistry 2002, 45, 5397, wherein A 1 , R 2 and n1 have the same meaning as described above. The compound represented by formula (54) and the compound represented by formula (54) are synthesized by a known method such as synthesis 2009, page 721, etc. [wherein A 1 , A 3 , R 2 , n and n1 Represents the same meaning as described above. ] Can be synthesized.
引き続き式(55)で表される化合物を、式(56)[式中R4は前記と同じ意味を表し、R50はC1〜C6アルキル基を表す。]で表される化合物又は式(57)[式中R4は前記と同じ意味を表し、R50はC1〜C6アルキル基を表す。]で表される化合物と反応させて、式(19)で表される化合物を合成することが出来る。 Subsequently, the compound represented by formula (55) is represented by formula (56), wherein R 4 represents the same meaning as described above, and R 50 represents a C 1 to C 6 alkyl group. Or a compound represented by formula (57): wherein R 4 represents the same meaning as described above, and R 50 represents a C 1 to C 6 alkyl group. And a compound represented by the formula (19) can be synthesized.
本反応では式(55)で表される化合物1当量に対して、式(56)で表される化合物又は式(57)で表される化合物を、0.5当量〜溶媒量の範囲で、用いることができる。 In this reaction, with respect to 1 equivalent of the compound represented by Formula (55), the compound represented by Formula (56) or the compound represented by Formula (57) is in the range of 0.5 equivalent to the amount of solvent. Can be used.
必要ならば塩酸、硫酸、p−トルエンスルホン酸等の酸又は、炭酸カリウム、トリエチルアミン、ピリジン、4−(ジメチルアミノ)ピリジン等の塩基を使用することができる。 If necessary, an acid such as hydrochloric acid, sulfuric acid or p-toluenesulfonic acid, or a base such as potassium carbonate, triethylamine, pyridine or 4- (dimethylamino) pyridine can be used.
本反応は、無溶媒でも実施することができるが、溶媒を用いてもよい。例えば、N,N−ジメチルホルムアミド、N,N−ジメチルアセトアミド、アセトニトリル、ジメチルスルホキシド、1,3−ジメチル−2−イミダゾリノン、水等の極性溶媒、メタノール、エタノール、プロパノール、2−プロパノール、エチレングリコール等のアルコール類、ジエチルエーテル、テトラヒドロフラン、ジフェニルエーテル等のエーテル類、ベンゼン、トルエン、キシレン等の芳香族炭化水素類、塩化メチレン、クロロホルム、四塩化炭素等のハロゲン化炭化水素類、ペンタン、n−ヘキサン等の脂肪族炭化水素類が挙げられる。これらの溶媒は単独で用いても、これらの内の2種類以上を混合して用いてもよい。 This reaction can be carried out without solvent, but a solvent may be used. For example, polar solvent such as N, N-dimethylformamide, N, N-dimethylacetamide, acetonitrile, dimethyl sulfoxide, 1,3-dimethyl-2-imidazolinone, water, methanol, ethanol, propanol, 2-propanol, ethylene glycol Alcohols such as diethyl ether, tetrahydrofuran and diphenyl ether, aromatic hydrocarbons such as benzene, toluene and xylene, halogenated hydrocarbons such as methylene chloride, chloroform and carbon tetrachloride, pentane and n-hexane And aliphatic hydrocarbons. These solvents may be used alone or as a mixture of two or more thereof.
反応温度は、−60℃から反応混合物の還流温度までの任意の温度を設定することができ、反応時間は、反応基質の濃度、反応温度によって変化するが、通常5分から100時間の範囲で任意に設定できる。 The reaction temperature can be set to any temperature from −60 ° C. to the reflux temperature of the reaction mixture, and the reaction time varies depending on the concentration of the reaction substrate and the reaction temperature, but is usually arbitrary in the range of 5 minutes to 100 hours. Can be set.
ここで用いられる式(56)で表される化合物又は式(57)で表される化合物の或るものは公知化合物であり、一部は市販品として入手できる。また、それ以外のものも文献記載の方法に準じて合成することができる。 Some of the compounds represented by formula (56) or the compounds represented by formula (57) used here are known compounds, and some of them are commercially available. Others can be synthesized according to the methods described in the literature.
製造法Bで用いられる式(39)で表される化合物は、例えば以下のようにして合成することが出来る。
The compound represented by the formula (39) used in the production method B can be synthesized, for example, as follows.
反応式2 Reaction formula 2
すなわち、式(18)で表される化合物と、エチルビニルエーテルを、文献既知の公知の方法、例えばヘテロサイクルス 2003年,60巻,879頁等に記載の方法に準じて反応させることにより、式(35)[式中A3、R4及びnは前記と同じ意味を表し、EEは−CH(CH3)OCH2CH3を表す。]で表される化合物を合成することができる。 That is, by reacting the compound represented by the formula (18) with ethyl vinyl ether according to a known method known in the literature, for example, the method described in Heterocycles 2003, Vol. (35) [wherein A 3 , R 4 and n represent the same meaning as described above, and EE represents —CH (CH 3 ) OCH 2 CH 3 . ] Can be synthesized.
次いで、式(35)で表される化合物を、文献既知の公知の方法に準じてN、N−ジメチルホルムアミドジメチルアセタール(DMFDMA)と反応させることにより、式(36)[式中A3、R4、n及びEEは前記と同じ意味を表す。]で表される化合物を容易に製造することができる。 Next, the compound represented by the formula (35) is reacted with N, N-dimethylformamide dimethyl acetal (DMFDMA) in accordance with a known method known in the literature to obtain a compound represented by the formula (36) [wherein A 3 , R 4 , n and EE represent the same meaning as described above. ] Can be easily produced.
引き続き、式(36)で表される化合物から上記製造法Aと同様の方法を用いて、式(37)[式中A3、R4、n及びEEは前記と同じ意味を表す。]で表される化合物及び式(38)[式中A3、R4、X1a、n及びEEは前記と同じ意味を表す。]で表される化合物を合成することができる。 Subsequently, from the compound represented by formula (36), using the same method as the above production method A, formula (37) [wherein A 3 , R 4 , n and EE represent the same meaning as described above. And a compound represented by formula (38): wherein A 3 , R 4 , X 1a , n and EE have the same meaning as described above. ] Can be synthesized.
さらに、式(38)で表される化合物から文献既知の公知の方法、例えばバイオオーガニック アンド メディシナル ケミストリー レター 2009年,19巻,3247頁等に記載の方法に準じて、酸と反応させることにより、式(39)[式中A3、R4、X1a及びnは前記と同じ意味を表す。]で表される化合物を合成することができる。 Furthermore, by reacting with an acid according to a known method known from the literature from a compound represented by formula (38), for example, the method described in Bioorganic and Medicinal Chemistry Letter 2009, Vol. 19, p. Formula (39) [wherein A 3 , R 4 , X 1a and n represent the same meaning as described above. ] Can be synthesized.
製造法Cで用いられる式(41)で表される化合物は、例えば以下のようにして合成することが出来る。 The compound represented by the formula (41) used in the production method C can be synthesized, for example, as follows.
反応式3 Reaction formula 3
すなわち、式(36)と式(7)で表される化合物を、上記製造法Aと同様の方法を用いて反応させることにより、式(40)[式中A3、R4、X1、n及びEEは前記と同じ意味を表す。]で表される化合物を合成することができる。 That is, by reacting the compounds represented by formula (36) and formula (7) using the same method as in the above production method A, formula (40) [wherein A 3 , R 4 , X 1 , n and EE represent the same meaning as described above. ] Can be synthesized.
次いで、式(40)で表される化合物を、上記反応式2と同様の方法を用いて反応させることにより、式(41)[式中A3、R4、X1及びnは前記と同じ意味を表す。]で表される化合物を合成することができる。 Next, the compound represented by the formula (40) is reacted using the same method as in the above reaction formula 2, whereby the formula (41) [wherein A 3 , R 4 , X 1 and n are the same as above. Represents meaning. ] Can be synthesized.
製造法Dで用いられる式(42)で表される化合物は、例えば以下のようにして合成することが出来る。 The compound represented by the formula (42) used in the production method D can be synthesized, for example, as follows.
反応式4 Reaction formula 4
すなわち、式(19)で表される化合物と、公知のハロゲン化剤を、文献既知の公知の方法、例えばジャーナル オブ オーガニック ケミストリー 1979年,44巻,2345頁等に記載の方法に準じて反応させることにより、式(42)で表される化合物を合成することができる。 That is, the compound represented by the formula (19) and a known halogenating agent are reacted according to a known method known in the literature, for example, the method described in Journal of Organic Chemistry 1979, 44, 2345. Thus, the compound represented by the formula (42) can be synthesized.
製造法Fで用いられる式(47)で表される化合物は、例えば以下のようにして合成することが出来る。 The compound represented by Formula (47) used in Production Method F can be synthesized, for example, as follows.
反応式5 Reaction formula 5
式(19)で表される化合物と、式(59)[式中X1は前記と同じ意味を表し、Jb2はハロゲン原子、−OH、−OSO2CH3、−OSO2CF3、ピラゾール−1−イル等の脱離基を表す。]で表される化合物を反応させることにより、式(47)で表される化合物を合成することができる。 A compound represented by formula (19) and formula (59) [wherein X 1 represents the same meaning as described above, J b2 represents a halogen atom, —OH, —OSO 2 CH 3 , —OSO 2 CF 3 , pyrazole; Represents a leaving group such as -1-yl. The compound represented by the formula (47) can be synthesized by reacting the compound represented by the formula:
本反応では式(19)で表される化合物1当量に対して、式(59)で表される化合物を、0.8〜5当量の範囲で、用いることができる。 In this reaction, the compound represented by the formula (59) can be used in the range of 0.8 to 5 equivalents with respect to 1 equivalent of the compound represented by the formula (19).
必要ならば水素化ナトリウム、n−ブチルリチウム、リチウムビス(トリメチルシリル)アミド、炭酸カリウム、トリエチルアミン、ピリジン、4−(ジメチルアミノ)ピリジン等の塩基を使用することができる。 If necessary, a base such as sodium hydride, n-butyllithium, lithium bis (trimethylsilyl) amide, potassium carbonate, triethylamine, pyridine, 4- (dimethylamino) pyridine and the like can be used.
本反応は、無溶媒でも実施することができるが、溶媒を用いてもよい。例えば、N,N−ジメチルホルムアミド、N,N−ジメチルアセトアミド、アセトニトリル、ジメチルスルホキシド、1,3−ジメチル−2−イミダゾリノン、水等の極性溶媒、メタノール、エタノール、プロパノール、2−プロパノール、エチレングリコール等のアルコール類、ジエチルエーテル、テトラヒドロフラン、ジフェニルエーテル等のエーテル類、ベンゼン、トルエン、キシレン等の芳香族炭化水素類、塩化メチレン、クロロホルム、四塩化炭素等のハロゲン化炭化水素類、ペンタン、n−ヘキサン等の脂肪族炭化水素類が挙げられる。これらの溶媒は単独で用いても、これらの内の2種類以上を混合して用いてもよい。 This reaction can be carried out without solvent, but a solvent may be used. For example, polar solvent such as N, N-dimethylformamide, N, N-dimethylacetamide, acetonitrile, dimethyl sulfoxide, 1,3-dimethyl-2-imidazolinone, water, methanol, ethanol, propanol, 2-propanol, ethylene glycol Alcohols such as diethyl ether, tetrahydrofuran and diphenyl ether, aromatic hydrocarbons such as benzene, toluene and xylene, halogenated hydrocarbons such as methylene chloride, chloroform and carbon tetrachloride, pentane and n-hexane And aliphatic hydrocarbons. These solvents may be used alone or as a mixture of two or more thereof.
反応温度は、−60℃から反応混合物の還流温度までの任意の温度を設定することができ、反応時間は、反応基質の濃度、反応温度によって変化するが、通常5分から100時間の範囲で任意に設定できる。 The reaction temperature can be set to any temperature from −60 ° C. to the reflux temperature of the reaction mixture, and the reaction time varies depending on the concentration of the reaction substrate and the reaction temperature, but is usually arbitrary in the range of 5 minutes to 100 hours. Can be set.
ここで用いられる式(59)で表される化合物の或るものは公知化合物であり、一部は市販品として入手できる。また、それ以外のものも文献記載の方法に準じて容易に合成することができる。 Some of the compounds represented by the formula (59) used here are known compounds, and some of them are commercially available. Others can be easily synthesized according to the methods described in the literature.
本発明に包含される活性化合物としては、具体的に例えば第1表乃至第3表に示す化合物が挙げられる。但し、第1表乃至第3表の化合物は例示のためのものであって、本発明はこれらのみに限定されるものではない。尚、表中、Meと記載される置換基はメチル基を表し、以下、Etとの記載はエチル基を表し、n−Pr及びPr−nはノルマルプロピル基を、i−Pr及びPr−iはイソプロピル基を、c−Pr及びPr−cはシクロプロピル基を、n−Bu及びBu−nはノルマルブチル基を、s−Bu及びBu−sはセカンダリーブチル基を、i−Bu及びBu−iはイソブチル基を、t−Bu及びBu−tはターシャリーブチル基を、c−Bu及びBu−cはシクロブチル基を、n−Pen及びPen−nはノルマルペンチル基を、c−Pen及びPen−cはシクロペンチル基を、n−Hex及びHex−nはノルマルヘキシル基を、c−Hex及びHex−cはシクロヘキシル基を、Heptはヘプチル基を、Octはオクチル基を、Phはフェニル基をそれぞれ表す。 Specific examples of the active compound included in the present invention include compounds shown in Tables 1 to 3. However, the compounds in Tables 1 to 3 are for illustrative purposes, and the present invention is not limited to these. In the table, the substituent described as Me represents a methyl group, hereinafter, Et represents an ethyl group, n-Pr and Pr-n represent normal propyl groups, i-Pr and Pr-i. Is an isopropyl group, c-Pr and Pr-c are cyclopropyl groups, n-Bu and Bu-n are normal butyl groups, s-Bu and Bu-s are secondary butyl groups, i-Bu and Bu- i is an isobutyl group, t-Bu and Bu-t are tertiary butyl groups, c-Bu and Bu-c are cyclobutyl groups, n-Pen and Pen-n are normal pentyl groups, c-Pen and Pen -C represents a cyclopentyl group, n-Hex and Hex-n represent a normal hexyl group, c-Hex and Hex-c represent a cyclohexyl group, Hept represents a heptyl group, Oct represents an octyl group, and Ph represents a hexyl group. It represents a sulfonyl group, respectively.
表中、D2−32a、D2−33a、D2−34a、D2−36a、D2−37a、D2−38a及びD2−92aで表される構造は下記の構造を表す。 In the table, the structures represented by D2-32a, D2-33a, D2-34a, D2-36a, D2-37a, D2-38a, and D2-92a represent the following structures.
〔第1表〕 [Table 1]
――――――――――――――――――
X1a X1
――――――――――――――――――
H CH2SMe
H CH2SEt
H CH2SCF3
H CH2SCH2CF3
H CH2S(O)Me
H CH2S(O)Et
H CH2S(O)CF3
H CH2S(O)CH2CF3
H CH2S(O)2Me
H CH2S(O)2Et
H CH2S(O)2CF3
H CH2S(O)2CH2CF3
H CH(Me)SMe
H CH(Me)SEt
H CH(Me)SCF3
H CH(Me)SCH2CF3
H CH(Me)S(O)Me
H CH(Me)S(O)Et
H CH(Me)S(O)CF3
H CH(Me)S(O)CH2CF3
H CH(Me)S(O)2Me
H CH(Me)S(O)2Et
H CH(Me)S(O)2CF3
H CH(Me)S(O)2CH2CF3
H CH(Et)SMe
H CH(Et)SEt
H CH(Et)SCF3
H CH(Et)SCH2CF3
H CH(Et)S(O)Me
H CH(Et)S(O)Et
H CH(Et)S(O)CF3
H CH(Et)S(O)CH2CF3
H CH(Et)S(O)2Me
H CH(Et)S(O)2Et
H CH(Et)S(O)2CF3
H CH(Et)S(O)2CH2CF3
H CH(n-Pr)SMe
H CH(n-Pr)SEt
H CH(n-Pr)SCF3
H CH(n-Pr)SCH2CF3
H CH(n-Pr)S(O)Me
H CH(n-Pr)S(O)Et
H CH(n-Pr)S(O)CF3
H CH(n-Pr)S(O)CH2CF3
H CH(n-Pr)S(O)2Me
H CH(n-Pr)S(O)2Et
H CH(n-Pr)S(O)2CF3
H CH(n-Pr)S(O)2CH2CF3
H CH(i-Pr)SMe
H CH(i-Pr)SEt
H CH(i-Pr)SCF3
H CH(i-Pr)SCH2CF3
H CH(i-Pr)S(O)Me
H CH(i-Pr)S(O)Et
H CH(i-Pr)S(O)CF3
H CH(i-Pr)S(O)CH2CF3
H CH(i-Pr)S(O)2Me
H CH(i-Pr)S(O)2Et
H CH(i-Pr)S(O)2CF3
H CH(i-Pr)S(O)2CH2CF3
H CH(n-Bu)SMe
H CH(n-Bu)SEt
H CH(n-Bu)SCF3
H CH(n-Bu)SCH2CF3
H CH(n-Bu)S(O)Me
H CH(n-Bu)S(O)Et
H CH(n-Bu)S(O)CF3
H CH(n-Bu)S(O)CH2CF3
H CH(n-Bu)S(O)2Me
H CH(n-Bu)S(O)2Et
H CH(n-Bu)S(O)2CF3
H CH(n-Bu)S(O)2CH2CF3
H CH(i-Bu)SMe
H CH(i-Bu)SEt
H CH(i-Bu)SCF3
H CH(i-Bu)SCH2CF3
H CH(i-Bu)S(O)Me
H CH(i-Bu)S(O)Et
H CH(i-Bu)S(O)CF3
H CH(i-Bu)S(O)CH2CF3
H CH(i-Bu)S(O)2Me
H CH(i-Bu)S(O)2Et
H CH(i-Bu)S(O)2CF3
H CH(i-Bu)S(O)2CH2CF3
H CH(s-Bu)SMe
H CH(s-Bu)SEt
H CH(s-Bu)SCF3
H CH(s-Bu)SCH2CF3
H CH(s-Bu)S(O)Me
H CH(s-Bu)S(O)Et
H CH(s-Bu)S(O)CF3
H CH(s-Bu)S(O)CH2CF3
H CH(s-Bu)S(O)2Me
H CH(s-Bu)S(O)2Et
H CH(s-Bu)S(O)2CF3
H CH(s-Bu)S(O)2CH2CF3
H CH(t-Bu)SMe
H CH(t-Bu)SEt
H CH(t-Bu)SCF3
H CH(t-Bu)SCH2CF3
H CH(t-Bu)S(O)Me
H CH(t-Bu)S(O)Et
H CH(t-Bu)S(O)CF3
H CH(t-Bu)S(O)CH2CF3
H CH(t-Bu)S(O)2Me
H CH(t-Bu)S(O)2Et
H CH(t-Bu)S(O)2CF3
H CH(t-Bu)S(O)2CH2CF3
H CH(CF3)SMe
H CH(CF3)SEt
H CH(CF3)SCF3
H CH(CF3)SCH2CF3
H CH(CF3)S(O)Me
H CH(CF3)S(O)Et
H CH(CF3)S(O)CF3
H CH(CF3)S(O)CH2CF3
H CH(CF3)S(O)2Me
H CH(CF3)S(O)2Et
H CH(CF3)S(O)2CF3
H CH(CF3)S(O)2CH2CF3
H CH2CH2SMe
H CH2CH2SEt
H CH2CH2SCF3
H CH2CH2SCH2CF3
H CH2CH2S(O)Me
H CH2CH2S(O)Et
H CH2CH2S(O)CF3
H CH2CH2S(O)CH2CF3
H CH2CH2S(O)2Me
H CH2CH2S(O)2Et
H CH2CH2S(O)2CF3
H CH2CH2S(O)2CH2CF3
H CH(Me)CH2SMe
H CH(Me)CH2SEt
H CH(Me)CH2SCF3
H CH(Me)CH2SCH2CF3
H CH(Me)CH2S(O)Me
H CH(Me)CH2S(O)Et
H CH(Me)CH2S(O)CF3
H CH(Me)CH2S(O)CH2CF3
H CH(Me)CH2S(O)2Me
H CH(Me)CH2S(O)2Et
H CH(Me)CH2S(O)2CF3
H CH(Me)CH2S(O)2CH2CF3
H CH(Et)CH2SMe
H CH(Et)CH2SEt
H CH(Et)CH2SCF3
H CH(Et)CH2SCH2CF3
H CH(Et)CH2S(O)Me
H CH(Et)CH2S(O)Et
H CH(Et)CH2S(O)CF3
H CH(Et)CH2S(O)CH2CF3
H CH(Et)CH2S(O)2Me
H CH(Et)CH2S(O)2Et
H CH(Et)CH2S(O)2CF3
H CH(Et)CH2S(O)2CH2CF3
H C(Me)2CH2SMe
H C(Me)2CH2SEt
H C(Me)2CH2SCF3
H C(Me)2CH2SCH2CF3
H C(Me)2CH2S(O)Me
H C(Me)2CH2S(O)Et
H C(Me)2CH2S(O)CF3
H C(Me)2CH2S(O)CH2CF3
H C(Me)2CH2S(O)2Me
H C(Me)2CH2S(O)2Et
H C(Me)2CH2S(O)2CF3
H C(Me)2CH2S(O)2CH2CF3
H CH2CH(Me)SMe
H CH2CH(Me)SEt
H CH2CH(Me)SCF3
H CH2CH(Me)SCH2CF3
H CH2CH(Me)S(O)Me
H CH2CH(Me)S(O)Et
H CH2CH(Me)S(O)CF3
H CH2CH(Me)S(O)CH2CF3
H CH2CH(Me)S(O)2Me
H CH2CH(Me)S(O)2Et
H CH2CH(Me)S(O)2CF3
H CH2CH(Me)S(O)2CH2CF3
H CH2CH(Et)SMe
H CH2CH(Et)SEt
H CH2CH(Et)SCF3
H CH2CH(Et)SCH2CF3
H CH2CH(Et)S(O)Me
H CH2CH(Et)S(O)Et
H CH2CH(Et)S(O)CF3
H CH2CH(Et)S(O)CH2CF3
H CH2CH(Et)S(O)2Me
H CH2CH(Et)S(O)2Et
H CH2CH(Et)S(O)2CF3
H CH2CH(Et)S(O)2CH2CF3
H CH(Me)CH(Me)SMe
H CH(Me)CH(Me)SEt
H CH(Me)CH(Me)SCF3
H CH(Me)CH(Me)SCH2CF3
H CH(Me)CH(Me)S(O)Me
H CH(Me)CH(Me)S(O)Et
H CH(Me)CH(Me)S(O)CF3
H CH(Me)CH(Me)S(O)CH2CF3
H CH(Me)CH(Me)S(O)2Me
H CH(Me)CH(Me)S(O)2Et
H CH(Me)CH(Me)S(O)2CF3
H CH(Me)CH(Me)S(O)2CH2CF3
Me CH2SMe
Me CH2SEt
Me CH2SCF3
Me CH2SCH2CF3
Me CH2S(O)Me
Me CH2S(O)Et
Me CH2S(O)CF3
Me CH2S(O)CH2CF3
Me CH2S(O)2Me
Me CH2S(O)2Et
Me CH2S(O)2CF3
Me CH2S(O)2CH2CF3
Me CH(Me)SMe
Me CH(Me)SEt
Me CH(Me)SCF3
Me CH(Me)SCH2CF3
Me CH(Me)S(O)Me
Me CH(Me)S(O)Et
Me CH(Me)S(O)CF3
Me CH(Me)S(O)CH2CF3
Me CH(Me)S(O)2Me
Me CH(Me)S(O)2Et
Me CH(Me)S(O)2CF3
Me CH(Me)S(O)2CH2CF3
Me CH(Et)SMe
Me CH(Et)SEt
Me CH(Et)SCF3
Me CH(Et)SCH2CF3
Me CH(Et)S(O)Me
Me CH(Et)S(O)Et
Me CH(Et)S(O)CF3
Me CH(Et)S(O)CH2CF3
Me CH(Et)S(O)2Me
Me CH(Et)S(O)2Et
Me CH(Et)S(O)2CF3
Me CH(Et)S(O)2CH2CF3
Me CH(n-Pr)SMe
Me CH(n-Pr)SEt
Me CH(n-Pr)SCF3
Me CH(n-Pr)SCH2CF3
Me CH(n-Pr)S(O)Me
Me CH(n-Pr)S(O)Et
Me CH(n-Pr)S(O)CF3
Me CH(n-Pr)S(O)CH2CF3
Me CH(n-Pr)S(O)2Me
Me CH(n-Pr)S(O)2Et
Me CH(n-Pr)S(O)2CF3
Me CH(n-Pr)S(O)2CH2CF3
Me CH(i-Pr)SMe
Me CH(i-Pr)SEt
Me CH(i-Pr)SCF3
Me CH(i-Pr)SCH2CF3
Me CH(i-Pr)S(O)Me
Me CH(i-Pr)S(O)Et
Me CH(i-Pr)S(O)CF3
Me CH(i-Pr)S(O)CH2CF3
Me CH(i-Pr)S(O)2Me
Me CH(i-Pr)S(O)2Et
Me CH(i-Pr)S(O)2CF3
Me CH(i-Pr)S(O)2CH2CF3
Me CH(n-Bu)SMe
Me CH(n-Bu)SEt
Me CH(n-Bu)SCF3
Me CH(n-Bu)SCH2CF3
Me CH(n-Bu)S(O)Me
Me CH(n-Bu)S(O)Et
Me CH(n-Bu)S(O)CF3
Me CH(n-Bu)S(O)CH2CF3
Me CH(n-Bu)S(O)2Me
Me CH(n-Bu)S(O)2Et
Me CH(n-Bu)S(O)2CF3
Me CH(n-Bu)S(O)2CH2CF3
Me CH(i-Bu)SMe
Me CH(i-Bu)SEt
Me CH(i-Bu)SCF3
Me CH(i-Bu)SCH2CF3
Me CH(i-Bu)S(O)Me
Me CH(i-Bu)S(O)Et
Me CH(i-Bu)S(O)CF3
Me CH(i-Bu)S(O)CH2CF3
Me CH(i-Bu)S(O)2Me
Me CH(i-Bu)S(O)2Et
Me CH(i-Bu)S(O)2CF3
Me CH(i-Bu)S(O)2CH2CF3
Me CH(s-Bu)SMe
Me CH(s-Bu)SEt
Me CH(s-Bu)SCF3
Me CH(s-Bu)SCH2CF3
Me CH(s-Bu)S(O)Me
Me CH(s-Bu)S(O)Et
Me CH(s-Bu)S(O)CF3
Me CH(s-Bu)S(O)CH2CF3
Me CH(s-Bu)S(O)2Me
Me CH(s-Bu)S(O)2Et
Me CH(s-Bu)S(O)2CF3
Me CH(s-Bu)S(O)2CH2CF3
Me CH(t-Bu)SMe
Me CH(t-Bu)SEt
Me CH(t-Bu)SCF3
Me CH(t-Bu)SCH2CF3
Me CH(t-Bu)S(O)Me
Me CH(t-Bu)S(O)Et
Me CH(t-Bu)S(O)CF3
Me CH(t-Bu)S(O)CH2CF3
Me CH(t-Bu)S(O)2Me
Me CH(t-Bu)S(O)2Et
Me CH(t-Bu)S(O)2CF3
Me CH(t-Bu)S(O)2CH2CF3
Me CH(CF3)SMe
Me CH(CF3)SEt
Me CH(CF3)SCF3
Me CH(CF3)SCH2CF3
Me CH(CF3)S(O)Me
Me CH(CF3)S(O)Et
Me CH(CF3)S(O)CF3
Me CH(CF3)S(O)CH2CF3
Me CH(CF3)S(O)2Me
Me CH(CF3)S(O)2Et
Me CH(CF3)S(O)2CF3
Me CH(CF3)S(O)2CH2CF3
Me CH2CH2SMe
Me CH2CH2SEt
Me CH2CH2SCF3
Me CH2CH2SCH2CF3
Me CH2CH2S(O)Me
Me CH2CH2S(O)Et
Me CH2CH2S(O)CF3
Me CH2CH2S(O)CH2CF3
Me CH2CH2S(O)2Me
Me CH2CH2S(O)2Et
Me CH2CH2S(O)2CF3
Me CH2CH2S(O)2CH2CF3
Me CH(Me)CH2SMe
Me CH(Me)CH2SEt
Me CH(Me)CH2SCF3
Me CH(Me)CH2SCH2CF3
Me CH(Me)CH2S(O)Me
Me CH(Me)CH2S(O)Et
Me CH(Me)CH2S(O)CF3
Me CH(Me)CH2S(O)CH2CF3
Me CH(Me)CH2S(O)2Me
Me CH(Me)CH2S(O)2Et
Me CH(Me)CH2S(O)2CF3
Me CH(Me)CH2S(O)2CH2CF3
Me CH(Et)CH2SMe
Me CH(Et)CH2SEt
Me CH(Et)CH2SCF3
Me CH(Et)CH2SCH2CF3
Me CH(Et)CH2S(O)Me
Me CH(Et)CH2S(O)Et
Me CH(Et)CH2S(O)CF3
Me CH(Et)CH2S(O)CH2CF3
Me CH(Et)CH2S(O)2Me
Me CH(Et)CH2S(O)2Et
Me CH(Et)CH2S(O)2CF3
Me CH(Et)CH2S(O)2CH2CF3
Me C(Me)2CH2SMe
Me C(Me)2CH2SEt
Me C(Me)2CH2SCF3
Me C(Me)2CH2SCH2CF3
Me C(Me)2CH2S(O)Me
Me C(Me)2CH2S(O)Et
Me C(Me)2CH2S(O)CF3
Me C(Me)2CH2S(O)CH2CF3
Me C(Me)2CH2S(O)2Me
Me C(Me)2CH2S(O)2Et
Me C(Me)2CH2S(O)2CF3
Me C(Me)2CH2S(O)2CH2CF3
Me CH2CH(Me)SMe
Me CH2CH(Me)SEt
Me CH2CH(Me)SCF3
Me CH2CH(Me)SCH2CF3
Me CH2CH(Me)S(O)Me
Me CH2CH(Me)S(O)Et
Me CH2CH(Me)S(O)CF3
Me CH2CH(Me)S(O)CH2CF3
Me CH2CH(Me)S(O)2Me
Me CH2CH(Me)S(O)2Et
Me CH2CH(Me)S(O)2CF3
Me CH2CH(Me)S(O)2CH2CF3
Me CH2CH(Et)SMe
Me CH2CH(Et)SEt
Me CH2CH(Et)SCF3
Me CH2CH(Et)SCH2CF3
Me CH2CH(Et)S(O)Me
Me CH2CH(Et)S(O)Et
Me CH2CH(Et)S(O)CF3
Me CH2CH(Et)S(O)CH2CF3
Me CH2CH(Et)S(O)2Me
Me CH2CH(Et)S(O)2Et
Me CH2CH(Et)S(O)2CF3
Me CH2CH(Et)S(O)2CH2CF3
Me CH(Me)CH(Me)SMe
Me CH(Me)CH(Me)SEt
Me CH(Me)CH(Me)SCF3
Me CH(Me)CH(Me)SCH2CF3
Me CH(Me)CH(Me)S(O)Me
Me CH(Me)CH(Me)S(O)Et
Me CH(Me)CH(Me)S(O)CF3
Me CH(Me)CH(Me)S(O)CH2CF3
Me CH(Me)CH(Me)S(O)2Me
Me CH(Me)CH(Me)S(O)2Et
Me CH(Me)CH(Me)S(O)2CF3
Me CH(Me)CH(Me)S(O)2CH2CF3
CH2CF3 CH2SMe
CH2CF3 CH2SEt
CH2CF3 CH2SCF3
CH2CF3 CH2SCH2CF3
CH2CF3 CH2S(O)Me
CH2CF3 CH2S(O)Et
CH2CF3 CH2S(O)CF3
CH2CF3 CH2S(O)CH2CF3
CH2CF3 CH2S(O)2Me
CH2CF3 CH2S(O)2Et
CH2CF3 CH2S(O)2CF3
CH2CF3 CH2S(O)2CH2CF3
CH2CF3 CH(Me)SMe
CH2CF3 CH(Me)SEt
CH2CF3 CH(Me)SCF3
CH2CF3 CH(Me)SCH2CF3
CH2CF3 CH(Me)S(O)Me
CH2CF3 CH(Me)S(O)Et
CH2CF3 CH(Me)S(O)CF3
CH2CF3 CH(Me)S(O)CH2CF3
CH2CF3 CH(Me)S(O)2Me
CH2CF3 CH(Me)S(O)2Et
CH2CF3 CH(Me)S(O)2CF3
CH2CF3 CH(Me)S(O)2CH2CF3
CH2CF3 CH(Et)SMe
CH2CF3 CH(Et)SEt
CH2CF3 CH(Et)SCF3
CH2CF3 CH(Et)SCH2CF3
CH2CF3 CH(Et)S(O)Me
CH2CF3 CH(Et)S(O)Et
CH2CF3 CH(Et)S(O)CF3
CH2CF3 CH(Et)S(O)CH2CF3
CH2CF3 CH(Et)S(O)2Me
CH2CF3 CH(Et)S(O)2Et
CH2CF3 CH(Et)S(O)2CF3
CH2CF3 CH(Et)S(O)2CH2CF3
CH2CF3 CH(n-Pr)SMe
CH2CF3 CH(n-Pr)SEt
CH2CF3 CH(n-Pr)SCF3
CH2CF3 CH(n-Pr)SCH2CF3
CH2CF3 CH(n-Pr)S(O)Me
CH2CF3 CH(n-Pr)S(O)Et
CH2CF3 CH(n-Pr)S(O)CF3
CH2CF3 CH(n-Pr)S(O)CH2CF3
CH2CF3 CH(n-Pr)S(O)2Me
CH2CF3 CH(n-Pr)S(O)2Et
CH2CF3 CH(n-Pr)S(O)2CF3
CH2CF3 CH(n-Pr)S(O)2CH2CF3
CH2CF3 CH(i-Pr)SMe
CH2CF3 CH(i-Pr)SEt
CH2CF3 CH(i-Pr)SCF3
CH2CF3 CH(i-Pr)SCH2CF3
CH2CF3 CH(i-Pr)S(O)Me
CH2CF3 CH(i-Pr)S(O)Et
CH2CF3 CH(i-Pr)S(O)CF3
CH2CF3 CH(i-Pr)S(O)CH2CF3
CH2CF3 CH(i-Pr)S(O)2Me
CH2CF3 CH(i-Pr)S(O)2Et
CH2CF3 CH(i-Pr)S(O)2CF3
CH2CF3 CH(i-Pr)S(O)2CH2CF3
CH2CF3 CH(n-Bu)SMe
CH2CF3 CH(n-Bu)SEt
CH2CF3 CH(n-Bu)SCF3
CH2CF3 CH(n-Bu)SCH2CF3
CH2CF3 CH(n-Bu)S(O)Me
CH2CF3 CH(n-Bu)S(O)Et
CH2CF3 CH(n-Bu)S(O)CF3
CH2CF3 CH(n-Bu)S(O)CH2CF3
CH2CF3 CH(n-Bu)S(O)2Me
CH2CF3 CH(n-Bu)S(O)2Et
CH2CF3 CH(n-Bu)S(O)2CF3
CH2CF3 CH(n-Bu)S(O)2CH2CF3
CH2CF3 CH(i-Bu)SMe
CH2CF3 CH(i-Bu)SEt
CH2CF3 CH(i-Bu)SCF3
CH2CF3 CH(i-Bu)SCH2CF3
CH2CF3 CH(i-Bu)S(O)Me
CH2CF3 CH(i-Bu)S(O)Et
CH2CF3 CH(i-Bu)S(O)CF3
CH2CF3 CH(i-Bu)S(O)CH2CF3
CH2CF3 CH(i-Bu)S(O)2Me
CH2CF3 CH(i-Bu)S(O)2Et
CH2CF3 CH(i-Bu)S(O)2CF3
CH2CF3 CH(i-Bu)S(O)2CH2CF3
CH2CF3 CH(s-Bu)SMe
CH2CF3 CH(s-Bu)SEt
CH2CF3 CH(s-Bu)SCF3
CH2CF3 CH(s-Bu)SCH2CF3
CH2CF3 CH(s-Bu)S(O)Me
CH2CF3 CH(s-Bu)S(O)Et
CH2CF3 CH(s-Bu)S(O)CF3
CH2CF3 CH(s-Bu)S(O)CH2CF3
CH2CF3 CH(s-Bu)S(O)2Me
CH2CF3 CH(s-Bu)S(O)2Et
CH2CF3 CH(s-Bu)S(O)2CF3
CH2CF3 CH(s-Bu)S(O)2CH2CF3
CH2CF3 CH(t-Bu)SMe
CH2CF3 CH(t-Bu)SEt
CH2CF3 CH(t-Bu)SCF3
CH2CF3 CH(t-Bu)SCH2CF3
CH2CF3 CH(t-Bu)S(O)Me
CH2CF3 CH(t-Bu)S(O)Et
CH2CF3 CH(t-Bu)S(O)CF3
CH2CF3 CH(t-Bu)S(O)CH2CF3
CH2CF3 CH(t-Bu)S(O)2Me
CH2CF3 CH(t-Bu)S(O)2Et
CH2CF3 CH(t-Bu)S(O)2CF3
CH2CF3 CH(t-Bu)S(O)2CH2CF3
CH2CF3 CH(CF3)SMe
CH2CF3 CH(CF3)SEt
CH2CF3 CH(CF3)SCF3
CH2CF3 CH(CF3)SCH2CF3
CH2CF3 CH(CF3)S(O)Me
CH2CF3 CH(CF3)S(O)Et
CH2CF3 CH(CF3)S(O)CF3
CH2CF3 CH(CF3)S(O)CH2CF3
CH2CF3 CH(CF3)S(O)2Me
CH2CF3 CH(CF3)S(O)2Et
CH2CF3 CH(CF3)S(O)2CF3
CH2CF3 CH(CF3)S(O)2CH2CF3
CH2CF3 CH2CH2SMe
CH2CF3 CH2CH2SEt
CH2CF3 CH2CH2SCF3
CH2CF3 CH2CH2SCH2CF3
CH2CF3 CH2CH2S(O)Me
CH2CF3 CH2CH2S(O)Et
CH2CF3 CH2CH2S(O)CF3
CH2CF3 CH2CH2S(O)CH2CF3
CH2CF3 CH2CH2S(O)2Me
CH2CF3 CH2CH2S(O)2Et
CH2CF3 CH2CH2S(O)2CF3
CH2CF3 CH2CH2S(O)2CH2CF3
CH2CF3 CH(Me)CH2SMe
CH2CF3 CH(Me)CH2SEt
CH2CF3 CH(Me)CH2SCF3
CH2CF3 CH(Me)CH2SCH2CF3
CH2CF3 CH(Me)CH2S(O)Me
CH2CF3 CH(Me)CH2S(O)Et
CH2CF3 CH(Me)CH2S(O)CF3
CH2CF3 CH(Me)CH2S(O)CH2CF3
CH2CF3 CH(Me)CH2S(O)2Me
CH2CF3 CH(Me)CH2S(O)2Et
CH2CF3 CH(Me)CH2S(O)2CF3
CH2CF3 CH(Me)CH2S(O)2CH2CF3
CH2CF3 CH(Et)CH2SMe
CH2CF3 CH(Et)CH2SEt
CH2CF3 CH(Et)CH2SCF3
CH2CF3 CH(Et)CH2SCH2CF3
CH2CF3 CH(Et)CH2S(O)Me
CH2CF3 CH(Et)CH2S(O)Et
CH2CF3 CH(Et)CH2S(O)CF3
CH2CF3 CH(Et)CH2S(O)CH2CF3
CH2CF3 CH(Et)CH2S(O)2Me
CH2CF3 CH(Et)CH2S(O)2Et
CH2CF3 CH(Et)CH2S(O)2CF3
CH2CF3 CH(Et)CH2S(O)2CH2CF3
CH2CF3 C(Me)2CH2SMe
CH2CF3 C(Me)2CH2SEt
CH2CF3 C(Me)2CH2SCF3
CH2CF3 C(Me)2CH2SCH2CF3
CH2CF3 C(Me)2CH2S(O)Me
CH2CF3 C(Me)2CH2S(O)Et
CH2CF3 C(Me)2CH2S(O)CF3
CH2CF3 C(Me)2CH2S(O)CH2CF3
CH2CF3 C(Me)2CH2S(O)2Me
CH2CF3 C(Me)2CH2S(O)2Et
CH2CF3 C(Me)2CH2S(O)2CF3
CH2CF3 C(Me)2CH2S(O)2CH2CF3
CH2CF3 CH2CH(Me)SMe
CH2CF3 CH2CH(Me)SEt
CH2CF3 CH2CH(Me)SCF3
CH2CF3 CH2CH(Me)SCH2CF3
CH2CF3 CH2CH(Me)S(O)Me
CH2CF3 CH2CH(Me)S(O)Et
CH2CF3 CH2CH(Me)S(O)CF3
CH2CF3 CH2CH(Me)S(O)CH2CF3
CH2CF3 CH2CH(Me)S(O)2Me
CH2CF3 CH2CH(Me)S(O)2Et
CH2CF3 CH2CH(Me)S(O)2CF3
CH2CF3 CH2CH(Me)S(O)2CH2CF3
CH2CF3 CH2CH(Et)SMe
CH2CF3 CH2CH(Et)SEt
CH2CF3 CH2CH(Et)SCF3
CH2CF3 CH2CH(Et)SCH2CF3
CH2CF3 CH2CH(Et)S(O)Me
CH2CF3 CH2CH(Et)S(O)Et
CH2CF3 CH2CH(Et)S(O)CF3
CH2CF3 CH2CH(Et)S(O)CH2CF3
CH2CF3 CH2CH(Et)S(O)2Me
CH2CF3 CH2CH(Et)S(O)2Et
CH2CF3 CH2CH(Et)S(O)2CF3
CH2CF3 CH2CH(Et)S(O)2CH2CF3
CH2CF3 CH(Me)CH(Me)SMe
CH2CF3 CH(Me)CH(Me)SEt
CH2CF3 CH(Me)CH(Me)SCF3
CH2CF3 CH(Me)CH(Me)SCH2CF3
CH2CF3 CH(Me)CH(Me)S(O)Me
CH2CF3 CH(Me)CH(Me)S(O)Et
CH2CF3 CH(Me)CH(Me)S(O)CF3
CH2CF3 CH(Me)CH(Me)S(O)CH2CF3
CH2CF3 CH(Me)CH(Me)S(O)2Me
CH2CF3 CH(Me)CH(Me)S(O)2Et
CH2CF3 CH(Me)CH(Me)S(O)2CF3
CH2CF3 CH(Me)CH(Me)S(O)2CH2CF3
CH2CN CH2SMe
CH2CN CH2SEt
CH2CN CH2SCF3
CH2CN CH2SCH2CF3
CH2CN CH2S(O)Me
CH2CN CH2S(O)Et
CH2CN CH2S(O)CF3
CH2CN CH2S(O)CH2CF3
CH2CN CH2S(O)2Me
CH2CN CH2S(O)2Et
CH2CN CH2S(O)2CF3
CH2CN CH2S(O)2CH2CF3
CH2CN CH(Me)SMe
CH2CN CH(Me)SEt
CH2CN CH(Me)SCF3
CH2CN CH(Me)SCH2CF3
CH2CN CH(Me)S(O)Me
CH2CN CH(Me)S(O)Et
CH2CN CH(Me)S(O)CF3
CH2CN CH(Me)S(O)CH2CF3
CH2CN CH(Me)S(O)2Me
CH2CN CH(Me)S(O)2Et
CH2CN CH(Me)S(O)2CF3
CH2CN CH(Me)S(O)2CH2CF3
CH2CN CH(Et)SMe
CH2CN CH(Et)SEt
CH2CN CH(Et)SCF3
CH2CN CH(Et)SCH2CF3
CH2CN CH(Et)S(O)Me
CH2CN CH(Et)S(O)Et
CH2CN CH(Et)S(O)CF3
CH2CN CH(Et)S(O)CH2CF3
CH2CN CH(Et)S(O)2Me
CH2CN CH(Et)S(O)2Et
CH2CN CH(Et)S(O)2CF3
CH2CN CH(Et)S(O)2CH2CF3
CH2CN CH(n-Pr)SMe
CH2CN CH(n-Pr)SEt
CH2CN CH(n-Pr)SCF3
CH2CN CH(n-Pr)SCH2CF3
CH2CN CH(n-Pr)S(O)Me
CH2CN CH(n-Pr)S(O)Et
CH2CN CH(n-Pr)S(O)CF3
CH2CN CH(n-Pr)S(O)CH2CF3
CH2CN CH(n-Pr)S(O)2Me
CH2CN CH(n-Pr)S(O)2Et
CH2CN CH(n-Pr)S(O)2CF3
CH2CN CH(n-Pr)S(O)2CH2CF3
CH2CN CH(i-Pr)SMe
CH2CN CH(i-Pr)SEt
CH2CN CH(i-Pr)SCF3
CH2CN CH(i-Pr)SCH2CF3
CH2CN CH(i-Pr)S(O)Me
CH2CN CH(i-Pr)S(O)Et
CH2CN CH(i-Pr)S(O)CF3
CH2CN CH(i-Pr)S(O)CH2CF3
CH2CN CH(i-Pr)S(O)2Me
CH2CN CH(i-Pr)S(O)2Et
CH2CN CH(i-Pr)S(O)2CF3
CH2CN CH(i-Pr)S(O)2CH2CF3
CH2CN CH(n-Bu)SMe
CH2CN CH(n-Bu)SEt
CH2CN CH(n-Bu)SCF3
CH2CN CH(n-Bu)SCH2CF3
CH2CN CH(n-Bu)S(O)Me
CH2CN CH(n-Bu)S(O)Et
CH2CN CH(n-Bu)S(O)CF3
CH2CN CH(n-Bu)S(O)CH2CF3
CH2CN CH(n-Bu)S(O)2Me
CH2CN CH(n-Bu)S(O)2Et
CH2CN CH(n-Bu)S(O)2CF3
CH2CN CH(n-Bu)S(O)2CH2CF3
CH2CN CH(i-Bu)SMe
CH2CN CH(i-Bu)SEt
CH2CN CH(i-Bu)SCF3
CH2CN CH(i-Bu)SCH2CF3
CH2CN CH(i-Bu)S(O)Me
CH2CN CH(i-Bu)S(O)Et
CH2CN CH(i-Bu)S(O)CF3
CH2CN CH(i-Bu)S(O)CH2CF3
CH2CN CH(i-Bu)S(O)2Me
CH2CN CH(i-Bu)S(O)2Et
CH2CN CH(i-Bu)S(O)2CF3
CH2CN CH(i-Bu)S(O)2CH2CF3
CH2CN CH(s-Bu)SMe
CH2CN CH(s-Bu)SEt
CH2CN CH(s-Bu)SCF3
CH2CN CH(s-Bu)SCH2CF3
CH2CN CH(s-Bu)S(O)Me
CH2CN CH(s-Bu)S(O)Et
CH2CN CH(s-Bu)S(O)CF3
CH2CN CH(s-Bu)S(O)CH2CF3
CH2CN CH(s-Bu)S(O)2Me
CH2CN CH(s-Bu)S(O)2Et
CH2CN CH(s-Bu)S(O)2CF3
CH2CN CH(s-Bu)S(O)2CH2CF3
CH2CN CH(t-Bu)SMe
CH2CN CH(t-Bu)SEt
CH2CN CH(t-Bu)SCF3
CH2CN CH(t-Bu)SCH2CF3
CH2CN CH(t-Bu)S(O)Me
CH2CN CH(t-Bu)S(O)Et
CH2CN CH(t-Bu)S(O)CF3
CH2CN CH(t-Bu)S(O)CH2CF3
CH2CN CH(t-Bu)S(O)2Me
CH2CN CH(t-Bu)S(O)2Et
CH2CN CH(t-Bu)S(O)2CF3
CH2CN CH(t-Bu)S(O)2CH2CF3
CH2CN CH(CF3)SMe
CH2CN CH(CF3)SEt
CH2CN CH(CF3)SCF3
CH2CN CH(CF3)SCH2CF3
CH2CN CH(CF3)S(O)Me
CH2CN CH(CF3)S(O)Et
CH2CN CH(CF3)S(O)CF3
CH2CN CH(CF3)S(O)CH2CF3
CH2CN CH(CF3)S(O)2Me
CH2CN CH(CF3)S(O)2Et
CH2CN CH(CF3)S(O)2CF3
CH2CN CH(CF3)S(O)2CH2CF3
CH2CN CH2CH2SMe
CH2CN CH2CH2SEt
CH2CN CH2CH2SCF3
CH2CN CH2CH2SCH2CF3
CH2CN CH2CH2S(O)Me
CH2CN CH2CH2S(O)Et
CH2CN CH2CH2S(O)CF3
CH2CN CH2CH2S(O)CH2CF3
CH2CN CH2CH2S(O)2Me
CH2CN CH2CH2S(O)2Et
CH2CN CH2CH2S(O)2CF3
CH2CN CH2CH2S(O)2CH2CF3
CH2CN CH(Me)CH2SMe
CH2CN CH(Me)CH2SEt
CH2CN CH(Me)CH2SCF3
CH2CN CH(Me)CH2SCH2CF3
CH2CN CH(Me)CH2S(O)Me
CH2CN CH(Me)CH2S(O)Et
CH2CN CH(Me)CH2S(O)CF3
CH2CN CH(Me)CH2S(O)CH2CF3
CH2CN CH(Me)CH2S(O)2Me
CH2CN CH(Me)CH2S(O)2Et
CH2CN CH(Me)CH2S(O)2CF3
CH2CN CH(Me)CH2S(O)2CH2CF3
CH2CN CH(Et)CH2SMe
CH2CN CH(Et)CH2SEt
CH2CN CH(Et)CH2SCF3
CH2CN CH(Et)CH2SCH2CF3
CH2CN CH(Et)CH2S(O)Me
CH2CN CH(Et)CH2S(O)Et
CH2CN CH(Et)CH2S(O)CF3
CH2CN CH(Et)CH2S(O)CH2CF3
CH2CN CH(Et)CH2S(O)2Me
CH2CN CH(Et)CH2S(O)2Et
CH2CN CH(Et)CH2S(O)2CF3
CH2CN CH(Et)CH2S(O)2CH2CF3
CH2CN C(Me)2CH2SMe
CH2CN C(Me)2CH2SEt
CH2CN C(Me)2CH2SCF3
CH2CN C(Me)2CH2SCH2CF3
CH2CN C(Me)2CH2S(O)Me
CH2CN C(Me)2CH2S(O)Et
CH2CN C(Me)2CH2S(O)CF3
CH2CN C(Me)2CH2S(O)CH2CF3
CH2CN C(Me)2CH2S(O)2Me
CH2CN C(Me)2CH2S(O)2Et
CH2CN C(Me)2CH2S(O)2CF3
CH2CN C(Me)2CH2S(O)2CH2CF3
CH2CN CH2CH(Me)SMe
CH2CN CH2CH(Me)SEt
CH2CN CH2CH(Me)SCF3
CH2CN CH2CH(Me)SCH2CF3
CH2CN CH2CH(Me)S(O)Me
CH2CN CH2CH(Me)S(O)Et
CH2CN CH2CH(Me)S(O)CF3
CH2CN CH2CH(Me)S(O)CH2CF3
CH2CN CH2CH(Me)S(O)2Me
CH2CN CH2CH(Me)S(O)2Et
CH2CN CH2CH(Me)S(O)2CF3
CH2CN CH2CH(Me)S(O)2CH2CF3
CH2CN CH2CH(Et)SMe
CH2CN CH2CH(Et)SEt
CH2CN CH2CH(Et)SCF3
CH2CN CH2CH(Et)SCH2CF3
CH2CN CH2CH(Et)S(O)Me
CH2CN CH2CH(Et)S(O)Et
CH2CN CH2CH(Et)S(O)CF3
CH2CN CH2CH(Et)S(O)CH2CF3
CH2CN CH2CH(Et)S(O)2Me
CH2CN CH2CH(Et)S(O)2Et
CH2CN CH2CH(Et)S(O)2CF3
CH2CN CH2CH(Et)S(O)2CH2CF3
CH2CN CH(Me)CH(Me)SMe
CH2CN CH(Me)CH(Me)SEt
CH2CN CH(Me)CH(Me)SCF3
CH2CN CH(Me)CH(Me)SCH2CF3
CH2CN CH(Me)CH(Me)S(O)Me
CH2CN CH(Me)CH(Me)S(O)Et
CH2CN CH(Me)CH(Me)S(O)CF3
CH2CN CH(Me)CH(Me)S(O)CH2CF3
CH2CN CH(Me)CH(Me)S(O)2Me
CH2CN CH(Me)CH(Me)S(O)2Et
CH2CN CH(Me)CH(Me)S(O)2CF3
CH2CN CH(Me)CH(Me)S(O)2CH2CF3
CH2CH=CH2 CH2SMe
CH2CH=CH2 CH2SEt
CH2CH=CH2 CH2SCF3
CH2CH=CH2 CH2SCH2CF3
CH2CH=CH2 CH2S(O)Me
CH2CH=CH2 CH2S(O)Et
CH2CH=CH2 CH2S(O)CF3
CH2CH=CH2 CH2S(O)CH2CF3
CH2CH=CH2 CH2S(O)2Me
CH2CH=CH2 CH2S(O)2Et
CH2CH=CH2 CH2S(O)2CF3
CH2CH=CH2 CH2S(O)2CH2CF3
CH2CH=CH2 CH(Me)SMe
CH2CH=CH2 CH(Me)SEt
CH2CH=CH2 CH(Me)SCF3
CH2CH=CH2 CH(Me)SCH2CF3
CH2CH=CH2 CH(Me)S(O)Me
CH2CH=CH2 CH(Me)S(O)Et
CH2CH=CH2 CH(Me)S(O)CF3
CH2CH=CH2 CH(Me)S(O)CH2CF3
CH2CH=CH2 CH(Me)S(O)2Me
CH2CH=CH2 CH(Me)S(O)2Et
CH2CH=CH2 CH(Me)S(O)2CF3
CH2CH=CH2 CH(Me)S(O)2CH2CF3
CH2CH=CH2 CH(Et)SMe
CH2CH=CH2 CH(Et)SEt
CH2CH=CH2 CH(Et)SCF3
CH2CH=CH2 CH(Et)SCH2CF3
CH2CH=CH2 CH(Et)S(O)Me
CH2CH=CH2 CH(Et)S(O)Et
CH2CH=CH2 CH(Et)S(O)CF3
CH2CH=CH2 CH(Et)S(O)CH2CF3
CH2CH=CH2 CH(Et)S(O)2Me
CH2CH=CH2 CH(Et)S(O)2Et
CH2CH=CH2 CH(Et)S(O)2CF3
CH2CH=CH2 CH(Et)S(O)2CH2CF3
CH2CH=CH2 CH(n-Pr)SMe
CH2CH=CH2 CH(n-Pr)SEt
CH2CH=CH2 CH(n-Pr)SCF3
CH2CH=CH2 CH(n-Pr)SCH2CF3
CH2CH=CH2 CH(n-Pr)S(O)Me
CH2CH=CH2 CH(n-Pr)S(O)Et
CH2CH=CH2 CH(n-Pr)S(O)CF3
CH2CH=CH2 CH(n-Pr)S(O)CH2CF3
CH2CH=CH2 CH(n-Pr)S(O)2Me
CH2CH=CH2 CH(n-Pr)S(O)2Et
CH2CH=CH2 CH(n-Pr)S(O)2CF3
CH2CH=CH2 CH(n-Pr)S(O)2CH2CF3
CH2CH=CH2 CH(i-Pr)SMe
CH2CH=CH2 CH(i-Pr)SEt
CH2CH=CH2 CH(i-Pr)SCF3
CH2CH=CH2 CH(i-Pr)SCH2CF3
CH2CH=CH2 CH(i-Pr)S(O)Me
CH2CH=CH2 CH(i-Pr)S(O)Et
CH2CH=CH2 CH(i-Pr)S(O)CF3
CH2CH=CH2 CH(i-Pr)S(O)CH2CF3
CH2CH=CH2 CH(i-Pr)S(O)2Me
CH2CH=CH2 CH(i-Pr)S(O)2Et
CH2CH=CH2 CH(i-Pr)S(O)2CF3
CH2CH=CH2 CH(i-Pr)S(O)2CH2CF3
CH2CH=CH2 CH(n-Bu)SMe
CH2CH=CH2 CH(n-Bu)SEt
CH2CH=CH2 CH(n-Bu)SCF3
CH2CH=CH2 CH(n-Bu)SCH2CF3
CH2CH=CH2 CH(n-Bu)S(O)Me
CH2CH=CH2 CH(n-Bu)S(O)Et
CH2CH=CH2 CH(n-Bu)S(O)CF3
CH2CH=CH2 CH(n-Bu)S(O)CH2CF3
CH2CH=CH2 CH(n-Bu)S(O)2Me
CH2CH=CH2 CH(n-Bu)S(O)2Et
CH2CH=CH2 CH(n-Bu)S(O)2CF3
CH2CH=CH2 CH(n-Bu)S(O)2CH2CF3
CH2CH=CH2 CH(i-Bu)SMe
CH2CH=CH2 CH(i-Bu)SEt
CH2CH=CH2 CH(i-Bu)SCF3
CH2CH=CH2 CH(i-Bu)SCH2CF3
CH2CH=CH2 CH(i-Bu)S(O)Me
CH2CH=CH2 CH(i-Bu)S(O)Et
CH2CH=CH2 CH(i-Bu)S(O)CF3
CH2CH=CH2 CH(i-Bu)S(O)CH2CF3
CH2CH=CH2 CH(i-Bu)S(O)2Me
CH2CH=CH2 CH(i-Bu)S(O)2Et
CH2CH=CH2 CH(i-Bu)S(O)2CF3
CH2CH=CH2 CH(i-Bu)S(O)2CH2CF3
CH2CH=CH2 CH(s-Bu)SMe
CH2CH=CH2 CH(s-Bu)SEt
CH2CH=CH2 CH(s-Bu)SCF3
CH2CH=CH2 CH(s-Bu)SCH2CF3
CH2CH=CH2 CH(s-Bu)S(O)Me
CH2CH=CH2 CH(s-Bu)S(O)Et
CH2CH=CH2 CH(s-Bu)S(O)CF3
CH2CH=CH2 CH(s-Bu)S(O)CH2CF3
CH2CH=CH2 CH(s-Bu)S(O)2Me
CH2CH=CH2 CH(s-Bu)S(O)2Et
CH2CH=CH2 CH(s-Bu)S(O)2CF3
CH2CH=CH2 CH(s-Bu)S(O)2CH2CF3
CH2CH=CH2 CH(t-Bu)SMe
CH2CH=CH2 CH(t-Bu)SEt
CH2CH=CH2 CH(t-Bu)SCF3
CH2CH=CH2 CH(t-Bu)SCH2CF3
CH2CH=CH2 CH(t-Bu)S(O)Me
CH2CH=CH2 CH(t-Bu)S(O)Et
CH2CH=CH2 CH(t-Bu)S(O)CF3
CH2CH=CH2 CH(t-Bu)S(O)CH2CF3
CH2CH=CH2 CH(t-Bu)S(O)2Me
CH2CH=CH2 CH(t-Bu)S(O)2Et
CH2CH=CH2 CH(t-Bu)S(O)2CF3
CH2CH=CH2 CH(t-Bu)S(O)2CH2CF3
CH2CH=CH2 CH(CF3)SMe
CH2CH=CH2 CH(CF3)SEt
CH2CH=CH2 CH(CF3)SCF3
CH2CH=CH2 CH(CF3)SCH2CF3
CH2CH=CH2 CH(CF3)S(O)Me
CH2CH=CH2 CH(CF3)S(O)Et
CH2CH=CH2 CH(CF3)S(O)CF3
CH2CH=CH2 CH(CF3)S(O)CH2CF3
CH2CH=CH2 CH(CF3)S(O)2Me
CH2CH=CH2 CH(CF3)S(O)2Et
CH2CH=CH2 CH(CF3)S(O)2CF3
CH2CH=CH2 CH(CF3)S(O)2CH2CF3
CH2CH=CH2 CH2CH2SMe
CH2CH=CH2 CH2CH2SEt
CH2CH=CH2 CH2CH2SCF3
CH2CH=CH2 CH2CH2SCH2CF3
CH2CH=CH2 CH2CH2S(O)Me
CH2CH=CH2 CH2CH2S(O)Et
CH2CH=CH2 CH2CH2S(O)CF3
CH2CH=CH2 CH2CH2S(O)CH2CF3
CH2CH=CH2 CH2CH2S(O)2Me
CH2CH=CH2 CH2CH2S(O)2Et
CH2CH=CH2 CH2CH2S(O)2CF3
CH2CH=CH2 CH2CH2S(O)2CH2CF3
CH2CH=CH2 CH(Me)CH2SMe
CH2CH=CH2 CH(Me)CH2SEt
CH2CH=CH2 CH(Me)CH2SCF3
CH2CH=CH2 CH(Me)CH2SCH2CF3
CH2CH=CH2 CH(Me)CH2S(O)Me
CH2CH=CH2 CH(Me)CH2S(O)Et
CH2CH=CH2 CH(Me)CH2S(O)CF3
CH2CH=CH2 CH(Me)CH2S(O)CH2CF3
CH2CH=CH2 CH(Me)CH2S(O)2Me
CH2CH=CH2 CH(Me)CH2S(O)2Et
CH2CH=CH2 CH(Me)CH2S(O)2CF3
CH2CH=CH2 CH(Me)CH2S(O)2CH2CF3
CH2CH=CH2 CH(Et)CH2SMe
CH2CH=CH2 CH(Et)CH2SEt
CH2CH=CH2 CH(Et)CH2SCF3
CH2CH=CH2 CH(Et)CH2SCH2CF3
CH2CH=CH2 CH(Et)CH2S(O)Me
CH2CH=CH2 CH(Et)CH2S(O)Et
CH2CH=CH2 CH(Et)CH2S(O)CF3
CH2CH=CH2 CH(Et)CH2S(O)CH2CF3
CH2CH=CH2 CH(Et)CH2S(O)2Me
CH2CH=CH2 CH(Et)CH2S(O)2Et
CH2CH=CH2 CH(Et)CH2S(O)2CF3
CH2CH=CH2 CH(Et)CH2S(O)2CH2CF3
CH2CH=CH2 C(Me)2CH2SMe
CH2CH=CH2 C(Me)2CH2SEt
CH2CH=CH2 C(Me)2CH2SCF3
CH2CH=CH2 C(Me)2CH2SCH2CF3
CH2CH=CH2 C(Me)2CH2S(O)Me
CH2CH=CH2 C(Me)2CH2S(O)Et
CH2CH=CH2 C(Me)2CH2S(O)CF3
CH2CH=CH2 C(Me)2CH2S(O)CH2CF3
CH2CH=CH2 C(Me)2CH2S(O)2Me
CH2CH=CH2 C(Me)2CH2S(O)2Et
CH2CH=CH2 C(Me)2CH2S(O)2CF3
CH2CH=CH2 C(Me)2CH2S(O)2CH2CF3
CH2CH=CH2 CH2CH(Me)SMe
CH2CH=CH2 CH2CH(Me)SEt
CH2CH=CH2 CH2CH(Me)SCF3
CH2CH=CH2 CH2CH(Me)SCH2CF3
CH2CH=CH2 CH2CH(Me)S(O)Me
CH2CH=CH2 CH2CH(Me)S(O)Et
CH2CH=CH2 CH2CH(Me)S(O)CF3
CH2CH=CH2 CH2CH(Me)S(O)CH2CF3
CH2CH=CH2 CH2CH(Me)S(O)2Me
CH2CH=CH2 CH2CH(Me)S(O)2Et
CH2CH=CH2 CH2CH(Me)S(O)2CF3
CH2CH=CH2 CH2CH(Me)S(O)2CH2CF3
CH2CH=CH2 CH2CH(Et)SMe
CH2CH=CH2 CH2CH(Et)SEt
CH2CH=CH2 CH2CH(Et)SCF3
CH2CH=CH2 CH2CH(Et)SCH2CF3
CH2CH=CH2 CH2CH(Et)S(O)Me
CH2CH=CH2 CH2CH(Et)S(O)Et
CH2CH=CH2 CH2CH(Et)S(O)CF3
CH2CH=CH2 CH2CH(Et)S(O)CH2CF3
CH2CH=CH2 CH2CH(Et)S(O)2Me
CH2CH=CH2 CH2CH(Et)S(O)2Et
CH2CH=CH2 CH2CH(Et)S(O)2CF3
CH2CH=CH2 CH2CH(Et)S(O)2CH2CF3
CH2CH=CH2 CH(Me)CH(Me)SMe
CH2CH=CH2 CH(Me)CH(Me)SEt
CH2CH=CH2 CH(Me)CH(Me)SCF3
CH2CH=CH2 CH(Me)CH(Me)SCH2CF3
CH2CH=CH2 CH(Me)CH(Me)S(O)Me
CH2CH=CH2 CH(Me)CH(Me)S(O)Et
CH2CH=CH2 CH(Me)CH(Me)S(O)CF3
CH2CH=CH2 CH(Me)CH(Me)S(O)CH2CF3
CH2CH=CH2 CH(Me)CH(Me)S(O)2Me
CH2CH=CH2 CH(Me)CH(Me)S(O)2Et
CH2CH=CH2 CH(Me)CH(Me)S(O)2CF3
CH2CH=CH2 CH(Me)CH(Me)S(O)2CH2CF3
CH2CH(OMe)2 CH2SMe
CH2CH(OMe)2 CH2SEt
CH2CH(OMe)2 CH2SCF3
CH2CH(OMe)2 CH2SCH2CF3
CH2CH(OMe)2 CH2S(O)Me
CH2CH(OMe)2 CH2S(O)Et
CH2CH(OMe)2 CH2S(O)CF3
CH2CH(OMe)2 CH2S(O)CH2CF3
CH2CH(OMe)2 CH2S(O)2Me
CH2CH(OMe)2 CH2S(O)2Et
CH2CH(OMe)2 CH2S(O)2CF3
CH2CH(OMe)2 CH2S(O)2CH2CF3
CH2CH(OMe)2 CH(Me)SMe
CH2CH(OMe)2 CH(Me)SEt
CH2CH(OMe)2 CH(Me)SCF3
CH2CH(OMe)2 CH(Me)SCH2CF3
CH2CH(OMe)2 CH(Me)S(O)Me
CH2CH(OMe)2 CH(Me)S(O)Et
CH2CH(OMe)2 CH(Me)S(O)CF3
CH2CH(OMe)2 CH(Me)S(O)CH2CF3
CH2CH(OMe)2 CH(Me)S(O)2Me
CH2CH(OMe)2 CH(Me)S(O)2Et
CH2CH(OMe)2 CH(Me)S(O)2CF3
CH2CH(OMe)2 CH(Me)S(O)2CH2CF3
CH2CH(OMe)2 CH(Et)SMe
CH2CH(OMe)2 CH(Et)SEt
CH2CH(OMe)2 CH(Et)SCF3
CH2CH(OMe)2 CH(Et)SCH2CF3
CH2CH(OMe)2 CH(Et)S(O)Me
CH2CH(OMe)2 CH(Et)S(O)Et
CH2CH(OMe)2 CH(Et)S(O)CF3
CH2CH(OMe)2 CH(Et)S(O)CH2CF3
CH2CH(OMe)2 CH(Et)S(O)2Me
CH2CH(OMe)2 CH(Et)S(O)2Et
CH2CH(OMe)2 CH(Et)S(O)2CF3
CH2CH(OMe)2 CH(Et)S(O)2CH2CF3
CH2CH(OMe)2 CH(n-Pr)SMe
CH2CH(OMe)2 CH(n-Pr)SEt
CH2CH(OMe)2 CH(n-Pr)SCF3
CH2CH(OMe)2 CH(n-Pr)SCH2CF3
CH2CH(OMe)2 CH(n-Pr)S(O)Me
CH2CH(OMe)2 CH(n-Pr)S(O)Et
CH2CH(OMe)2 CH(n-Pr)S(O)CF3
CH2CH(OMe)2 CH(n-Pr)S(O)CH2CF3
CH2CH(OMe)2 CH(n-Pr)S(O)2Me
CH2CH(OMe)2 CH(n-Pr)S(O)2Et
CH2CH(OMe)2 CH(n-Pr)S(O)2CF3
CH2CH(OMe)2 CH(n-Pr)S(O)2CH2CF3
CH2CH(OMe)2 CH(i-Pr)SMe
CH2CH(OMe)2 CH(i-Pr)SEt
CH2CH(OMe)2 CH(i-Pr)SCF3
CH2CH(OMe)2 CH(i-Pr)SCH2CF3
CH2CH(OMe)2 CH(i-Pr)S(O)Me
CH2CH(OMe)2 CH(i-Pr)S(O)Et
CH2CH(OMe)2 CH(i-Pr)S(O)CF3
CH2CH(OMe)2 CH(i-Pr)S(O)CH2CF3
CH2CH(OMe)2 CH(i-Pr)S(O)2Me
CH2CH(OMe)2 CH(i-Pr)S(O)2Et
CH2CH(OMe)2 CH(i-Pr)S(O)2CF3
CH2CH(OMe)2 CH(i-Pr)S(O)2CH2CF3
CH2CH(OMe)2 CH(n-Bu)SMe
CH2CH(OMe)2 CH(n-Bu)SEt
CH2CH(OMe)2 CH(n-Bu)SCF3
CH2CH(OMe)2 CH(n-Bu)SCH2CF3
CH2CH(OMe)2 CH(n-Bu)S(O)Me
CH2CH(OMe)2 CH(n-Bu)S(O)Et
CH2CH(OMe)2 CH(n-Bu)S(O)CF3
CH2CH(OMe)2 CH(n-Bu)S(O)CH2CF3
CH2CH(OMe)2 CH(n-Bu)S(O)2Me
CH2CH(OMe)2 CH(n-Bu)S(O)2Et
CH2CH(OMe)2 CH(n-Bu)S(O)2CF3
CH2CH(OMe)2 CH(n-Bu)S(O)2CH2CF3
CH2CH(OMe)2 CH(i-Bu)SMe
CH2CH(OMe)2 CH(i-Bu)SEt
CH2CH(OMe)2 CH(i-Bu)SCF3
CH2CH(OMe)2 CH(i-Bu)SCH2CF3
CH2CH(OMe)2 CH(i-Bu)S(O)Me
CH2CH(OMe)2 CH(i-Bu)S(O)Et
CH2CH(OMe)2 CH(i-Bu)S(O)CF3
CH2CH(OMe)2 CH(i-Bu)S(O)CH2CF3
CH2CH(OMe)2 CH(i-Bu)S(O)2Me
CH2CH(OMe)2 CH(i-Bu)S(O)2Et
CH2CH(OMe)2 CH(i-Bu)S(O)2CF3
CH2CH(OMe)2 CH(i-Bu)S(O)2CH2CF3
CH2CH(OMe)2 CH(s-Bu)SMe
CH2CH(OMe)2 CH(s-Bu)SEt
CH2CH(OMe)2 CH(s-Bu)SCF3
CH2CH(OMe)2 CH(s-Bu)SCH2CF3
CH2CH(OMe)2 CH(s-Bu)S(O)Me
CH2CH(OMe)2 CH(s-Bu)S(O)Et
CH2CH(OMe)2 CH(s-Bu)S(O)CF3
CH2CH(OMe)2 CH(s-Bu)S(O)CH2CF3
CH2CH(OMe)2 CH(s-Bu)S(O)2Me
CH2CH(OMe)2 CH(s-Bu)S(O)2Et
CH2CH(OMe)2 CH(s-Bu)S(O)2CF3
CH2CH(OMe)2 CH(s-Bu)S(O)2CH2CF3
CH2CH(OMe)2 CH(t-Bu)SMe
CH2CH(OMe)2 CH(t-Bu)SEt
CH2CH(OMe)2 CH(t-Bu)SCF3
CH2CH(OMe)2 CH(t-Bu)SCH2CF3
CH2CH(OMe)2 CH(t-Bu)S(O)Me
CH2CH(OMe)2 CH(t-Bu)S(O)Et
CH2CH(OMe)2 CH(t-Bu)S(O)CF3
CH2CH(OMe)2 CH(t-Bu)S(O)CH2CF3
CH2CH(OMe)2 CH(t-Bu)S(O)2Me
CH2CH(OMe)2 CH(t-Bu)S(O)2Et
CH2CH(OMe)2 CH(t-Bu)S(O)2CF3
CH2CH(OMe)2 CH(t-Bu)S(O)2CH2CF3
CH2CH(OMe)2 CH(CF3)SMe
CH2CH(OMe)2 CH(CF3)SEt
CH2CH(OMe)2 CH(CF3)SCF3
CH2CH(OMe)2 CH(CF3)SCH2CF3
CH2CH(OMe)2 CH(CF3)S(O)Me
CH2CH(OMe)2 CH(CF3)S(O)Et
CH2CH(OMe)2 CH(CF3)S(O)CF3
CH2CH(OMe)2 CH(CF3)S(O)CH2CF3
CH2CH(OMe)2 CH(CF3)S(O)2Me
CH2CH(OMe)2 CH(CF3)S(O)2Et
CH2CH(OMe)2 CH(CF3)S(O)2CF3
CH2CH(OMe)2 CH(CF3)S(O)2CH2CF3
CH2CH(OMe)2 CH2CH2SMe
CH2CH(OMe)2 CH2CH2SEt
CH2CH(OMe)2 CH2CH2SCF3
CH2CH(OMe)2 CH2CH2SCH2CF3
CH2CH(OMe)2 CH2CH2S(O)Me
CH2CH(OMe)2 CH2CH2S(O)Et
CH2CH(OMe)2 CH2CH2S(O)CF3
CH2CH(OMe)2 CH2CH2S(O)CH2CF3
CH2CH(OMe)2 CH2CH2S(O)2Me
CH2CH(OMe)2 CH2CH2S(O)2Et
CH2CH(OMe)2 CH2CH2S(O)2CF3
CH2CH(OMe)2 CH2CH2S(O)2CH2CF3
CH2CH(OMe)2 CH(Me)CH2SMe
CH2CH(OMe)2 CH(Me)CH2SEt
CH2CH(OMe)2 CH(Me)CH2SCF3
CH2CH(OMe)2 CH(Me)CH2SCH2CF3
CH2CH(OMe)2 CH(Me)CH2S(O)Me
CH2CH(OMe)2 CH(Me)CH2S(O)Et
CH2CH(OMe)2 CH(Me)CH2S(O)CF3
CH2CH(OMe)2 CH(Me)CH2S(O)CH2CF3
CH2CH(OMe)2 CH(Me)CH2S(O)2Me
CH2CH(OMe)2 CH(Me)CH2S(O)2Et
CH2CH(OMe)2 CH(Me)CH2S(O)2CF3
CH2CH(OMe)2 CH(Me)CH2S(O)2CH2CF3
CH2CH(OMe)2 CH(Et)CH2SMe
CH2CH(OMe)2 CH(Et)CH2SEt
CH2CH(OMe)2 CH(Et)CH2SCF3
CH2CH(OMe)2 CH(Et)CH2SCH2CF3
CH2CH(OMe)2 CH(Et)CH2S(O)Me
CH2CH(OMe)2 CH(Et)CH2S(O)Et
CH2CH(OMe)2 CH(Et)CH2S(O)CF3
CH2CH(OMe)2 CH(Et)CH2S(O)CH2CF3
CH2CH(OMe)2 CH(Et)CH2S(O)2Me
CH2CH(OMe)2 CH(Et)CH2S(O)2Et
CH2CH(OMe)2 CH(Et)CH2S(O)2CF3
CH2CH(OMe)2 CH(Et)CH2S(O)2CH2CF3
CH2CH(OMe)2 C(Me)2CH2SMe
CH2CH(OMe)2 C(Me)2CH2SEt
CH2CH(OMe)2 C(Me)2CH2SCF3
CH2CH(OMe)2 C(Me)2CH2SCH2CF3
CH2CH(OMe)2 C(Me)2CH2S(O)Me
CH2CH(OMe)2 C(Me)2CH2S(O)Et
CH2CH(OMe)2 C(Me)2CH2S(O)CF3
CH2CH(OMe)2 C(Me)2CH2S(O)CH2CF3
CH2CH(OMe)2 C(Me)2CH2S(O)2Me
CH2CH(OMe)2 C(Me)2CH2S(O)2Et
CH2CH(OMe)2 C(Me)2CH2S(O)2CF3
CH2CH(OMe)2 C(Me)2CH2S(O)2CH2CF3
CH2CH(OMe)2 CH2CH(Me)SMe
CH2CH(OMe)2 CH2CH(Me)SEt
CH2CH(OMe)2 CH2CH(Me)SCF3
CH2CH(OMe)2 CH2CH(Me)SCH2CF3
CH2CH(OMe)2 CH2CH(Me)S(O)Me
CH2CH(OMe)2 CH2CH(Me)S(O)Et
CH2CH(OMe)2 CH2CH(Me)S(O)CF3
CH2CH(OMe)2 CH2CH(Me)S(O)CH2CF3
CH2CH(OMe)2 CH2CH(Me)S(O)2Me
CH2CH(OMe)2 CH2CH(Me)S(O)2Et
CH2CH(OMe)2 CH2CH(Me)S(O)2CF3
CH2CH(OMe)2 CH2CH(Me)S(O)2CH2CF3
CH2CH(OMe)2 CH2CH(Et)SMe
CH2CH(OMe)2 CH2CH(Et)SEt
CH2CH(OMe)2 CH2CH(Et)SCF3
CH2CH(OMe)2 CH2CH(Et)SCH2CF3
CH2CH(OMe)2 CH2CH(Et)S(O)Me
CH2CH(OMe)2 CH2CH(Et)S(O)Et
CH2CH(OMe)2 CH2CH(Et)S(O)CF3
CH2CH(OMe)2 CH2CH(Et)S(O)CH2CF3
CH2CH(OMe)2 CH2CH(Et)S(O)2Me
CH2CH(OMe)2 CH2CH(Et)S(O)2Et
CH2CH(OMe)2 CH2CH(Et)S(O)2CF3
CH2CH(OMe)2 CH2CH(Et)S(O)2CH2CF3
CH2CH(OMe)2 CH(Me)CH(Me)SMe
CH2CH(OMe)2 CH(Me)CH(Me)SEt
CH2CH(OMe)2 CH(Me)CH(Me)SCF3
CH2CH(OMe)2 CH(Me)CH(Me)SCH2CF3
CH2CH(OMe)2 CH(Me)CH(Me)S(O)Me
CH2CH(OMe)2 CH(Me)CH(Me)S(O)Et
CH2CH(OMe)2 CH(Me)CH(Me)S(O)CF3
CH2CH(OMe)2 CH(Me)CH(Me)S(O)CH2CF3
CH2CH(OMe)2 CH(Me)CH(Me)S(O)2Me
CH2CH(OMe)2 CH(Me)CH(Me)S(O)2Et
CH2CH(OMe)2 CH(Me)CH(Me)S(O)2CF3
CH2CH(OMe)2 CH(Me)CH(Me)S(O)2CH2CF3
CH(Me)OEt CH2SMe
CH(Me)OEt CH2SEt
CH(Me)OEt CH2SCF3
CH(Me)OEt CH2SCH2CF3
CH(Me)OEt CH2S(O)Me
CH(Me)OEt CH2S(O)Et
CH(Me)OEt CH2S(O)CF3
CH(Me)OEt CH2S(O)CH2CF3
CH(Me)OEt CH2S(O)2Me
CH(Me)OEt CH2S(O)2Et
CH(Me)OEt CH2S(O)2CF3
CH(Me)OEt CH2S(O)2CH2CF3
CH(Me)OEt CH(Me)SMe
CH(Me)OEt CH(Me)SEt
CH(Me)OEt CH(Me)SCF3
CH(Me)OEt CH(Me)SCH2CF3
CH(Me)OEt CH(Me)S(O)Me
CH(Me)OEt CH(Me)S(O)Et
CH(Me)OEt CH(Me)S(O)CF3
CH(Me)OEt CH(Me)S(O)CH2CF3
CH(Me)OEt CH(Me)S(O)2Me
CH(Me)OEt CH(Me)S(O)2Et
CH(Me)OEt CH(Me)S(O)2CF3
CH(Me)OEt CH(Me)S(O)2CH2CF3
CH(Me)OEt CH(Et)SMe
CH(Me)OEt CH(Et)SEt
CH(Me)OEt CH(Et)SCF3
CH(Me)OEt CH(Et)SCH2CF3
CH(Me)OEt CH(Et)S(O)Me
CH(Me)OEt CH(Et)S(O)Et
CH(Me)OEt CH(Et)S(O)CF3
CH(Me)OEt CH(Et)S(O)CH2CF3
CH(Me)OEt CH(Et)S(O)2Me
CH(Me)OEt CH(Et)S(O)2Et
CH(Me)OEt CH(Et)S(O)2CF3
CH(Me)OEt CH(Et)S(O)2CH2CF3
CH(Me)OEt CH(n-Pr)SMe
CH(Me)OEt CH(n-Pr)SEt
CH(Me)OEt CH(n-Pr)SCF3
CH(Me)OEt CH(n-Pr)SCH2CF3
CH(Me)OEt CH(n-Pr)S(O)Me
CH(Me)OEt CH(n-Pr)S(O)Et
CH(Me)OEt CH(n-Pr)S(O)CF3
CH(Me)OEt CH(n-Pr)S(O)CH2CF3
CH(Me)OEt CH(n-Pr)S(O)2Me
CH(Me)OEt CH(n-Pr)S(O)2Et
CH(Me)OEt CH(n-Pr)S(O)2CF3
CH(Me)OEt CH(n-Pr)S(O)2CH2CF3
CH(Me)OEt CH(i-Pr)SMe
CH(Me)OEt CH(i-Pr)SEt
CH(Me)OEt CH(i-Pr)SCF3
CH(Me)OEt CH(i-Pr)SCH2CF3
CH(Me)OEt CH(i-Pr)S(O)Me
CH(Me)OEt CH(i-Pr)S(O)Et
CH(Me)OEt CH(i-Pr)S(O)CF3
CH(Me)OEt CH(i-Pr)S(O)CH2CF3
CH(Me)OEt CH(i-Pr)S(O)2Me
CH(Me)OEt CH(i-Pr)S(O)2Et
CH(Me)OEt CH(i-Pr)S(O)2CF3
CH(Me)OEt CH(i-Pr)S(O)2CH2CF3
CH(Me)OEt CH(n-Bu)SMe
CH(Me)OEt CH(n-Bu)SEt
CH(Me)OEt CH(n-Bu)SCF3
CH(Me)OEt CH(n-Bu)SCH2CF3
CH(Me)OEt CH(n-Bu)S(O)Me
CH(Me)OEt CH(n-Bu)S(O)Et
CH(Me)OEt CH(n-Bu)S(O)CF3
CH(Me)OEt CH(n-Bu)S(O)CH2CF3
CH(Me)OEt CH(n-Bu)S(O)2Me
CH(Me)OEt CH(n-Bu)S(O)2Et
CH(Me)OEt CH(n-Bu)S(O)2CF3
CH(Me)OEt CH(n-Bu)S(O)2CH2CF3
CH(Me)OEt CH(i-Bu)SMe
CH(Me)OEt CH(i-Bu)SEt
CH(Me)OEt CH(i-Bu)SCF3
CH(Me)OEt CH(i-Bu)SCH2CF3
CH(Me)OEt CH(i-Bu)S(O)Me
CH(Me)OEt CH(i-Bu)S(O)Et
CH(Me)OEt CH(i-Bu)S(O)CF3
CH(Me)OEt CH(i-Bu)S(O)CH2CF3
CH(Me)OEt CH(i-Bu)S(O)2Me
CH(Me)OEt CH(i-Bu)S(O)2Et
CH(Me)OEt CH(i-Bu)S(O)2CF3
CH(Me)OEt CH(i-Bu)S(O)2CH2CF3
CH(Me)OEt CH(s-Bu)SMe
CH(Me)OEt CH(s-Bu)SEt
CH(Me)OEt CH(s-Bu)SCF3
CH(Me)OEt CH(s-Bu)SCH2CF3
CH(Me)OEt CH(s-Bu)S(O)Me
CH(Me)OEt CH(s-Bu)S(O)Et
CH(Me)OEt CH(s-Bu)S(O)CF3
CH(Me)OEt CH(s-Bu)S(O)CH2CF3
CH(Me)OEt CH(s-Bu)S(O)2Me
CH(Me)OEt CH(s-Bu)S(O)2Et
CH(Me)OEt CH(s-Bu)S(O)2CF3
CH(Me)OEt CH(s-Bu)S(O)2CH2CF3
CH(Me)OEt CH(t-Bu)SMe
CH(Me)OEt CH(t-Bu)SEt
CH(Me)OEt CH(t-Bu)SCF3
CH(Me)OEt CH(t-Bu)SCH2CF3
CH(Me)OEt CH(t-Bu)S(O)Me
CH(Me)OEt CH(t-Bu)S(O)Et
CH(Me)OEt CH(t-Bu)S(O)CF3
CH(Me)OEt CH(t-Bu)S(O)CH2CF3
CH(Me)OEt CH(t-Bu)S(O)2Me
CH(Me)OEt CH(t-Bu)S(O)2Et
CH(Me)OEt CH(t-Bu)S(O)2CF3
CH(Me)OEt CH(t-Bu)S(O)2CH2CF3
CH(Me)OEt CH(CF3)SMe
CH(Me)OEt CH(CF3)SEt
CH(Me)OEt CH(CF3)SCF3
CH(Me)OEt CH(CF3)SCH2CF3
CH(Me)OEt CH(CF3)S(O)Me
CH(Me)OEt CH(CF3)S(O)Et
CH(Me)OEt CH(CF3)S(O)CF3
CH(Me)OEt CH(CF3)S(O)CH2CF3
CH(Me)OEt CH(CF3)S(O)2Me
CH(Me)OEt CH(CF3)S(O)2Et
CH(Me)OEt CH(CF3)S(O)2CF3
CH(Me)OEt CH(CF3)S(O)2CH2CF3
CH(Me)OEt CH2CH2SMe
CH(Me)OEt CH2CH2SEt
CH(Me)OEt CH2CH2SCF3
CH(Me)OEt CH2CH2SCH2CF3
CH(Me)OEt CH2CH2S(O)Me
CH(Me)OEt CH2CH2S(O)Et
CH(Me)OEt CH2CH2S(O)CF3
CH(Me)OEt CH2CH2S(O)CH2CF3
CH(Me)OEt CH2CH2S(O)2Me
CH(Me)OEt CH2CH2S(O)2Et
CH(Me)OEt CH2CH2S(O)2CF3
CH(Me)OEt CH2CH2S(O)2CH2CF3
CH(Me)OEt CH(Me)CH2SMe
CH(Me)OEt CH(Me)CH2SEt
CH(Me)OEt CH(Me)CH2SCF3
CH(Me)OEt CH(Me)CH2SCH2CF3
CH(Me)OEt CH(Me)CH2S(O)Me
CH(Me)OEt CH(Me)CH2S(O)Et
CH(Me)OEt CH(Me)CH2S(O)CF3
CH(Me)OEt CH(Me)CH2S(O)CH2CF3
CH(Me)OEt CH(Me)CH2S(O)2Me
CH(Me)OEt CH(Me)CH2S(O)2Et
CH(Me)OEt CH(Me)CH2S(O)2CF3
CH(Me)OEt CH(Me)CH2S(O)2CH2CF3
CH(Me)OEt CH(Et)CH2SMe
CH(Me)OEt CH(Et)CH2SEt
CH(Me)OEt CH(Et)CH2SCF3
CH(Me)OEt CH(Et)CH2SCH2CF3
CH(Me)OEt CH(Et)CH2S(O)Me
CH(Me)OEt CH(Et)CH2S(O)Et
CH(Me)OEt CH(Et)CH2S(O)CF3
CH(Me)OEt CH(Et)CH2S(O)CH2CF3
CH(Me)OEt CH(Et)CH2S(O)2Me
CH(Me)OEt CH(Et)CH2S(O)2Et
CH(Me)OEt CH(Et)CH2S(O)2CF3
CH(Me)OEt CH(Et)CH2S(O)2CH2CF3
CH(Me)OEt C(Me)2CH2SMe
CH(Me)OEt C(Me)2CH2SEt
CH(Me)OEt C(Me)2CH2SCF3
CH(Me)OEt C(Me)2CH2SCH2CF3
CH(Me)OEt C(Me)2CH2S(O)Me
CH(Me)OEt C(Me)2CH2S(O)Et
CH(Me)OEt C(Me)2CH2S(O)CF3
CH(Me)OEt C(Me)2CH2S(O)CH2CF3
CH(Me)OEt C(Me)2CH2S(O)2Me
CH(Me)OEt C(Me)2CH2S(O)2Et
CH(Me)OEt C(Me)2CH2S(O)2CF3
CH(Me)OEt C(Me)2CH2S(O)2CH2CF3
CH(Me)OEt CH2CH(Me)SMe
CH(Me)OEt CH2CH(Me)SEt
CH(Me)OEt CH2CH(Me)SCF3
CH(Me)OEt CH2CH(Me)SCH2CF3
CH(Me)OEt CH2CH(Me)S(O)Me
CH(Me)OEt CH2CH(Me)S(O)Et
CH(Me)OEt CH2CH(Me)S(O)CF3
CH(Me)OEt CH2CH(Me)S(O)CH2CF3
CH(Me)OEt CH2CH(Me)S(O)2Me
CH(Me)OEt CH2CH(Me)S(O)2Et
CH(Me)OEt CH2CH(Me)S(O)2CF3
CH(Me)OEt CH2CH(Me)S(O)2CH2CF3
CH(Me)OEt CH2CH(Et)SMe
CH(Me)OEt CH2CH(Et)SEt
CH(Me)OEt CH2CH(Et)SCF3
CH(Me)OEt CH2CH(Et)SCH2CF3
CH(Me)OEt CH2CH(Et)S(O)Me
CH(Me)OEt CH2CH(Et)S(O)Et
CH(Me)OEt CH2CH(Et)S(O)CF3
CH(Me)OEt CH2CH(Et)S(O)CH2CF3
CH(Me)OEt CH2CH(Et)S(O)2Me
CH(Me)OEt CH2CH(Et)S(O)2Et
CH(Me)OEt CH2CH(Et)S(O)2CF3
CH(Me)OEt CH2CH(Et)S(O)2CH2CF3
CH(Me)OEt CH(Me)CH(Me)SMe
CH(Me)OEt CH(Me)CH(Me)SEt
CH(Me)OEt CH(Me)CH(Me)SCF3
CH(Me)OEt CH(Me)CH(Me)SCH2CF3
CH(Me)OEt CH(Me)CH(Me)S(O)Me
CH(Me)OEt CH(Me)CH(Me)S(O)Et
CH(Me)OEt CH(Me)CH(Me)S(O)CF3
CH(Me)OEt CH(Me)CH(Me)S(O)CH2CF3
CH(Me)OEt CH(Me)CH(Me)S(O)2Me
CH(Me)OEt CH(Me)CH(Me)S(O)2Et
CH(Me)OEt CH(Me)CH(Me)S(O)2CF3
CH(Me)OEt CH(Me)CH(Me)S(O)2CH2CF3
S(O)2Me CH2SMe
S(O)2Me CH2SEt
S(O)2Me CH2SCF3
S(O)2Me CH2SCH2CF3
S(O)2Me CH2S(O)Me
S(O)2Me CH2S(O)Et
S(O)2Me CH2S(O)CF3
S(O)2Me CH2S(O)CH2CF3
S(O)2Me CH2S(O)2Me
S(O)2Me CH2S(O)2Et
S(O)2Me CH2S(O)2CF3
S(O)2Me CH2S(O)2CH2CF3
S(O)2Me CH(Me)SMe
S(O)2Me CH(Me)SEt
S(O)2Me CH(Me)SCF3
S(O)2Me CH(Me)SCH2CF3
S(O)2Me CH(Me)S(O)Me
S(O)2Me CH(Me)S(O)Et
S(O)2Me CH(Me)S(O)CF3
S(O)2Me CH(Me)S(O)CH2CF3
S(O)2Me CH(Me)S(O)2Me
S(O)2Me CH(Me)S(O)2Et
S(O)2Me CH(Me)S(O)2CF3
S(O)2Me CH(Me)S(O)2CH2CF3
S(O)2Me CH(Et)SMe
S(O)2Me CH(Et)SEt
S(O)2Me CH(Et)SCF3
S(O)2Me CH(Et)SCH2CF3
S(O)2Me CH(Et)S(O)Me
S(O)2Me CH(Et)S(O)Et
S(O)2Me CH(Et)S(O)CF3
S(O)2Me CH(Et)S(O)CH2CF3
S(O)2Me CH(Et)S(O)2Me
S(O)2Me CH(Et)S(O)2Et
S(O)2Me CH(Et)S(O)2CF3
S(O)2Me CH(Et)S(O)2CH2CF3
S(O)2Me CH(n-Pr)SMe
S(O)2Me CH(n-Pr)SEt
S(O)2Me CH(n-Pr)SCF3
S(O)2Me CH(n-Pr)SCH2CF3
S(O)2Me CH(n-Pr)S(O)Me
S(O)2Me CH(n-Pr)S(O)Et
S(O)2Me CH(n-Pr)S(O)CF3
S(O)2Me CH(n-Pr)S(O)CH2CF3
S(O)2Me CH(n-Pr)S(O)2Me
S(O)2Me CH(n-Pr)S(O)2Et
S(O)2Me CH(n-Pr)S(O)2CF3
S(O)2Me CH(n-Pr)S(O)2CH2CF3
S(O)2Me CH(i-Pr)SMe
S(O)2Me CH(i-Pr)SEt
S(O)2Me CH(i-Pr)SCF3
S(O)2Me CH(i-Pr)SCH2CF3
S(O)2Me CH(i-Pr)S(O)Me
S(O)2Me CH(i-Pr)S(O)Et
S(O)2Me CH(i-Pr)S(O)CF3
S(O)2Me CH(i-Pr)S(O)CH2CF3
S(O)2Me CH(i-Pr)S(O)2Me
S(O)2Me CH(i-Pr)S(O)2Et
S(O)2Me CH(i-Pr)S(O)2CF3
S(O)2Me CH(i-Pr)S(O)2CH2CF3
S(O)2Me CH(n-Bu)SMe
S(O)2Me CH(n-Bu)SEt
S(O)2Me CH(n-Bu)SCF3
S(O)2Me CH(n-Bu)SCH2CF3
S(O)2Me CH(n-Bu)S(O)Me
S(O)2Me CH(n-Bu)S(O)Et
S(O)2Me CH(n-Bu)S(O)CF3
S(O)2Me CH(n-Bu)S(O)CH2CF3
S(O)2Me CH(n-Bu)S(O)2Me
S(O)2Me CH(n-Bu)S(O)2Et
S(O)2Me CH(n-Bu)S(O)2CF3
S(O)2Me CH(n-Bu)S(O)2CH2CF3
S(O)2Me CH(i-Bu)SMe
S(O)2Me CH(i-Bu)SEt
S(O)2Me CH(i-Bu)SCF3
S(O)2Me CH(i-Bu)SCH2CF3
S(O)2Me CH(i-Bu)S(O)Me
S(O)2Me CH(i-Bu)S(O)Et
S(O)2Me CH(i-Bu)S(O)CF3
S(O)2Me CH(i-Bu)S(O)CH2CF3
S(O)2Me CH(i-Bu)S(O)2Me
S(O)2Me CH(i-Bu)S(O)2Et
S(O)2Me CH(i-Bu)S(O)2CF3
S(O)2Me CH(i-Bu)S(O)2CH2CF3
S(O)2Me CH(s-Bu)SMe
S(O)2Me CH(s-Bu)SEt
S(O)2Me CH(s-Bu)SCF3
S(O)2Me CH(s-Bu)SCH2CF3
S(O)2Me CH(s-Bu)S(O)Me
S(O)2Me CH(s-Bu)S(O)Et
S(O)2Me CH(s-Bu)S(O)CF3
S(O)2Me CH(s-Bu)S(O)CH2CF3
S(O)2Me CH(s-Bu)S(O)2Me
S(O)2Me CH(s-Bu)S(O)2Et
S(O)2Me CH(s-Bu)S(O)2CF3
S(O)2Me CH(s-Bu)S(O)2CH2CF3
S(O)2Me CH(t-Bu)SMe
S(O)2Me CH(t-Bu)SEt
S(O)2Me CH(t-Bu)SCF3
S(O)2Me CH(t-Bu)SCH2CF3
S(O)2Me CH(t-Bu)S(O)Me
S(O)2Me CH(t-Bu)S(O)Et
S(O)2Me CH(t-Bu)S(O)CF3
S(O)2Me CH(t-Bu)S(O)CH2CF3
S(O)2Me CH(t-Bu)S(O)2Me
S(O)2Me CH(t-Bu)S(O)2Et
S(O)2Me CH(t-Bu)S(O)2CF3
S(O)2Me CH(t-Bu)S(O)2CH2CF3
S(O)2Me CH(CF3)SMe
S(O)2Me CH(CF3)SEt
S(O)2Me CH(CF3)SCF3
S(O)2Me CH(CF3)SCH2CF3
S(O)2Me CH(CF3)S(O)Me
S(O)2Me CH(CF3)S(O)Et
S(O)2Me CH(CF3)S(O)CF3
S(O)2Me CH(CF3)S(O)CH2CF3
S(O)2Me CH(CF3)S(O)2Me
S(O)2Me CH(CF3)S(O)2Et
S(O)2Me CH(CF3)S(O)2CF3
S(O)2Me CH(CF3)S(O)2CH2CF3
S(O)2Me CH2CH2SMe
S(O)2Me CH2CH2SEt
S(O)2Me CH2CH2SCF3
S(O)2Me CH2CH2SCH2CF3
S(O)2Me CH2CH2S(O)Me
S(O)2Me CH2CH2S(O)Et
S(O)2Me CH2CH2S(O)CF3
S(O)2Me CH2CH2S(O)CH2CF3
S(O)2Me CH2CH2S(O)2Me
S(O)2Me CH2CH2S(O)2Et
S(O)2Me CH2CH2S(O)2CF3
S(O)2Me CH2CH2S(O)2CH2CF3
S(O)2Me CH(Me)CH2SMe
S(O)2Me CH(Me)CH2SEt
S(O)2Me CH(Me)CH2SCF3
S(O)2Me CH(Me)CH2SCH2CF3
S(O)2Me CH(Me)CH2S(O)Me
S(O)2Me CH(Me)CH2S(O)Et
S(O)2Me CH(Me)CH2S(O)CF3
S(O)2Me CH(Me)CH2S(O)CH2CF3
S(O)2Me CH(Me)CH2S(O)2Me
S(O)2Me CH(Me)CH2S(O)2Et
S(O)2Me CH(Me)CH2S(O)2CF3
S(O)2Me CH(Me)CH2S(O)2CH2CF3
S(O)2Me CH(Et)CH2SMe
S(O)2Me CH(Et)CH2SEt
S(O)2Me CH(Et)CH2SCF3
S(O)2Me CH(Et)CH2SCH2CF3
S(O)2Me CH(Et)CH2S(O)Me
S(O)2Me CH(Et)CH2S(O)Et
S(O)2Me CH(Et)CH2S(O)CF3
S(O)2Me CH(Et)CH2S(O)CH2CF3
S(O)2Me CH(Et)CH2S(O)2Me
S(O)2Me CH(Et)CH2S(O)2Et
S(O)2Me CH(Et)CH2S(O)2CF3
S(O)2Me CH(Et)CH2S(O)2CH2CF3
S(O)2Me C(Me)2CH2SMe
S(O)2Me C(Me)2CH2SEt
S(O)2Me C(Me)2CH2SCF3
S(O)2Me C(Me)2CH2SCH2CF3
S(O)2Me C(Me)2CH2S(O)Me
S(O)2Me C(Me)2CH2S(O)Et
S(O)2Me C(Me)2CH2S(O)CF3
S(O)2Me C(Me)2CH2S(O)CH2CF3
S(O)2Me C(Me)2CH2S(O)2Me
S(O)2Me C(Me)2CH2S(O)2Et
S(O)2Me C(Me)2CH2S(O)2CF3
S(O)2Me C(Me)2CH2S(O)2CH2CF3
S(O)2Me CH2CH(Me)SMe
S(O)2Me CH2CH(Me)SEt
S(O)2Me CH2CH(Me)SCF3
S(O)2Me CH2CH(Me)SCH2CF3
S(O)2Me CH2CH(Me)S(O)Me
S(O)2Me CH2CH(Me)S(O)Et
S(O)2Me CH2CH(Me)S(O)CF3
S(O)2Me CH2CH(Me)S(O)CH2CF3
S(O)2Me CH2CH(Me)S(O)2Me
S(O)2Me CH2CH(Me)S(O)2Et
S(O)2Me CH2CH(Me)S(O)2CF3
S(O)2Me CH2CH(Me)S(O)2CH2CF3
S(O)2Me CH2CH(Et)SMe
S(O)2Me CH2CH(Et)SEt
S(O)2Me CH2CH(Et)SCF3
S(O)2Me CH2CH(Et)SCH2CF3
S(O)2Me CH2CH(Et)S(O)Me
S(O)2Me CH2CH(Et)S(O)Et
S(O)2Me CH2CH(Et)S(O)CF3
S(O)2Me CH2CH(Et)S(O)CH2CF3
S(O)2Me CH2CH(Et)S(O)2Me
S(O)2Me CH2CH(Et)S(O)2Et
S(O)2Me CH2CH(Et)S(O)2CF3
S(O)2Me CH2CH(Et)S(O)2CH2CF3
S(O)2Me CH(Me)CH(Me)SMe
S(O)2Me CH(Me)CH(Me)SEt
S(O)2Me CH(Me)CH(Me)SCF3
S(O)2Me CH(Me)CH(Me)SCH2CF3
S(O)2Me CH(Me)CH(Me)S(O)Me
S(O)2Me CH(Me)CH(Me)S(O)Et
S(O)2Me CH(Me)CH(Me)S(O)CF3
S(O)2Me CH(Me)CH(Me)S(O)CH2CF3
S(O)2Me CH(Me)CH(Me)S(O)2Me
S(O)2Me CH(Me)CH(Me)S(O)2Et
S(O)2Me CH(Me)CH(Me)S(O)2CF3
S(O)2Me CH(Me)CH(Me)S(O)2CH2CF3
D2-32a CH2SMe
D2-32a CH2SEt
D2-32a CH2SCF3
D2-32a CH2SCH2CF3
D2-32a CH2S(O)Me
D2-32a CH2S(O)Et
D2-32a CH2S(O)CF3
D2-32a CH2S(O)CH2CF3
D2-32a CH2S(O)2Me
D2-32a CH2S(O)2Et
D2-32a CH2S(O)2CF3
D2-32a CH2S(O)2CH2CF3
D2-32a CH(Me)SMe
D2-32a CH(Me)SEt
D2-32a CH(Me)SCF3
D2-32a CH(Me)SCH2CF3
D2-32a CH(Me)S(O)Me
D2-32a CH(Me)S(O)Et
D2-32a CH(Me)S(O)CF3
D2-32a CH(Me)S(O)CH2CF3
D2-32a CH(Me)S(O)2Me
D2-32a CH(Me)S(O)2Et
D2-32a CH(Me)S(O)2CF3
D2-32a CH(Me)S(O)2CH2CF3
D2-32a CH(Et)SMe
D2-32a CH(Et)SEt
D2-32a CH(Et)SCF3
D2-32a CH(Et)SCH2CF3
D2-32a CH(Et)S(O)Me
D2-32a CH(Et)S(O)Et
D2-32a CH(Et)S(O)CF3
D2-32a CH(Et)S(O)CH2CF3
D2-32a CH(Et)S(O)2Me
D2-32a CH(Et)S(O)2Et
D2-32a CH(Et)S(O)2CF3
D2-32a CH(Et)S(O)2CH2CF3
D2-32a CH(n-Pr)SMe
D2-32a CH(n-Pr)SEt
D2-32a CH(n-Pr)SCF3
D2-32a CH(n-Pr)SCH2CF3
D2-32a CH(n-Pr)S(O)Me
D2-32a CH(n-Pr)S(O)Et
D2-32a CH(n-Pr)S(O)CF3
D2-32a CH(n-Pr)S(O)CH2CF3
D2-32a CH(n-Pr)S(O)2Me
D2-32a CH(n-Pr)S(O)2Et
D2-32a CH(n-Pr)S(O)2CF3
D2-32a CH(n-Pr)S(O)2CH2CF3
D2-32a CH(i-Pr)SMe
D2-32a CH(i-Pr)SEt
D2-32a CH(i-Pr)SCF3
D2-32a CH(i-Pr)SCH2CF3
D2-32a CH(i-Pr)S(O)Me
D2-32a CH(i-Pr)S(O)Et
D2-32a CH(i-Pr)S(O)CF3
D2-32a CH(i-Pr)S(O)CH2CF3
D2-32a CH(i-Pr)S(O)2Me
D2-32a CH(i-Pr)S(O)2Et
D2-32a CH(i-Pr)S(O)2CF3
D2-32a CH(i-Pr)S(O)2CH2CF3
D2-32a CH(n-Bu)SMe
D2-32a CH(n-Bu)SEt
D2-32a CH(n-Bu)SCF3
D2-32a CH(n-Bu)SCH2CF3
D2-32a CH(n-Bu)S(O)Me
D2-32a CH(n-Bu)S(O)Et
D2-32a CH(n-Bu)S(O)CF3
D2-32a CH(n-Bu)S(O)CH2CF3
D2-32a CH(n-Bu)S(O)2Me
D2-32a CH(n-Bu)S(O)2Et
D2-32a CH(n-Bu)S(O)2CF3
D2-32a CH(n-Bu)S(O)2CH2CF3
D2-32a CH(i-Bu)SMe
D2-32a CH(i-Bu)SEt
D2-32a CH(i-Bu)SCF3
D2-32a CH(i-Bu)SCH2CF3
D2-32a CH(i-Bu)S(O)Me
D2-32a CH(i-Bu)S(O)Et
D2-32a CH(i-Bu)S(O)CF3
D2-32a CH(i-Bu)S(O)CH2CF3
D2-32a CH(i-Bu)S(O)2Me
D2-32a CH(i-Bu)S(O)2Et
D2-32a CH(i-Bu)S(O)2CF3
D2-32a CH(i-Bu)S(O)2CH2CF3
D2-32a CH(s-Bu)SMe
D2-32a CH(s-Bu)SEt
D2-32a CH(s-Bu)SCF3
D2-32a CH(s-Bu)SCH2CF3
D2-32a CH(s-Bu)S(O)Me
D2-32a CH(s-Bu)S(O)Et
D2-32a CH(s-Bu)S(O)CF3
D2-32a CH(s-Bu)S(O)CH2CF3
D2-32a CH(s-Bu)S(O)2Me
D2-32a CH(s-Bu)S(O)2Et
D2-32a CH(s-Bu)S(O)2CF3
D2-32a CH(s-Bu)S(O)2CH2CF3
D2-32a CH(t-Bu)SMe
D2-32a CH(t-Bu)SEt
D2-32a CH(t-Bu)SCF3
D2-32a CH(t-Bu)SCH2CF3
D2-32a CH(t-Bu)S(O)Me
D2-32a CH(t-Bu)S(O)Et
D2-32a CH(t-Bu)S(O)CF3
D2-32a CH(t-Bu)S(O)CH2CF3
D2-32a CH(t-Bu)S(O)2Me
D2-32a CH(t-Bu)S(O)2Et
D2-32a CH(t-Bu)S(O)2CF3
D2-32a CH(t-Bu)S(O)2CH2CF3
D2-32a CH(CF3)SMe
D2-32a CH(CF3)SEt
D2-32a CH(CF3)SCF3
D2-32a CH(CF3)SCH2CF3
D2-32a CH(CF3)S(O)Me
D2-32a CH(CF3)S(O)Et
D2-32a CH(CF3)S(O)CF3
D2-32a CH(CF3)S(O)CH2CF3
D2-32a CH(CF3)S(O)2Me
D2-32a CH(CF3)S(O)2Et
D2-32a CH(CF3)S(O)2CF3
D2-32a CH(CF3)S(O)2CH2CF3
D2-32a CH2CH2SMe
D2-32a CH2CH2SEt
D2-32a CH2CH2SCF3
D2-32a CH2CH2SCH2CF3
D2-32a CH2CH2S(O)Me
D2-32a CH2CH2S(O)Et
D2-32a CH2CH2S(O)CF3
D2-32a CH2CH2S(O)CH2CF3
D2-32a CH2CH2S(O)2Me
D2-32a CH2CH2S(O)2Et
D2-32a CH2CH2S(O)2CF3
D2-32a CH2CH2S(O)2CH2CF3
D2-32a CH(Me)CH2SMe
D2-32a CH(Me)CH2SEt
D2-32a CH(Me)CH2SCF3
D2-32a CH(Me)CH2SCH2CF3
D2-32a CH(Me)CH2S(O)Me
D2-32a CH(Me)CH2S(O)Et
D2-32a CH(Me)CH2S(O)CF3
D2-32a CH(Me)CH2S(O)CH2CF3
D2-32a CH(Me)CH2S(O)2Me
D2-32a CH(Me)CH2S(O)2Et
D2-32a CH(Me)CH2S(O)2CF3
D2-32a CH(Me)CH2S(O)2CH2CF3
D2-32a CH(Et)CH2SMe
D2-32a CH(Et)CH2SEt
D2-32a CH(Et)CH2SCF3
D2-32a CH(Et)CH2SCH2CF3
D2-32a CH(Et)CH2S(O)Me
D2-32a CH(Et)CH2S(O)Et
D2-32a CH(Et)CH2S(O)CF3
D2-32a CH(Et)CH2S(O)CH2CF3
D2-32a CH(Et)CH2S(O)2Me
D2-32a CH(Et)CH2S(O)2Et
D2-32a CH(Et)CH2S(O)2CF3
D2-32a CH(Et)CH2S(O)2CH2CF3
D2-32a C(Me)2CH2SMe
D2-32a C(Me)2CH2SEt
D2-32a C(Me)2CH2SCF3
D2-32a C(Me)2CH2SCH2CF3
D2-32a C(Me)2CH2S(O)Me
D2-32a C(Me)2CH2S(O)Et
D2-32a C(Me)2CH2S(O)CF3
D2-32a C(Me)2CH2S(O)CH2CF3
D2-32a C(Me)2CH2S(O)2Me
D2-32a C(Me)2CH2S(O)2Et
D2-32a C(Me)2CH2S(O)2CF3
D2-32a C(Me)2CH2S(O)2CH2CF3
D2-32a CH2CH(Me)SMe
D2-32a CH2CH(Me)SEt
D2-32a CH2CH(Me)SCF3
D2-32a CH2CH(Me)SCH2CF3
D2-32a CH2CH(Me)S(O)Me
D2-32a CH2CH(Me)S(O)Et
D2-32a CH2CH(Me)S(O)CF3
D2-32a CH2CH(Me)S(O)CH2CF3
D2-32a CH2CH(Me)S(O)2Me
D2-32a CH2CH(Me)S(O)2Et
D2-32a CH2CH(Me)S(O)2CF3
D2-32a CH2CH(Me)S(O)2CH2CF3
D2-32a CH2CH(Et)SMe
D2-32a CH2CH(Et)SEt
D2-32a CH2CH(Et)SCF3
D2-32a CH2CH(Et)SCH2CF3
D2-32a CH2CH(Et)S(O)Me
D2-32a CH2CH(Et)S(O)Et
D2-32a CH2CH(Et)S(O)CF3
D2-32a CH2CH(Et)S(O)CH2CF3
D2-32a CH2CH(Et)S(O)2Me
D2-32a CH2CH(Et)S(O)2Et
D2-32a CH2CH(Et)S(O)2CF3
D2-32a CH2CH(Et)S(O)2CH2CF3
D2-32a CH(Me)CH(Me)SMe
D2-32a CH(Me)CH(Me)SEt
D2-32a CH(Me)CH(Me)SCF3
D2-32a CH(Me)CH(Me)SCH2CF3
D2-32a CH(Me)CH(Me)S(O)Me
D2-32a CH(Me)CH(Me)S(O)Et
D2-32a CH(Me)CH(Me)S(O)CF3
D2-32a CH(Me)CH(Me)S(O)CH2CF3
D2-32a CH(Me)CH(Me)S(O)2Me
D2-32a CH(Me)CH(Me)S(O)2Et
D2-32a CH(Me)CH(Me)S(O)2CF3
D2-32a CH(Me)CH(Me)S(O)2CH2CF3
D2-33a CH2SMe
D2-33a CH2SEt
D2-33a CH2SCF3
D2-33a CH2SCH2CF3
D2-33a CH2S(O)Me
D2-33a CH2S(O)Et
D2-33a CH2S(O)CF3
D2-33a CH2S(O)CH2CF3
D2-33a CH2S(O)2Me
D2-33a CH2S(O)2Et
D2-33a CH2S(O)2CF3
D2-33a CH2S(O)2CH2CF3
D2-33a CH(Me)SMe
D2-33a CH(Me)SEt
D2-33a CH(Me)SCF3
D2-33a CH(Me)SCH2CF3
D2-33a CH(Me)S(O)Me
D2-33a CH(Me)S(O)Et
D2-33a CH(Me)S(O)CF3
D2-33a CH(Me)S(O)CH2CF3
D2-33a CH(Me)S(O)2Me
D2-33a CH(Me)S(O)2Et
D2-33a CH(Me)S(O)2CF3
D2-33a CH(Me)S(O)2CH2CF3
D2-33a CH(Et)SMe
D2-33a CH(Et)SEt
D2-33a CH(Et)SCF3
D2-33a CH(Et)SCH2CF3
D2-33a CH(Et)S(O)Me
D2-33a CH(Et)S(O)Et
D2-33a CH(Et)S(O)CF3
D2-33a CH(Et)S(O)CH2CF3
D2-33a CH(Et)S(O)2Me
D2-33a CH(Et)S(O)2Et
D2-33a CH(Et)S(O)2CF3
D2-33a CH(Et)S(O)2CH2CF3
D2-33a CH(n-Pr)SMe
D2-33a CH(n-Pr)SEt
D2-33a CH(n-Pr)SCF3
D2-33a CH(n-Pr)SCH2CF3
D2-33a CH(n-Pr)S(O)Me
D2-33a CH(n-Pr)S(O)Et
D2-33a CH(n-Pr)S(O)CF3
D2-33a CH(n-Pr)S(O)CH2CF3
D2-33a CH(n-Pr)S(O)2Me
D2-33a CH(n-Pr)S(O)2Et
D2-33a CH(n-Pr)S(O)2CF3
D2-33a CH(n-Pr)S(O)2CH2CF3
D2-33a CH(i-Pr)SMe
D2-33a CH(i-Pr)SEt
D2-33a CH(i-Pr)SCF3
D2-33a CH(i-Pr)SCH2CF3
D2-33a CH(i-Pr)S(O)Me
D2-33a CH(i-Pr)S(O)Et
D2-33a CH(i-Pr)S(O)CF3
D2-33a CH(i-Pr)S(O)CH2CF3
D2-33a CH(i-Pr)S(O)2Me
D2-33a CH(i-Pr)S(O)2Et
D2-33a CH(i-Pr)S(O)2CF3
D2-33a CH(i-Pr)S(O)2CH2CF3
D2-33a CH(n-Bu)SMe
D2-33a CH(n-Bu)SEt
D2-33a CH(n-Bu)SCF3
D2-33a CH(n-Bu)SCH2CF3
D2-33a CH(n-Bu)S(O)Me
D2-33a CH(n-Bu)S(O)Et
D2-33a CH(n-Bu)S(O)CF3
D2-33a CH(n-Bu)S(O)CH2CF3
D2-33a CH(n-Bu)S(O)2Me
D2-33a CH(n-Bu)S(O)2Et
D2-33a CH(n-Bu)S(O)2CF3
D2-33a CH(n-Bu)S(O)2CH2CF3
D2-33a CH(i-Bu)SMe
D2-33a CH(i-Bu)SEt
D2-33a CH(i-Bu)SCF3
D2-33a CH(i-Bu)SCH2CF3
D2-33a CH(i-Bu)S(O)Me
D2-33a CH(i-Bu)S(O)Et
D2-33a CH(i-Bu)S(O)CF3
D2-33a CH(i-Bu)S(O)CH2CF3
D2-33a CH(i-Bu)S(O)2Me
D2-33a CH(i-Bu)S(O)2Et
D2-33a CH(i-Bu)S(O)2CF3
D2-33a CH(i-Bu)S(O)2CH2CF3
D2-33a CH(s-Bu)SMe
D2-33a CH(s-Bu)SEt
D2-33a CH(s-Bu)SCF3
D2-33a CH(s-Bu)SCH2CF3
D2-33a CH(s-Bu)S(O)Me
D2-33a CH(s-Bu)S(O)Et
D2-33a CH(s-Bu)S(O)CF3
D2-33a CH(s-Bu)S(O)CH2CF3
D2-33a CH(s-Bu)S(O)2Me
D2-33a CH(s-Bu)S(O)2Et
D2-33a CH(s-Bu)S(O)2CF3
D2-33a CH(s-Bu)S(O)2CH2CF3
D2-33a CH(t-Bu)SMe
D2-33a CH(t-Bu)SEt
D2-33a CH(t-Bu)SCF3
D2-33a CH(t-Bu)SCH2CF3
D2-33a CH(t-Bu)S(O)Me
D2-33a CH(t-Bu)S(O)Et
D2-33a CH(t-Bu)S(O)CF3
D2-33a CH(t-Bu)S(O)CH2CF3
D2-33a CH(t-Bu)S(O)2Me
D2-33a CH(t-Bu)S(O)2Et
D2-33a CH(t-Bu)S(O)2CF3
D2-33a CH(t-Bu)S(O)2CH2CF3
D2-33a CH(CF3)SMe
D2-33a CH(CF3)SEt
D2-33a CH(CF3)SCF3
D2-33a CH(CF3)SCH2CF3
D2-33a CH(CF3)S(O)Me
D2-33a CH(CF3)S(O)Et
D2-33a CH(CF3)S(O)CF3
D2-33a CH(CF3)S(O)CH2CF3
D2-33a CH(CF3)S(O)2Me
D2-33a CH(CF3)S(O)2Et
D2-33a CH(CF3)S(O)2CF3
D2-33a CH(CF3)S(O)2CH2CF3
D2-33a CH2CH2SMe
D2-33a CH2CH2SEt
D2-33a CH2CH2SCF3
D2-33a CH2CH2SCH2CF3
D2-33a CH2CH2S(O)Me
D2-33a CH2CH2S(O)Et
D2-33a CH2CH2S(O)CF3
D2-33a CH2CH2S(O)CH2CF3
D2-33a CH2CH2S(O)2Me
D2-33a CH2CH2S(O)2Et
D2-33a CH2CH2S(O)2CF3
D2-33a CH2CH2S(O)2CH2CF3
D2-33a CH(Me)CH2SMe
D2-33a CH(Me)CH2SEt
D2-33a CH(Me)CH2SCF3
D2-33a CH(Me)CH2SCH2CF3
D2-33a CH(Me)CH2S(O)Me
D2-33a CH(Me)CH2S(O)Et
D2-33a CH(Me)CH2S(O)CF3
D2-33a CH(Me)CH2S(O)CH2CF3
D2-33a CH(Me)CH2S(O)2Me
D2-33a CH(Me)CH2S(O)2Et
D2-33a CH(Me)CH2S(O)2CF3
D2-33a CH(Me)CH2S(O)2CH2CF3
D2-33a CH(Et)CH2SMe
D2-33a CH(Et)CH2SEt
D2-33a CH(Et)CH2SCF3
D2-33a CH(Et)CH2SCH2CF3
D2-33a CH(Et)CH2S(O)Me
D2-33a CH(Et)CH2S(O)Et
D2-33a CH(Et)CH2S(O)CF3
D2-33a CH(Et)CH2S(O)CH2CF3
D2-33a CH(Et)CH2S(O)2Me
D2-33a CH(Et)CH2S(O)2Et
D2-33a CH(Et)CH2S(O)2CF3
D2-33a CH(Et)CH2S(O)2CH2CF3
D2-33a C(Me)2CH2SMe
D2-33a C(Me)2CH2SEt
D2-33a C(Me)2CH2SCF3
D2-33a C(Me)2CH2SCH2CF3
D2-33a C(Me)2CH2S(O)Me
D2-33a C(Me)2CH2S(O)Et
D2-33a C(Me)2CH2S(O)CF3
D2-33a C(Me)2CH2S(O)CH2CF3
D2-33a C(Me)2CH2S(O)2Me
D2-33a C(Me)2CH2S(O)2Et
D2-33a C(Me)2CH2S(O)2CF3
D2-33a C(Me)2CH2S(O)2CH2CF3
D2-33a CH2CH(Me)SMe
D2-33a CH2CH(Me)SEt
D2-33a CH2CH(Me)SCF3
D2-33a CH2CH(Me)SCH2CF3
D2-33a CH2CH(Me)S(O)Me
D2-33a CH2CH(Me)S(O)Et
D2-33a CH2CH(Me)S(O)CF3
D2-33a CH2CH(Me)S(O)CH2CF3
D2-33a CH2CH(Me)S(O)2Me
D2-33a CH2CH(Me)S(O)2Et
D2-33a CH2CH(Me)S(O)2CF3
D2-33a CH2CH(Me)S(O)2CH2CF3
D2-33a CH2CH(Et)SMe
D2-33a CH2CH(Et)SEt
D2-33a CH2CH(Et)SCF3
D2-33a CH2CH(Et)SCH2CF3
D2-33a CH2CH(Et)S(O)Me
D2-33a CH2CH(Et)S(O)Et
D2-33a CH2CH(Et)S(O)CF3
D2-33a CH2CH(Et)S(O)CH2CF3
D2-33a CH2CH(Et)S(O)2Me
D2-33a CH2CH(Et)S(O)2Et
D2-33a CH2CH(Et)S(O)2CF3
D2-33a CH2CH(Et)S(O)2CH2CF3
D2-33a CH(Me)CH(Me)SMe
D2-33a CH(Me)CH(Me)SEt
D2-33a CH(Me)CH(Me)SCF3
D2-33a CH(Me)CH(Me)SCH2CF3
D2-33a CH(Me)CH(Me)S(O)Me
D2-33a CH(Me)CH(Me)S(O)Et
D2-33a CH(Me)CH(Me)S(O)CF3
D2-33a CH(Me)CH(Me)S(O)CH2CF3
D2-33a CH(Me)CH(Me)S(O)2Me
D2-33a CH(Me)CH(Me)S(O)2Et
D2-33a CH(Me)CH(Me)S(O)2CF3
D2-33a CH(Me)CH(Me)S(O)2CH2CF3
D2-34a CH2SMe
D2-34a CH2SEt
D2-34a CH2SCF3
D2-34a CH2SCH2CF3
D2-34a CH2S(O)Me
D2-34a CH2S(O)Et
D2-34a CH2S(O)CF3
D2-34a CH2S(O)CH2CF3
D2-34a CH2S(O)2Me
D2-34a CH2S(O)2Et
D2-34a CH2S(O)2CF3
D2-34a CH2S(O)2CH2CF3
D2-34a CH(Me)SMe
D2-34a CH(Me)SEt
D2-34a CH(Me)SCF3
D2-34a CH(Me)SCH2CF3
D2-34a CH(Me)S(O)Me
D2-34a CH(Me)S(O)Et
D2-34a CH(Me)S(O)CF3
D2-34a CH(Me)S(O)CH2CF3
D2-34a CH(Me)S(O)2Me
D2-34a CH(Me)S(O)2Et
D2-34a CH(Me)S(O)2CF3
D2-34a CH(Me)S(O)2CH2CF3
D2-34a CH(Et)SMe
D2-34a CH(Et)SEt
D2-34a CH(Et)SCF3
D2-34a CH(Et)SCH2CF3
D2-34a CH(Et)S(O)Me
D2-34a CH(Et)S(O)Et
D2-34a CH(Et)S(O)CF3
D2-34a CH(Et)S(O)CH2CF3
D2-34a CH(Et)S(O)2Me
D2-34a CH(Et)S(O)2Et
D2-34a CH(Et)S(O)2CF3
D2-34a CH(Et)S(O)2CH2CF3
D2-34a CH(n-Pr)SMe
D2-34a CH(n-Pr)SEt
D2-34a CH(n-Pr)SCF3
D2-34a CH(n-Pr)SCH2CF3
D2-34a CH(n-Pr)S(O)Me
D2-34a CH(n-Pr)S(O)Et
D2-34a CH(n-Pr)S(O)CF3
D2-34a CH(n-Pr)S(O)CH2CF3
D2-34a CH(n-Pr)S(O)2Me
D2-34a CH(n-Pr)S(O)2Et
D2-34a CH(n-Pr)S(O)2CF3
D2-34a CH(n-Pr)S(O)2CH2CF3
D2-34a CH(i-Pr)SMe
D2-34a CH(i-Pr)SEt
D2-34a CH(i-Pr)SCF3
D2-34a CH(i-Pr)SCH2CF3
D2-34a CH(i-Pr)S(O)Me
D2-34a CH(i-Pr)S(O)Et
D2-34a CH(i-Pr)S(O)CF3
D2-34a CH(i-Pr)S(O)CH2CF3
D2-34a CH(i-Pr)S(O)2Me
D2-34a CH(i-Pr)S(O)2Et
D2-34a CH(i-Pr)S(O)2CF3
D2-34a CH(i-Pr)S(O)2CH2CF3
D2-34a CH(n-Bu)SMe
D2-34a CH(n-Bu)SEt
D2-34a CH(n-Bu)SCF3
D2-34a CH(n-Bu)SCH2CF3
D2-34a CH(n-Bu)S(O)Me
D2-34a CH(n-Bu)S(O)Et
D2-34a CH(n-Bu)S(O)CF3
D2-34a CH(n-Bu)S(O)CH2CF3
D2-34a CH(n-Bu)S(O)2Me
D2-34a CH(n-Bu)S(O)2Et
D2-34a CH(n-Bu)S(O)2CF3
D2-34a CH(n-Bu)S(O)2CH2CF3
D2-34a CH(i-Bu)SMe
D2-34a CH(i-Bu)SEt
D2-34a CH(i-Bu)SCF3
D2-34a CH(i-Bu)SCH2CF3
D2-34a CH(i-Bu)S(O)Me
D2-34a CH(i-Bu)S(O)Et
D2-34a CH(i-Bu)S(O)CF3
D2-34a CH(i-Bu)S(O)CH2CF3
D2-34a CH(i-Bu)S(O)2Me
D2-34a CH(i-Bu)S(O)2Et
D2-34a CH(i-Bu)S(O)2CF3
D2-34a CH(i-Bu)S(O)2CH2CF3
D2-34a CH(s-Bu)SMe
D2-34a CH(s-Bu)SEt
D2-34a CH(s-Bu)SCF3
D2-34a CH(s-Bu)SCH2CF3
D2-34a CH(s-Bu)S(O)Me
D2-34a CH(s-Bu)S(O)Et
D2-34a CH(s-Bu)S(O)CF3
D2-34a CH(s-Bu)S(O)CH2CF3
D2-34a CH(s-Bu)S(O)2Me
D2-34a CH(s-Bu)S(O)2Et
D2-34a CH(s-Bu)S(O)2CF3
D2-34a CH(s-Bu)S(O)2CH2CF3
D2-34a CH(t-Bu)SMe
D2-34a CH(t-Bu)SEt
D2-34a CH(t-Bu)SCF3
D2-34a CH(t-Bu)SCH2CF3
D2-34a CH(t-Bu)S(O)Me
D2-34a CH(t-Bu)S(O)Et
D2-34a CH(t-Bu)S(O)CF3
D2-34a CH(t-Bu)S(O)CH2CF3
D2-34a CH(t-Bu)S(O)2Me
D2-34a CH(t-Bu)S(O)2Et
D2-34a CH(t-Bu)S(O)2CF3
D2-34a CH(t-Bu)S(O)2CH2CF3
D2-34a CH(CF3)SMe
D2-34a CH(CF3)SEt
D2-34a CH(CF3)SCF3
D2-34a CH(CF3)SCH2CF3
D2-34a CH(CF3)S(O)Me
D2-34a CH(CF3)S(O)Et
D2-34a CH(CF3)S(O)CF3
D2-34a CH(CF3)S(O)CH2CF3
D2-34a CH(CF3)S(O)2Me
D2-34a CH(CF3)S(O)2Et
D2-34a CH(CF3)S(O)2CF3
D2-34a CH(CF3)S(O)2CH2CF3
D2-34a CH2CH2SMe
D2-34a CH2CH2SEt
D2-34a CH2CH2SCF3
D2-34a CH2CH2SCH2CF3
D2-34a CH2CH2S(O)Me
D2-34a CH2CH2S(O)Et
D2-34a CH2CH2S(O)CF3
D2-34a CH2CH2S(O)CH2CF3
D2-34a CH2CH2S(O)2Me
D2-34a CH2CH2S(O)2Et
D2-34a CH2CH2S(O)2CF3
D2-34a CH2CH2S(O)2CH2CF3
D2-34a CH(Me)CH2SMe
D2-34a CH(Me)CH2SEt
D2-34a CH(Me)CH2SCF3
D2-34a CH(Me)CH2SCH2CF3
D2-34a CH(Me)CH2S(O)Me
D2-34a CH(Me)CH2S(O)Et
D2-34a CH(Me)CH2S(O)CF3
D2-34a CH(Me)CH2S(O)CH2CF3
D2-34a CH(Me)CH2S(O)2Me
D2-34a CH(Me)CH2S(O)2Et
D2-34a CH(Me)CH2S(O)2CF3
D2-34a CH(Me)CH2S(O)2CH2CF3
D2-34a CH(Et)CH2SMe
D2-34a CH(Et)CH2SEt
D2-34a CH(Et)CH2SCF3
D2-34a CH(Et)CH2SCH2CF3
D2-34a CH(Et)CH2S(O)Me
D2-34a CH(Et)CH2S(O)Et
D2-34a CH(Et)CH2S(O)CF3
D2-34a CH(Et)CH2S(O)CH2CF3
D2-34a CH(Et)CH2S(O)2Me
D2-34a CH(Et)CH2S(O)2Et
D2-34a CH(Et)CH2S(O)2CF3
D2-34a CH(Et)CH2S(O)2CH2CF3
D2-34a C(Me)2CH2SMe
D2-34a C(Me)2CH2SEt
D2-34a C(Me)2CH2SCF3
D2-34a C(Me)2CH2SCH2CF3
D2-34a C(Me)2CH2S(O)Me
D2-34a C(Me)2CH2S(O)Et
D2-34a C(Me)2CH2S(O)CF3
D2-34a C(Me)2CH2S(O)CH2CF3
D2-34a C(Me)2CH2S(O)2Me
D2-34a C(Me)2CH2S(O)2Et
D2-34a C(Me)2CH2S(O)2CF3
D2-34a C(Me)2CH2S(O)2CH2CF3
D2-34a CH2CH(Me)SMe
D2-34a CH2CH(Me)SEt
D2-34a CH2CH(Me)SCF3
D2-34a CH2CH(Me)SCH2CF3
D2-34a CH2CH(Me)S(O)Me
D2-34a CH2CH(Me)S(O)Et
D2-34a CH2CH(Me)S(O)CF3
D2-34a CH2CH(Me)S(O)CH2CF3
D2-34a CH2CH(Me)S(O)2Me
D2-34a CH2CH(Me)S(O)2Et
D2-34a CH2CH(Me)S(O)2CF3
D2-34a CH2CH(Me)S(O)2CH2CF3
D2-34a CH2CH(Et)SMe
D2-34a CH2CH(Et)SEt
D2-34a CH2CH(Et)SCF3
D2-34a CH2CH(Et)SCH2CF3
D2-34a CH2CH(Et)S(O)Me
D2-34a CH2CH(Et)S(O)Et
D2-34a CH2CH(Et)S(O)CF3
D2-34a CH2CH(Et)S(O)CH2CF3
D2-34a CH2CH(Et)S(O)2Me
D2-34a CH2CH(Et)S(O)2Et
D2-34a CH2CH(Et)S(O)2CF3
D2-34a CH2CH(Et)S(O)2CH2CF3
D2-34a CH(Me)CH(Me)SMe
D2-34a CH(Me)CH(Me)SEt
D2-34a CH(Me)CH(Me)SCF3
D2-34a CH(Me)CH(Me)SCH2CF3
D2-34a CH(Me)CH(Me)S(O)Me
D2-34a CH(Me)CH(Me)S(O)Et
D2-34a CH(Me)CH(Me)S(O)CF3
D2-34a CH(Me)CH(Me)S(O)CH2CF3
D2-34a CH(Me)CH(Me)S(O)2Me
D2-34a CH(Me)CH(Me)S(O)2Et
D2-34a CH(Me)CH(Me)S(O)2CF3
D2-34a CH(Me)CH(Me)S(O)2CH2CF3
D2-36a CH2SMe
D2-36a CH2SEt
D2-36a CH2SCF3
D2-36a CH2SCH2CF3
D2-36a CH2S(O)Me
D2-36a CH2S(O)Et
D2-36a CH2S(O)CF3
D2-36a CH2S(O)CH2CF3
D2-36a CH2S(O)2Me
D2-36a CH2S(O)2Et
D2-36a CH2S(O)2CF3
D2-36a CH2S(O)2CH2CF3
D2-36a CH(Me)SMe
D2-36a CH(Me)SEt
D2-36a CH(Me)SCF3
D2-36a CH(Me)SCH2CF3
D2-36a CH(Me)S(O)Me
D2-36a CH(Me)S(O)Et
D2-36a CH(Me)S(O)CF3
D2-36a CH(Me)S(O)CH2CF3
D2-36a CH(Me)S(O)2Me
D2-36a CH(Me)S(O)2Et
D2-36a CH(Me)S(O)2CF3
D2-36a CH(Me)S(O)2CH2CF3
D2-36a CH(Et)SMe
D2-36a CH(Et)SEt
D2-36a CH(Et)SCF3
D2-36a CH(Et)SCH2CF3
D2-36a CH(Et)S(O)Me
D2-36a CH(Et)S(O)Et
D2-36a CH(Et)S(O)CF3
D2-36a CH(Et)S(O)CH2CF3
D2-36a CH(Et)S(O)2Me
D2-36a CH(Et)S(O)2Et
D2-36a CH(Et)S(O)2CF3
D2-36a CH(Et)S(O)2CH2CF3
D2-36a CH(n-Pr)SMe
D2-36a CH(n-Pr)SEt
D2-36a CH(n-Pr)SCF3
D2-36a CH(n-Pr)SCH2CF3
D2-36a CH(n-Pr)S(O)Me
D2-36a CH(n-Pr)S(O)Et
D2-36a CH(n-Pr)S(O)CF3
D2-36a CH(n-Pr)S(O)CH2CF3
D2-36a CH(n-Pr)S(O)2Me
D2-36a CH(n-Pr)S(O)2Et
D2-36a CH(n-Pr)S(O)2CF3
D2-36a CH(n-Pr)S(O)2CH2CF3
D2-36a CH(i-Pr)SMe
D2-36a CH(i-Pr)SEt
D2-36a CH(i-Pr)SCF3
D2-36a CH(i-Pr)SCH2CF3
D2-36a CH(i-Pr)S(O)Me
D2-36a CH(i-Pr)S(O)Et
D2-36a CH(i-Pr)S(O)CF3
D2-36a CH(i-Pr)S(O)CH2CF3
D2-36a CH(i-Pr)S(O)2Me
D2-36a CH(i-Pr)S(O)2Et
D2-36a CH(i-Pr)S(O)2CF3
D2-36a CH(i-Pr)S(O)2CH2CF3
D2-36a CH(n-Bu)SMe
D2-36a CH(n-Bu)SEt
D2-36a CH(n-Bu)SCF3
D2-36a CH(n-Bu)SCH2CF3
D2-36a CH(n-Bu)S(O)Me
D2-36a CH(n-Bu)S(O)Et
D2-36a CH(n-Bu)S(O)CF3
D2-36a CH(n-Bu)S(O)CH2CF3
D2-36a CH(n-Bu)S(O)2Me
D2-36a CH(n-Bu)S(O)2Et
D2-36a CH(n-Bu)S(O)2CF3
D2-36a CH(n-Bu)S(O)2CH2CF3
D2-36a CH(i-Bu)SMe
D2-36a CH(i-Bu)SEt
D2-36a CH(i-Bu)SCF3
D2-36a CH(i-Bu)SCH2CF3
D2-36a CH(i-Bu)S(O)Me
D2-36a CH(i-Bu)S(O)Et
D2-36a CH(i-Bu)S(O)CF3
D2-36a CH(i-Bu)S(O)CH2CF3
D2-36a CH(i-Bu)S(O)2Me
D2-36a CH(i-Bu)S(O)2Et
D2-36a CH(i-Bu)S(O)2CF3
D2-36a CH(i-Bu)S(O)2CH2CF3
D2-36a CH(s-Bu)SMe
D2-36a CH(s-Bu)SEt
D2-36a CH(s-Bu)SCF3
D2-36a CH(s-Bu)SCH2CF3
D2-36a CH(s-Bu)S(O)Me
D2-36a CH(s-Bu)S(O)Et
D2-36a CH(s-Bu)S(O)CF3
D2-36a CH(s-Bu)S(O)CH2CF3
D2-36a CH(s-Bu)S(O)2Me
D2-36a CH(s-Bu)S(O)2Et
D2-36a CH(s-Bu)S(O)2CF3
D2-36a CH(s-Bu)S(O)2CH2CF3
D2-36a CH(t-Bu)SMe
D2-36a CH(t-Bu)SEt
D2-36a CH(t-Bu)SCF3
D2-36a CH(t-Bu)SCH2CF3
D2-36a CH(t-Bu)S(O)Me
D2-36a CH(t-Bu)S(O)Et
D2-36a CH(t-Bu)S(O)CF3
D2-36a CH(t-Bu)S(O)CH2CF3
D2-36a CH(t-Bu)S(O)2Me
D2-36a CH(t-Bu)S(O)2Et
D2-36a CH(t-Bu)S(O)2CF3
D2-36a CH(t-Bu)S(O)2CH2CF3
D2-36a CH(CF3)SMe
D2-36a CH(CF3)SEt
D2-36a CH(CF3)SCF3
D2-36a CH(CF3)SCH2CF3
D2-36a CH(CF3)S(O)Me
D2-36a CH(CF3)S(O)Et
D2-36a CH(CF3)S(O)CF3
D2-36a CH(CF3)S(O)CH2CF3
D2-36a CH(CF3)S(O)2Me
D2-36a CH(CF3)S(O)2Et
D2-36a CH(CF3)S(O)2CF3
D2-36a CH(CF3)S(O)2CH2CF3
D2-36a CH2CH2SMe
D2-36a CH2CH2SEt
D2-36a CH2CH2SCF3
D2-36a CH2CH2SCH2CF3
D2-36a CH2CH2S(O)Me
D2-36a CH2CH2S(O)Et
D2-36a CH2CH2S(O)CF3
D2-36a CH2CH2S(O)CH2CF3
D2-36a CH2CH2S(O)2Me
D2-36a CH2CH2S(O)2Et
D2-36a CH2CH2S(O)2CF3
D2-36a CH2CH2S(O)2CH2CF3
D2-36a CH(Me)CH2SMe
D2-36a CH(Me)CH2SEt
D2-36a CH(Me)CH2SCF3
D2-36a CH(Me)CH2SCH2CF3
D2-36a CH(Me)CH2S(O)Me
D2-36a CH(Me)CH2S(O)Et
D2-36a CH(Me)CH2S(O)CF3
D2-36a CH(Me)CH2S(O)CH2CF3
D2-36a CH(Me)CH2S(O)2Me
D2-36a CH(Me)CH2S(O)2Et
D2-36a CH(Me)CH2S(O)2CF3
D2-36a CH(Me)CH2S(O)2CH2CF3
D2-36a CH(Et)CH2SMe
D2-36a CH(Et)CH2SEt
D2-36a CH(Et)CH2SCF3
D2-36a CH(Et)CH2SCH2CF3
D2-36a CH(Et)CH2S(O)Me
D2-36a CH(Et)CH2S(O)Et
D2-36a CH(Et)CH2S(O)CF3
D2-36a CH(Et)CH2S(O)CH2CF3
D2-36a CH(Et)CH2S(O)2Me
D2-36a CH(Et)CH2S(O)2Et
D2-36a CH(Et)CH2S(O)2CF3
D2-36a CH(Et)CH2S(O)2CH2CF3
D2-36a C(Me)2CH2SMe
D2-36a C(Me)2CH2SEt
D2-36a C(Me)2CH2SCF3
D2-36a C(Me)2CH2SCH2CF3
D2-36a C(Me)2CH2S(O)Me
D2-36a C(Me)2CH2S(O)Et
D2-36a C(Me)2CH2S(O)CF3
D2-36a C(Me)2CH2S(O)CH2CF3
D2-36a C(Me)2CH2S(O)2Me
D2-36a C(Me)2CH2S(O)2Et
D2-36a C(Me)2CH2S(O)2CF3
D2-36a C(Me)2CH2S(O)2CH2CF3
D2-36a CH2CH(Me)SMe
D2-36a CH2CH(Me)SEt
D2-36a CH2CH(Me)SCF3
D2-36a CH2CH(Me)SCH2CF3
D2-36a CH2CH(Me)S(O)Me
D2-36a CH2CH(Me)S(O)Et
D2-36a CH2CH(Me)S(O)CF3
D2-36a CH2CH(Me)S(O)CH2CF3
D2-36a CH2CH(Me)S(O)2Me
D2-36a CH2CH(Me)S(O)2Et
D2-36a CH2CH(Me)S(O)2CF3
D2-36a CH2CH(Me)S(O)2CH2CF3
D2-36a CH2CH(Et)SMe
D2-36a CH2CH(Et)SEt
D2-36a CH2CH(Et)SCF3
D2-36a CH2CH(Et)SCH2CF3
D2-36a CH2CH(Et)S(O)Me
D2-36a CH2CH(Et)S(O)Et
D2-36a CH2CH(Et)S(O)CF3
D2-36a CH2CH(Et)S(O)CH2CF3
D2-36a CH2CH(Et)S(O)2Me
D2-36a CH2CH(Et)S(O)2Et
D2-36a CH2CH(Et)S(O)2CF3
D2-36a CH2CH(Et)S(O)2CH2CF3
D2-36a CH(Me)CH(Me)SMe
D2-36a CH(Me)CH(Me)SEt
D2-36a CH(Me)CH(Me)SCF3
D2-36a CH(Me)CH(Me)SCH2CF3
D2-36a CH(Me)CH(Me)S(O)Me
D2-36a CH(Me)CH(Me)S(O)Et
D2-36a CH(Me)CH(Me)S(O)CF3
D2-36a CH(Me)CH(Me)S(O)CH2CF3
D2-36a CH(Me)CH(Me)S(O)2Me
D2-36a CH(Me)CH(Me)S(O)2Et
D2-36a CH(Me)CH(Me)S(O)2CF3
D2-36a CH(Me)CH(Me)S(O)2CH2CF3
D2-37a CH2SMe
D2-37a CH2SEt
D2-37a CH2SCF3
D2-37a CH2SCH2CF3
D2-37a CH2S(O)Me
D2-37a CH2S(O)Et
D2-37a CH2S(O)CF3
D2-37a CH2S(O)CH2CF3
D2-37a CH2S(O)2Me
D2-37a CH2S(O)2Et
D2-37a CH2S(O)2CF3
D2-37a CH2S(O)2CH2CF3
D2-37a CH(Me)SMe
D2-37a CH(Me)SEt
D2-37a CH(Me)SCF3
D2-37a CH(Me)SCH2CF3
D2-37a CH(Me)S(O)Me
D2-37a CH(Me)S(O)Et
D2-37a CH(Me)S(O)CF3
D2-37a CH(Me)S(O)CH2CF3
D2-37a CH(Me)S(O)2Me
D2-37a CH(Me)S(O)2Et
D2-37a CH(Me)S(O)2CF3
D2-37a CH(Me)S(O)2CH2CF3
D2-37a CH(Et)SMe
D2-37a CH(Et)SEt
D2-37a CH(Et)SCF3
D2-37a CH(Et)SCH2CF3
D2-37a CH(Et)S(O)Me
D2-37a CH(Et)S(O)Et
D2-37a CH(Et)S(O)CF3
D2-37a CH(Et)S(O)CH2CF3
D2-37a CH(Et)S(O)2Me
D2-37a CH(Et)S(O)2Et
D2-37a CH(Et)S(O)2CF3
D2-37a CH(Et)S(O)2CH2CF3
D2-37a CH(n-Pr)SMe
D2-37a CH(n-Pr)SEt
D2-37a CH(n-Pr)SCF3
D2-37a CH(n-Pr)SCH2CF3
D2-37a CH(n-Pr)S(O)Me
D2-37a CH(n-Pr)S(O)Et
D2-37a CH(n-Pr)S(O)CF3
D2-37a CH(n-Pr)S(O)CH2CF3
D2-37a CH(n-Pr)S(O)2Me
D2-37a CH(n-Pr)S(O)2Et
D2-37a CH(n-Pr)S(O)2CF3
D2-37a CH(n-Pr)S(O)2CH2CF3
D2-37a CH(i-Pr)SMe
D2-37a CH(i-Pr)SEt
D2-37a CH(i-Pr)SCF3
D2-37a CH(i-Pr)SCH2CF3
D2-37a CH(i-Pr)S(O)Me
D2-37a CH(i-Pr)S(O)Et
D2-37a CH(i-Pr)S(O)CF3
D2-37a CH(i-Pr)S(O)CH2CF3
D2-37a CH(i-Pr)S(O)2Me
D2-37a CH(i-Pr)S(O)2Et
D2-37a CH(i-Pr)S(O)2CF3
D2-37a CH(i-Pr)S(O)2CH2CF3
D2-37a CH(n-Bu)SMe
D2-37a CH(n-Bu)SEt
D2-37a CH(n-Bu)SCF3
D2-37a CH(n-Bu)SCH2CF3
D2-37a CH(n-Bu)S(O)Me
D2-37a CH(n-Bu)S(O)Et
D2-37a CH(n-Bu)S(O)CF3
D2-37a CH(n-Bu)S(O)CH2CF3
D2-37a CH(n-Bu)S(O)2Me
D2-37a CH(n-Bu)S(O)2Et
D2-37a CH(n-Bu)S(O)2CF3
D2-37a CH(n-Bu)S(O)2CH2CF3
D2-37a CH(i-Bu)SMe
D2-37a CH(i-Bu)SEt
D2-37a CH(i-Bu)SCF3
D2-37a CH(i-Bu)SCH2CF3
D2-37a CH(i-Bu)S(O)Me
D2-37a CH(i-Bu)S(O)Et
D2-37a CH(i-Bu)S(O)CF3
D2-37a CH(i-Bu)S(O)CH2CF3
D2-37a CH(i-Bu)S(O)2Me
D2-37a CH(i-Bu)S(O)2Et
D2-37a CH(i-Bu)S(O)2CF3
D2-37a CH(i-Bu)S(O)2CH2CF3
D2-37a CH(s-Bu)SMe
D2-37a CH(s-Bu)SEt
D2-37a CH(s-Bu)SCF3
D2-37a CH(s-Bu)SCH2CF3
D2-37a CH(s-Bu)S(O)Me
D2-37a CH(s-Bu)S(O)Et
D2-37a CH(s-Bu)S(O)CF3
D2-37a CH(s-Bu)S(O)CH2CF3
D2-37a CH(s-Bu)S(O)2Me
D2-37a CH(s-Bu)S(O)2Et
D2-37a CH(s-Bu)S(O)2CF3
D2-37a CH(s-Bu)S(O)2CH2CF3
D2-37a CH(t-Bu)SMe
D2-37a CH(t-Bu)SEt
D2-37a CH(t-Bu)SCF3
D2-37a CH(t-Bu)SCH2CF3
D2-37a CH(t-Bu)S(O)Me
D2-37a CH(t-Bu)S(O)Et
D2-37a CH(t-Bu)S(O)CF3
D2-37a CH(t-Bu)S(O)CH2CF3
D2-37a CH(t-Bu)S(O)2Me
D2-37a CH(t-Bu)S(O)2Et
D2-37a CH(t-Bu)S(O)2CF3
D2-37a CH(t-Bu)S(O)2CH2CF3
D2-37a CH(CF3)SMe
D2-37a CH(CF3)SEt
D2-37a CH(CF3)SCF3
D2-37a CH(CF3)SCH2CF3
D2-37a CH(CF3)S(O)Me
D2-37a CH(CF3)S(O)Et
D2-37a CH(CF3)S(O)CF3
D2-37a CH(CF3)S(O)CH2CF3
D2-37a CH(CF3)S(O)2Me
D2-37a CH(CF3)S(O)2Et
D2-37a CH(CF3)S(O)2CF3
D2-37a CH(CF3)S(O)2CH2CF3
D2-37a CH2CH2SMe
D2-37a CH2CH2SEt
D2-37a CH2CH2SCF3
D2-37a CH2CH2SCH2CF3
D2-37a CH2CH2S(O)Me
D2-37a CH2CH2S(O)Et
D2-37a CH2CH2S(O)CF3
D2-37a CH2CH2S(O)CH2CF3
D2-37a CH2CH2S(O)2Me
D2-37a CH2CH2S(O)2Et
D2-37a CH2CH2S(O)2CF3
D2-37a CH2CH2S(O)2CH2CF3
D2-37a CH(Me)CH2SMe
D2-37a CH(Me)CH2SEt
D2-37a CH(Me)CH2SCF3
D2-37a CH(Me)CH2SCH2CF3
D2-37a CH(Me)CH2S(O)Me
D2-37a CH(Me)CH2S(O)Et
D2-37a CH(Me)CH2S(O)CF3
D2-37a CH(Me)CH2S(O)CH2CF3
D2-37a CH(Me)CH2S(O)2Me
D2-37a CH(Me)CH2S(O)2Et
D2-37a CH(Me)CH2S(O)2CF3
D2-37a CH(Me)CH2S(O)2CH2CF3
D2-37a CH(Et)CH2SMe
D2-37a CH(Et)CH2SEt
D2-37a CH(Et)CH2SCF3
D2-37a CH(Et)CH2SCH2CF3
D2-37a CH(Et)CH2S(O)Me
D2-37a CH(Et)CH2S(O)Et
D2-37a CH(Et)CH2S(O)CF3
D2-37a CH(Et)CH2S(O)CH2CF3
D2-37a CH(Et)CH2S(O)2Me
D2-37a CH(Et)CH2S(O)2Et
D2-37a CH(Et)CH2S(O)2CF3
D2-37a CH(Et)CH2S(O)2CH2CF3
D2-37a C(Me)2CH2SMe
D2-37a C(Me)2CH2SEt
D2-37a C(Me)2CH2SCF3
D2-37a C(Me)2CH2SCH2CF3
D2-37a C(Me)2CH2S(O)Me
D2-37a C(Me)2CH2S(O)Et
D2-37a C(Me)2CH2S(O)CF3
D2-37a C(Me)2CH2S(O)CH2CF3
D2-37a C(Me)2CH2S(O)2Me
D2-37a C(Me)2CH2S(O)2Et
D2-37a C(Me)2CH2S(O)2CF3
D2-37a C(Me)2CH2S(O)2CH2CF3
D2-37a CH2CH(Me)SMe
D2-37a CH2CH(Me)SEt
D2-37a CH2CH(Me)SCF3
D2-37a CH2CH(Me)SCH2CF3
D2-37a CH2CH(Me)S(O)Me
D2-37a CH2CH(Me)S(O)Et
D2-37a CH2CH(Me)S(O)CF3
D2-37a CH2CH(Me)S(O)CH2CF3
D2-37a CH2CH(Me)S(O)2Me
D2-37a CH2CH(Me)S(O)2Et
D2-37a CH2CH(Me)S(O)2CF3
D2-37a CH2CH(Me)S(O)2CH2CF3
D2-37a CH2CH(Et)SMe
D2-37a CH2CH(Et)SEt
D2-37a CH2CH(Et)SCF3
D2-37a CH2CH(Et)SCH2CF3
D2-37a CH2CH(Et)S(O)Me
D2-37a CH2CH(Et)S(O)Et
D2-37a CH2CH(Et)S(O)CF3
D2-37a CH2CH(Et)S(O)CH2CF3
D2-37a CH2CH(Et)S(O)2Me
D2-37a CH2CH(Et)S(O)2Et
D2-37a CH2CH(Et)S(O)2CF3
D2-37a CH2CH(Et)S(O)2CH2CF3
D2-37a CH(Me)CH(Me)SMe
D2-37a CH(Me)CH(Me)SEt
D2-37a CH(Me)CH(Me)SCF3
D2-37a CH(Me)CH(Me)SCH2CF3
D2-37a CH(Me)CH(Me)S(O)Me
D2-37a CH(Me)CH(Me)S(O)Et
D2-37a CH(Me)CH(Me)S(O)CF3
D2-37a CH(Me)CH(Me)S(O)CH2CF3
D2-37a CH(Me)CH(Me)S(O)2Me
D2-37a CH(Me)CH(Me)S(O)2Et
D2-37a CH(Me)CH(Me)S(O)2CF3
D2-37a CH(Me)CH(Me)S(O)2CH2CF3
D2-38a CH2SMe
D2-38a CH2SEt
D2-38a CH2SCF3
D2-38a CH2SCH2CF3
D2-38a CH2S(O)Me
D2-38a CH2S(O)Et
D2-38a CH2S(O)CF3
D2-38a CH2S(O)CH2CF3
D2-38a CH2S(O)2Me
D2-38a CH2S(O)2Et
D2-38a CH2S(O)2CF3
D2-38a CH2S(O)2CH2CF3
D2-38a CH(Me)SMe
D2-38a CH(Me)SEt
D2-38a CH(Me)SCF3
D2-38a CH(Me)SCH2CF3
D2-38a CH(Me)S(O)Me
D2-38a CH(Me)S(O)Et
D2-38a CH(Me)S(O)CF3
D2-38a CH(Me)S(O)CH2CF3
D2-38a CH(Me)S(O)2Me
D2-38a CH(Me)S(O)2Et
D2-38a CH(Me)S(O)2CF3
D2-38a CH(Me)S(O)2CH2CF3
D2-38a CH(Et)SMe
D2-38a CH(Et)SEt
D2-38a CH(Et)SCF3
D2-38a CH(Et)SCH2CF3
D2-38a CH(Et)S(O)Me
D2-38a CH(Et)S(O)Et
D2-38a CH(Et)S(O)CF3
D2-38a CH(Et)S(O)CH2CF3
D2-38a CH(Et)S(O)2Me
D2-38a CH(Et)S(O)2Et
D2-38a CH(Et)S(O)2CF3
D2-38a CH(Et)S(O)2CH2CF3
D2-38a CH(n-Pr)SMe
D2-38a CH(n-Pr)SEt
D2-38a CH(n-Pr)SCF3
D2-38a CH(n-Pr)SCH2CF3
D2-38a CH(n-Pr)S(O)Me
D2-38a CH(n-Pr)S(O)Et
D2-38a CH(n-Pr)S(O)CF3
D2-38a CH(n-Pr)S(O)CH2CF3
D2-38a CH(n-Pr)S(O)2Me
D2-38a CH(n-Pr)S(O)2Et
D2-38a CH(n-Pr)S(O)2CF3
D2-38a CH(n-Pr)S(O)2CH2CF3
D2-38a CH(i-Pr)SMe
D2-38a CH(i-Pr)SEt
D2-38a CH(i-Pr)SCF3
D2-38a CH(i-Pr)SCH2CF3
D2-38a CH(i-Pr)S(O)Me
D2-38a CH(i-Pr)S(O)Et
D2-38a CH(i-Pr)S(O)CF3
D2-38a CH(i-Pr)S(O)CH2CF3
D2-38a CH(i-Pr)S(O)2Me
D2-38a CH(i-Pr)S(O)2Et
D2-38a CH(i-Pr)S(O)2CF3
D2-38a CH(i-Pr)S(O)2CH2CF3
D2-38a CH(n-Bu)SMe
D2-38a CH(n-Bu)SEt
D2-38a CH(n-Bu)SCF3
D2-38a CH(n-Bu)SCH2CF3
D2-38a CH(n-Bu)S(O)Me
D2-38a CH(n-Bu)S(O)Et
D2-38a CH(n-Bu)S(O)CF3
D2-38a CH(n-Bu)S(O)CH2CF3
D2-38a CH(n-Bu)S(O)2Me
D2-38a CH(n-Bu)S(O)2Et
D2-38a CH(n-Bu)S(O)2CF3
D2-38a CH(n-Bu)S(O)2CH2CF3
D2-38a CH(i-Bu)SMe
D2-38a CH(i-Bu)SEt
D2-38a CH(i-Bu)SCF3
D2-38a CH(i-Bu)SCH2CF3
D2-38a CH(i-Bu)S(O)Me
D2-38a CH(i-Bu)S(O)Et
D2-38a CH(i-Bu)S(O)CF3
D2-38a CH(i-Bu)S(O)CH2CF3
D2-38a CH(i-Bu)S(O)2Me
D2-38a CH(i-Bu)S(O)2Et
D2-38a CH(i-Bu)S(O)2CF3
D2-38a CH(i-Bu)S(O)2CH2CF3
D2-38a CH(s-Bu)SMe
D2-38a CH(s-Bu)SEt
D2-38a CH(s-Bu)SCF3
D2-38a CH(s-Bu)SCH2CF3
D2-38a CH(s-Bu)S(O)Me
D2-38a CH(s-Bu)S(O)Et
D2-38a CH(s-Bu)S(O)CF3
D2-38a CH(s-Bu)S(O)CH2CF3
D2-38a CH(s-Bu)S(O)2Me
D2-38a CH(s-Bu)S(O)2Et
D2-38a CH(s-Bu)S(O)2CF3
D2-38a CH(s-Bu)S(O)2CH2CF3
D2-38a CH(t-Bu)SMe
D2-38a CH(t-Bu)SEt
D2-38a CH(t-Bu)SCF3
D2-38a CH(t-Bu)SCH2CF3
D2-38a CH(t-Bu)S(O)Me
D2-38a CH(t-Bu)S(O)Et
D2-38a CH(t-Bu)S(O)CF3
D2-38a CH(t-Bu)S(O)CH2CF3
D2-38a CH(t-Bu)S(O)2Me
D2-38a CH(t-Bu)S(O)2Et
D2-38a CH(t-Bu)S(O)2CF3
D2-38a CH(t-Bu)S(O)2CH2CF3
D2-38a CH(CF3)SMe
D2-38a CH(CF3)SEt
D2-38a CH(CF3)SCF3
D2-38a CH(CF3)SCH2CF3
D2-38a CH(CF3)S(O)Me
D2-38a CH(CF3)S(O)Et
D2-38a CH(CF3)S(O)CF3
D2-38a CH(CF3)S(O)CH2CF3
D2-38a CH(CF3)S(O)2Me
D2-38a CH(CF3)S(O)2Et
D2-38a CH(CF3)S(O)2CF3
D2-38a CH(CF3)S(O)2CH2CF3
D2-38a CH2CH2SMe
D2-38a CH2CH2SEt
D2-38a CH2CH2SCF3
D2-38a CH2CH2SCH2CF3
D2-38a CH2CH2S(O)Me
D2-38a CH2CH2S(O)Et
D2-38a CH2CH2S(O)CF3
D2-38a CH2CH2S(O)CH2CF3
D2-38a CH2CH2S(O)2Me
D2-38a CH2CH2S(O)2Et
D2-38a CH2CH2S(O)2CF3
D2-38a CH2CH2S(O)2CH2CF3
D2-38a CH(Me)CH2SMe
D2-38a CH(Me)CH2SEt
D2-38a CH(Me)CH2SCF3
D2-38a CH(Me)CH2SCH2CF3
D2-38a CH(Me)CH2S(O)Me
D2-38a CH(Me)CH2S(O)Et
D2-38a CH(Me)CH2S(O)CF3
D2-38a CH(Me)CH2S(O)CH2CF3
D2-38a CH(Me)CH2S(O)2Me
D2-38a CH(Me)CH2S(O)2Et
D2-38a CH(Me)CH2S(O)2CF3
D2-38a CH(Me)CH2S(O)2CH2CF3
D2-38a CH(Et)CH2SMe
D2-38a CH(Et)CH2SEt
D2-38a CH(Et)CH2SCF3
D2-38a CH(Et)CH2SCH2CF3
D2-38a CH(Et)CH2S(O)Me
D2-38a CH(Et)CH2S(O)Et
D2-38a CH(Et)CH2S(O)CF3
D2-38a CH(Et)CH2S(O)CH2CF3
D2-38a CH(Et)CH2S(O)2Me
D2-38a CH(Et)CH2S(O)2Et
D2-38a CH(Et)CH2S(O)2CF3
D2-38a CH(Et)CH2S(O)2CH2CF3
D2-38a C(Me)2CH2SMe
D2-38a C(Me)2CH2SEt
D2-38a C(Me)2CH2SCF3
D2-38a C(Me)2CH2SCH2CF3
D2-38a C(Me)2CH2S(O)Me
D2-38a C(Me)2CH2S(O)Et
D2-38a C(Me)2CH2S(O)CF3
D2-38a C(Me)2CH2S(O)CH2CF3
D2-38a C(Me)2CH2S(O)2Me
D2-38a C(Me)2CH2S(O)2Et
D2-38a C(Me)2CH2S(O)2CF3
D2-38a C(Me)2CH2S(O)2CH2CF3
D2-38a CH2CH(Me)SMe
D2-38a CH2CH(Me)SEt
D2-38a CH2CH(Me)SCF3
D2-38a CH2CH(Me)SCH2CF3
D2-38a CH2CH(Me)S(O)Me
D2-38a CH2CH(Me)S(O)Et
D2-38a CH2CH(Me)S(O)CF3
D2-38a CH2CH(Me)S(O)CH2CF3
D2-38a CH2CH(Me)S(O)2Me
D2-38a CH2CH(Me)S(O)2Et
D2-38a CH2CH(Me)S(O)2CF3
D2-38a CH2CH(Me)S(O)2CH2CF3
D2-38a CH2CH(Et)SMe
D2-38a CH2CH(Et)SEt
D2-38a CH2CH(Et)SCF3
D2-38a CH2CH(Et)SCH2CF3
D2-38a CH2CH(Et)S(O)Me
D2-38a CH2CH(Et)S(O)Et
D2-38a CH2CH(Et)S(O)CF3
D2-38a CH2CH(Et)S(O)CH2CF3
D2-38a CH2CH(Et)S(O)2Me
D2-38a CH2CH(Et)S(O)2Et
D2-38a CH2CH(Et)S(O)2CF3
D2-38a CH2CH(Et)S(O)2CH2CF3
D2-38a CH(Me)CH(Me)SMe
D2-38a CH(Me)CH(Me)SEt
D2-38a CH(Me)CH(Me)SCF3
D2-38a CH(Me)CH(Me)SCH2CF3
D2-38a CH(Me)CH(Me)S(O)Me
D2-38a CH(Me)CH(Me)S(O)Et
D2-38a CH(Me)CH(Me)S(O)CF3
D2-38a CH(Me)CH(Me)S(O)CH2CF3
D2-38a CH(Me)CH(Me)S(O)2Me
D2-38a CH(Me)CH(Me)S(O)2Et
D2-38a CH(Me)CH(Me)S(O)2CF3
D2-38a CH(Me)CH(Me)S(O)2CH2CF3
D2-92a CH2SMe
D2-92a CH2SEt
D2-92a CH2SCF3
D2-92a CH2SCH2CF3
D2-92a CH2S(O)Me
D2-92a CH2S(O)Et
D2-92a CH2S(O)CF3
D2-92a CH2S(O)CH2CF3
D2-92a CH2S(O)2Me
D2-92a CH2S(O)2Et
D2-92a CH2S(O)2CF3
D2-92a CH2S(O)2CH2CF3
D2-92a CH(Me)SMe
D2-92a CH(Me)SEt
D2-92a CH(Me)SCF3
D2-92a CH(Me)SCH2CF3
D2-92a CH(Me)S(O)Me
D2-92a CH(Me)S(O)Et
D2-92a CH(Me)S(O)CF3
D2-92a CH(Me)S(O)CH2CF3
D2-92a CH(Me)S(O)2Me
D2-92a CH(Me)S(O)2Et
D2-92a CH(Me)S(O)2CF3
D2-92a CH(Me)S(O)2CH2CF3
D2-92a CH(Et)SMe
D2-92a CH(Et)SEt
D2-92a CH(Et)SCF3
D2-92a CH(Et)SCH2CF3
D2-92a CH(Et)S(O)Me
D2-92a CH(Et)S(O)Et
D2-92a CH(Et)S(O)CF3
D2-92a CH(Et)S(O)CH2CF3
D2-92a CH(Et)S(O)2Me
D2-92a CH(Et)S(O)2Et
D2-92a CH(Et)S(O)2CF3
D2-92a CH(Et)S(O)2CH2CF3
D2-92a CH(n-Pr)SMe
D2-92a CH(n-Pr)SEt
D2-92a CH(n-Pr)SCF3
D2-92a CH(n-Pr)SCH2CF3
D2-92a CH(n-Pr)S(O)Me
D2-92a CH(n-Pr)S(O)Et
D2-92a CH(n-Pr)S(O)CF3
D2-92a CH(n-Pr)S(O)CH2CF3
D2-92a CH(n-Pr)S(O)2Me
D2-92a CH(n-Pr)S(O)2Et
D2-92a CH(n-Pr)S(O)2CF3
D2-92a CH(n-Pr)S(O)2CH2CF3
D2-92a CH(i-Pr)SMe
D2-92a CH(i-Pr)SEt
D2-92a CH(i-Pr)SCF3
D2-92a CH(i-Pr)SCH2CF3
D2-92a CH(i-Pr)S(O)Me
D2-92a CH(i-Pr)S(O)Et
D2-92a CH(i-Pr)S(O)CF3
D2-92a CH(i-Pr)S(O)CH2CF3
D2-92a CH(i-Pr)S(O)2Me
D2-92a CH(i-Pr)S(O)2Et
D2-92a CH(i-Pr)S(O)2CF3
D2-92a CH(i-Pr)S(O)2CH2CF3
D2-92a CH(n-Bu)SMe
D2-92a CH(n-Bu)SEt
D2-92a CH(n-Bu)SCF3
D2-92a CH(n-Bu)SCH2CF3
D2-92a CH(n-Bu)S(O)Me
D2-92a CH(n-Bu)S(O)Et
D2-92a CH(n-Bu)S(O)CF3
D2-92a CH(n-Bu)S(O)CH2CF3
D2-92a CH(n-Bu)S(O)2Me
D2-92a CH(n-Bu)S(O)2Et
D2-92a CH(n-Bu)S(O)2CF3
D2-92a CH(n-Bu)S(O)2CH2CF3
D2-92a CH(i-Bu)SMe
D2-92a CH(i-Bu)SEt
D2-92a CH(i-Bu)SCF3
D2-92a CH(i-Bu)SCH2CF3
D2-92a CH(i-Bu)S(O)Me
D2-92a CH(i-Bu)S(O)Et
D2-92a CH(i-Bu)S(O)CF3
D2-92a CH(i-Bu)S(O)CH2CF3
D2-92a CH(i-Bu)S(O)2Me
D2-92a CH(i-Bu)S(O)2Et
D2-92a CH(i-Bu)S(O)2CF3
D2-92a CH(i-Bu)S(O)2CH2CF3
D2-92a CH(s-Bu)SMe
D2-92a CH(s-Bu)SEt
D2-92a CH(s-Bu)SCF3
D2-92a CH(s-Bu)SCH2CF3
D2-92a CH(s-Bu)S(O)Me
D2-92a CH(s-Bu)S(O)Et
D2-92a CH(s-Bu)S(O)CF3
D2-92a CH(s-Bu)S(O)CH2CF3
D2-92a CH(s-Bu)S(O)2Me
D2-92a CH(s-Bu)S(O)2Et
D2-92a CH(s-Bu)S(O)2CF3
D2-92a CH(s-Bu)S(O)2CH2CF3
D2-92a CH(t-Bu)SMe
D2-92a CH(t-Bu)SEt
D2-92a CH(t-Bu)SCF3
D2-92a CH(t-Bu)SCH2CF3
D2-92a CH(t-Bu)S(O)Me
D2-92a CH(t-Bu)S(O)Et
D2-92a CH(t-Bu)S(O)CF3
D2-92a CH(t-Bu)S(O)CH2CF3
D2-92a CH(t-Bu)S(O)2Me
D2-92a CH(t-Bu)S(O)2Et
D2-92a CH(t-Bu)S(O)2CF3
D2-92a CH(t-Bu)S(O)2CH2CF3
D2-92a CH(CF3)SMe
D2-92a CH(CF3)SEt
D2-92a CH(CF3)SCF3
D2-92a CH(CF3)SCH2CF3
D2-92a CH(CF3)S(O)Me
D2-92a CH(CF3)S(O)Et
D2-92a CH(CF3)S(O)CF3
D2-92a CH(CF3)S(O)CH2CF3
D2-92a CH(CF3)S(O)2Me
D2-92a CH(CF3)S(O)2Et
D2-92a CH(CF3)S(O)2CF3
D2-92a CH(CF3)S(O)2CH2CF3
D2-92a CH2CH2SMe
D2-92a CH2CH2SEt
D2-92a CH2CH2SCF3
D2-92a CH2CH2SCH2CF3
D2-92a CH2CH2S(O)Me
D2-92a CH2CH2S(O)Et
D2-92a CH2CH2S(O)CF3
D2-92a CH2CH2S(O)CH2CF3
D2-92a CH2CH2S(O)2Me
D2-92a CH2CH2S(O)2Et
D2-92a CH2CH2S(O)2CF3
D2-92a CH2CH2S(O)2CH2CF3
D2-92a CH(Me)CH2SMe
D2-92a CH(Me)CH2SEt
D2-92a CH(Me)CH2SCF3
D2-92a CH(Me)CH2SCH2CF3
D2-92a CH(Me)CH2S(O)Me
D2-92a CH(Me)CH2S(O)Et
D2-92a CH(Me)CH2S(O)CF3
D2-92a CH(Me)CH2S(O)CH2CF3
D2-92a CH(Me)CH2S(O)2Me
D2-92a CH(Me)CH2S(O)2Et
D2-92a CH(Me)CH2S(O)2CF3
D2-92a CH(Me)CH2S(O)2CH2CF3
D2-92a CH(Et)CH2SMe
D2-92a CH(Et)CH2SEt
D2-92a CH(Et)CH2SCF3
D2-92a CH(Et)CH2SCH2CF3
D2-92a CH(Et)CH2S(O)Me
D2-92a CH(Et)CH2S(O)Et
D2-92a CH(Et)CH2S(O)CF3
D2-92a CH(Et)CH2S(O)CH2CF3
D2-92a CH(Et)CH2S(O)2Me
D2-92a CH(Et)CH2S(O)2Et
D2-92a CH(Et)CH2S(O)2CF3
D2-92a CH(Et)CH2S(O)2CH2CF3
D2-92a C(Me)2CH2SMe
D2-92a C(Me)2CH2SEt
D2-92a C(Me)2CH2SCF3
D2-92a C(Me)2CH2SCH2CF3
D2-92a C(Me)2CH2S(O)Me
D2-92a C(Me)2CH2S(O)Et
D2-92a C(Me)2CH2S(O)CF3
D2-92a C(Me)2CH2S(O)CH2CF3
D2-92a C(Me)2CH2S(O)2Me
D2-92a C(Me)2CH2S(O)2Et
D2-92a C(Me)2CH2S(O)2CF3
D2-92a C(Me)2CH2S(O)2CH2CF3
D2-92a CH2CH(Me)SMe
D2-92a CH2CH(Me)SEt
D2-92a CH2CH(Me)SCF3
D2-92a CH2CH(Me)SCH2CF3
D2-92a CH2CH(Me)S(O)Me
D2-92a CH2CH(Me)S(O)Et
D2-92a CH2CH(Me)S(O)CF3
D2-92a CH2CH(Me)S(O)CH2CF3
D2-92a CH2CH(Me)S(O)2Me
D2-92a CH2CH(Me)S(O)2Et
D2-92a CH2CH(Me)S(O)2CF3
D2-92a CH2CH(Me)S(O)2CH2CF3
D2-92a CH2CH(Et)SMe
D2-92a CH2CH(Et)SEt
D2-92a CH2CH(Et)SCF3
D2-92a CH2CH(Et)SCH2CF3
D2-92a CH2CH(Et)S(O)Me
D2-92a CH2CH(Et)S(O)Et
D2-92a CH2CH(Et)S(O)CF3
D2-92a CH2CH(Et)S(O)CH2CF3
D2-92a CH2CH(Et)S(O)2Me
D2-92a CH2CH(Et)S(O)2Et
D2-92a CH2CH(Et)S(O)2CF3
D2-92a CH2CH(Et)S(O)2CH2CF3
D2-92a CH(Me)CH(Me)SMe
D2-92a CH(Me)CH(Me)SEt
D2-92a CH(Me)CH(Me)SCF3
D2-92a CH(Me)CH(Me)SCH2CF3
D2-92a CH(Me)CH(Me)S(O)Me
D2-92a CH(Me)CH(Me)S(O)Et
D2-92a CH(Me)CH(Me)S(O)CF3
D2-92a CH(Me)CH(Me)S(O)CH2CF3
D2-92a CH(Me)CH(Me)S(O)2Me
D2-92a CH(Me)CH(Me)S(O)2Et
D2-92a CH(Me)CH(Me)S(O)2CF3
D2-92a CH(Me)CH(Me)S(O)2CH2CF3
CH(Me)SMe CH2SMe
CH(Me)SMe CH2SEt
CH(Me)SMe CH2SCF3
CH(Me)SMe CH2SCH2CF3
CH(Me)SMe CH2S(O)Me
CH(Me)SMe CH2S(O)Et
CH(Me)SMe CH2S(O)CF3
CH(Me)SMe CH2S(O)CH2CF3
CH(Me)SMe CH2S(O)2Me
CH(Me)SMe CH2S(O)2Et
CH(Me)SMe CH2S(O)2CF3
CH(Me)SMe CH2S(O)2CH2CF3
CH(Me)SMe CH(Me)SMe
CH(Me)SMe CH(Me)SEt
CH(Me)SMe CH(Me)SCF3
CH(Me)SMe CH(Me)SCH2CF3
CH(Me)SMe CH(Me)S(O)Me
CH(Me)SMe CH(Me)S(O)Et
CH(Me)SMe CH(Me)S(O)CF3
CH(Me)SMe CH(Me)S(O)CH2CF3
CH(Me)SMe CH(Me)S(O)2Me
CH(Me)SMe CH(Me)S(O)2Et
CH(Me)SMe CH(Me)S(O)2CF3
CH(Me)SMe CH(Me)S(O)2CH2CF3
CH(Me)SMe CH(Et)SMe
CH(Me)SMe CH(Et)SEt
CH(Me)SMe CH(Et)SCF3
CH(Me)SMe CH(Et)SCH2CF3
CH(Me)SMe CH(Et)S(O)Me
CH(Me)SMe CH(Et)S(O)Et
CH(Me)SMe CH(Et)S(O)CF3
CH(Me)SMe CH(Et)S(O)CH2CF3
CH(Me)SMe CH(Et)S(O)2Me
CH(Me)SMe CH(Et)S(O)2Et
CH(Me)SMe CH(Et)S(O)2CF3
CH(Me)SMe CH(Et)S(O)2CH2CF3
CH(Me)SMe CH(n-Pr)SMe
CH(Me)SMe CH(n-Pr)SEt
CH(Me)SMe CH(n-Pr)SCF3
CH(Me)SMe CH(n-Pr)SCH2CF3
CH(Me)SMe CH(n-Pr)S(O)Me
CH(Me)SMe CH(n-Pr)S(O)Et
CH(Me)SMe CH(n-Pr)S(O)CF3
CH(Me)SMe CH(n-Pr)S(O)CH2CF3
CH(Me)SMe CH(n-Pr)S(O)2Me
CH(Me)SMe CH(n-Pr)S(O)2Et
CH(Me)SMe CH(n-Pr)S(O)2CF3
CH(Me)SMe CH(n-Pr)S(O)2CH2CF3
CH(Me)SMe CH(i-Pr)SMe
CH(Me)SMe CH(i-Pr)SEt
CH(Me)SMe CH(i-Pr)SCF3
CH(Me)SMe CH(i-Pr)SCH2CF3
CH(Me)SMe CH(i-Pr)S(O)Me
CH(Me)SMe CH(i-Pr)S(O)Et
CH(Me)SMe CH(i-Pr)S(O)CF3
CH(Me)SMe CH(i-Pr)S(O)CH2CF3
CH(Me)SMe CH(i-Pr)S(O)2Me
CH(Me)SMe CH(i-Pr)S(O)2Et
CH(Me)SMe CH(i-Pr)S(O)2CF3
CH(Me)SMe CH(i-Pr)S(O)2CH2CF3
CH(Me)SMe CH(n-Bu)SMe
CH(Me)SMe CH(n-Bu)SEt
CH(Me)SMe CH(n-Bu)SCF3
CH(Me)SMe CH(n-Bu)SCH2CF3
CH(Me)SMe CH(n-Bu)S(O)Me
CH(Me)SMe CH(n-Bu)S(O)Et
CH(Me)SMe CH(n-Bu)S(O)CF3
CH(Me)SMe CH(n-Bu)S(O)CH2CF3
CH(Me)SMe CH(n-Bu)S(O)2Me
CH(Me)SMe CH(n-Bu)S(O)2Et
CH(Me)SMe CH(n-Bu)S(O)2CF3
CH(Me)SMe CH(n-Bu)S(O)2CH2CF3
CH(Me)SMe CH(i-Bu)SMe
CH(Me)SMe CH(i-Bu)SEt
CH(Me)SMe CH(i-Bu)SCF3
CH(Me)SMe CH(i-Bu)SCH2CF3
CH(Me)SMe CH(i-Bu)S(O)Me
CH(Me)SMe CH(i-Bu)S(O)Et
CH(Me)SMe CH(i-Bu)S(O)CF3
CH(Me)SMe CH(i-Bu)S(O)CH2CF3
CH(Me)SMe CH(i-Bu)S(O)2Me
CH(Me)SMe CH(i-Bu)S(O)2Et
CH(Me)SMe CH(i-Bu)S(O)2CF3
CH(Me)SMe CH(i-Bu)S(O)2CH2CF3
CH(Me)SMe CH(s-Bu)SMe
CH(Me)SMe CH(s-Bu)SEt
CH(Me)SMe CH(s-Bu)SCF3
CH(Me)SMe CH(s-Bu)SCH2CF3
CH(Me)SMe CH(s-Bu)S(O)Me
CH(Me)SMe CH(s-Bu)S(O)Et
CH(Me)SMe CH(s-Bu)S(O)CF3
CH(Me)SMe CH(s-Bu)S(O)CH2CF3
CH(Me)SMe CH(s-Bu)S(O)2Me
CH(Me)SMe CH(s-Bu)S(O)2Et
CH(Me)SMe CH(s-Bu)S(O)2CF3
CH(Me)SMe CH(s-Bu)S(O)2CH2CF3
CH(Me)SMe CH(t-Bu)SMe
CH(Me)SMe CH(t-Bu)SEt
CH(Me)SMe CH(t-Bu)SCF3
CH(Me)SMe CH(t-Bu)SCH2CF3
CH(Me)SMe CH(t-Bu)S(O)Me
CH(Me)SMe CH(t-Bu)S(O)Et
CH(Me)SMe CH(t-Bu)S(O)CF3
CH(Me)SMe CH(t-Bu)S(O)CH2CF3
CH(Me)SMe CH(t-Bu)S(O)2Me
CH(Me)SMe CH(t-Bu)S(O)2Et
CH(Me)SMe CH(t-Bu)S(O)2CF3
CH(Me)SMe CH(t-Bu)S(O)2CH2CF3
CH(Me)SMe CH(CF3)SMe
CH(Me)SMe CH(CF3)SEt
CH(Me)SMe CH(CF3)SCF3
CH(Me)SMe CH(CF3)SCH2CF3
CH(Me)SMe CH(CF3)S(O)Me
CH(Me)SMe CH(CF3)S(O)Et
CH(Me)SMe CH(CF3)S(O)CF3
CH(Me)SMe CH(CF3)S(O)CH2CF3
CH(Me)SMe CH(CF3)S(O)2Me
CH(Me)SMe CH(CF3)S(O)2Et
CH(Me)SMe CH(CF3)S(O)2CF3
CH(Me)SMe CH(CF3)S(O)2CH2CF3
CH(Me)SMe CH2CH2SMe
CH(Me)SMe CH2CH2SEt
CH(Me)SMe CH2CH2SCF3
CH(Me)SMe CH2CH2SCH2CF3
CH(Me)SMe CH2CH2S(O)Me
CH(Me)SMe CH2CH2S(O)Et
CH(Me)SMe CH2CH2S(O)CF3
CH(Me)SMe CH2CH2S(O)CH2CF3
CH(Me)SMe CH2CH2S(O)2Me
CH(Me)SMe CH2CH2S(O)2Et
CH(Me)SMe CH2CH2S(O)2CF3
CH(Me)SMe CH2CH2S(O)2CH2CF3
CH(Me)SMe CH(Me)CH2SMe
CH(Me)SMe CH(Me)CH2SEt
CH(Me)SMe CH(Me)CH2SCF3
CH(Me)SMe CH(Me)CH2SCH2CF3
CH(Me)SMe CH(Me)CH2S(O)Me
CH(Me)SMe CH(Me)CH2S(O)Et
CH(Me)SMe CH(Me)CH2S(O)CF3
CH(Me)SMe CH(Me)CH2S(O)CH2CF3
CH(Me)SMe CH(Me)CH2S(O)2Me
CH(Me)SMe CH(Me)CH2S(O)2Et
CH(Me)SMe CH(Me)CH2S(O)2CF3
CH(Me)SMe CH(Me)CH2S(O)2CH2CF3
CH(Me)SMe CH(Et)CH2SMe
CH(Me)SMe CH(Et)CH2SEt
CH(Me)SMe CH(Et)CH2SCF3
CH(Me)SMe CH(Et)CH2SCH2CF3
CH(Me)SMe CH(Et)CH2S(O)Me
CH(Me)SMe CH(Et)CH2S(O)Et
CH(Me)SMe CH(Et)CH2S(O)CF3
CH(Me)SMe CH(Et)CH2S(O)CH2CF3
CH(Me)SMe CH(Et)CH2S(O)2Me
CH(Me)SMe CH(Et)CH2S(O)2Et
CH(Me)SMe CH(Et)CH2S(O)2CF3
CH(Me)SMe CH(Et)CH2S(O)2CH2CF3
CH(Me)SMe C(Me)2CH2SMe
CH(Me)SMe C(Me)2CH2SEt
CH(Me)SMe C(Me)2CH2SCF3
CH(Me)SMe C(Me)2CH2SCH2CF3
CH(Me)SMe C(Me)2CH2S(O)Me
CH(Me)SMe C(Me)2CH2S(O)Et
CH(Me)SMe C(Me)2CH2S(O)CF3
CH(Me)SMe C(Me)2CH2S(O)CH2CF3
CH(Me)SMe C(Me)2CH2S(O)2Me
CH(Me)SMe C(Me)2CH2S(O)2Et
CH(Me)SMe C(Me)2CH2S(O)2CF3
CH(Me)SMe C(Me)2CH2S(O)2CH2CF3
CH(Me)SMe CH2CH(Me)SMe
CH(Me)SMe CH2CH(Me)SEt
CH(Me)SMe CH2CH(Me)SCF3
CH(Me)SMe CH2CH(Me)SCH2CF3
CH(Me)SMe CH2CH(Me)S(O)Me
CH(Me)SMe CH2CH(Me)S(O)Et
CH(Me)SMe CH2CH(Me)S(O)CF3
CH(Me)SMe CH2CH(Me)S(O)CH2CF3
CH(Me)SMe CH2CH(Me)S(O)2Me
CH(Me)SMe CH2CH(Me)S(O)2Et
CH(Me)SMe CH2CH(Me)S(O)2CF3
CH(Me)SMe CH2CH(Me)S(O)2CH2CF3
CH(Me)SMe CH2CH(Et)SMe
CH(Me)SMe CH2CH(Et)SEt
CH(Me)SMe CH2CH(Et)SCF3
CH(Me)SMe CH2CH(Et)SCH2CF3
CH(Me)SMe CH2CH(Et)S(O)Me
CH(Me)SMe CH2CH(Et)S(O)Et
CH(Me)SMe CH2CH(Et)S(O)CF3
CH(Me)SMe CH2CH(Et)S(O)CH2CF3
CH(Me)SMe CH2CH(Et)S(O)2Me
CH(Me)SMe CH2CH(Et)S(O)2Et
CH(Me)SMe CH2CH(Et)S(O)2CF3
CH(Me)SMe CH2CH(Et)S(O)2CH2CF3
CH(Me)SMe CH(Me)CH(Me)SMe
CH(Me)SMe CH(Me)CH(Me)SEt
CH(Me)SMe CH(Me)CH(Me)SCF3
CH(Me)SMe CH(Me)CH(Me)SCH2CF3
CH(Me)SMe CH(Me)CH(Me)S(O)Me
CH(Me)SMe CH(Me)CH(Me)S(O)Et
CH(Me)SMe CH(Me)CH(Me)S(O)CF3
CH(Me)SMe CH(Me)CH(Me)S(O)CH2CF3
CH(Me)SMe CH(Me)CH(Me)S(O)2Me
CH(Me)SMe CH(Me)CH(Me)S(O)2Et
CH(Me)SMe CH(Me)CH(Me)S(O)2CF3
CH(Me)SMe CH(Me)CH(Me)S(O)2CH2CF3
C(O)Me CH2SMe
C(O)Me CH2SEt
C(O)Me CH2SCF3
C(O)Me CH2SCH2CF3
C(O)Me CH2S(O)Me
C(O)Me CH2S(O)Et
C(O)Me CH2S(O)CF3
C(O)Me CH2S(O)CH2CF3
C(O)Me CH2S(O)2Me
C(O)Me CH2S(O)2Et
C(O)Me CH2S(O)2CF3
C(O)Me CH2S(O)2CH2CF3
C(O)Me CH(Me)SMe
C(O)Me CH(Me)SEt
C(O)Me CH(Me)SCF3
C(O)Me CH(Me)SCH2CF3
C(O)Me CH(Me)S(O)Me
C(O)Me CH(Me)S(O)Et
C(O)Me CH(Me)S(O)CF3
C(O)Me CH(Me)S(O)CH2CF3
C(O)Me CH(Me)S(O)2Me
C(O)Me CH(Me)S(O)2Et
C(O)Me CH(Me)S(O)2CF3
C(O)Me CH(Me)S(O)2CH2CF3
C(O)Me CH(Et)SMe
C(O)Me CH(Et)SEt
C(O)Me CH(Et)SCF3
C(O)Me CH(Et)SCH2CF3
C(O)Me CH(Et)S(O)Me
C(O)Me CH(Et)S(O)Et
C(O)Me CH(Et)S(O)CF3
C(O)Me CH(Et)S(O)CH2CF3
C(O)Me CH(Et)S(O)2Me
C(O)Me CH(Et)S(O)2Et
C(O)Me CH(Et)S(O)2CF3
C(O)Me CH(Et)S(O)2CH2CF3
C(O)Me CH(n-Pr)SMe
C(O)Me CH(n-Pr)SEt
C(O)Me CH(n-Pr)SCF3
C(O)Me CH(n-Pr)SCH2CF3
C(O)Me CH(n-Pr)S(O)Me
C(O)Me CH(n-Pr)S(O)Et
C(O)Me CH(n-Pr)S(O)CF3
C(O)Me CH(n-Pr)S(O)CH2CF3
C(O)Me CH(n-Pr)S(O)2Me
C(O)Me CH(n-Pr)S(O)2Et
C(O)Me CH(n-Pr)S(O)2CF3
C(O)Me CH(n-Pr)S(O)2CH2CF3
C(O)Me CH(i-Pr)SMe
C(O)Me CH(i-Pr)SEt
C(O)Me CH(i-Pr)SCF3
C(O)Me CH(i-Pr)SCH2CF3
C(O)Me CH(i-Pr)S(O)Me
C(O)Me CH(i-Pr)S(O)Et
C(O)Me CH(i-Pr)S(O)CF3
C(O)Me CH(i-Pr)S(O)CH2CF3
C(O)Me CH(i-Pr)S(O)2Me
C(O)Me CH(i-Pr)S(O)2Et
C(O)Me CH(i-Pr)S(O)2CF3
C(O)Me CH(i-Pr)S(O)2CH2CF3
C(O)Me CH(n-Bu)SMe
C(O)Me CH(n-Bu)SEt
C(O)Me CH(n-Bu)SCF3
C(O)Me CH(n-Bu)SCH2CF3
C(O)Me CH(n-Bu)S(O)Me
C(O)Me CH(n-Bu)S(O)Et
C(O)Me CH(n-Bu)S(O)CF3
C(O)Me CH(n-Bu)S(O)CH2CF3
C(O)Me CH(n-Bu)S(O)2Me
C(O)Me CH(n-Bu)S(O)2Et
C(O)Me CH(n-Bu)S(O)2CF3
C(O)Me CH(n-Bu)S(O)2CH2CF3
C(O)Me CH(i-Bu)SMe
C(O)Me CH(i-Bu)SEt
C(O)Me CH(i-Bu)SCF3
C(O)Me CH(i-Bu)SCH2CF3
C(O)Me CH(i-Bu)S(O)Me
C(O)Me CH(i-Bu)S(O)Et
C(O)Me CH(i-Bu)S(O)CF3
C(O)Me CH(i-Bu)S(O)CH2CF3
C(O)Me CH(i-Bu)S(O)2Me
C(O)Me CH(i-Bu)S(O)2Et
C(O)Me CH(i-Bu)S(O)2CF3
C(O)Me CH(i-Bu)S(O)2CH2CF3
C(O)Me CH(s-Bu)SMe
C(O)Me CH(s-Bu)SEt
C(O)Me CH(s-Bu)SCF3
C(O)Me CH(s-Bu)SCH2CF3
C(O)Me CH(s-Bu)S(O)Me
C(O)Me CH(s-Bu)S(O)Et
C(O)Me CH(s-Bu)S(O)CF3
C(O)Me CH(s-Bu)S(O)CH2CF3
C(O)Me CH(s-Bu)S(O)2Me
C(O)Me CH(s-Bu)S(O)2Et
C(O)Me CH(s-Bu)S(O)2CF3
C(O)Me CH(s-Bu)S(O)2CH2CF3
C(O)Me CH(t-Bu)SMe
C(O)Me CH(t-Bu)SEt
C(O)Me CH(t-Bu)SCF3
C(O)Me CH(t-Bu)SCH2CF3
C(O)Me CH(t-Bu)S(O)Me
C(O)Me CH(t-Bu)S(O)Et
C(O)Me CH(t-Bu)S(O)CF3
C(O)Me CH(t-Bu)S(O)CH2CF3
C(O)Me CH(t-Bu)S(O)2Me
C(O)Me CH(t-Bu)S(O)2Et
C(O)Me CH(t-Bu)S(O)2CF3
C(O)Me CH(t-Bu)S(O)2CH2CF3
C(O)Me CH(CF3)SMe
C(O)Me CH(CF3)SEt
C(O)Me CH(CF3)SCF3
C(O)Me CH(CF3)SCH2CF3
C(O)Me CH(CF3)S(O)Me
C(O)Me CH(CF3)S(O)Et
C(O)Me CH(CF3)S(O)CF3
C(O)Me CH(CF3)S(O)CH2CF3
C(O)Me CH(CF3)S(O)2Me
C(O)Me CH(CF3)S(O)2Et
C(O)Me CH(CF3)S(O)2CF3
C(O)Me CH(CF3)S(O)2CH2CF3
C(O)Me CH2CH2SMe
C(O)Me CH2CH2SEt
C(O)Me CH2CH2SCF3
C(O)Me CH2CH2SCH2CF3
C(O)Me CH2CH2S(O)Me
C(O)Me CH2CH2S(O)Et
C(O)Me CH2CH2S(O)CF3
C(O)Me CH2CH2S(O)CH2CF3
C(O)Me CH2CH2S(O)2Me
C(O)Me CH2CH2S(O)2Et
C(O)Me CH2CH2S(O)2CF3
C(O)Me CH2CH2S(O)2CH2CF3
C(O)Me CH(Me)CH2SMe
C(O)Me CH(Me)CH2SEt
C(O)Me CH(Me)CH2SCF3
C(O)Me CH(Me)CH2SCH2CF3
C(O)Me CH(Me)CH2S(O)Me
C(O)Me CH(Me)CH2S(O)Et
C(O)Me CH(Me)CH2S(O)CF3
C(O)Me CH(Me)CH2S(O)CH2CF3
C(O)Me CH(Me)CH2S(O)2Me
C(O)Me CH(Me)CH2S(O)2Et
C(O)Me CH(Me)CH2S(O)2CF3
C(O)Me CH(Me)CH2S(O)2CH2CF3
C(O)Me CH(Et)CH2SMe
C(O)Me CH(Et)CH2SEt
C(O)Me CH(Et)CH2SCF3
C(O)Me CH(Et)CH2SCH2CF3
C(O)Me CH(Et)CH2S(O)Me
C(O)Me CH(Et)CH2S(O)Et
C(O)Me CH(Et)CH2S(O)CF3
C(O)Me CH(Et)CH2S(O)CH2CF3
C(O)Me CH(Et)CH2S(O)2Me
C(O)Me CH(Et)CH2S(O)2Et
C(O)Me CH(Et)CH2S(O)2CF3
C(O)Me CH(Et)CH2S(O)2CH2CF3
C(O)Me C(Me)2CH2SMe
C(O)Me C(Me)2CH2SEt
C(O)Me C(Me)2CH2SCF3
C(O)Me C(Me)2CH2SCH2CF3
C(O)Me C(Me)2CH2S(O)Me
C(O)Me C(Me)2CH2S(O)Et
C(O)Me C(Me)2CH2S(O)CF3
C(O)Me C(Me)2CH2S(O)CH2CF3
C(O)Me C(Me)2CH2S(O)2Me
C(O)Me C(Me)2CH2S(O)2Et
C(O)Me C(Me)2CH2S(O)2CF3
C(O)Me C(Me)2CH2S(O)2CH2CF3
C(O)Me CH2CH(Me)SMe
C(O)Me CH2CH(Me)SEt
C(O)Me CH2CH(Me)SCF3
C(O)Me CH2CH(Me)SCH2CF3
C(O)Me CH2CH(Me)S(O)Me
C(O)Me CH2CH(Me)S(O)Et
C(O)Me CH2CH(Me)S(O)CF3
C(O)Me CH2CH(Me)S(O)CH2CF3
C(O)Me CH2CH(Me)S(O)2Me
C(O)Me CH2CH(Me)S(O)2Et
C(O)Me CH2CH(Me)S(O)2CF3
C(O)Me CH2CH(Me)S(O)2CH2CF3
C(O)Me CH2CH(Et)SMe
C(O)Me CH2CH(Et)SEt
C(O)Me CH2CH(Et)SCF3
C(O)Me CH2CH(Et)SCH2CF3
C(O)Me CH2CH(Et)S(O)Me
C(O)Me CH2CH(Et)S(O)Et
C(O)Me CH2CH(Et)S(O)CF3
C(O)Me CH2CH(Et)S(O)CH2CF3
C(O)Me CH2CH(Et)S(O)2Me
C(O)Me CH2CH(Et)S(O)2Et
C(O)Me CH2CH(Et)S(O)2CF3
C(O)Me CH2CH(Et)S(O)2CH2CF3
C(O)Me CH(Me)CH(Me)SMe
C(O)Me CH(Me)CH(Me)SEt
C(O)Me CH(Me)CH(Me)SCF3
C(O)Me CH(Me)CH(Me)SCH2CF3
C(O)Me CH(Me)CH(Me)S(O)Me
C(O)Me CH(Me)CH(Me)S(O)Et
C(O)Me CH(Me)CH(Me)S(O)CF3
C(O)Me CH(Me)CH(Me)S(O)CH2CF3
C(O)Me CH(Me)CH(Me)S(O)2Me
C(O)Me CH(Me)CH(Me)S(O)2Et
C(O)Me CH(Me)CH(Me)S(O)2CF3
C(O)Me CH(Me)CH(Me)S(O)2CH2CF3
C(O)OMe CH2SMe
C(O)OMe CH2SEt
C(O)OMe CH2SCF3
C(O)OMe CH2SCH2CF3
C(O)OMe CH2S(O)Me
C(O)OMe CH2S(O)Et
C(O)OMe CH2S(O)CF3
C(O)OMe CH2S(O)CH2CF3
C(O)OMe CH2S(O)2Me
C(O)OMe CH2S(O)2Et
C(O)OMe CH2S(O)2CF3
C(O)OMe CH2S(O)2CH2CF3
C(O)OMe CH(Me)SMe
C(O)OMe CH(Me)SEt
C(O)OMe CH(Me)SCF3
C(O)OMe CH(Me)SCH2CF3
C(O)OMe CH(Me)S(O)Me
C(O)OMe CH(Me)S(O)Et
C(O)OMe CH(Me)S(O)CF3
C(O)OMe CH(Me)S(O)CH2CF3
C(O)OMe CH(Me)S(O)2Me
C(O)OMe CH(Me)S(O)2Et
C(O)OMe CH(Me)S(O)2CF3
C(O)OMe CH(Me)S(O)2CH2CF3
C(O)OMe CH(Et)SMe
C(O)OMe CH(Et)SEt
C(O)OMe CH(Et)SCF3
C(O)OMe CH(Et)SCH2CF3
C(O)OMe CH(Et)S(O)Me
C(O)OMe CH(Et)S(O)Et
C(O)OMe CH(Et)S(O)CF3
C(O)OMe CH(Et)S(O)CH2CF3
C(O)OMe CH(Et)S(O)2Me
C(O)OMe CH(Et)S(O)2Et
C(O)OMe CH(Et)S(O)2CF3
C(O)OMe CH(Et)S(O)2CH2CF3
C(O)OMe CH(n-Pr)SMe
C(O)OMe CH(n-Pr)SEt
C(O)OMe CH(n-Pr)SCF3
C(O)OMe CH(n-Pr)SCH2CF3
C(O)OMe CH(n-Pr)S(O)Me
C(O)OMe CH(n-Pr)S(O)Et
C(O)OMe CH(n-Pr)S(O)CF3
C(O)OMe CH(n-Pr)S(O)CH2CF3
C(O)OMe CH(n-Pr)S(O)2Me
C(O)OMe CH(n-Pr)S(O)2Et
C(O)OMe CH(n-Pr)S(O)2CF3
C(O)OMe CH(n-Pr)S(O)2CH2CF3
C(O)OMe CH(i-Pr)SMe
C(O)OMe CH(i-Pr)SEt
C(O)OMe CH(i-Pr)SCF3
C(O)OMe CH(i-Pr)SCH2CF3
C(O)OMe CH(i-Pr)S(O)Me
C(O)OMe CH(i-Pr)S(O)Et
C(O)OMe CH(i-Pr)S(O)CF3
C(O)OMe CH(i-Pr)S(O)CH2CF3
C(O)OMe CH(i-Pr)S(O)2Me
C(O)OMe CH(i-Pr)S(O)2Et
C(O)OMe CH(i-Pr)S(O)2CF3
C(O)OMe CH(i-Pr)S(O)2CH2CF3
C(O)OMe CH(n-Bu)SMe
C(O)OMe CH(n-Bu)SEt
C(O)OMe CH(n-Bu)SCF3
C(O)OMe CH(n-Bu)SCH2CF3
C(O)OMe CH(n-Bu)S(O)Me
C(O)OMe CH(n-Bu)S(O)Et
C(O)OMe CH(n-Bu)S(O)CF3
C(O)OMe CH(n-Bu)S(O)CH2CF3
C(O)OMe CH(n-Bu)S(O)2Me
C(O)OMe CH(n-Bu)S(O)2Et
C(O)OMe CH(n-Bu)S(O)2CF3
C(O)OMe CH(n-Bu)S(O)2CH2CF3
C(O)OMe CH(i-Bu)SMe
C(O)OMe CH(i-Bu)SEt
C(O)OMe CH(i-Bu)SCF3
C(O)OMe CH(i-Bu)SCH2CF3
C(O)OMe CH(i-Bu)S(O)Me
C(O)OMe CH(i-Bu)S(O)Et
C(O)OMe CH(i-Bu)S(O)CF3
C(O)OMe CH(i-Bu)S(O)CH2CF3
C(O)OMe CH(i-Bu)S(O)2Me
C(O)OMe CH(i-Bu)S(O)2Et
C(O)OMe CH(i-Bu)S(O)2CF3
C(O)OMe CH(i-Bu)S(O)2CH2CF3
C(O)OMe CH(s-Bu)SMe
C(O)OMe CH(s-Bu)SEt
C(O)OMe CH(s-Bu)SCF3
C(O)OMe CH(s-Bu)SCH2CF3
C(O)OMe CH(s-Bu)S(O)Me
C(O)OMe CH(s-Bu)S(O)Et
C(O)OMe CH(s-Bu)S(O)CF3
C(O)OMe CH(s-Bu)S(O)CH2CF3
C(O)OMe CH(s-Bu)S(O)2Me
C(O)OMe CH(s-Bu)S(O)2Et
C(O)OMe CH(s-Bu)S(O)2CF3
C(O)OMe CH(s-Bu)S(O)2CH2CF3
C(O)OMe CH(t-Bu)SMe
C(O)OMe CH(t-Bu)SEt
C(O)OMe CH(t-Bu)SCF3
C(O)OMe CH(t-Bu)SCH2CF3
C(O)OMe CH(t-Bu)S(O)Me
C(O)OMe CH(t-Bu)S(O)Et
C(O)OMe CH(t-Bu)S(O)CF3
C(O)OMe CH(t-Bu)S(O)CH2CF3
C(O)OMe CH(t-Bu)S(O)2Me
C(O)OMe CH(t-Bu)S(O)2Et
C(O)OMe CH(t-Bu)S(O)2CF3
C(O)OMe CH(t-Bu)S(O)2CH2CF3
C(O)OMe CH(CF3)SMe
C(O)OMe CH(CF3)SEt
C(O)OMe CH(CF3)SCF3
C(O)OMe CH(CF3)SCH2CF3
C(O)OMe CH(CF3)S(O)Me
C(O)OMe CH(CF3)S(O)Et
C(O)OMe CH(CF3)S(O)CF3
C(O)OMe CH(CF3)S(O)CH2CF3
C(O)OMe CH(CF3)S(O)2Me
C(O)OMe CH(CF3)S(O)2Et
C(O)OMe CH(CF3)S(O)2CF3
C(O)OMe CH(CF3)S(O)2CH2CF3
C(O)OMe CH2CH2SMe
C(O)OMe CH2CH2SEt
C(O)OMe CH2CH2SCF3
C(O)OMe CH2CH2SCH2CF3
C(O)OMe CH2CH2S(O)Me
C(O)OMe CH2CH2S(O)Et
C(O)OMe CH2CH2S(O)CF3
C(O)OMe CH2CH2S(O)CH2CF3
C(O)OMe CH2CH2S(O)2Me
C(O)OMe CH2CH2S(O)2Et
C(O)OMe CH2CH2S(O)2CF3
C(O)OMe CH2CH2S(O)2CH2CF3
C(O)OMe CH(Me)CH2SMe
C(O)OMe CH(Me)CH2SEt
C(O)OMe CH(Me)CH2SCF3
C(O)OMe CH(Me)CH2SCH2CF3
C(O)OMe CH(Me)CH2S(O)Me
C(O)OMe CH(Me)CH2S(O)Et
C(O)OMe CH(Me)CH2S(O)CF3
C(O)OMe CH(Me)CH2S(O)CH2CF3
C(O)OMe CH(Me)CH2S(O)2Me
C(O)OMe CH(Me)CH2S(O)2Et
C(O)OMe CH(Me)CH2S(O)2CF3
C(O)OMe CH(Me)CH2S(O)2CH2CF3
C(O)OMe CH(Et)CH2SMe
C(O)OMe CH(Et)CH2SEt
C(O)OMe CH(Et)CH2SCF3
C(O)OMe CH(Et)CH2SCH2CF3
C(O)OMe CH(Et)CH2S(O)Me
C(O)OMe CH(Et)CH2S(O)Et
C(O)OMe CH(Et)CH2S(O)CF3
C(O)OMe CH(Et)CH2S(O)CH2CF3
C(O)OMe CH(Et)CH2S(O)2Me
C(O)OMe CH(Et)CH2S(O)2Et
C(O)OMe CH(Et)CH2S(O)2CF3
C(O)OMe CH(Et)CH2S(O)2CH2CF3
C(O)OMe C(Me)2CH2SMe
C(O)OMe C(Me)2CH2SEt
C(O)OMe C(Me)2CH2SCF3
C(O)OMe C(Me)2CH2SCH2CF3
C(O)OMe C(Me)2CH2S(O)Me
C(O)OMe C(Me)2CH2S(O)Et
C(O)OMe C(Me)2CH2S(O)CF3
C(O)OMe C(Me)2CH2S(O)CH2CF3
C(O)OMe C(Me)2CH2S(O)2Me
C(O)OMe C(Me)2CH2S(O)2Et
C(O)OMe C(Me)2CH2S(O)2CF3
C(O)OMe C(Me)2CH2S(O)2CH2CF3
C(O)OMe CH2CH(Me)SMe
C(O)OMe CH2CH(Me)SEt
C(O)OMe CH2CH(Me)SCF3
C(O)OMe CH2CH(Me)SCH2CF3
C(O)OMe CH2CH(Me)S(O)Me
C(O)OMe CH2CH(Me)S(O)Et
C(O)OMe CH2CH(Me)S(O)CF3
C(O)OMe CH2CH(Me)S(O)CH2CF3
C(O)OMe CH2CH(Me)S(O)2Me
C(O)OMe CH2CH(Me)S(O)2Et
C(O)OMe CH2CH(Me)S(O)2CF3
C(O)OMe CH2CH(Me)S(O)2CH2CF3
C(O)OMe CH2CH(Et)SMe
C(O)OMe CH2CH(Et)SEt
C(O)OMe CH2CH(Et)SCF3
C(O)OMe CH2CH(Et)SCH2CF3
C(O)OMe CH2CH(Et)S(O)Me
C(O)OMe CH2CH(Et)S(O)Et
C(O)OMe CH2CH(Et)S(O)CF3
C(O)OMe CH2CH(Et)S(O)CH2CF3
C(O)OMe CH2CH(Et)S(O)2Me
C(O)OMe CH2CH(Et)S(O)2Et
C(O)OMe CH2CH(Et)S(O)2CF3
C(O)OMe CH2CH(Et)S(O)2CH2CF3
C(O)OMe CH(Me)CH(Me)SMe
C(O)OMe CH(Me)CH(Me)SEt
C(O)OMe CH(Me)CH(Me)SCF3
C(O)OMe CH(Me)CH(Me)SCH2CF3
C(O)OMe CH(Me)CH(Me)S(O)Me
C(O)OMe CH(Me)CH(Me)S(O)Et
C(O)OMe CH(Me)CH(Me)S(O)CF3
C(O)OMe CH(Me)CH(Me)S(O)CH2CF3
C(O)OMe CH(Me)CH(Me)S(O)2Me
C(O)OMe CH(Me)CH(Me)S(O)2Et
C(O)OMe CH(Me)CH(Me)S(O)2CF3
C(O)OMe CH(Me)CH(Me)S(O)2CH2CF3
CH2OMe CH2SMe
CH2OMe CH2SEt
CH2OMe CH2SCF3
CH2OMe CH2SCH2CF3
CH2OMe CH2S(O)Me
CH2OMe CH2S(O)Et
CH2OMe CH2S(O)CF3
CH2OMe CH2S(O)CH2CF3
CH2OMe CH2S(O)2Me
CH2OMe CH2S(O)2Et
CH2OMe CH2S(O)2CF3
CH2OMe CH2S(O)2CH2CF3
CH2OMe CH(Me)SMe
CH2OMe CH(Me)SEt
CH2OMe CH(Me)SCF3
CH2OMe CH(Me)SCH2CF3
CH2OMe CH(Me)S(O)Me
CH2OMe CH(Me)S(O)Et
CH2OMe CH(Me)S(O)CF3
CH2OMe CH(Me)S(O)CH2CF3
CH2OMe CH(Me)S(O)2Me
CH2OMe CH(Me)S(O)2Et
CH2OMe CH(Me)S(O)2CF3
CH2OMe CH(Me)S(O)2CH2CF3
CH2OMe CH(Et)SMe
CH2OMe CH(Et)SEt
CH2OMe CH(Et)SCF3
CH2OMe CH(Et)SCH2CF3
CH2OMe CH(Et)S(O)Me
CH2OMe CH(Et)S(O)Et
CH2OMe CH(Et)S(O)CF3
CH2OMe CH(Et)S(O)CH2CF3
CH2OMe CH(Et)S(O)2Me
CH2OMe CH(Et)S(O)2Et
CH2OMe CH(Et)S(O)2CF3
CH2OMe CH(Et)S(O)2CH2CF3
CH2OMe CH(n-Pr)SMe
CH2OMe CH(n-Pr)SEt
CH2OMe CH(n-Pr)SCF3
CH2OMe CH(n-Pr)SCH2CF3
CH2OMe CH(n-Pr)S(O)Me
CH2OMe CH(n-Pr)S(O)Et
CH2OMe CH(n-Pr)S(O)CF3
CH2OMe CH(n-Pr)S(O)CH2CF3
CH2OMe CH(n-Pr)S(O)2Me
CH2OMe CH(n-Pr)S(O)2Et
CH2OMe CH(n-Pr)S(O)2CF3
CH2OMe CH(n-Pr)S(O)2CH2CF3
CH2OMe CH(i-Pr)SMe
CH2OMe CH(i-Pr)SEt
CH2OMe CH(i-Pr)SCF3
CH2OMe CH(i-Pr)SCH2CF3
CH2OMe CH(i-Pr)S(O)Me
CH2OMe CH(i-Pr)S(O)Et
CH2OMe CH(i-Pr)S(O)CF3
CH2OMe CH(i-Pr)S(O)CH2CF3
CH2OMe CH(i-Pr)S(O)2Me
CH2OMe CH(i-Pr)S(O)2Et
CH2OMe CH(i-Pr)S(O)2CF3
CH2OMe CH(i-Pr)S(O)2CH2CF3
CH2OMe CH(n-Bu)SMe
CH2OMe CH(n-Bu)SEt
CH2OMe CH(n-Bu)SCF3
CH2OMe CH(n-Bu)SCH2CF3
CH2OMe CH(n-Bu)S(O)Me
CH2OMe CH(n-Bu)S(O)Et
CH2OMe CH(n-Bu)S(O)CF3
CH2OMe CH(n-Bu)S(O)CH2CF3
CH2OMe CH(n-Bu)S(O)2Me
CH2OMe CH(n-Bu)S(O)2Et
CH2OMe CH(n-Bu)S(O)2CF3
CH2OMe CH(n-Bu)S(O)2CH2CF3
CH2OMe CH(i-Bu)SMe
CH2OMe CH(i-Bu)SEt
CH2OMe CH(i-Bu)SCF3
CH2OMe CH(i-Bu)SCH2CF3
CH2OMe CH(i-Bu)S(O)Me
CH2OMe CH(i-Bu)S(O)Et
CH2OMe CH(i-Bu)S(O)CF3
CH2OMe CH(i-Bu)S(O)CH2CF3
CH2OMe CH(i-Bu)S(O)2Me
CH2OMe CH(i-Bu)S(O)2Et
CH2OMe CH(i-Bu)S(O)2CF3
CH2OMe CH(i-Bu)S(O)2CH2CF3
CH2OMe CH(s-Bu)SMe
CH2OMe CH(s-Bu)SEt
CH2OMe CH(s-Bu)SCF3
CH2OMe CH(s-Bu)SCH2CF3
CH2OMe CH(s-Bu)S(O)Me
CH2OMe CH(s-Bu)S(O)Et
CH2OMe CH(s-Bu)S(O)CF3
CH2OMe CH(s-Bu)S(O)CH2CF3
CH2OMe CH(s-Bu)S(O)2Me
CH2OMe CH(s-Bu)S(O)2Et
CH2OMe CH(s-Bu)S(O)2CF3
CH2OMe CH(s-Bu)S(O)2CH2CF3
CH2OMe CH(t-Bu)SMe
CH2OMe CH(t-Bu)SEt
CH2OMe CH(t-Bu)SCF3
CH2OMe CH(t-Bu)SCH2CF3
CH2OMe CH(t-Bu)S(O)Me
CH2OMe CH(t-Bu)S(O)Et
CH2OMe CH(t-Bu)S(O)CF3
CH2OMe CH(t-Bu)S(O)CH2CF3
CH2OMe CH(t-Bu)S(O)2Me
CH2OMe CH(t-Bu)S(O)2Et
CH2OMe CH(t-Bu)S(O)2CF3
CH2OMe CH(t-Bu)S(O)2CH2CF3
CH2OMe CH(CF3)SMe
CH2OMe CH(CF3)SEt
CH2OMe CH(CF3)SCF3
CH2OMe CH(CF3)SCH2CF3
CH2OMe CH(CF3)S(O)Me
CH2OMe CH(CF3)S(O)Et
CH2OMe CH(CF3)S(O)CF3
CH2OMe CH(CF3)S(O)CH2CF3
CH2OMe CH(CF3)S(O)2Me
CH2OMe CH(CF3)S(O)2Et
CH2OMe CH(CF3)S(O)2CF3
CH2OMe CH(CF3)S(O)2CH2CF3
CH2OMe CH2CH2SMe
CH2OMe CH2CH2SEt
CH2OMe CH2CH2SCF3
CH2OMe CH2CH2SCH2CF3
CH2OMe CH2CH2S(O)Me
CH2OMe CH2CH2S(O)Et
CH2OMe CH2CH2S(O)CF3
CH2OMe CH2CH2S(O)CH2CF3
CH2OMe CH2CH2S(O)2Me
CH2OMe CH2CH2S(O)2Et
CH2OMe CH2CH2S(O)2CF3
CH2OMe CH2CH2S(O)2CH2CF3
CH2OMe CH(Me)CH2SMe
CH2OMe CH(Me)CH2SEt
CH2OMe CH(Me)CH2SCF3
CH2OMe CH(Me)CH2SCH2CF3
CH2OMe CH(Me)CH2S(O)Me
CH2OMe CH(Me)CH2S(O)Et
CH2OMe CH(Me)CH2S(O)CF3
CH2OMe CH(Me)CH2S(O)CH2CF3
CH2OMe CH(Me)CH2S(O)2Me
CH2OMe CH(Me)CH2S(O)2Et
CH2OMe CH(Me)CH2S(O)2CF3
CH2OMe CH(Me)CH2S(O)2CH2CF3
CH2OMe CH(Et)CH2SMe
CH2OMe CH(Et)CH2SEt
CH2OMe CH(Et)CH2SCF3
CH2OMe CH(Et)CH2SCH2CF3
CH2OMe CH(Et)CH2S(O)Me
CH2OMe CH(Et)CH2S(O)Et
CH2OMe CH(Et)CH2S(O)CF3
CH2OMe CH(Et)CH2S(O)CH2CF3
CH2OMe CH(Et)CH2S(O)2Me
CH2OMe CH(Et)CH2S(O)2Et
CH2OMe CH(Et)CH2S(O)2CF3
CH2OMe CH(Et)CH2S(O)2CH2CF3
CH2OMe C(Me)2CH2SMe
CH2OMe C(Me)2CH2SEt
CH2OMe C(Me)2CH2SCF3
CH2OMe C(Me)2CH2SCH2CF3
CH2OMe C(Me)2CH2S(O)Me
CH2OMe C(Me)2CH2S(O)Et
CH2OMe C(Me)2CH2S(O)CF3
CH2OMe C(Me)2CH2S(O)CH2CF3
CH2OMe C(Me)2CH2S(O)2Me
CH2OMe C(Me)2CH2S(O)2Et
CH2OMe C(Me)2CH2S(O)2CF3
CH2OMe C(Me)2CH2S(O)2CH2CF3
CH2OMe CH2CH(Me)SMe
CH2OMe CH2CH(Me)SEt
CH2OMe CH2CH(Me)SCF3
CH2OMe CH2CH(Me)SCH2CF3
CH2OMe CH2CH(Me)S(O)Me
CH2OMe CH2CH(Me)S(O)Et
CH2OMe CH2CH(Me)S(O)CF3
CH2OMe CH2CH(Me)S(O)CH2CF3
CH2OMe CH2CH(Me)S(O)2Me
CH2OMe CH2CH(Me)S(O)2Et
CH2OMe CH2CH(Me)S(O)2CF3
CH2OMe CH2CH(Me)S(O)2CH2CF3
CH2OMe CH2CH(Et)SMe
CH2OMe CH2CH(Et)SEt
CH2OMe CH2CH(Et)SCF3
CH2OMe CH2CH(Et)SCH2CF3
CH2OMe CH2CH(Et)S(O)Me
CH2OMe CH2CH(Et)S(O)Et
CH2OMe CH2CH(Et)S(O)CF3
CH2OMe CH2CH(Et)S(O)CH2CF3
CH2OMe CH2CH(Et)S(O)2Me
CH2OMe CH2CH(Et)S(O)2Et
CH2OMe CH2CH(Et)S(O)2CF3
CH2OMe CH2CH(Et)S(O)2CH2CF3
CH2OMe CH(Me)CH(Me)SMe
CH2OMe CH(Me)CH(Me)SEt
CH2OMe CH(Me)CH(Me)SCF3
CH2OMe CH(Me)CH(Me)SCH2CF3
CH2OMe CH(Me)CH(Me)S(O)Me
CH2OMe CH(Me)CH(Me)S(O)Et
CH2OMe CH(Me)CH(Me)S(O)CF3
CH2OMe CH(Me)CH(Me)S(O)CH2CF3
CH2OMe CH(Me)CH(Me)S(O)2Me
CH2OMe CH(Me)CH(Me)S(O)2Et
CH2OMe CH(Me)CH(Me)S(O)2CF3
CH2OMe CH(Me)CH(Me)S(O)2CH2CF3
CH2SMe CH2SMe
CH2SEt CH2SMe
CH2S(O)Me CH2SMe
CH2S(O)Et CH2SMe
CH2S(O)2Me CH2SMe
CH2S(O)2Et CH2SMe
CH(Me)SMe CH2SMe
CH(Me)SEt CH2SMe
CH(Me)S(O)Me CH2SMe
CH(Me)S(O)Et CH2SMe
CH(Me)S(O)2Me CH2SMe
CH(Me)S(O)2Et CH2SMe
CH(Et)SMe CH2SMe
CH(Et)SEt CH2SMe
CH(Et)S(O)Me CH2SMe
CH(Et)S(O)Et CH2SMe
CH(Et)S(O)2Me CH2SMe
CH(Et)S(O)2Et CH2SMe
CH(n-Pr)SMe CH2SMe
CH(n-Pr)SEt CH2SMe
CH(n-Pr)S(O)Me CH2SMe
CH(n-Pr)S(O)Et CH2SMe
CH(n-Pr)S(O)2Me CH2SMe
CH(n-Pr)S(O)2Et CH2SMe
CH(i-Pr)SMe CH2SMe
CH(i-Pr)SEt CH2SMe
CH(i-Pr)S(O)Me CH2SMe
CH(i-Pr)S(O)Et CH2SMe
CH(i-Pr)S(O)2Me CH2SMe
CH(i-Pr)S(O)2Et CH2SMe
CH(n-Bu)SMe CH2SMe
CH(n-Bu)SEt CH2SMe
CH(n-Bu)S(O)Me CH2SMe
CH(n-Bu)S(O)Et CH2SMe
CH(n-Bu)S(O)2Me CH2SMe
CH(n-Bu)S(O)2Et CH2SMe
CH(i-Bu)SMe CH2SMe
CH(i-Bu)SEt CH2SMe
CH(i-Bu)S(O)Me CH2SMe
CH(i-Bu)S(O)Et CH2SMe
CH(i-Bu)S(O)2Me CH2SMe
CH(i-Bu)S(O)2Et CH2SMe
CH(s-Bu)SMe CH2SMe
CH(s-Bu)SEt CH2SMe
CH(s-Bu)S(O)Me CH2SMe
CH(s-Bu)S(O)Et CH2SMe
CH(s-Bu)S(O)2Me CH2SMe
CH(s-Bu)S(O)2Et CH2SMe
CH(t-Bu)SMe CH2SMe
CH(t-Bu)SEt CH2SMe
CH(t-Bu)S(O)Me CH2SMe
CH(t-Bu)S(O)Et CH2SMe
CH(t-Bu)S(O)2Me CH2SMe
CH(t-Bu)S(O)2Et CH2SMe
CH2CH2SMe CH2SMe
CH2CH2SEt CH2SMe
CH2CH2S(O)2Me CH2SMe
CH2CH2S(O)2Et CH2SMe
CH(Me)CH2SMe CH2SMe
CH(Me)CH2SEt CH2SMe
CH(Me)CH2S(O)Me CH2SMe
CH(Me)CH2S(O)Et CH2SMe
CH(Me)CH2S(O)2Me CH2SMe
CH(Me)CH2S(O)2Et CH2SMe
CH(Et)CH2SMe CH2SMe
CH(Et)CH2SEt CH2SMe
CH(Et)CH2S(O)Me CH2SMe
CH(Et)CH2S(O)Et CH2SMe
CH(Et)CH2S(O)2Me CH2SMe
CH(Et)CH2S(O)2Et CH2SMe
C(Me)2CH2SMe CH2SMe
C(Me)2CH2SEt CH2SMe
C(Me)2CH2S(O)Me CH2SMe
C(Me)2CH2S(O)Et CH2SMe
C(Me)2CH2S(O)2Me CH2SMe
C(Me)2CH2S(O)2Et CH2SMe
CH2CH(Me)SMe CH2SMe
CH2CH(Me)SEt CH2SMe
CH2CH(Me)S(O)Me CH2SMe
CH2CH(Me)S(O)Et CH2SMe
CH2CH(Me)S(O)2Me CH2SMe
CH2CH(Me)S(O)2Et CH2SMe
CH2CH(Et)SMe CH2SMe
CH2CH(Et)SEt CH2SMe
CH2CH(Et)S(O)Me CH2SMe
CH2CH(Et)S(O)Et CH2SMe
CH2CH(Et)S(O)2Me CH2SMe
CH2CH(Et)S(O)2Et CH2SMe
CH(Me)CH(Me)SMe CH2SMe
CH(Me)CH(Me)SEt CH2SMe
CH(Me)CH(Me)S(O)Me CH2SMe
CH(Me)CH(Me)S(O)Et CH2SMe
CH(Me)CH(Me)S(O)2Me CH2SMe
CH(Me)CH(Me)S(O)2Et CH2SMe
CH2SMe CH2S(O)Me
CH2SEt CH2S(O)Me
CH2S(O)Me CH2S(O)Me
CH2S(O)Et CH2S(O)Me
CH2S(O)2Me CH2S(O)Me
CH2S(O)2Et CH2S(O)Me
CH(Me)SMe CH2S(O)Me
CH(Me)SEt CH2S(O)Me
CH(Me)S(O)Me CH2S(O)Me
CH(Me)S(O)Et CH2S(O)Me
CH(Me)S(O)2Me CH2S(O)Me
CH(Me)S(O)2Et CH2S(O)Me
CH(Et)SMe CH2S(O)Me
CH(Et)SEt CH2S(O)Me
CH(Et)S(O)Me CH2S(O)Me
CH(Et)S(O)Et CH2S(O)Me
CH(Et)S(O)2Me CH2S(O)Me
CH(Et)S(O)2Et CH2S(O)Me
CH(n-Pr)SMe CH2S(O)Me
CH(n-Pr)SEt CH2S(O)Me
CH(n-Pr)S(O)Me CH2S(O)Me
CH(n-Pr)S(O)Et CH2S(O)Me
CH(n-Pr)S(O)2Me CH2S(O)Me
CH(n-Pr)S(O)2Et CH2S(O)Me
CH(i-Pr)SMe CH2S(O)Me
CH(i-Pr)SEt CH2S(O)Me
CH(i-Pr)S(O)Me CH2S(O)Me
CH(i-Pr)S(O)Et CH2S(O)Me
CH(i-Pr)S(O)2Me CH2S(O)Me
CH(i-Pr)S(O)2Et CH2S(O)Me
CH(n-Bu)SMe CH2S(O)Me
CH(n-Bu)SEt CH2S(O)Me
CH(n-Bu)S(O)Me CH2S(O)Me
CH(n-Bu)S(O)Et CH2S(O)Me
CH(n-Bu)S(O)2Me CH2S(O)Me
CH(n-Bu)S(O)2Et CH2S(O)Me
CH(i-Bu)SMe CH2S(O)Me
CH(i-Bu)SEt CH2S(O)Me
CH(i-Bu)S(O)Me CH2S(O)Me
CH(i-Bu)S(O)Et CH2S(O)Me
CH(i-Bu)S(O)2Me CH2S(O)Me
CH(i-Bu)S(O)2Et CH2S(O)Me
CH(s-Bu)SMe CH2S(O)Me
CH(s-Bu)SEt CH2S(O)Me
CH(s-Bu)S(O)Me CH2S(O)Me
CH(s-Bu)S(O)Et CH2S(O)Me
CH(s-Bu)S(O)2Me CH2S(O)Me
CH(s-Bu)S(O)2Et CH2S(O)Me
CH(t-Bu)SMe CH2S(O)Me
CH(t-Bu)SEt CH2S(O)Me
CH(t-Bu)S(O)Me CH2S(O)Me
CH(t-Bu)S(O)Et CH2S(O)Me
CH(t-Bu)S(O)2Me CH2S(O)Me
CH(t-Bu)S(O)2Et CH2S(O)Me
CH2CH2SMe CH2S(O)Me
CH2CH2SEt CH2S(O)Me
CH2CH2S(O)2Me CH2S(O)Me
CH2CH2S(O)2Et CH2S(O)Me
CH(Me)CH2SMe CH2S(O)Me
CH(Me)CH2SEt CH2S(O)Me
CH(Me)CH2S(O)Me CH2S(O)Me
CH(Me)CH2S(O)Et CH2S(O)Me
CH(Me)CH2S(O)2Me CH2S(O)Me
CH(Me)CH2S(O)2Et CH2S(O)Me
CH(Et)CH2SMe CH2S(O)Me
CH(Et)CH2SEt CH2S(O)Me
CH(Et)CH2S(O)Me CH2S(O)Me
CH(Et)CH2S(O)Et CH2S(O)Me
CH(Et)CH2S(O)2Me CH2S(O)Me
CH(Et)CH2S(O)2Et CH2S(O)Me
C(Me)2CH2SMe CH2S(O)Me
C(Me)2CH2SEt CH2S(O)Me
C(Me)2CH2S(O)Me CH2S(O)Me
C(Me)2CH2S(O)Et CH2S(O)Me
C(Me)2CH2S(O)2Me CH2S(O)Me
C(Me)2CH2S(O)2Et CH2S(O)Me
CH2CH(Me)SMe CH2S(O)Me
CH2CH(Me)SEt CH2S(O)Me
CH2CH(Me)S(O)Me CH2S(O)Me
CH2CH(Me)S(O)Et CH2S(O)Me
CH2CH(Me)S(O)2Me CH2S(O)Me
CH2CH(Me)S(O)2Et CH2S(O)Me
CH2CH(Et)SMe CH2S(O)Me
CH2CH(Et)SEt CH2S(O)Me
CH2CH(Et)S(O)Me CH2S(O)Me
CH2CH(Et)S(O)Et CH2S(O)Me
CH2CH(Et)S(O)2Me CH2S(O)Me
CH2CH(Et)S(O)2Et CH2S(O)Me
CH(Me)CH(Me)SMe CH2S(O)Me
CH(Me)CH(Me)SEt CH2S(O)Me
CH(Me)CH(Me)S(O)Me CH2S(O)Me
CH(Me)CH(Me)S(O)Et CH2S(O)Me
CH(Me)CH(Me)S(O)2Me CH2S(O)Me
CH(Me)CH(Me)S(O)2Et CH2S(O)Me
CH2SMe CH2S(O)2Me
CH2SEt CH2S(O)2Me
CH2S(O)Me CH2S(O)2Me
CH2S(O)Et CH2S(O)2Me
CH2S(O)2Me CH2S(O)2Me
CH2S(O)2Et CH2S(O)2Me
CH(Me)SMe CH2S(O)2Me
CH(Me)SEt CH2S(O)2Me
CH(Me)S(O)Me CH2S(O)2Me
CH(Me)S(O)Et CH2S(O)2Me
CH(Me)S(O)2Me CH2S(O)2Me
CH(Me)S(O)2Et CH2S(O)2Me
CH(Et)SMe CH2S(O)2Me
CH(Et)SEt CH2S(O)2Me
CH(Et)S(O)Me CH2S(O)2Me
CH(Et)S(O)Et CH2S(O)2Me
CH(Et)S(O)2Me CH2S(O)2Me
CH(Et)S(O)2Et CH2S(O)2Me
CH(n-Pr)SMe CH2S(O)2Me
CH(n-Pr)SEt CH2S(O)2Me
CH(n-Pr)S(O)Me CH2S(O)2Me
CH(n-Pr)S(O)Et CH2S(O)2Me
CH(n-Pr)S(O)2Me CH2S(O)2Me
CH(n-Pr)S(O)2Et CH2S(O)2Me
CH(i-Pr)SMe CH2S(O)2Me
CH(i-Pr)SEt CH2S(O)2Me
CH(i-Pr)S(O)Me CH2S(O)2Me
CH(i-Pr)S(O)Et CH2S(O)2Me
CH(i-Pr)S(O)2Me CH2S(O)2Me
CH(i-Pr)S(O)2Et CH2S(O)2Me
CH(n-Bu)SMe CH2S(O)2Me
CH(n-Bu)SEt CH2S(O)2Me
CH(n-Bu)S(O)Me CH2S(O)2Me
CH(n-Bu)S(O)Et CH2S(O)2Me
CH(n-Bu)S(O)2Me CH2S(O)2Me
CH(n-Bu)S(O)2Et CH2S(O)2Me
CH(i-Bu)SMe CH2S(O)2Me
CH(i-Bu)SEt CH2S(O)2Me
CH(i-Bu)S(O)Me CH2S(O)2Me
CH(i-Bu)S(O)Et CH2S(O)2Me
CH(i-Bu)S(O)2Me CH2S(O)2Me
CH(i-Bu)S(O)2Et CH2S(O)2Me
CH(s-Bu)SMe CH2S(O)2Me
CH(s-Bu)SEt CH2S(O)2Me
CH(s-Bu)S(O)Me CH2S(O)2Me
CH(s-Bu)S(O)Et CH2S(O)2Me
CH(s-Bu)S(O)2Me CH2S(O)2Me
CH(s-Bu)S(O)2Et CH2S(O)2Me
CH(t-Bu)SMe CH2S(O)2Me
CH(t-Bu)SEt CH2S(O)2Me
CH(t-Bu)S(O)Me CH2S(O)2Me
CH(t-Bu)S(O)Et CH2S(O)2Me
CH(t-Bu)S(O)2Me CH2S(O)2Me
CH(t-Bu)S(O)2Et CH2S(O)2Me
CH2CH2SMe CH2S(O)2Me
CH2CH2SEt CH2S(O)2Me
CH2CH2S(O)2Me CH2S(O)2Me
CH2CH2S(O)2Et CH2S(O)2Me
CH(Me)CH2SMe CH2S(O)2Me
CH(Me)CH2SEt CH2S(O)2Me
CH(Me)CH2S(O)Me CH2S(O)2Me
CH(Me)CH2S(O)Et CH2S(O)2Me
CH(Me)CH2S(O)2Me CH2S(O)2Me
CH(Me)CH2S(O)2Et CH2S(O)2Me
CH(Et)CH2SMe CH2S(O)2Me
CH(Et)CH2SEt CH2S(O)2Me
CH(Et)CH2S(O)Me CH2S(O)2Me
CH(Et)CH2S(O)Et CH2S(O)2Me
CH(Et)CH2S(O)2Me CH2S(O)2Me
CH(Et)CH2S(O)2Et CH2S(O)2Me
C(Me)2CH2SMe CH2S(O)2Me
C(Me)2CH2SEt CH2S(O)2Me
C(Me)2CH2S(O)Me CH2S(O)2Me
C(Me)2CH2S(O)Et CH2S(O)2Me
C(Me)2CH2S(O)2Me CH2S(O)2Me
C(Me)2CH2S(O)2Et CH2S(O)2Me
CH2CH(Me)SMe CH2S(O)2Me
CH2CH(Me)SEt CH2S(O)2Me
CH2CH(Me)S(O)Me CH2S(O)2Me
CH2CH(Me)S(O)Et CH2S(O)2Me
CH2CH(Me)S(O)2Me CH2S(O)2Me
CH2CH(Me)S(O)2Et CH2S(O)2Me
CH2CH(Et)SMe CH2S(O)2Me
CH2CH(Et)SEt CH2S(O)2Me
CH2CH(Et)S(O)Me CH2S(O)2Me
CH2CH(Et)S(O)Et CH2S(O)2Me
CH2CH(Et)S(O)2Me CH2S(O)2Me
CH2CH(Et)S(O)2Et CH2S(O)2Me
CH(Me)CH(Me)SMe CH2S(O)2Me
CH(Me)CH(Me)SEt CH2S(O)2Me
CH(Me)CH(Me)S(O)Me CH2S(O)2Me
CH(Me)CH(Me)S(O)Et CH2S(O)2Me
CH(Me)CH(Me)S(O)2Me CH2S(O)2Me
CH(Me)CH(Me)S(O)2Et CH2S(O)2Me
CH2SMe SMe
CH2SEt SMe
CH2S(O)Me SMe
CH2S(O)Et SMe
CH2S(O)2Me SMe
CH2S(O)2Et SMe
CH(Me)SMe SMe
CH(Me)SEt SMe
CH(Me)S(O)Me SMe
CH(Me)S(O)Et SMe
CH(Me)S(O)2Me SMe
CH(Me)S(O)2Et SMe
CH(Et)SMe SMe
CH(Et)SEt SMe
CH(Et)S(O)Me SMe
CH(Et)S(O)Et SMe
CH(Et)S(O)2Me SMe
CH(Et)S(O)2Et SMe
CH(n-Pr)SMe SMe
CH(n-Pr)SEt SMe
CH(n-Pr)S(O)Me SMe
CH(n-Pr)S(O)Et SMe
CH(n-Pr)S(O)2Me SMe
CH(n-Pr)S(O)2Et SMe
CH(i-Pr)SMe SMe
CH(i-Pr)SEt SMe
CH(i-Pr)S(O)Me SMe
CH(i-Pr)S(O)Et SMe
CH(i-Pr)S(O)2Me SMe
CH(i-Pr)S(O)2Et SMe
CH(n-Bu)SMe SMe
CH(n-Bu)SEt SMe
CH(n-Bu)S(O)Me SMe
CH(n-Bu)S(O)Et SMe
CH(n-Bu)S(O)2Me SMe
CH(n-Bu)S(O)2Et SMe
CH(i-Bu)SMe SMe
CH(i-Bu)SEt SMe
CH(i-Bu)S(O)Me SMe
CH(i-Bu)S(O)Et SMe
CH(i-Bu)S(O)2Me SMe
CH(i-Bu)S(O)2Et SMe
CH(s-Bu)SMe SMe
CH(s-Bu)SEt SMe
CH(s-Bu)S(O)Me SMe
CH(s-Bu)S(O)Et SMe
CH(s-Bu)S(O)2Me SMe
CH(s-Bu)S(O)2Et SMe
CH(t-Bu)SMe SMe
CH(t-Bu)SEt SMe
CH(t-Bu)S(O)Me SMe
CH(t-Bu)S(O)Et SMe
CH(t-Bu)S(O)2Me SMe
CH(t-Bu)S(O)2Et SMe
CH2CH2SMe SMe
CH2CH2SEt SMe
CH2CH2S(O)2Me SMe
CH2CH2S(O)2Et SMe
CH(Me)CH2SMe SMe
CH(Me)CH2SEt SMe
CH(Me)CH2S(O)Me SMe
CH(Me)CH2S(O)Et SMe
CH(Me)CH2S(O)2Me SMe
CH(Me)CH2S(O)2Et SMe
CH(Et)CH2SMe SMe
CH(Et)CH2SEt SMe
CH(Et)CH2S(O)Me SMe
CH(Et)CH2S(O)Et SMe
CH(Et)CH2S(O)2Me SMe
CH(Et)CH2S(O)2Et SMe
C(Me)2CH2SMe SMe
C(Me)2CH2SEt SMe
C(Me)2CH2S(O)Me SMe
C(Me)2CH2S(O)Et SMe
C(Me)2CH2S(O)2Me SMe
C(Me)2CH2S(O)2Et SMe
CH2CH(Me)SMe SMe
CH2CH(Me)SEt SMe
CH2CH(Me)S(O)Me SMe
CH2CH(Me)S(O)Et SMe
CH2CH(Me)S(O)2Me SMe
CH2CH(Me)S(O)2Et SMe
CH2CH(Et)SMe SMe
CH2CH(Et)SEt SMe
CH2CH(Et)S(O)Me SMe
CH2CH(Et)S(O)Et SMe
CH2CH(Et)S(O)2Me SMe
CH2CH(Et)S(O)2Et SMe
CH(Me)CH(Me)SMe SMe
CH(Me)CH(Me)SEt SMe
CH(Me)CH(Me)S(O)Me SMe
CH(Me)CH(Me)S(O)Et SMe
CH(Me)CH(Me)S(O)2Me SMe
CH(Me)CH(Me)S(O)2Et SMe
CH2SMe S(O)Me
CH2SEt S(O)Me
CH2S(O)Me S(O)Me
CH2S(O)Et S(O)Me
CH2S(O)2Me S(O)Me
CH2S(O)2Et S(O)Me
CH(Me)SMe S(O)Me
CH(Me)SEt S(O)Me
CH(Me)S(O)Me S(O)Me
CH(Me)S(O)Et S(O)Me
CH(Me)S(O)2Me S(O)Me
CH(Me)S(O)2Et S(O)Me
CH(Et)SMe S(O)Me
CH(Et)SEt S(O)Me
CH(Et)S(O)Me S(O)Me
CH(Et)S(O)Et S(O)Me
CH(Et)S(O)2Me S(O)Me
CH(Et)S(O)2Et S(O)Me
CH(n-Pr)SMe S(O)Me
CH(n-Pr)SEt S(O)Me
CH(n-Pr)S(O)Me S(O)Me
CH(n-Pr)S(O)Et S(O)Me
CH(n-Pr)S(O)2Me S(O)Me
CH(n-Pr)S(O)2Et S(O)Me
CH(i-Pr)SMe S(O)Me
CH(i-Pr)SEt S(O)Me
CH(i-Pr)S(O)Me S(O)Me
CH(i-Pr)S(O)Et S(O)Me
CH(i-Pr)S(O)2Me S(O)Me
CH(i-Pr)S(O)2Et S(O)Me
CH(n-Bu)SMe S(O)Me
CH(n-Bu)SEt S(O)Me
CH(n-Bu)S(O)Me S(O)Me
CH(n-Bu)S(O)Et S(O)Me
CH(n-Bu)S(O)2Me S(O)Me
CH(n-Bu)S(O)2Et S(O)Me
CH(i-Bu)SMe S(O)Me
CH(i-Bu)SEt S(O)Me
CH(i-Bu)S(O)Me S(O)Me
CH(i-Bu)S(O)Et S(O)Me
CH(i-Bu)S(O)2Me S(O)Me
CH(i-Bu)S(O)2Et S(O)Me
CH(s-Bu)SMe S(O)Me
CH(s-Bu)SEt S(O)Me
CH(s-Bu)S(O)Me S(O)Me
CH(s-Bu)S(O)Et S(O)Me
CH(s-Bu)S(O)2Me S(O)Me
CH(s-Bu)S(O)2Et S(O)Me
CH(t-Bu)SMe S(O)Me
CH(t-Bu)SEt S(O)Me
CH(t-Bu)S(O)Me S(O)Me
CH(t-Bu)S(O)Et S(O)Me
CH(t-Bu)S(O)2Me S(O)Me
CH(t-Bu)S(O)2Et S(O)Me
CH2CH2SMe S(O)Me
CH2CH2SEt S(O)Me
CH2CH2S(O)2Me S(O)Me
CH2CH2S(O)2Et S(O)Me
CH(Me)CH2SMe S(O)Me
CH(Me)CH2SEt S(O)Me
CH(Me)CH2S(O)Me S(O)Me
CH(Me)CH2S(O)Et S(O)Me
CH(Me)CH2S(O)2Me S(O)Me
CH(Me)CH2S(O)2Et S(O)Me
CH(Et)CH2SMe S(O)Me
CH(Et)CH2SEt S(O)Me
CH(Et)CH2S(O)Me S(O)Me
CH(Et)CH2S(O)Et S(O)Me
CH(Et)CH2S(O)2Me S(O)Me
CH(Et)CH2S(O)2Et S(O)Me
C(Me)2CH2SMe S(O)Me
C(Me)2CH2SEt S(O)Me
C(Me)2CH2S(O)Me S(O)Me
C(Me)2CH2S(O)Et S(O)Me
C(Me)2CH2S(O)2Me S(O)Me
C(Me)2CH2S(O)2Et S(O)Me
CH2CH(Me)SMe S(O)Me
CH2CH(Me)SEt S(O)Me
CH2CH(Me)S(O)Me S(O)Me
CH2CH(Me)S(O)Et S(O)Me
CH2CH(Me)S(O)2Me S(O)Me
CH2CH(Me)S(O)2Et S(O)Me
CH2CH(Et)SMe S(O)Me
CH2CH(Et)SEt S(O)Me
CH2CH(Et)S(O)Me S(O)Me
CH2CH(Et)S(O)Et S(O)Me
CH2CH(Et)S(O)2Me S(O)Me
CH2CH(Et)S(O)2Et S(O)Me
CH(Me)CH(Me)SMe S(O)Me
CH(Me)CH(Me)SEt S(O)Me
CH(Me)CH(Me)S(O)Me S(O)Me
CH(Me)CH(Me)S(O)Et S(O)Me
CH(Me)CH(Me)S(O)2Me S(O)Me
CH(Me)CH(Me)S(O)2Et S(O)Me
CH2SMe S(O)2Me
CH2SEt S(O)2Me
CH2S(O)Me S(O)2Me
CH2S(O)Et S(O)2Me
CH2S(O)2Me S(O)2Me
CH2S(O)2Et S(O)2Me
CH(Me)SMe S(O)2Me
CH(Me)SEt S(O)2Me
CH(Me)S(O)Me S(O)2Me
CH(Me)S(O)Et S(O)2Me
CH(Me)S(O)2Me S(O)2Me
CH(Me)S(O)2Et S(O)2Me
CH(Et)SMe S(O)2Me
CH(Et)SEt S(O)2Me
CH(Et)S(O)Me S(O)2Me
CH(Et)S(O)Et S(O)2Me
CH(Et)S(O)2Me S(O)2Me
CH(Et)S(O)2Et S(O)2Me
CH(n-Pr)SMe S(O)2Me
CH(n-Pr)SEt S(O)2Me
CH(n-Pr)S(O)Me S(O)2Me
CH(n-Pr)S(O)Et S(O)2Me
CH(n-Pr)S(O)2Me S(O)2Me
CH(n-Pr)S(O)2Et S(O)2Me
CH(i-Pr)SMe S(O)2Me
CH(i-Pr)SEt S(O)2Me
CH(i-Pr)S(O)Me S(O)2Me
CH(i-Pr)S(O)Et S(O)2Me
CH(i-Pr)S(O)2Me S(O)2Me
CH(i-Pr)S(O)2Et S(O)2Me
CH(n-Bu)SMe S(O)2Me
CH(n-Bu)SEt S(O)2Me
CH(n-Bu)S(O)Me S(O)2Me
CH(n-Bu)S(O)Et S(O)2Me
CH(n-Bu)S(O)2Me S(O)2Me
CH(n-Bu)S(O)2Et S(O)2Me
CH(i-Bu)SMe S(O)2Me
CH(i-Bu)SEt S(O)2Me
CH(i-Bu)S(O)Me S(O)2Me
CH(i-Bu)S(O)Et S(O)2Me
CH(i-Bu)S(O)2Me S(O)2Me
CH(i-Bu)S(O)2Et S(O)2Me
CH(s-Bu)SMe S(O)2Me
CH(s-Bu)SEt S(O)2Me
CH(s-Bu)S(O)Me S(O)2Me
CH(s-Bu)S(O)Et S(O)2Me
CH(s-Bu)S(O)2Me S(O)2Me
CH(s-Bu)S(O)2Et S(O)2Me
CH(t-Bu)SMe S(O)2Me
CH(t-Bu)SEt S(O)2Me
CH(t-Bu)S(O)Me S(O)2Me
CH(t-Bu)S(O)Et S(O)2Me
CH(t-Bu)S(O)2Me S(O)2Me
CH(t-Bu)S(O)2Et S(O)2Me
CH2CH2SMe S(O)2Me
CH2CH2SEt S(O)2Me
CH2CH2S(O)2Me S(O)2Me
CH2CH2S(O)2Et S(O)2Me
CH(Me)CH2SMe S(O)2Me
CH(Me)CH2SEt S(O)2Me
CH(Me)CH2S(O)Me S(O)2Me
CH(Me)CH2S(O)Et S(O)2Me
CH(Me)CH2S(O)2Me S(O)2Me
CH(Me)CH2S(O)2Et S(O)2Me
CH(Et)CH2SMe S(O)2Me
CH(Et)CH2SEt S(O)2Me
CH(Et)CH2S(O)Me S(O)2Me
CH(Et)CH2S(O)Et S(O)2Me
CH(Et)CH2S(O)2Me S(O)2Me
CH(Et)CH2S(O)2Et S(O)2Me
C(Me)2CH2SMe S(O)2Me
C(Me)2CH2SEt S(O)2Me
C(Me)2CH2S(O)Me S(O)2Me
C(Me)2CH2S(O)Et S(O)2Me
C(Me)2CH2S(O)2Me S(O)2Me
C(Me)2CH2S(O)2Et S(O)2Me
CH2CH(Me)SMe S(O)2Me
CH2CH(Me)SEt S(O)2Me
CH2CH(Me)S(O)Me S(O)2Me
CH2CH(Me)S(O)Et S(O)2Me
CH2CH(Me)S(O)2Me S(O)2Me
CH2CH(Me)S(O)2Et S(O)2Me
CH2CH(Et)SMe S(O)2Me
CH2CH(Et)SEt S(O)2Me
CH2CH(Et)S(O)Me S(O)2Me
CH2CH(Et)S(O)Et S(O)2Me
CH2CH(Et)S(O)2Me S(O)2Me
CH2CH(Et)S(O)2Et S(O)2Me
CH(Me)CH(Me)SMe S(O)2Me
CH(Me)CH(Me)SEt S(O)2Me
CH(Me)CH(Me)S(O)Me S(O)2Me
CH(Me)CH(Me)S(O)Et S(O)2Me
CH(Me)CH(Me)S(O)2Me S(O)2Me
CH(Me)CH(Me)S(O)2Et S(O)2Me
CH2SMe H
CH2SEt H
CH2S(O)Me H
CH2S(O)Et H
CH2S(O)2Me H
CH2S(O)2Et H
CH(Me)SMe H
CH(Me)SEt H
CH(Me)S(O)Me H
CH(Me)S(O)Et H
CH(Me)S(O)2Me H
CH(Me)S(O)2Et H
CH(Et)SMe H
CH(Et)SEt H
CH(Et)S(O)Me H
CH(Et)S(O)Et H
CH(Et)S(O)2Me H
CH(Et)S(O)2Et H
CH(n-Pr)SMe H
CH(n-Pr)SEt H
CH(n-Pr)S(O)Me H
CH(n-Pr)S(O)Et H
CH(n-Pr)S(O)2Me H
CH(n-Pr)S(O)2Et H
CH(i-Pr)SMe H
CH(i-Pr)SEt H
CH(i-Pr)S(O)Me H
CH(i-Pr)S(O)Et H
CH(i-Pr)S(O)2Me H
CH(i-Pr)S(O)2Et H
CH(n-Bu)SMe H
CH(n-Bu)SEt H
CH(n-Bu)S(O)Me H
CH(n-Bu)S(O)Et H
CH(n-Bu)S(O)2Me H
CH(n-Bu)S(O)2Et H
CH(i-Bu)SMe H
CH(i-Bu)SEt H
CH(i-Bu)S(O)Me H
CH(i-Bu)S(O)Et H
CH(i-Bu)S(O)2Me H
CH(i-Bu)S(O)2Et H
CH(s-Bu)SMe H
CH(s-Bu)SEt H
CH(s-Bu)S(O)Me H
CH(s-Bu)S(O)Et H
CH(s-Bu)S(O)2Me H
CH(s-Bu)S(O)2Et H
CH(t-Bu)SMe H
CH(t-Bu)SEt H
CH(t-Bu)S(O)Me H
CH(t-Bu)S(O)Et H
CH(t-Bu)S(O)2Me H
CH(t-Bu)S(O)2Et H
CH2CH2SMe H
CH2CH2SEt H
CH2CH2S(O)2Me H
CH2CH2S(O)2Et H
CH(Me)CH2SMe H
CH(Me)CH2SEt H
CH(Me)CH2S(O)Me H
CH(Me)CH2S(O)Et H
CH(Me)CH2S(O)2Me H
CH(Me)CH2S(O)2Et H
CH(Et)CH2SMe H
CH(Et)CH2SEt H
CH(Et)CH2S(O)Me H
CH(Et)CH2S(O)Et H
CH(Et)CH2S(O)2Me H
CH(Et)CH2S(O)2Et H
C(Me)2CH2SMe H
C(Me)2CH2SEt H
C(Me)2CH2S(O)Me H
C(Me)2CH2S(O)Et H
C(Me)2CH2S(O)2Me H
C(Me)2CH2S(O)2Et H
CH2CH(Me)SMe H
CH2CH(Me)SEt H
CH2CH(Me)S(O)Me H
CH2CH(Me)S(O)Et H
CH2CH(Me)S(O)2Me H
CH2CH(Me)S(O)2Et H
CH2CH(Et)SMe H
CH2CH(Et)SEt H
CH2CH(Et)S(O)Me H
CH2CH(Et)S(O)Et H
CH2CH(Et)S(O)2Me H
CH2CH(Et)S(O)2Et H
CH(Me)CH(Me)SMe H
CH(Me)CH(Me)SEt H
CH(Me)CH(Me)S(O)Me H
CH(Me)CH(Me)S(O)Et H
CH(Me)CH(Me)S(O)2Me H
CH(Me)CH(Me)S(O)2Et H
CH2SMe Me
CH2SEt Me
CH2S(O)Me Me
CH2S(O)Et Me
CH2S(O)2Me Me
CH2S(O)2Et Me
CH(Me)SMe Me
CH(Me)SEt Me
CH(Me)S(O)Me Me
CH(Me)S(O)Et Me
CH(Me)S(O)2Me Me
CH(Me)S(O)2Et Me
CH(Et)SMe Me
CH(Et)SEt Me
CH(Et)S(O)Me Me
CH(Et)S(O)Et Me
CH(Et)S(O)2Me Me
CH(Et)S(O)2Et Me
CH(n-Pr)SMe Me
CH(n-Pr)SEt Me
CH(n-Pr)S(O)Me Me
CH(n-Pr)S(O)Et Me
CH(n-Pr)S(O)2Me Me
CH(n-Pr)S(O)2Et Me
CH(i-Pr)SMe Me
CH(i-Pr)SEt Me
CH(i-Pr)S(O)Me Me
CH(i-Pr)S(O)Et Me
CH(i-Pr)S(O)2Me Me
CH(i-Pr)S(O)2Et Me
CH(n-Bu)SMe Me
CH(n-Bu)SEt Me
CH(n-Bu)S(O)Me Me
CH(n-Bu)S(O)Et Me
CH(n-Bu)S(O)2Me Me
CH(n-Bu)S(O)2Et Me
CH(i-Bu)SMe Me
CH(i-Bu)SEt Me
CH(i-Bu)S(O)Me Me
CH(i-Bu)S(O)Et Me
CH(i-Bu)S(O)2Me Me
CH(i-Bu)S(O)2Et Me
CH(s-Bu)SMe Me
CH(s-Bu)SEt Me
CH(s-Bu)S(O)Me Me
CH(s-Bu)S(O)Et Me
CH(s-Bu)S(O)2Me Me
CH(s-Bu)S(O)2Et Me
CH(t-Bu)SMe Me
CH(t-Bu)SEt Me
CH(t-Bu)S(O)Me Me
CH(t-Bu)S(O)Et Me
CH(t-Bu)S(O)2Me Me
CH(t-Bu)S(O)2Et Me
CH2CH2SMe Me
CH2CH2SEt Me
CH2CH2S(O)2Me Me
CH2CH2S(O)2Et Me
CH(Me)CH2SMe Me
CH(Me)CH2SEt Me
CH(Me)CH2S(O)Me Me
CH(Me)CH2S(O)Et Me
CH(Me)CH2S(O)2Me Me
CH(Me)CH2S(O)2Et Me
CH(Et)CH2SMe Me
CH(Et)CH2SEt Me
CH(Et)CH2S(O)Me Me
CH(Et)CH2S(O)Et Me
CH(Et)CH2S(O)2Me Me
CH(Et)CH2S(O)2Et Me
C(Me)2CH2SMe Me
C(Me)2CH2SEt Me
C(Me)2CH2S(O)Me Me
C(Me)2CH2S(O)Et Me
C(Me)2CH2S(O)2Me Me
C(Me)2CH2S(O)2Et Me
CH2CH(Me)SMe Me
CH2CH(Me)SEt Me
CH2CH(Me)S(O)Me Me
CH2CH(Me)S(O)Et Me
CH2CH(Me)S(O)2Me Me
CH2CH(Me)S(O)2Et Me
CH2CH(Et)SMe Me
CH2CH(Et)SEt Me
CH2CH(Et)S(O)Me Me
CH2CH(Et)S(O)Et Me
CH2CH(Et)S(O)2Me Me
CH2CH(Et)S(O)2Et Me
CH(Me)CH(Me)SMe Me
CH(Me)CH(Me)SEt Me
CH(Me)CH(Me)S(O)Me Me
CH(Me)CH(Me)S(O)Et Me
CH(Me)CH(Me)S(O)2Me Me
CH(Me)CH(Me)S(O)2Et Me
CH2SMe CF3
CH2SEt CF3
CH2S(O)Me CF3
CH2S(O)Et CF3
CH2S(O)2Me CF3
CH2S(O)2Et CF3
CH(Me)SMe CF3
CH(Me)SEt CF3
CH(Me)S(O)Me CF3
CH(Me)S(O)Et CF3
CH(Me)S(O)2Me CF3
CH(Me)S(O)2Et CF3
CH(Et)SMe CF3
CH(Et)SEt CF3
CH(Et)S(O)Me CF3
CH(Et)S(O)Et CF3
CH(Et)S(O)2Me CF3
CH(Et)S(O)2Et CF3
CH(n-Pr)SMe CF3
CH(n-Pr)SEt CF3
CH(n-Pr)S(O)Me CF3
CH(n-Pr)S(O)Et CF3
CH(n-Pr)S(O)2Me CF3
CH(n-Pr)S(O)2Et CF3
CH(i-Pr)SMe CF3
CH(i-Pr)SEt CF3
CH(i-Pr)S(O)Me CF3
CH(i-Pr)S(O)Et CF3
CH(i-Pr)S(O)2Me CF3
CH(i-Pr)S(O)2Et CF3
CH(n-Bu)SMe CF3
CH(n-Bu)SEt CF3
CH(n-Bu)S(O)Me CF3
CH(n-Bu)S(O)Et CF3
CH(n-Bu)S(O)2Me CF3
CH(n-Bu)S(O)2Et CF3
CH(i-Bu)SMe CF3
CH(i-Bu)SEt CF3
CH(i-Bu)S(O)Me CF3
CH(i-Bu)S(O)Et CF3
CH(i-Bu)S(O)2Me CF3
CH(i-Bu)S(O)2Et CF3
CH(s-Bu)SMe CF3
CH(s-Bu)SEt CF3
CH(s-Bu)S(O)Me CF3
CH(s-Bu)S(O)Et CF3
CH(s-Bu)S(O)2Me CF3
CH(s-Bu)S(O)2Et CF3
CH(t-Bu)SMe CF3
CH(t-Bu)SEt CF3
CH(t-Bu)S(O)Me CF3
CH(t-Bu)S(O)Et CF3
CH(t-Bu)S(O)2Me CF3
CH(t-Bu)S(O)2Et CF3
CH2CH2SMe CF3
CH2CH2SEt CF3
CH2CH2S(O)2Me CF3
CH2CH2S(O)2Et CF3
CH(Me)CH2SMe CF3
CH(Me)CH2SEt CF3
CH(Me)CH2S(O)Me CF3
CH(Me)CH2S(O)Et CF3
CH(Me)CH2S(O)2Me CF3
CH(Me)CH2S(O)2Et CF3
CH(Et)CH2SMe CF3
CH(Et)CH2SEt CF3
CH(Et)CH2S(O)Me CF3
CH(Et)CH2S(O)Et CF3
CH(Et)CH2S(O)2Me CF3
CH(Et)CH2S(O)2Et CF3
C(Me)2CH2SMe CF3
C(Me)2CH2SEt CF3
C(Me)2CH2S(O)Me CF3
C(Me)2CH2S(O)Et CF3
C(Me)2CH2S(O)2Me CF3
C(Me)2CH2S(O)2Et CF3
CH2CH(Me)SMe CF3
CH2CH(Me)SEt CF3
CH2CH(Me)S(O)Me CF3
CH2CH(Me)S(O)Et CF3
CH2CH(Me)S(O)2Me CF3
CH2CH(Me)S(O)2Et CF3
CH2CH(Et)SMe CF3
CH2CH(Et)SEt CF3
CH2CH(Et)S(O)Me CF3
CH2CH(Et)S(O)Et CF3
CH2CH(Et)S(O)2Me CF3
CH2CH(Et)S(O)2Et CF3
CH(Me)CH(Me)SMe CF3
CH(Me)CH(Me)SEt CF3
CH(Me)CH(Me)S(O)Me CF3
CH(Me)CH(Me)S(O)Et CF3
CH(Me)CH(Me)S(O)2Me CF3
CH(Me)CH(Me)S(O)2Et CF3
CH2SMe CN
CH2SEt CN
CH2S(O)Me CN
CH2S(O)Et CN
CH2S(O)2Me CN
CH2S(O)2Et CN
CH(Me)SMe CN
CH(Me)SEt CN
CH(Me)S(O)Me CN
CH(Me)S(O)Et CN
CH(Me)S(O)2Me CN
CH(Me)S(O)2Et CN
CH(Et)SMe CN
CH(Et)SEt CN
CH(Et)S(O)Me CN
CH(Et)S(O)Et CN
CH(Et)S(O)2Me CN
CH(Et)S(O)2Et CN
CH(n-Pr)SMe CN
CH(n-Pr)SEt CN
CH(n-Pr)S(O)Me CN
CH(n-Pr)S(O)Et CN
CH(n-Pr)S(O)2Me CN
CH(n-Pr)S(O)2Et CN
CH(i-Pr)SMe CN
CH(i-Pr)SEt CN
CH(i-Pr)S(O)Me CN
CH(i-Pr)S(O)Et CN
CH(i-Pr)S(O)2Me CN
CH(i-Pr)S(O)2Et CN
CH(n-Bu)SMe CN
CH(n-Bu)SEt CN
CH(n-Bu)S(O)Me CN
CH(n-Bu)S(O)Et CN
CH(n-Bu)S(O)2Me CN
CH(n-Bu)S(O)2Et CN
CH(i-Bu)SMe CN
CH(i-Bu)SEt CN
CH(i-Bu)S(O)Me CN
CH(i-Bu)S(O)Et CN
CH(i-Bu)S(O)2Me CN
CH(i-Bu)S(O)2Et CN
CH(s-Bu)SMe CN
CH(s-Bu)SEt CN
CH(s-Bu)S(O)Me CN
CH(s-Bu)S(O)Et CN
CH(s-Bu)S(O)2Me CN
CH(s-Bu)S(O)2Et CN
CH(t-Bu)SMe CN
CH(t-Bu)SEt CN
CH(t-Bu)S(O)Me CN
CH(t-Bu)S(O)Et CN
CH(t-Bu)S(O)2Me CN
CH(t-Bu)S(O)2Et CN
CH2CH2SMe CN
CH2CH2SEt CN
CH2CH2S(O)2Me CN
CH2CH2S(O)2Et CN
CH(Me)CH2SMe CN
CH(Me)CH2SEt CN
CH(Me)CH2S(O)Me CN
CH(Me)CH2S(O)Et CN
CH(Me)CH2S(O)2Me CN
CH(Me)CH2S(O)2Et CN
CH(Et)CH2SMe CN
CH(Et)CH2SEt CN
CH(Et)CH2S(O)Me CN
CH(Et)CH2S(O)Et CN
CH(Et)CH2S(O)2Me CN
CH(Et)CH2S(O)2Et CN
C(Me)2CH2SMe CN
C(Me)2CH2SEt CN
C(Me)2CH2S(O)Me CN
C(Me)2CH2S(O)Et CN
C(Me)2CH2S(O)2Me CN
C(Me)2CH2S(O)2Et CN
CH2CH(Me)SMe CN
CH2CH(Me)SEt CN
CH2CH(Me)S(O)Me CN
CH2CH(Me)S(O)Et CN
CH2CH(Me)S(O)2Me CN
CH2CH(Me)S(O)2Et CN
CH2CH(Et)SMe CN
CH2CH(Et)SEt CN
CH2CH(Et)S(O)Me CN
CH2CH(Et)S(O)Et CN
CH2CH(Et)S(O)2Me CN
CH2CH(Et)S(O)2Et CN
CH(Me)CH(Me)SMe CN
CH(Me)CH(Me)SEt CN
CH(Me)CH(Me)S(O)Me CN
CH(Me)CH(Me)S(O)Et CN
CH(Me)CH(Me)S(O)2Me CN
CH(Me)CH(Me)S(O)2Et CN
CH2SMe Cl
CH2SEt Cl
CH2S(O)Me Cl
CH2S(O)Et Cl
CH2S(O)2Me Cl
CH2S(O)2Et Cl
CH(Me)SMe Cl
CH(Me)SEt Cl
CH(Me)S(O)Me Cl
CH(Me)S(O)Et Cl
CH(Me)S(O)2Me Cl
CH(Me)S(O)2Et Cl
CH(Et)SMe Cl
CH(Et)SEt Cl
CH(Et)S(O)Me Cl
CH(Et)S(O)Et Cl
CH(Et)S(O)2Me Cl
CH(Et)S(O)2Et Cl
CH(n-Pr)SMe Cl
CH(n-Pr)SEt Cl
CH(n-Pr)S(O)Me Cl
CH(n-Pr)S(O)Et Cl
CH(n-Pr)S(O)2Me Cl
CH(n-Pr)S(O)2Et Cl
CH(i-Pr)SMe Cl
CH(i-Pr)SEt Cl
CH(i-Pr)S(O)Me Cl
CH(i-Pr)S(O)Et Cl
CH(i-Pr)S(O)2Me Cl
CH(i-Pr)S(O)2Et Cl
CH(n-Bu)SMe Cl
CH(n-Bu)SEt Cl
CH(n-Bu)S(O)Me Cl
CH(n-Bu)S(O)Et Cl
CH(n-Bu)S(O)2Me Cl
CH(n-Bu)S(O)2Et Cl
CH(i-Bu)SMe Cl
CH(i-Bu)SEt Cl
CH(i-Bu)S(O)Me Cl
CH(i-Bu)S(O)Et Cl
CH(i-Bu)S(O)2Me Cl
CH(i-Bu)S(O)2Et Cl
CH(s-Bu)SMe Cl
CH(s-Bu)SEt Cl
CH(s-Bu)S(O)Me Cl
CH(s-Bu)S(O)Et Cl
CH(s-Bu)S(O)2Me Cl
CH(s-Bu)S(O)2Et Cl
CH(t-Bu)SMe Cl
CH(t-Bu)SEt Cl
CH(t-Bu)S(O)Me Cl
CH(t-Bu)S(O)Et Cl
CH(t-Bu)S(O)2Me Cl
CH(t-Bu)S(O)2Et Cl
CH2CH2SMe Cl
CH2CH2SEt Cl
CH2CH2S(O)2Me Cl
CH2CH2S(O)2Et Cl
CH(Me)CH2SMe Cl
CH(Me)CH2SEt Cl
CH(Me)CH2S(O)Me Cl
CH(Me)CH2S(O)Et Cl
CH(Me)CH2S(O)2Me Cl
CH(Me)CH2S(O)2Et Cl
CH(Et)CH2SMe Cl
CH(Et)CH2SEt Cl
CH(Et)CH2S(O)Me Cl
CH(Et)CH2S(O)Et Cl
CH(Et)CH2S(O)2Me Cl
CH(Et)CH2S(O)2Et Cl
C(Me)2CH2SMe Cl
C(Me)2CH2SEt Cl
C(Me)2CH2S(O)Me Cl
C(Me)2CH2S(O)Et Cl
C(Me)2CH2S(O)2Me Cl
C(Me)2CH2S(O)2Et Cl
CH2CH(Me)SMe Cl
CH2CH(Me)SEt Cl
CH2CH(Me)S(O)Me Cl
CH2CH(Me)S(O)Et Cl
CH2CH(Me)S(O)2Me Cl
CH2CH(Me)S(O)2Et Cl
CH2CH(Et)SMe Cl
CH2CH(Et)SEt Cl
CH2CH(Et)S(O)Me Cl
CH2CH(Et)S(O)Et Cl
CH2CH(Et)S(O)2Me Cl
CH2CH(Et)S(O)2Et Cl
CH(Me)CH(Me)SMe Cl
CH(Me)CH(Me)SEt Cl
CH(Me)CH(Me)S(O)Me Cl
CH(Me)CH(Me)S(O)Et Cl
CH(Me)CH(Me)S(O)2Me Cl
CH(Me)CH(Me)S(O)2Et Cl
CH2SMe C(O)OMe
CH2SEt C(O)OMe
CH2S(O)Me C(O)OMe
CH2S(O)Et C(O)OMe
CH2S(O)2Me C(O)OMe
CH2S(O)2Et C(O)OMe
CH(Me)SMe C(O)OMe
CH(Me)SEt C(O)OMe
CH(Me)S(O)Me C(O)OMe
CH(Me)S(O)Et C(O)OMe
CH(Me)S(O)2Me C(O)OMe
CH(Me)S(O)2Et C(O)OMe
CH(Et)SMe C(O)OMe
CH(Et)SEt C(O)OMe
CH(Et)S(O)Me C(O)OMe
CH(Et)S(O)Et C(O)OMe
CH(Et)S(O)2Me C(O)OMe
CH(Et)S(O)2Et C(O)OMe
CH(n-Pr)SMe C(O)OMe
CH(n-Pr)SEt C(O)OMe
CH(n-Pr)S(O)Me C(O)OMe
CH(n-Pr)S(O)Et C(O)OMe
CH(n-Pr)S(O)2Me C(O)OMe
CH(n-Pr)S(O)2Et C(O)OMe
CH(i-Pr)SMe C(O)OMe
CH(i-Pr)SEt C(O)OMe
CH(i-Pr)S(O)Me C(O)OMe
CH(i-Pr)S(O)Et C(O)OMe
CH(i-Pr)S(O)2Me C(O)OMe
CH(i-Pr)S(O)2Et C(O)OMe
CH(n-Bu)SMe C(O)OMe
CH(n-Bu)SEt C(O)OMe
CH(n-Bu)S(O)Me C(O)OMe
CH(n-Bu)S(O)Et C(O)OMe
CH(n-Bu)S(O)2Me C(O)OMe
CH(n-Bu)S(O)2Et C(O)OMe
CH(i-Bu)SMe C(O)OMe
CH(i-Bu)SEt C(O)OMe
CH(i-Bu)S(O)Me C(O)OMe
CH(i-Bu)S(O)Et C(O)OMe
CH(i-Bu)S(O)2Me C(O)OMe
CH(i-Bu)S(O)2Et C(O)OMe
CH(s-Bu)SMe C(O)OMe
CH(s-Bu)SEt C(O)OMe
CH(s-Bu)S(O)Me C(O)OMe
CH(s-Bu)S(O)Et C(O)OMe
CH(s-Bu)S(O)2Me C(O)OMe
CH(s-Bu)S(O)2Et C(O)OMe
CH(t-Bu)SMe C(O)OMe
CH(t-Bu)SEt C(O)OMe
CH(t-Bu)S(O)Me C(O)OMe
CH(t-Bu)S(O)Et C(O)OMe
CH(t-Bu)S(O)2Me C(O)OMe
CH(t-Bu)S(O)2Et C(O)OMe
CH2CH2SMe C(O)OMe
CH2CH2SEt C(O)OMe
CH2CH2S(O)2Me C(O)OMe
CH2CH2S(O)2Et C(O)OMe
CH(Me)CH2SMe C(O)OMe
CH(Me)CH2SEt C(O)OMe
CH(Me)CH2S(O)Me C(O)OMe
CH(Me)CH2S(O)Et C(O)OMe
CH(Me)CH2S(O)2Me C(O)OMe
CH(Me)CH2S(O)2Et C(O)OMe
CH(Et)CH2SMe C(O)OMe
CH(Et)CH2SEt C(O)OMe
CH(Et)CH2S(O)Me C(O)OMe
CH(Et)CH2S(O)Et C(O)OMe
CH(Et)CH2S(O)2Me C(O)OMe
CH(Et)CH2S(O)2Et C(O)OMe
C(Me)2CH2SMe C(O)OMe
C(Me)2CH2SEt C(O)OMe
C(Me)2CH2S(O)Me C(O)OMe
C(Me)2CH2S(O)Et C(O)OMe
C(Me)2CH2S(O)2Me C(O)OMe
C(Me)2CH2S(O)2Et C(O)OMe
CH2CH(Me)SMe C(O)OMe
CH2CH(Me)SEt C(O)OMe
CH2CH(Me)S(O)Me C(O)OMe
CH2CH(Me)S(O)Et C(O)OMe
CH2CH(Me)S(O)2Me C(O)OMe
CH2CH(Me)S(O)2Et C(O)OMe
CH2CH(Et)SMe C(O)OMe
CH2CH(Et)SEt C(O)OMe
CH2CH(Et)S(O)Me C(O)OMe
CH2CH(Et)S(O)Et C(O)OMe
CH2CH(Et)S(O)2Me C(O)OMe
CH2CH(Et)S(O)2Et C(O)OMe
CH(Me)CH(Me)SMe C(O)OMe
CH(Me)CH(Me)SEt C(O)OMe
CH(Me)CH(Me)S(O)Me C(O)OMe
CH(Me)CH(Me)S(O)Et C(O)OMe
CH(Me)CH(Me)S(O)2Me C(O)OMe
CH(Me)CH(Me)S(O)2Et C(O)OMe
CH2OMe CH2SMe
CH2OMe CH2SEt
CH2OMe CH2SCF3
CH2OMe CH2SCH2CF3
CH2OMe CH2S(O)Me
CH2OMe CH2S(O)Et
CH2OMe CH2S(O)CF3
CH2OMe CH2S(O)CH2CF3
CH2OMe CH2S(O)2Me
CH2OMe CH2S(O)2Et
CH2OMe CH2S(O)2CF3
CH2OMe CH2S(O)2CH2CF3
CH2OMe CH(Me)SMe
CH2OMe CH(Me)SEt
CH2OMe CH(Me)SCF3
CH2OMe CH(Me)SCH2CF3
CH2OMe CH(Me)S(O)Me
CH2OMe CH(Me)S(O)Et
CH2OMe CH(Me)S(O)CF3
CH2OMe CH(Me)S(O)CH2CF3
CH2OMe CH(Me)S(O)2Me
CH2OMe CH(Me)S(O)2Et
CH2OMe CH(Me)S(O)2CF3
CH2OMe CH(Me)S(O)2CH2CF3
CH2OMe CH(Et)SMe
CH2OMe CH(Et)SEt
CH2OMe CH(Et)SCF3
CH2OMe CH(Et)SCH2CF3
CH2OMe CH(Et)S(O)Me
CH2OMe CH(Et)S(O)Et
CH2OMe CH(Et)S(O)CF3
CH2OMe CH(Et)S(O)CH2CF3
CH2OMe CH(Et)S(O)2Me
CH2OMe CH(Et)S(O)2Et
CH2OMe CH(Et)S(O)2CF3
CH2OMe CH(Et)S(O)2CH2CF3
CH2OMe CH(n-Pr)SMe
CH2OMe CH(n-Pr)SEt
CH2OMe CH(n-Pr)SCF3
CH2OMe CH(n-Pr)SCH2CF3
CH2OMe CH(n-Pr)S(O)Me
CH2OMe CH(n-Pr)S(O)Et
CH2OMe CH(n-Pr)S(O)CF3
CH2OMe CH(n-Pr)S(O)CH2CF3
CH2OMe CH(n-Pr)S(O)2Me
CH2OMe CH(n-Pr)S(O)2Et
CH2OMe CH(n-Pr)S(O)2CF3
CH2OMe CH(n-Pr)S(O)2CH2CF3
CH2OMe CH(i-Pr)SMe
CH2OMe CH(i-Pr)SEt
CH2OMe CH(i-Pr)SCF3
CH2OMe CH(i-Pr)SCH2CF3
CH2OMe CH(i-Pr)S(O)Me
CH2OMe CH(i-Pr)S(O)Et
CH2OMe CH(i-Pr)S(O)CF3
CH2OMe CH(i-Pr)S(O)CH2CF3
CH2OMe CH(i-Pr)S(O)2Me
CH2OMe CH(i-Pr)S(O)2Et
CH2OMe CH(i-Pr)S(O)2CF3
CH2OMe CH(i-Pr)S(O)2CH2CF3
CH2OMe CH(n-Bu)SMe
CH2OMe CH(n-Bu)SEt
CH2OMe CH(n-Bu)SCF3
CH2OMe CH(n-Bu)SCH2CF3
CH2OMe CH(n-Bu)S(O)Me
CH2OMe CH(n-Bu)S(O)Et
CH2OMe CH(n-Bu)S(O)CF3
CH2OMe CH(n-Bu)S(O)CH2CF3
CH2OMe CH(n-Bu)S(O)2Me
CH2OMe CH(n-Bu)S(O)2Et
CH2OMe CH(n-Bu)S(O)2CF3
CH2OMe CH(n-Bu)S(O)2CH2CF3
CH2OMe CH(i-Bu)SMe
CH2OMe CH(i-Bu)SEt
CH2OMe CH(i-Bu)SCF3
CH2OMe CH(i-Bu)SCH2CF3
CH2OMe CH(i-Bu)S(O)Me
CH2OMe CH(i-Bu)S(O)Et
CH2OMe CH(i-Bu)S(O)CF3
CH2OMe CH(i-Bu)S(O)CH2CF3
CH2OMe CH(i-Bu)S(O)2Me
CH2OMe CH(i-Bu)S(O)2Et
CH2OMe CH(i-Bu)S(O)2CF3
CH2OMe CH(i-Bu)S(O)2CH2CF3
CH2OMe CH(s-Bu)SMe
CH2OMe CH(s-Bu)SEt
CH2OMe CH(s-Bu)SCF3
CH2OMe CH(s-Bu)SCH2CF3
CH2OMe CH(s-Bu)S(O)Me
CH2OMe CH(s-Bu)S(O)Et
CH2OMe CH(s-Bu)S(O)CF3
CH2OMe CH(s-Bu)S(O)CH2CF3
CH2OMe CH(s-Bu)S(O)2Me
CH2OMe CH(s-Bu)S(O)2Et
CH2OMe CH(s-Bu)S(O)2CF3
CH2OMe CH(s-Bu)S(O)2CH2CF3
CH2OMe CH(t-Bu)SMe
CH2OMe CH(t-Bu)SEt
CH2OMe CH(t-Bu)SCF3
CH2OMe CH(t-Bu)SCH2CF3
CH2OMe CH(t-Bu)S(O)Me
CH2OMe CH(t-Bu)S(O)Et
CH2OMe CH(t-Bu)S(O)CF3
CH2OMe CH(t-Bu)S(O)CH2CF3
CH2OMe CH(t-Bu)S(O)2Me
CH2OMe CH(t-Bu)S(O)2Et
CH2OMe CH(t-Bu)S(O)2CF3
CH2OMe CH(t-Bu)S(O)2CH2CF3
CH2OMe CH(CF3)SMe
CH2OMe CH(CF3)SEt
CH2OMe CH(CF3)SCF3
CH2OMe CH(CF3)SCH2CF3
CH2OMe CH(CF3)S(O)Me
CH2OMe CH(CF3)S(O)Et
CH2OMe CH(CF3)S(O)CF3
CH2OMe CH(CF3)S(O)CH2CF3
CH2OMe CH(CF3)S(O)2Me
CH2OMe CH(CF3)S(O)2Et
CH2OMe CH(CF3)S(O)2CF3
CH2OMe CH(CF3)S(O)2CH2CF3
CH2OMe CH2CH2SMe
CH2OMe CH2CH2SEt
CH2OMe CH2CH2SCF3
CH2OMe CH2CH2SCH2CF3
CH2OMe CH2CH2S(O)Me
CH2OMe CH2CH2S(O)Et
CH2OMe CH2CH2S(O)CF3
CH2OMe CH2CH2S(O)CH2CF3
CH2OMe CH2CH2S(O)2Me
CH2OMe CH2CH2S(O)2Et
CH2OMe CH2CH2S(O)2CF3
CH2OMe CH2CH2S(O)2CH2CF3
CH2OMe CH(Me)CH2SMe
CH2OMe CH(Me)CH2SEt
CH2OMe CH(Me)CH2SCF3
CH2OMe CH(Me)CH2SCH2CF3
CH2OMe CH(Me)CH2S(O)Me
CH2OMe CH(Me)CH2S(O)Et
CH2OMe CH(Me)CH2S(O)CF3
CH2OMe CH(Me)CH2S(O)CH2CF3
CH2OMe CH(Me)CH2S(O)2Me
CH2OMe CH(Me)CH2S(O)2Et
CH2OMe CH(Me)CH2S(O)2CF3
CH2OMe CH(Me)CH2S(O)2CH2CF3
CH2OMe CH(Et)CH2SMe
CH2OMe CH(Et)CH2SEt
CH2OMe CH(Et)CH2SCF3
CH2OMe CH(Et)CH2SCH2CF3
CH2OMe CH(Et)CH2S(O)Me
CH2OMe CH(Et)CH2S(O)Et
CH2OMe CH(Et)CH2S(O)CF3
CH2OMe CH(Et)CH2S(O)CH2CF3
CH2OMe CH(Et)CH2S(O)2Me
CH2OMe CH(Et)CH2S(O)2Et
CH2OMe CH(Et)CH2S(O)2CF3
CH2OMe CH(Et)CH2S(O)2CH2CF3
CH2OMe C(Me)2CH2SMe
CH2OMe C(Me)2CH2SEt
CH2OMe C(Me)2CH2SCF3
CH2OMe C(Me)2CH2SCH2CF3
CH2OMe C(Me)2CH2S(O)Me
CH2OMe C(Me)2CH2S(O)Et
CH2OMe C(Me)2CH2S(O)CF3
CH2OMe C(Me)2CH2S(O)CH2CF3
CH2OMe C(Me)2CH2S(O)2Me
CH2OMe C(Me)2CH2S(O)2Et
CH2OMe C(Me)2CH2S(O)2CF3
CH2OMe C(Me)2CH2S(O)2CH2CF3
CH2OMe CH2CH(Me)SMe
CH2OMe CH2CH(Me)SEt
CH2OMe CH2CH(Me)SCF3
CH2OMe CH2CH(Me)SCH2CF3
CH2OMe CH2CH(Me)S(O)Me
CH2OMe CH2CH(Me)S(O)Et
CH2OMe CH2CH(Me)S(O)CF3
CH2OMe CH2CH(Me)S(O)CH2CF3
CH2OMe CH2CH(Me)S(O)2Me
CH2OMe CH2CH(Me)S(O)2Et
CH2OMe CH2CH(Me)S(O)2CF3
CH2OMe CH2CH(Me)S(O)2CH2CF3
CH2OMe CH2CH(Et)SMe
CH2OMe CH2CH(Et)SEt
CH2OMe CH2CH(Et)SCF3
CH2OMe CH2CH(Et)SCH2CF3
CH2OMe CH2CH(Et)S(O)Me
CH2OMe CH2CH(Et)S(O)Et
CH2OMe CH2CH(Et)S(O)CF3
CH2OMe CH2CH(Et)S(O)CH2CF3
CH2OMe CH2CH(Et)S(O)2Me
CH2OMe CH2CH(Et)S(O)2Et
CH2OMe CH2CH(Et)S(O)2CF3
CH2OMe CH2CH(Et)S(O)2CH2CF3
CH2OMe CH(Me)CH(Me)SMe
CH2OMe CH(Me)CH(Me)SEt
CH2OMe CH(Me)CH(Me)SCF3
CH2OMe CH(Me)CH(Me)SCH2CF3
CH2OMe CH(Me)CH(Me)S(O)Me
CH2OMe CH(Me)CH(Me)S(O)Et
CH2OMe CH(Me)CH(Me)S(O)CF3
CH2OMe CH(Me)CH(Me)S(O)CH2CF3
CH2OMe CH(Me)CH(Me)S(O)2Me
CH2OMe CH(Me)CH(Me)S(O)2Et
CH2OMe CH(Me)CH(Me)S(O)2CF3
CH2OMe CH(Me)CH(Me)S(O)2CH2CF3
CH2C(=NOMe)Me CH2SMe
CH2C(=NOMe)Me CH2SEt
CH2C(=NOMe)Me CH2SCF3
CH2C(=NOMe)Me CH2SCH2CF3
CH2C(=NOMe)Me CH2S(O)Me
CH2C(=NOMe)Me CH2S(O)Et
CH2C(=NOMe)Me CH2S(O)CF3
CH2C(=NOMe)Me CH2S(O)CH2CF3
CH2C(=NOMe)Me CH2S(O)2Me
CH2C(=NOMe)Me CH2S(O)2Et
CH2C(=NOMe)Me CH2S(O)2CF3
CH2C(=NOMe)Me CH2S(O)2CH2CF3
CH2C(=NOMe)Me CH(Me)SMe
CH2C(=NOMe)Me CH(Me)SEt
CH2C(=NOMe)Me CH(Me)SCF3
CH2C(=NOMe)Me CH(Me)SCH2CF3
CH2C(=NOMe)Me CH(Me)S(O)Me
CH2C(=NOMe)Me CH(Me)S(O)Et
CH2C(=NOMe)Me CH(Me)S(O)CF3
CH2C(=NOMe)Me CH(Me)S(O)CH2CF3
CH2C(=NOMe)Me CH(Me)S(O)2Me
CH2C(=NOMe)Me CH(Me)S(O)2Et
CH2C(=NOMe)Me CH(Me)S(O)2CF3
CH2C(=NOMe)Me CH(Me)S(O)2CH2CF3
CH2C(=NOMe)Me CH(Et)SMe
CH2C(=NOMe)Me CH(Et)SEt
CH2C(=NOMe)Me CH(Et)SCF3
CH2C(=NOMe)Me CH(Et)SCH2CF3
CH2C(=NOMe)Me CH(Et)S(O)Me
CH2C(=NOMe)Me CH(Et)S(O)Et
CH2C(=NOMe)Me CH(Et)S(O)CF3
CH2C(=NOMe)Me CH(Et)S(O)CH2CF3
CH2C(=NOMe)Me CH(Et)S(O)2Me
CH2C(=NOMe)Me CH(Et)S(O)2Et
CH2C(=NOMe)Me CH(Et)S(O)2CF3
CH2C(=NOMe)Me CH(Et)S(O)2CH2CF3
CH2C(=NOMe)Me CH(n-Pr)SMe
CH2C(=NOMe)Me CH(n-Pr)SEt
CH2C(=NOMe)Me CH(n-Pr)SCF3
CH2C(=NOMe)Me CH(n-Pr)SCH2CF3
CH2C(=NOMe)Me CH(n-Pr)S(O)Me
CH2C(=NOMe)Me CH(n-Pr)S(O)Et
CH2C(=NOMe)Me CH(n-Pr)S(O)CF3
CH2C(=NOMe)Me CH(n-Pr)S(O)CH2CF3
CH2C(=NOMe)Me CH(n-Pr)S(O)2Me
CH2C(=NOMe)Me CH(n-Pr)S(O)2Et
CH2C(=NOMe)Me CH(n-Pr)S(O)2CF3
CH2C(=NOMe)Me CH(n-Pr)S(O)2CH2CF3
CH2C(=NOMe)Me CH(i-Pr)SMe
CH2C(=NOMe)Me CH(i-Pr)SEt
CH2C(=NOMe)Me CH(i-Pr)SCF3
CH2C(=NOMe)Me CH(i-Pr)SCH2CF3
CH2C(=NOMe)Me CH(i-Pr)S(O)Me
CH2C(=NOMe)Me CH(i-Pr)S(O)Et
CH2C(=NOMe)Me CH(i-Pr)S(O)CF3
CH2C(=NOMe)Me CH(i-Pr)S(O)CH2CF3
CH2C(=NOMe)Me CH(i-Pr)S(O)2Me
CH2C(=NOMe)Me CH(i-Pr)S(O)2Et
CH2C(=NOMe)Me CH(i-Pr)S(O)2CF3
CH2C(=NOMe)Me CH(i-Pr)S(O)2CH2CF3
CH2C(=NOMe)Me CH(n-Bu)SMe
CH2C(=NOMe)Me CH(n-Bu)SEt
CH2C(=NOMe)Me CH(n-Bu)SCF3
CH2C(=NOMe)Me CH(n-Bu)SCH2CF3
CH2C(=NOMe)Me CH(n-Bu)S(O)Me
CH2C(=NOMe)Me CH(n-Bu)S(O)Et
CH2C(=NOMe)Me CH(n-Bu)S(O)CF3
CH2C(=NOMe)Me CH(n-Bu)S(O)CH2CF3
CH2C(=NOMe)Me CH(n-Bu)S(O)2Me
CH2C(=NOMe)Me CH(n-Bu)S(O)2Et
CH2C(=NOMe)Me CH(n-Bu)S(O)2CF3
CH2C(=NOMe)Me CH(n-Bu)S(O)2CH2CF3
CH2C(=NOMe)Me CH(i-Bu)SMe
CH2C(=NOMe)Me CH(i-Bu)SEt
CH2C(=NOMe)Me CH(i-Bu)SCF3
CH2C(=NOMe)Me CH(i-Bu)SCH2CF3
CH2C(=NOMe)Me CH(i-Bu)S(O)Me
CH2C(=NOMe)Me CH(i-Bu)S(O)Et
CH2C(=NOMe)Me CH(i-Bu)S(O)CF3
CH2C(=NOMe)Me CH(i-Bu)S(O)CH2CF3
CH2C(=NOMe)Me CH(i-Bu)S(O)2Me
CH2C(=NOMe)Me CH(i-Bu)S(O)2Et
CH2C(=NOMe)Me CH(i-Bu)S(O)2CF3
CH2C(=NOMe)Me CH(i-Bu)S(O)2CH2CF3
CH2C(=NOMe)Me CH(s-Bu)SMe
CH2C(=NOMe)Me CH(s-Bu)SEt
CH2C(=NOMe)Me CH(s-Bu)SCF3
CH2C(=NOMe)Me CH(s-Bu)SCH2CF3
CH2C(=NOMe)Me CH(s-Bu)S(O)Me
CH2C(=NOMe)Me CH(s-Bu)S(O)Et
CH2C(=NOMe)Me CH(s-Bu)S(O)CF3
CH2C(=NOMe)Me CH(s-Bu)S(O)CH2CF3
CH2C(=NOMe)Me CH(s-Bu)S(O)2Me
CH2C(=NOMe)Me CH(s-Bu)S(O)2Et
CH2C(=NOMe)Me CH(s-Bu)S(O)2CF3
CH2C(=NOMe)Me CH(s-Bu)S(O)2CH2CF3
CH2C(=NOMe)Me CH(t-Bu)SMe
CH2C(=NOMe)Me CH(t-Bu)SEt
CH2C(=NOMe)Me CH(t-Bu)SCF3
CH2C(=NOMe)Me CH(t-Bu)SCH2CF3
CH2C(=NOMe)Me CH(t-Bu)S(O)Me
CH2C(=NOMe)Me CH(t-Bu)S(O)Et
CH2C(=NOMe)Me CH(t-Bu)S(O)CF3
CH2C(=NOMe)Me CH(t-Bu)S(O)CH2CF3
CH2C(=NOMe)Me CH(t-Bu)S(O)2Me
CH2C(=NOMe)Me CH(t-Bu)S(O)2Et
CH2C(=NOMe)Me CH(t-Bu)S(O)2CF3
CH2C(=NOMe)Me CH(t-Bu)S(O)2CH2CF3
CH2C(=NOMe)Me CH(CF3)SMe
CH2C(=NOMe)Me CH(CF3)SEt
CH2C(=NOMe)Me CH(CF3)SCF3
CH2C(=NOMe)Me CH(CF3)SCH2CF3
CH2C(=NOMe)Me CH(CF3)S(O)Me
CH2C(=NOMe)Me CH(CF3)S(O)Et
CH2C(=NOMe)Me CH(CF3)S(O)CF3
CH2C(=NOMe)Me CH(CF3)S(O)CH2CF3
CH2C(=NOMe)Me CH(CF3)S(O)2Me
CH2C(=NOMe)Me CH(CF3)S(O)2Et
CH2C(=NOMe)Me CH(CF3)S(O)2CF3
CH2C(=NOMe)Me CH(CF3)S(O)2CH2CF3
CH2C(=NOMe)Me CH2CH2SMe
CH2C(=NOMe)Me CH2CH2SEt
CH2C(=NOMe)Me CH2CH2SCF3
CH2C(=NOMe)Me CH2CH2SCH2CF3
CH2C(=NOMe)Me CH2CH2S(O)Me
CH2C(=NOMe)Me CH2CH2S(O)Et
CH2C(=NOMe)Me CH2CH2S(O)CF3
CH2C(=NOMe)Me CH2CH2S(O)CH2CF3
CH2C(=NOMe)Me CH2CH2S(O)2Me
CH2C(=NOMe)Me CH2CH2S(O)2Et
CH2C(=NOMe)Me CH2CH2S(O)2CF3
CH2C(=NOMe)Me CH2CH2S(O)2CH2CF3
CH2C(=NOMe)Me CH(Me)CH2SMe
CH2C(=NOMe)Me CH(Me)CH2SEt
CH2C(=NOMe)Me CH(Me)CH2SCF3
CH2C(=NOMe)Me CH(Me)CH2SCH2CF3
CH2C(=NOMe)Me CH(Me)CH2S(O)Me
CH2C(=NOMe)Me CH(Me)CH2S(O)Et
CH2C(=NOMe)Me CH(Me)CH2S(O)CF3
CH2C(=NOMe)Me CH(Me)CH2S(O)CH2CF3
CH2C(=NOMe)Me CH(Me)CH2S(O)2Me
CH2C(=NOMe)Me CH(Me)CH2S(O)2Et
CH2C(=NOMe)Me CH(Me)CH2S(O)2CF3
CH2C(=NOMe)Me CH(Me)CH2S(O)2CH2CF3
CH2C(=NOMe)Me CH(Et)CH2SMe
CH2C(=NOMe)Me CH(Et)CH2SEt
CH2C(=NOMe)Me CH(Et)CH2SCF3
CH2C(=NOMe)Me CH(Et)CH2SCH2CF3
CH2C(=NOMe)Me CH(Et)CH2S(O)Me
CH2C(=NOMe)Me CH(Et)CH2S(O)Et
CH2C(=NOMe)Me CH(Et)CH2S(O)CF3
CH2C(=NOMe)Me CH(Et)CH2S(O)CH2CF3
CH2C(=NOMe)Me CH(Et)CH2S(O)2Me
CH2C(=NOMe)Me CH(Et)CH2S(O)2Et
CH2C(=NOMe)Me CH(Et)CH2S(O)2CF3
CH2C(=NOMe)Me CH(Et)CH2S(O)2CH2CF3
CH2C(=NOMe)Me C(Me)2CH2SMe
CH2C(=NOMe)Me C(Me)2CH2SEt
CH2C(=NOMe)Me C(Me)2CH2SCF3
CH2C(=NOMe)Me C(Me)2CH2SCH2CF3
CH2C(=NOMe)Me C(Me)2CH2S(O)Me
CH2C(=NOMe)Me C(Me)2CH2S(O)Et
CH2C(=NOMe)Me C(Me)2CH2S(O)CF3
CH2C(=NOMe)Me C(Me)2CH2S(O)CH2CF3
CH2C(=NOMe)Me C(Me)2CH2S(O)2Me
CH2C(=NOMe)Me C(Me)2CH2S(O)2Et
CH2C(=NOMe)Me C(Me)2CH2S(O)2CF3
CH2C(=NOMe)Me C(Me)2CH2S(O)2CH2CF3
CH2C(=NOMe)Me CH2CH(Me)SMe
CH2C(=NOMe)Me CH2CH(Me)SEt
CH2C(=NOMe)Me CH2CH(Me)SCF3
CH2C(=NOMe)Me CH2CH(Me)SCH2CF3
CH2C(=NOMe)Me CH2CH(Me)S(O)Me
CH2C(=NOMe)Me CH2CH(Me)S(O)Et
CH2C(=NOMe)Me CH2CH(Me)S(O)CF3
CH2C(=NOMe)Me CH2CH(Me)S(O)CH2CF3
CH2C(=NOMe)Me CH2CH(Me)S(O)2Me
CH2C(=NOMe)Me CH2CH(Me)S(O)2Et
CH2C(=NOMe)Me CH2CH(Me)S(O)2CF3
CH2C(=NOMe)Me CH2CH(Me)S(O)2CH2CF3
CH2C(=NOMe)Me CH2CH(Et)SMe
CH2C(=NOMe)Me CH2CH(Et)SEt
CH2C(=NOMe)Me CH2CH(Et)SCF3
CH2C(=NOMe)Me CH2CH(Et)SCH2CF3
CH2C(=NOMe)Me CH2CH(Et)S(O)Me
CH2C(=NOMe)Me CH2CH(Et)S(O)Et
CH2C(=NOMe)Me CH2CH(Et)S(O)CF3
CH2C(=NOMe)Me CH2CH(Et)S(O)CH2CF3
CH2C(=NOMe)Me CH2CH(Et)S(O)2Me
CH2C(=NOMe)Me CH2CH(Et)S(O)2Et
CH2C(=NOMe)Me CH2CH(Et)S(O)2CF3
CH2C(=NOMe)Me CH2CH(Et)S(O)2CH2CF3
CH2C(=NOMe)Me CH(Me)CH(Me)SMe
CH2C(=NOMe)Me CH(Me)CH(Me)SEt
CH2C(=NOMe)Me CH(Me)CH(Me)SCF3
CH2C(=NOMe)Me CH(Me)CH(Me)SCH2CF3
CH2C(=NOMe)Me CH(Me)CH(Me)S(O)Me
CH2C(=NOMe)Me CH(Me)CH(Me)S(O)Et
CH2C(=NOMe)Me CH(Me)CH(Me)S(O)CF3
CH2C(=NOMe)Me CH(Me)CH(Me)S(O)CH2CF3
CH2C(=NOMe)Me CH(Me)CH(Me)S(O)2Me
CH2C(=NOMe)Me CH(Me)CH(Me)S(O)2Et
CH2C(=NOMe)Me CH(Me)CH(Me)S(O)2CF3
CH2C(=NOMe)Me CH(Me)CH(Me)S(O)2CH2CF3
――――――――――――――――――
〔第2表〕
――――――――――――――――――
X1a X1
――――――――――――――――――
H CH2SMe
H CH2SEt
H CH2SCFThree
H CH2SCH2CFThree
H CH2S (O) Me
H CH2S (O) Et
H CH2S (O) CFThree
H CH2S (O) CH2CFThree
H CH2S (O)2Me
H CH2S (O)2Et
H CH2S (O)2CFThree
H CH2S (O)2CH2CFThree
H CH (Me) SMe
H CH (Me) SEt
H CH (Me) SCFThree
H CH (Me) SCH2CFThree
H CH (Me) S (O) Me
H CH (Me) S (O) Et
H CH (Me) S (O) CFThree
H CH (Me) S (O) CH2CFThree
H CH (Me) S (O)2Me
H CH (Me) S (O)2Et
H CH (Me) S (O)2CFThree
H CH (Me) S (O)2CH2CFThree
H CH (Et) SMe
H CH (Et) SEt
H CH (Et) SCFThree
H CH (Et) SCH2CFThree
H CH (Et) S (O) Me
H CH (Et) S (O) Et
H CH (Et) S (O) CFThree
H CH (Et) S (O) CH2CFThree
H CH (Et) S (O)2Me
H CH (Et) S (O)2Et
H CH (Et) S (O)2CFThree
H CH (Et) S (O)2CH2CFThree
H CH (n-Pr) SMe
H CH (n-Pr) SEt
H CH (n-Pr) SCFThree
H CH (n-Pr) SCH2CFThree
H CH (n-Pr) S (O) Me
H CH (n-Pr) S (O) Et
H CH (n-Pr) S (O) CFThree
H CH (n-Pr) S (O) CH2CFThree
H CH (n-Pr) S (O)2Me
H CH (n-Pr) S (O)2Et
H CH (n-Pr) S (O)2CFThree
H CH (n-Pr) S (O)2CH2CFThree
H CH (i-Pr) SMe
H CH (i-Pr) SEt
H CH (i-Pr) SCFThree
H CH (i-Pr) SCH2CFThree
H CH (i-Pr) S (O) Me
H CH (i-Pr) S (O) Et
H CH (i-Pr) S (O) CFThree
H CH (i-Pr) S (O) CH2CFThree
H CH (i-Pr) S (O)2Me
H CH (i-Pr) S (O)2Et
H CH (i-Pr) S (O)2CFThree
H CH (i-Pr) S (O)2CH2CFThree
H CH (n-Bu) SMe
H CH (n-Bu) SEt
H CH (n-Bu) SCFThree
H CH (n-Bu) SCH2CFThree
H CH (n-Bu) S (O) Me
H CH (n-Bu) S (O) Et
H CH (n-Bu) S (O) CFThree
H CH (n-Bu) S (O) CH2CFThree
H CH (n-Bu) S (O)2Me
H CH (n-Bu) S (O)2Et
H CH (n-Bu) S (O)2CFThree
H CH (n-Bu) S (O)2CH2CFThree
H CH (i-Bu) SMe
H CH (i-Bu) SEt
H CH (i-Bu) SCFThree
H CH (i-Bu) SCH2CFThree
H CH (i-Bu) S (O) Me
H CH (i-Bu) S (O) Et
H CH (i-Bu) S (O) CFThree
H CH (i-Bu) S (O) CH2CFThree
H CH (i-Bu) S (O)2Me
H CH (i-Bu) S (O)2Et
H CH (i-Bu) S (O)2CFThree
H CH (i-Bu) S (O)2CH2CFThree
H CH (s-Bu) SMe
H CH (s-Bu) SEt
H CH (s-Bu) SCFThree
H CH (s-Bu) SCH2CFThree
H CH (s-Bu) S (O) Me
H CH (s-Bu) S (O) Et
H CH (s-Bu) S (O) CFThree
H CH (s-Bu) S (O) CH2CFThree
H CH (s-Bu) S (O)2Me
H CH (s-Bu) S (O)2Et
H CH (s-Bu) S (O)2CFThree
H CH (s-Bu) S (O)2CH2CFThree
H CH (t-Bu) SMe
H CH (t-Bu) SEt
H CH (t-Bu) SCFThree
H CH (t-Bu) SCH2CFThree
H CH (t-Bu) S (O) Me
H CH (t-Bu) S (O) Et
H CH (t-Bu) S (O) CFThree
H CH (t-Bu) S (O) CH2CFThree
H CH (t-Bu) S (O)2Me
H CH (t-Bu) S (O)2Et
H CH (t-Bu) S (O)2CFThree
H CH (t-Bu) S (O)2CH2CFThree
H CH (CFThreeSMe
H CH (CFThree) SEt
H CH (CFThree) SCFThree
H CH (CFThree) SCH2CFThree
H CH (CFThree) S (O) Me
H CH (CFThree) S (O) Et
H CH (CFThree) S (O) CFThree
H CH (CFThree) S (O) CH2CFThree
H CH (CFThree) S (O)2Me
H CH (CFThree) S (O)2Et
H CH (CFThree) S (O)2CFThree
H CH (CFThree) S (O)2CH2CFThree
H CH2CH2SMe
H CH2CH2SEt
H CH2CH2SCFThree
H CH2CH2SCH2CFThree
H CH2CH2S (O) Me
H CH2CH2S (O) Et
H CH2CH2S (O) CFThree
H CH2CH2S (O) CH2CFThree
H CH2CH2S (O)2Me
H CH2CH2S (O)2Et
H CH2CH2S (O)2CFThree
H CH2CH2S (O)2CH2CFThree
H CH (Me) CH2SMe
H CH (Me) CH2SEt
H CH (Me) CH2SCFThree
H CH (Me) CH2SCH2CFThree
H CH (Me) CH2S (O) Me
H CH (Me) CH2S (O) Et
H CH (Me) CH2S (O) CFThree
H CH (Me) CH2S (O) CH2CFThree
H CH (Me) CH2S (O)2Me
H CH (Me) CH2S (O)2Et
H CH (Me) CH2S (O)2CFThree
H CH (Me) CH2S (O)2CH2CFThree
H CH (Et) CH2SMe
H CH (Et) CH2SEt
H CH (Et) CH2SCFThree
H CH (Et) CH2SCH2CFThree
H CH (Et) CH2S (O) Me
H CH (Et) CH2S (O) Et
H CH (Et) CH2S (O) CFThree
H CH (Et) CH2S (O) CH2CFThree
H CH (Et) CH2S (O)2Me
H CH (Et) CH2S (O)2Et
H CH (Et) CH2S (O)2CFThree
H CH (Et) CH2S (O)2CH2CFThree
H C (Me)2CH2SMe
H C (Me)2CH2SEt
H C (Me)2CH2SCFThree
H C (Me)2CH2SCH2CFThree
H C (Me)2CH2S (O) Me
H C (Me)2CH2S (O) Et
H C (Me)2CH2S (O) CFThree
H C (Me)2CH2S (O) CH2CFThree
H C (Me)2CH2S (O)2Me
H C (Me)2CH2S (O)2Et
H C (Me)2CH2S (O)2CFThree
H C (Me)2CH2S (O)2CH2CFThree
H CH2CH (Me) SMe
H CH2CH (Me) SEt
H CH2CH (Me) SCFThree
H CH2CH (Me) SCH2CFThree
H CH2CH (Me) S (O) Me
H CH2CH (Me) S (O) Et
H CH2CH (Me) S (O) CFThree
H CH2CH (Me) S (O) CH2CFThree
H CH2CH (Me) S (O)2Me
H CH2CH (Me) S (O)2Et
H CH2CH (Me) S (O)2CFThree
H CH2CH (Me) S (O)2CH2CFThree
H CH2CH (Et) SMe
H CH2CH (Et) SEt
H CH2CH (Et) SCFThree
H CH2CH (Et) SCH2CFThree
H CH2CH (Et) S (O) Me
H CH2CH (Et) S (O) Et
H CH2CH (Et) S (O) CFThree
H CH2CH (Et) S (O) CH2CFThree
H CH2CH (Et) S (O)2Me
H CH2CH (Et) S (O)2Et
H CH2CH (Et) S (O)2CFThree
H CH2CH (Et) S (O)2CH2CFThree
H CH (Me) CH (Me) SMe
H CH (Me) CH (Me) SEt
H CH (Me) CH (Me) SCFThree
H CH (Me) CH (Me) SCH2CFThree
H CH (Me) CH (Me) S (O) Me
H CH (Me) CH (Me) S (O) Et
H CH (Me) CH (Me) S (O) CFThree
H CH (Me) CH (Me) S (O) CH2CFThree
H CH (Me) CH (Me) S (O)2Me
H CH (Me) CH (Me) S (O)2Et
H CH (Me) CH (Me) S (O)2CFThree
H CH (Me) CH (Me) S (O)2CH2CFThree
Me CH2SMe
Me CH2SEt
Me CH2SCFThree
Me CH2SCH2CFThree
Me CH2S (O) Me
Me CH2S (O) Et
Me CH2S (O) CFThree
Me CH2S (O) CH2CFThree
Me CH2S (O)2Me
Me CH2S (O)2Et
Me CH2S (O)2CFThree
Me CH2S (O)2CH2CFThree
Me CH (Me) SMe
Me CH (Me) SEt
Me CH (Me) SCFThree
Me CH (Me) SCH2CFThree
Me CH (Me) S (O) Me
Me CH (Me) S (O) Et
Me CH (Me) S (O) CFThree
Me CH (Me) S (O) CH2CFThree
Me CH (Me) S (O)2Me
Me CH (Me) S (O)2Et
Me CH (Me) S (O)2CFThree
Me CH (Me) S (O)2CH2CFThree
Me CH (Et) SMe
Me CH (Et) SEt
Me CH (Et) SCFThree
Me CH (Et) SCH2CFThree
Me CH (Et) S (O) Me
Me CH (Et) S (O) Et
Me CH (Et) S (O) CFThree
Me CH (Et) S (O) CH2CFThree
Me CH (Et) S (O)2Me
Me CH (Et) S (O)2Et
Me CH (Et) S (O)2CFThree
Me CH (Et) S (O)2CH2CFThree
Me CH (n-Pr) SMe
Me CH (n-Pr) SEt
Me CH (n-Pr) SCFThree
Me CH (n-Pr) SCH2CFThree
Me CH (n-Pr) S (O) Me
Me CH (n-Pr) S (O) Et
Me CH (n-Pr) S (O) CFThree
Me CH (n-Pr) S (O) CH2CFThree
Me CH (n-Pr) S (O)2Me
Me CH (n-Pr) S (O)2Et
Me CH (n-Pr) S (O)2CFThree
Me CH (n-Pr) S (O)2CH2CFThree
Me CH (i-Pr) SMe
Me CH (i-Pr) SEt
Me CH (i-Pr) SCFThree
Me CH (i-Pr) SCH2CFThree
Me CH (i-Pr) S (O) Me
Me CH (i-Pr) S (O) Et
Me CH (i-Pr) S (O) CFThree
Me CH (i-Pr) S (O) CH2CFThree
Me CH (i-Pr) S (O)2Me
Me CH (i-Pr) S (O)2Et
Me CH (i-Pr) S (O)2CFThree
Me CH (i-Pr) S (O)2CH2CFThree
Me CH (n-Bu) SMe
Me CH (n-Bu) SEt
Me CH (n-Bu) SCFThree
Me CH (n-Bu) SCH2CFThree
Me CH (n-Bu) S (O) Me
Me CH (n-Bu) S (O) Et
Me CH (n-Bu) S (O) CFThree
Me CH (n-Bu) S (O) CH2CFThree
Me CH (n-Bu) S (O)2Me
Me CH (n-Bu) S (O)2Et
Me CH (n-Bu) S (O)2CFThree
Me CH (n-Bu) S (O)2CH2CFThree
Me CH (i-Bu) SMe
Me CH (i-Bu) SEt
Me CH (i-Bu) SCFThree
Me CH (i-Bu) SCH2CFThree
Me CH (i-Bu) S (O) Me
Me CH (i-Bu) S (O) Et
Me CH (i-Bu) S (O) CFThree
Me CH (i-Bu) S (O) CH2CFThree
Me CH (i-Bu) S (O)2Me
Me CH (i-Bu) S (O)2Et
Me CH (i-Bu) S (O)2CFThree
Me CH (i-Bu) S (O)2CH2CFThree
Me CH (s-Bu) SMe
Me CH (s-Bu) SEt
Me CH (s-Bu) SCFThree
Me CH (s-Bu) SCH2CFThree
Me CH (s-Bu) S (O) Me
Me CH (s-Bu) S (O) Et
Me CH (s-Bu) S (O) CFThree
Me CH (s-Bu) S (O) CH2CFThree
Me CH (s-Bu) S (O)2Me
Me CH (s-Bu) S (O)2Et
Me CH (s-Bu) S (O)2CFThree
Me CH (s-Bu) S (O)2CH2CFThree
Me CH (t-Bu) SMe
Me CH (t-Bu) SEt
Me CH (t-Bu) SCFThree
Me CH (t-Bu) SCH2CFThree
Me CH (t-Bu) S (O) Me
Me CH (t-Bu) S (O) Et
Me CH (t-Bu) S (O) CFThree
Me CH (t-Bu) S (O) CH2CFThree
Me CH (t-Bu) S (O)2Me
Me CH (t-Bu) S (O)2Et
Me CH (t-Bu) S (O)2CFThree
Me CH (t-Bu) S (O)2CH2CFThree
Me CH (CFThreeSMe
Me CH (CFThree) SEt
Me CH (CFThree) SCFThree
Me CH (CFThree) SCH2CFThree
Me CH (CFThree) S (O) Me
Me CH (CFThree) S (O) Et
Me CH (CFThree) S (O) CFThree
Me CH (CFThree) S (O) CH2CFThree
Me CH (CFThree) S (O)2Me
Me CH (CFThree) S (O)2Et
Me CH (CFThree) S (O)2CFThree
Me CH (CFThree) S (O)2CH2CFThree
Me CH2CH2SMe
Me CH2CH2SEt
Me CH2CH2SCFThree
Me CH2CH2SCH2CFThree
Me CH2CH2S (O) Me
Me CH2CH2S (O) Et
Me CH2CH2S (O) CFThree
Me CH2CH2S (O) CH2CFThree
Me CH2CH2S (O)2Me
Me CH2CH2S (O)2Et
Me CH2CH2S (O)2CFThree
Me CH2CH2S (O)2CH2CFThree
Me CH (Me) CH2SMe
Me CH (Me) CH2SEt
Me CH (Me) CH2SCFThree
Me CH (Me) CH2SCH2CFThree
Me CH (Me) CH2S (O) Me
Me CH (Me) CH2S (O) Et
Me CH (Me) CH2S (O) CFThree
Me CH (Me) CH2S (O) CH2CFThree
Me CH (Me) CH2S (O)2Me
Me CH (Me) CH2S (O)2Et
Me CH (Me) CH2S (O)2CFThree
Me CH (Me) CH2S (O)2CH2CFThree
Me CH (Et) CH2SMe
Me CH (Et) CH2SEt
Me CH (Et) CH2SCFThree
Me CH (Et) CH2SCH2CFThree
Me CH (Et) CH2S (O) Me
Me CH (Et) CH2S (O) Et
Me CH (Et) CH2S (O) CFThree
Me CH (Et) CH2S (O) CH2CFThree
Me CH (Et) CH2S (O)2Me
Me CH (Et) CH2S (O)2Et
Me CH (Et) CH2S (O)2CFThree
Me CH (Et) CH2S (O)2CH2CFThree
Me C (Me)2CH2SMe
Me C (Me)2CH2SEt
Me C (Me)2CH2SCFThree
Me C (Me)2CH2SCH2CFThree
Me C (Me)2CH2S (O) Me
Me C (Me)2CH2S (O) Et
Me C (Me)2CH2S (O) CFThree
Me C (Me)2CH2S (O) CH2CFThree
Me C (Me)2CH2S (O)2Me
Me C (Me)2CH2S (O)2Et
Me C (Me)2CH2S (O)2CFThree
Me C (Me)2CH2S (O)2CH2CFThree
Me CH2CH (Me) SMe
Me CH2CH (Me) SEt
Me CH2CH (Me) SCFThree
Me CH2CH (Me) SCH2CFThree
Me CH2CH (Me) S (O) Me
Me CH2CH (Me) S (O) Et
Me CH2CH (Me) S (O) CFThree
Me CH2CH (Me) S (O) CH2CFThree
Me CH2CH (Me) S (O)2Me
Me CH2CH (Me) S (O)2Et
Me CH2CH (Me) S (O)2CFThree
Me CH2CH (Me) S (O)2CH2CFThree
Me CH2CH (Et) SMe
Me CH2CH (Et) SEt
Me CH2CH (Et) SCFThree
Me CH2CH (Et) SCH2CFThree
Me CH2CH (Et) S (O) Me
Me CH2CH (Et) S (O) Et
Me CH2CH (Et) S (O) CFThree
Me CH2CH (Et) S (O) CH2CFThree
Me CH2CH (Et) S (O)2Me
Me CH2CH (Et) S (O)2Et
Me CH2CH (Et) S (O)2CFThree
Me CH2CH (Et) S (O)2CH2CFThree
Me CH (Me) CH (Me) SMe
Me CH (Me) CH (Me) SEt
Me CH (Me) CH (Me) SCFThree
Me CH (Me) CH (Me) SCH2CFThree
Me CH (Me) CH (Me) S (O) Me
Me CH (Me) CH (Me) S (O) Et
Me CH (Me) CH (Me) S (O) CFThree
Me CH (Me) CH (Me) S (O) CH2CFThree
Me CH (Me) CH (Me) S (O)2Me
Me CH (Me) CH (Me) S (O)2Et
Me CH (Me) CH (Me) S (O)2CFThree
Me CH (Me) CH (Me) S (O)2CH2CFThree
CH2CFThree CH2SMe
CH2CFThree CH2SEt
CH2CFThree CH2SCFThree
CH2CFThree CH2SCH2CFThree
CH2CFThree CH2S (O) Me
CH2CFThree CH2S (O) Et
CH2CFThree CH2S (O) CFThree
CH2CFThree CH2S (O) CH2CFThree
CH2CFThree CH2S (O)2Me
CH2CFThree CH2S (O)2Et
CH2CFThree CH2S (O)2CFThree
CH2CFThree CH2S (O)2CH2CFThree
CH2CFThree CH (Me) SMe
CH2CFThree CH (Me) SEt
CH2CFThree CH (Me) SCFThree
CH2CFThree CH (Me) SCH2CFThree
CH2CFThree CH (Me) S (O) Me
CH2CFThree CH (Me) S (O) Et
CH2CFThree CH (Me) S (O) CFThree
CH2CFThree CH (Me) S (O) CH2CFThree
CH2CFThree CH (Me) S (O)2Me
CH2CFThree CH (Me) S (O)2Et
CH2CFThree CH (Me) S (O)2CFThree
CH2CFThree CH (Me) S (O)2CH2CFThree
CH2CFThree CH (Et) SMe
CH2CFThree CH (Et) SEt
CH2CFThree CH (Et) SCFThree
CH2CFThree CH (Et) SCH2CFThree
CH2CFThree CH (Et) S (O) Me
CH2CFThree CH (Et) S (O) Et
CH2CFThree CH (Et) S (O) CFThree
CH2CFThree CH (Et) S (O) CH2CFThree
CH2CFThree CH (Et) S (O)2Me
CH2CFThree CH (Et) S (O)2Et
CH2CFThree CH (Et) S (O)2CFThree
CH2CFThree CH (Et) S (O)2CH2CFThree
CH2CFThree CH (n-Pr) SMe
CH2CFThree CH (n-Pr) SEt
CH2CFThree CH (n-Pr) SCFThree
CH2CFThree CH (n-Pr) SCH2CFThree
CH2CFThree CH (n-Pr) S (O) Me
CH2CFThree CH (n-Pr) S (O) Et
CH2CFThree CH (n-Pr) S (O) CFThree
CH2CFThree CH (n-Pr) S (O) CH2CFThree
CH2CFThree CH (n-Pr) S (O)2Me
CH2CFThree CH (n-Pr) S (O)2Et
CH2CFThree CH (n-Pr) S (O)2CFThree
CH2CFThree CH (n-Pr) S (O)2CH2CFThree
CH2CFThree CH (i-Pr) SMe
CH2CFThree CH (i-Pr) SEt
CH2CFThree CH (i-Pr) SCFThree
CH2CFThree CH (i-Pr) SCH2CFThree
CH2CFThree CH (i-Pr) S (O) Me
CH2CFThree CH (i-Pr) S (O) Et
CH2CFThree CH (i-Pr) S (O) CFThree
CH2CFThree CH (i-Pr) S (O) CH2CFThree
CH2CFThree CH (i-Pr) S (O)2Me
CH2CFThree CH (i-Pr) S (O)2Et
CH2CFThree CH (i-Pr) S (O)2CFThree
CH2CFThree CH (i-Pr) S (O)2CH2CFThree
CH2CFThree CH (n-Bu) SMe
CH2CFThree CH (n-Bu) SEt
CH2CFThree CH (n-Bu) SCFThree
CH2CFThree CH (n-Bu) SCH2CFThree
CH2CFThree CH (n-Bu) S (O) Me
CH2CFThree CH (n-Bu) S (O) Et
CH2CFThree CH (n-Bu) S (O) CFThree
CH2CFThree CH (n-Bu) S (O) CH2CFThree
CH2CFThree CH (n-Bu) S (O)2Me
CH2CFThree CH (n-Bu) S (O)2Et
CH2CFThree CH (n-Bu) S (O)2CFThree
CH2CFThree CH (n-Bu) S (O)2CH2CFThree
CH2CFThree CH (i-Bu) SMe
CH2CFThree CH (i-Bu) SEt
CH2CFThree CH (i-Bu) SCFThree
CH2CFThree CH (i-Bu) SCH2CFThree
CH2CFThree CH (i-Bu) S (O) Me
CH2CFThree CH (i-Bu) S (O) Et
CH2CFThree CH (i-Bu) S (O) CFThree
CH2CFThree CH (i-Bu) S (O) CH2CFThree
CH2CFThree CH (i-Bu) S (O)2Me
CH2CFThree CH (i-Bu) S (O)2Et
CH2CFThree CH (i-Bu) S (O)2CFThree
CH2CFThree CH (i-Bu) S (O)2CH2CFThree
CH2CFThree CH (s-Bu) SMe
CH2CFThree CH (s-Bu) SEt
CH2CFThree CH (s-Bu) SCFThree
CH2CFThree CH (s-Bu) SCH2CFThree
CH2CFThree CH (s-Bu) S (O) Me
CH2CFThree CH (s-Bu) S (O) Et
CH2CFThree CH (s-Bu) S (O) CFThree
CH2CFThree CH (s-Bu) S (O) CH2CFThree
CH2CFThree CH (s-Bu) S (O)2Me
CH2CFThree CH (s-Bu) S (O)2Et
CH2CFThree CH (s-Bu) S (O)2CFThree
CH2CFThree CH (s-Bu) S (O)2CH2CFThree
CH2CFThree CH (t-Bu) SMe
CH2CFThree CH (t-Bu) SEt
CH2CFThree CH (t-Bu) SCFThree
CH2CFThree CH (t-Bu) SCH2CFThree
CH2CFThree CH (t-Bu) S (O) Me
CH2CFThree CH (t-Bu) S (O) Et
CH2CFThree CH (t-Bu) S (O) CFThree
CH2CFThree CH (t-Bu) S (O) CH2CFThree
CH2CFThree CH (t-Bu) S (O)2Me
CH2CFThree CH (t-Bu) S (O)2Et
CH2CFThree CH (t-Bu) S (O)2CFThree
CH2CFThree CH (t-Bu) S (O)2CH2CFThree
CH2CFThree CH (CFThreeSMe
CH2CFThree CH (CFThree) SEt
CH2CFThree CH (CFThree) SCFThree
CH2CFThree CH (CFThree) SCH2CFThree
CH2CFThree CH (CFThree) S (O) Me
CH2CFThree CH (CFThree) S (O) Et
CH2CFThree CH (CFThree) S (O) CFThree
CH2CFThree CH (CFThree) S (O) CH2CFThree
CH2CFThree CH (CFThree) S (O)2Me
CH2CFThree CH (CFThree) S (O)2Et
CH2CFThree CH (CFThree) S (O)2CFThree
CH2CFThree CH (CFThree) S (O)2CH2CFThree
CH2CFThree CH2CH2SMe
CH2CFThree CH2CH2SEt
CH2CFThree CH2CH2SCFThree
CH2CFThree CH2CH2SCH2CFThree
CH2CFThree CH2CH2S (O) Me
CH2CFThree CH2CH2S (O) Et
CH2CFThree CH2CH2S (O) CFThree
CH2CFThree CH2CH2S (O) CH2CFThree
CH2CFThree CH2CH2S (O)2Me
CH2CFThree CH2CH2S (O)2Et
CH2CFThree CH2CH2S (O)2CFThree
CH2CFThree CH2CH2S (O)2CH2CFThree
CH2CFThree CH (Me) CH2SMe
CH2CFThree CH (Me) CH2SEt
CH2CFThree CH (Me) CH2SCFThree
CH2CFThree CH (Me) CH2SCH2CFThree
CH2CFThree CH (Me) CH2S (O) Me
CH2CFThree CH (Me) CH2S (O) Et
CH2CFThree CH (Me) CH2S (O) CFThree
CH2CFThree CH (Me) CH2S (O) CH2CFThree
CH2CFThree CH (Me) CH2S (O)2Me
CH2CFThree CH (Me) CH2S (O)2Et
CH2CFThree CH (Me) CH2S (O)2CFThree
CH2CFThree CH (Me) CH2S (O)2CH2CFThree
CH2CFThree CH (Et) CH2SMe
CH2CFThree CH (Et) CH2SEt
CH2CFThree CH (Et) CH2SCFThree
CH2CFThree CH (Et) CH2SCH2CFThree
CH2CFThree CH (Et) CH2S (O) Me
CH2CFThree CH (Et) CH2S (O) Et
CH2CFThree CH (Et) CH2S (O) CFThree
CH2CFThree CH (Et) CH2S (O) CH2CFThree
CH2CFThree CH (Et) CH2S (O)2Me
CH2CFThree CH (Et) CH2S (O)2Et
CH2CFThree CH (Et) CH2S (O)2CFThree
CH2CFThree CH (Et) CH2S (O)2CH2CFThree
CH2CFThree C (Me)2CH2SMe
CH2CFThree C (Me)2CH2SEt
CH2CFThree C (Me)2CH2SCFThree
CH2CFThree C (Me)2CH2SCH2CFThree
CH2CFThree C (Me)2CH2S (O) Me
CH2CFThree C (Me)2CH2S (O) Et
CH2CFThree C (Me)2CH2S (O) CFThree
CH2CFThree C (Me)2CH2S (O) CH2CFThree
CH2CFThree C (Me)2CH2S (O)2Me
CH2CFThree C (Me)2CH2S (O)2Et
CH2CFThree C (Me)2CH2S (O)2CFThree
CH2CFThree C (Me)2CH2S (O)2CH2CFThree
CH2CFThree CH2CH (Me) SMe
CH2CFThree CH2CH (Me) SEt
CH2CFThree CH2CH (Me) SCFThree
CH2CFThree CH2CH (Me) SCH2CFThree
CH2CFThree CH2CH (Me) S (O) Me
CH2CFThree CH2CH (Me) S (O) Et
CH2CFThree CH2CH (Me) S (O) CFThree
CH2CFThree CH2CH (Me) S (O) CH2CFThree
CH2CFThree CH2CH (Me) S (O)2Me
CH2CFThree CH2CH (Me) S (O)2Et
CH2CFThree CH2CH (Me) S (O)2CFThree
CH2CFThree CH2CH (Me) S (O)2CH2CFThree
CH2CFThree CH2CH (Et) SMe
CH2CFThree CH2CH (Et) SEt
CH2CFThree CH2CH (Et) SCFThree
CH2CFThree CH2CH (Et) SCH2CFThree
CH2CFThree CH2CH (Et) S (O) Me
CH2CFThree CH2CH (Et) S (O) Et
CH2CFThree CH2CH (Et) S (O) CFThree
CH2CFThree CH2CH (Et) S (O) CH2CFThree
CH2CFThree CH2CH (Et) S (O)2Me
CH2CFThree CH2CH (Et) S (O)2Et
CH2CFThree CH2CH (Et) S (O)2CFThree
CH2CFThree CH2CH (Et) S (O)2CH2CFThree
CH2CFThree CH (Me) CH (Me) SMe
CH2CFThree CH (Me) CH (Me) SEt
CH2CFThree CH (Me) CH (Me) SCFThree
CH2CFThree CH (Me) CH (Me) SCH2CFThree
CH2CFThree CH (Me) CH (Me) S (O) Me
CH2CFThree CH (Me) CH (Me) S (O) Et
CH2CFThree CH (Me) CH (Me) S (O) CFThree
CH2CFThree CH (Me) CH (Me) S (O) CH2CFThree
CH2CFThree CH (Me) CH (Me) S (O)2Me
CH2CFThree CH (Me) CH (Me) S (O)2Et
CH2CFThree CH (Me) CH (Me) S (O)2CFThree
CH2CFThree CH (Me) CH (Me) S (O)2CH2CFThree
CH2CN CH2SMe
CH2CN CH2SEt
CH2CN CH2SCFThree
CH2CN CH2SCH2CFThree
CH2CN CH2S (O) Me
CH2CN CH2S (O) Et
CH2CN CH2S (O) CFThree
CH2CN CH2S (O) CH2CFThree
CH2CN CH2S (O)2Me
CH2CN CH2S (O)2Et
CH2CN CH2S (O)2CFThree
CH2CN CH2S (O)2CH2CFThree
CH2CN CH (Me) SMe
CH2CN CH (Me) SEt
CH2CN CH (Me) SCFThree
CH2CN CH (Me) SCH2CFThree
CH2CN CH (Me) S (O) Me
CH2CN CH (Me) S (O) Et
CH2CN CH (Me) S (O) CFThree
CH2CN CH (Me) S (O) CH2CFThree
CH2CN CH (Me) S (O)2Me
CH2CN CH (Me) S (O)2Et
CH2CN CH (Me) S (O)2CFThree
CH2CN CH (Me) S (O)2CH2CFThree
CH2CN CH (Et) SMe
CH2CN CH (Et) SEt
CH2CN CH (Et) SCFThree
CH2CN CH (Et) SCH2CFThree
CH2CN CH (Et) S (O) Me
CH2CN CH (Et) S (O) Et
CH2CN CH (Et) S (O) CFThree
CH2CN CH (Et) S (O) CH2CFThree
CH2CN CH (Et) S (O)2Me
CH2CN CH (Et) S (O)2Et
CH2CN CH (Et) S (O)2CFThree
CH2CN CH (Et) S (O)2CH2CFThree
CH2CN CH (n-Pr) SMe
CH2CN CH (n-Pr) SEt
CH2CN CH (n-Pr) SCFThree
CH2CN CH (n-Pr) SCH2CFThree
CH2CN CH (n-Pr) S (O) Me
CH2CN CH (n-Pr) S (O) Et
CH2CN CH (n-Pr) S (O) CFThree
CH2CN CH (n-Pr) S (O) CH2CFThree
CH2CN CH (n-Pr) S (O)2Me
CH2CN CH (n-Pr) S (O)2Et
CH2CN CH (n-Pr) S (O)2CFThree
CH2CN CH (n-Pr) S (O)2CH2CFThree
CH2CN CH (i-Pr) SMe
CH2CN CH (i-Pr) SEt
CH2CN CH (i-Pr) SCFThree
CH2CN CH (i-Pr) SCH2CFThree
CH2CN CH (i-Pr) S (O) Me
CH2CN CH (i-Pr) S (O) Et
CH2CN CH (i-Pr) S (O) CFThree
CH2CN CH (i-Pr) S (O) CH2CFThree
CH2CN CH (i-Pr) S (O)2Me
CH2CN CH (i-Pr) S (O)2Et
CH2CN CH (i-Pr) S (O)2CFThree
CH2CN CH (i-Pr) S (O)2CH2CFThree
CH2CN CH (n-Bu) SMe
CH2CN CH (n-Bu) SEt
CH2CN CH (n-Bu) SCFThree
CH2CN CH (n-Bu) SCH2CFThree
CH2CN CH (n-Bu) S (O) Me
CH2CN CH (n-Bu) S (O) Et
CH2CN CH (n-Bu) S (O) CFThree
CH2CN CH (n-Bu) S (O) CH2CFThree
CH2CN CH (n-Bu) S (O)2Me
CH2CN CH (n-Bu) S (O)2Et
CH2CN CH (n-Bu) S (O)2CFThree
CH2CN CH (n-Bu) S (O)2CH2CFThree
CH2CN CH (i-Bu) SMe
CH2CN CH (i-Bu) SEt
CH2CN CH (i-Bu) SCFThree
CH2CN CH (i-Bu) SCH2CFThree
CH2CN CH (i-Bu) S (O) Me
CH2CN CH (i-Bu) S (O) Et
CH2CN CH (i-Bu) S (O) CFThree
CH2CN CH (i-Bu) S (O) CH2CFThree
CH2CN CH (i-Bu) S (O)2Me
CH2CN CH (i-Bu) S (O)2Et
CH2CN CH (i-Bu) S (O)2CFThree
CH2CN CH (i-Bu) S (O)2CH2CFThree
CH2CN CH (s-Bu) SMe
CH2CN CH (s-Bu) SEt
CH2CN CH (s-Bu) SCFThree
CH2CN CH (s-Bu) SCH2CFThree
CH2CN CH (s-Bu) S (O) Me
CH2CN CH (s-Bu) S (O) Et
CH2CN CH (s-Bu) S (O) CFThree
CH2CN CH (s-Bu) S (O) CH2CFThree
CH2CN CH (s-Bu) S (O)2Me
CH2CN CH (s-Bu) S (O)2Et
CH2CN CH (s-Bu) S (O)2CFThree
CH2CN CH (s-Bu) S (O)2CH2CFThree
CH2CN CH (t-Bu) SMe
CH2CN CH (t-Bu) SEt
CH2CN CH (t-Bu) SCFThree
CH2CN CH (t-Bu) SCH2CFThree
CH2CN CH (t-Bu) S (O) Me
CH2CN CH (t-Bu) S (O) Et
CH2CN CH (t-Bu) S (O) CFThree
CH2CN CH (t-Bu) S (O) CH2CFThree
CH2CN CH (t-Bu) S (O)2Me
CH2CN CH (t-Bu) S (O)2Et
CH2CN CH (t-Bu) S (O)2CFThree
CH2CN CH (t-Bu) S (O)2CH2CFThree
CH2CN CH (CFThreeSMe
CH2CN CH (CFThree) SEt
CH2CN CH (CFThree) SCFThree
CH2CN CH (CFThree) SCH2CFThree
CH2CN CH (CFThree) S (O) Me
CH2CN CH (CFThree) S (O) Et
CH2CN CH (CFThree) S (O) CFThree
CH2CN CH (CFThree) S (O) CH2CFThree
CH2CN CH (CFThree) S (O)2Me
CH2CN CH (CFThree) S (O)2Et
CH2CN CH (CFThree) S (O)2CFThree
CH2CN CH (CFThree) S (O)2CH2CFThree
CH2CN CH2CH2SMe
CH2CN CH2CH2SEt
CH2CN CH2CH2SCFThree
CH2CN CH2CH2SCH2CFThree
CH2CN CH2CH2S (O) Me
CH2CN CH2CH2S (O) Et
CH2CN CH2CH2S (O) CFThree
CH2CN CH2CH2S (O) CH2CFThree
CH2CN CH2CH2S (O)2Me
CH2CN CH2CH2S (O)2Et
CH2CN CH2CH2S (O)2CFThree
CH2CN CH2CH2S (O)2CH2CFThree
CH2CN CH (Me) CH2SMe
CH2CN CH (Me) CH2SEt
CH2CN CH (Me) CH2SCFThree
CH2CN CH (Me) CH2SCH2CFThree
CH2CN CH (Me) CH2S (O) Me
CH2CN CH (Me) CH2S (O) Et
CH2CN CH (Me) CH2S (O) CFThree
CH2CN CH (Me) CH2S (O) CH2CFThree
CH2CN CH (Me) CH2S (O)2Me
CH2CN CH (Me) CH2S (O)2Et
CH2CN CH (Me) CH2S (O)2CFThree
CH2CN CH (Me) CH2S (O)2CH2CFThree
CH2CN CH (Et) CH2SMe
CH2CN CH (Et) CH2SEt
CH2CN CH (Et) CH2SCFThree
CH2CN CH (Et) CH2SCH2CFThree
CH2CN CH (Et) CH2S (O) Me
CH2CN CH (Et) CH2S (O) Et
CH2CN CH (Et) CH2S (O) CFThree
CH2CN CH (Et) CH2S (O) CH2CFThree
CH2CN CH (Et) CH2S (O)2Me
CH2CN CH (Et) CH2S (O)2Et
CH2CN CH (Et) CH2S (O)2CFThree
CH2CN CH (Et) CH2S (O)2CH2CFThree
CH2CN C (Me)2CH2SMe
CH2CN C (Me)2CH2SEt
CH2CN C (Me)2CH2SCFThree
CH2CN C (Me)2CH2SCH2CFThree
CH2CN C (Me)2CH2S (O) Me
CH2CN C (Me)2CH2S (O) Et
CH2CN C (Me)2CH2S (O) CFThree
CH2CN C (Me)2CH2S (O) CH2CFThree
CH2CN C (Me)2CH2S (O)2Me
CH2CN C (Me)2CH2S (O)2Et
CH2CN C (Me)2CH2S (O)2CFThree
CH2CN C (Me)2CH2S (O)2CH2CFThree
CH2CN CH2CH (Me) SMe
CH2CN CH2CH (Me) SEt
CH2CN CH2CH (Me) SCFThree
CH2CN CH2CH (Me) SCH2CFThree
CH2CN CH2CH (Me) S (O) Me
CH2CN CH2CH (Me) S (O) Et
CH2CN CH2CH (Me) S (O) CFThree
CH2CN CH2CH (Me) S (O) CH2CFThree
CH2CN CH2CH (Me) S (O)2Me
CH2CN CH2CH (Me) S (O)2Et
CH2CN CH2CH (Me) S (O)2CFThree
CH2CN CH2CH (Me) S (O)2CH2CFThree
CH2CN CH2CH (Et) SMe
CH2CN CH2CH (Et) SEt
CH2CN CH2CH (Et) SCFThree
CH2CN CH2CH (Et) SCH2CFThree
CH2CN CH2CH (Et) S (O) Me
CH2CN CH2CH (Et) S (O) Et
CH2CN CH2CH (Et) S (O) CFThree
CH2CN CH2CH (Et) S (O) CH2CFThree
CH2CN CH2CH (Et) S (O)2Me
CH2CN CH2CH (Et) S (O)2Et
CH2CN CH2CH (Et) S (O)2CFThree
CH2CN CH2CH (Et) S (O)2CH2CFThree
CH2CN CH (Me) CH (Me) SMe
CH2CN CH (Me) CH (Me) SEt
CH2CN CH (Me) CH (Me) SCFThree
CH2CN CH (Me) CH (Me) SCH2CFThree
CH2CN CH (Me) CH (Me) S (O) Me
CH2CN CH (Me) CH (Me) S (O) Et
CH2CN CH (Me) CH (Me) S (O) CFThree
CH2CN CH (Me) CH (Me) S (O) CH2CFThree
CH2CN CH (Me) CH (Me) S (O)2Me
CH2CN CH (Me) CH (Me) S (O)2Et
CH2CN CH (Me) CH (Me) S (O)2CFThree
CH2CN CH (Me) CH (Me) S (O)2CH2CFThree
CH2CH = CH2 CH2SMe
CH2CH = CH2 CH2SEt
CH2CH = CH2 CH2SCFThree
CH2CH = CH2 CH2SCH2CFThree
CH2CH = CH2 CH2S (O) Me
CH2CH = CH2 CH2S (O) Et
CH2CH = CH2 CH2S (O) CFThree
CH2CH = CH2 CH2S (O) CH2CFThree
CH2CH = CH2 CH2S (O)2Me
CH2CH = CH2 CH2S (O)2Et
CH2CH = CH2 CH2S (O)2CFThree
CH2CH = CH2 CH2S (O)2CH2CFThree
CH2CH = CH2 CH (Me) SMe
CH2CH = CH2 CH (Me) SEt
CH2CH = CH2 CH (Me) SCFThree
CH2CH = CH2 CH (Me) SCH2CFThree
CH2CH = CH2 CH (Me) S (O) Me
CH2CH = CH2 CH (Me) S (O) Et
CH2CH = CH2 CH (Me) S (O) CFThree
CH2CH = CH2 CH (Me) S (O) CH2CFThree
CH2CH = CH2 CH (Me) S (O)2Me
CH2CH = CH2 CH (Me) S (O)2Et
CH2CH = CH2 CH (Me) S (O)2CFThree
CH2CH = CH2 CH (Me) S (O)2CH2CFThree
CH2CH = CH2 CH (Et) SMe
CH2CH = CH2 CH (Et) SEt
CH2CH = CH2 CH (Et) SCFThree
CH2CH = CH2 CH (Et) SCH2CFThree
CH2CH = CH2 CH (Et) S (O) Me
CH2CH = CH2 CH (Et) S (O) Et
CH2CH = CH2 CH (Et) S (O) CFThree
CH2CH = CH2 CH (Et) S (O) CH2CFThree
CH2CH = CH2 CH (Et) S (O)2Me
CH2CH = CH2 CH (Et) S (O)2Et
CH2CH = CH2 CH (Et) S (O)2CFThree
CH2CH = CH2 CH (Et) S (O)2CH2CFThree
CH2CH = CH2 CH (n-Pr) SMe
CH2CH = CH2 CH (n-Pr) SEt
CH2CH = CH2 CH (n-Pr) SCFThree
CH2CH = CH2 CH (n-Pr) SCH2CFThree
CH2CH = CH2 CH (n-Pr) S (O) Me
CH2CH = CH2 CH (n-Pr) S (O) Et
CH2CH = CH2 CH (n-Pr) S (O) CFThree
CH2CH = CH2 CH (n-Pr) S (O) CH2CFThree
CH2CH = CH2 CH (n-Pr) S (O)2Me
CH2CH = CH2 CH (n-Pr) S (O)2Et
CH2CH = CH2 CH (n-Pr) S (O)2CFThree
CH2CH = CH2 CH (n-Pr) S (O)2CH2CFThree
CH2CH = CH2 CH (i-Pr) SMe
CH2CH = CH2 CH (i-Pr) SEt
CH2CH = CH2 CH (i-Pr) SCFThree
CH2CH = CH2 CH (i-Pr) SCH2CFThree
CH2CH = CH2 CH (i-Pr) S (O) Me
CH2CH = CH2 CH (i-Pr) S (O) Et
CH2CH = CH2 CH (i-Pr) S (O) CFThree
CH2CH = CH2 CH (i-Pr) S (O) CH2CFThree
CH2CH = CH2 CH (i-Pr) S (O)2Me
CH2CH = CH2 CH (i-Pr) S (O)2Et
CH2CH = CH2 CH (i-Pr) S (O)2CFThree
CH2CH = CH2 CH (i-Pr) S (O)2CH2CFThree
CH2CH = CH2 CH (n-Bu) SMe
CH2CH = CH2 CH (n-Bu) SEt
CH2CH = CH2 CH (n-Bu) SCFThree
CH2CH = CH2 CH (n-Bu) SCH2CFThree
CH2CH = CH2 CH (n-Bu) S (O) Me
CH2CH = CH2 CH (n-Bu) S (O) Et
CH2CH = CH2 CH (n-Bu) S (O) CFThree
CH2CH = CH2 CH (n-Bu) S (O) CH2CFThree
CH2CH = CH2 CH (n-Bu) S (O)2Me
CH2CH = CH2 CH (n-Bu) S (O)2Et
CH2CH = CH2 CH (n-Bu) S (O)2CFThree
CH2CH = CH2 CH (n-Bu) S (O)2CH2CFThree
CH2CH = CH2 CH (i-Bu) SMe
CH2CH = CH2 CH (i-Bu) SEt
CH2CH = CH2 CH (i-Bu) SCFThree
CH2CH = CH2 CH (i-Bu) SCH2CFThree
CH2CH = CH2 CH (i-Bu) S (O) Me
CH2CH = CH2 CH (i-Bu) S (O) Et
CH2CH = CH2 CH (i-Bu) S (O) CFThree
CH2CH = CH2 CH (i-Bu) S (O) CH2CFThree
CH2CH = CH2 CH (i-Bu) S (O)2Me
CH2CH = CH2 CH (i-Bu) S (O)2Et
CH2CH = CH2 CH (i-Bu) S (O)2CFThree
CH2CH = CH2 CH (i-Bu) S (O)2CH2CFThree
CH2CH = CH2 CH (s-Bu) SMe
CH2CH = CH2 CH (s-Bu) SEt
CH2CH = CH2 CH (s-Bu) SCFThree
CH2CH = CH2 CH (s-Bu) SCH2CFThree
CH2CH = CH2 CH (s-Bu) S (O) Me
CH2CH = CH2 CH (s-Bu) S (O) Et
CH2CH = CH2 CH (s-Bu) S (O) CFThree
CH2CH = CH2 CH (s-Bu) S (O) CH2CFThree
CH2CH = CH2 CH (s-Bu) S (O)2Me
CH2CH = CH2 CH (s-Bu) S (O)2Et
CH2CH = CH2 CH (s-Bu) S (O)2CFThree
CH2CH = CH2 CH (s-Bu) S (O)2CH2CFThree
CH2CH = CH2 CH (t-Bu) SMe
CH2CH = CH2 CH (t-Bu) SEt
CH2CH = CH2 CH (t-Bu) SCFThree
CH2CH = CH2 CH (t-Bu) SCH2CFThree
CH2CH = CH2 CH (t-Bu) S (O) Me
CH2CH = CH2 CH (t-Bu) S (O) Et
CH2CH = CH2 CH (t-Bu) S (O) CFThree
CH2CH = CH2 CH (t-Bu) S (O) CH2CFThree
CH2CH = CH2 CH (t-Bu) S (O)2Me
CH2CH = CH2 CH (t-Bu) S (O)2Et
CH2CH = CH2 CH (t-Bu) S (O)2CFThree
CH2CH = CH2 CH (t-Bu) S (O)2CH2CFThree
CH2CH = CH2 CH (CFThreeSMe
CH2CH = CH2 CH (CFThree) SEt
CH2CH = CH2 CH (CFThree) SCFThree
CH2CH = CH2 CH (CFThree) SCH2CFThree
CH2CH = CH2 CH (CFThree) S (O) Me
CH2CH = CH2 CH (CFThree) S (O) Et
CH2CH = CH2 CH (CFThree) S (O) CFThree
CH2CH = CH2 CH (CFThree) S (O) CH2CFThree
CH2CH = CH2 CH (CFThree) S (O)2Me
CH2CH = CH2 CH (CFThree) S (O)2Et
CH2CH = CH2 CH (CFThree) S (O)2CFThree
CH2CH = CH2 CH (CFThree) S (O)2CH2CFThree
CH2CH = CH2 CH2CH2SMe
CH2CH = CH2 CH2CH2SEt
CH2CH = CH2 CH2CH2SCFThree
CH2CH = CH2 CH2CH2SCH2CFThree
CH2CH = CH2 CH2CH2S (O) Me
CH2CH = CH2 CH2CH2S (O) Et
CH2CH = CH2 CH2CH2S (O) CFThree
CH2CH = CH2 CH2CH2S (O) CH2CFThree
CH2CH = CH2 CH2CH2S (O)2Me
CH2CH = CH2 CH2CH2S (O)2Et
CH2CH = CH2 CH2CH2S (O)2CFThree
CH2CH = CH2 CH2CH2S (O)2CH2CFThree
CH2CH = CH2 CH (Me) CH2SMe
CH2CH = CH2 CH (Me) CH2SEt
CH2CH = CH2 CH (Me) CH2SCFThree
CH2CH = CH2 CH (Me) CH2SCH2CFThree
CH2CH = CH2 CH (Me) CH2S (O) Me
CH2CH = CH2 CH (Me) CH2S (O) Et
CH2CH = CH2 CH (Me) CH2S (O) CFThree
CH2CH = CH2 CH (Me) CH2S (O) CH2CFThree
CH2CH = CH2 CH (Me) CH2S (O)2Me
CH2CH = CH2 CH (Me) CH2S (O)2Et
CH2CH = CH2 CH (Me) CH2S (O)2CFThree
CH2CH = CH2 CH (Me) CH2S (O)2CH2CFThree
CH2CH = CH2 CH (Et) CH2SMe
CH2CH = CH2 CH (Et) CH2SEt
CH2CH = CH2 CH (Et) CH2SCFThree
CH2CH = CH2 CH (Et) CH2SCH2CFThree
CH2CH = CH2 CH (Et) CH2S (O) Me
CH2CH = CH2 CH (Et) CH2S (O) Et
CH2CH = CH2 CH (Et) CH2S (O) CFThree
CH2CH = CH2 CH (Et) CH2S (O) CH2CFThree
CH2CH = CH2 CH (Et) CH2S (O)2Me
CH2CH = CH2 CH (Et) CH2S (O)2Et
CH2CH = CH2 CH (Et) CH2S (O)2CFThree
CH2CH = CH2 CH (Et) CH2S (O)2CH2CFThree
CH2CH = CH2 C (Me)2CH2SMe
CH2CH = CH2 C (Me)2CH2SEt
CH2CH = CH2 C (Me)2CH2SCFThree
CH2CH = CH2 C (Me)2CH2SCH2CFThree
CH2CH = CH2 C (Me)2CH2S (O) Me
CH2CH = CH2 C (Me)2CH2S (O) Et
CH2CH = CH2 C (Me)2CH2S (O) CFThree
CH2CH = CH2 C (Me)2CH2S (O) CH2CFThree
CH2CH = CH2 C (Me)2CH2S (O)2Me
CH2CH = CH2 C (Me)2CH2S (O)2Et
CH2CH = CH2 C (Me)2CH2S (O)2CFThree
CH2CH = CH2 C (Me)2CH2S (O)2CH2CFThree
CH2CH = CH2 CH2CH (Me) SMe
CH2CH = CH2 CH2CH (Me) SEt
CH2CH = CH2 CH2CH (Me) SCFThree
CH2CH = CH2 CH2CH (Me) SCH2CFThree
CH2CH = CH2 CH2CH (Me) S (O) Me
CH2CH = CH2 CH2CH (Me) S (O) Et
CH2CH = CH2 CH2CH (Me) S (O) CFThree
CH2CH = CH2 CH2CH (Me) S (O) CH2CFThree
CH2CH = CH2 CH2CH (Me) S (O)2Me
CH2CH = CH2 CH2CH (Me) S (O)2Et
CH2CH = CH2 CH2CH (Me) S (O)2CFThree
CH2CH = CH2 CH2CH (Me) S (O)2CH2CFThree
CH2CH = CH2 CH2CH (Et) SMe
CH2CH = CH2 CH2CH (Et) SEt
CH2CH = CH2 CH2CH (Et) SCFThree
CH2CH = CH2 CH2CH (Et) SCH2CFThree
CH2CH = CH2 CH2CH (Et) S (O) Me
CH2CH = CH2 CH2CH (Et) S (O) Et
CH2CH = CH2 CH2CH (Et) S (O) CFThree
CH2CH = CH2 CH2CH (Et) S (O) CH2CFThree
CH2CH = CH2 CH2CH (Et) S (O)2Me
CH2CH = CH2 CH2CH (Et) S (O)2Et
CH2CH = CH2 CH2CH (Et) S (O)2CFThree
CH2CH = CH2 CH2CH (Et) S (O)2CH2CFThree
CH2CH = CH2 CH (Me) CH (Me) SMe
CH2CH = CH2 CH (Me) CH (Me) SEt
CH2CH = CH2 CH (Me) CH (Me) SCFThree
CH2CH = CH2 CH (Me) CH (Me) SCH2CFThree
CH2CH = CH2 CH (Me) CH (Me) S (O) Me
CH2CH = CH2 CH (Me) CH (Me) S (O) Et
CH2CH = CH2 CH (Me) CH (Me) S (O) CFThree
CH2CH = CH2 CH (Me) CH (Me) S (O) CH2CFThree
CH2CH = CH2 CH (Me) CH (Me) S (O)2Me
CH2CH = CH2 CH (Me) CH (Me) S (O)2Et
CH2CH = CH2 CH (Me) CH (Me) S (O)2CFThree
CH2CH = CH2 CH (Me) CH (Me) S (O)2CH2CFThree
CH2CH (OMe)2 CH2SMe
CH2CH (OMe)2 CH2SEt
CH2CH (OMe)2 CH2SCFThree
CH2CH (OMe)2 CH2SCH2CFThree
CH2CH (OMe)2 CH2S (O) Me
CH2CH (OMe)2 CH2S (O) Et
CH2CH (OMe)2 CH2S (O) CFThree
CH2CH (OMe)2 CH2S (O) CH2CFThree
CH2CH (OMe)2 CH2S (O)2Me
CH2CH (OMe)2 CH2S (O)2Et
CH2CH (OMe)2 CH2S (O)2CFThree
CH2CH (OMe)2 CH2S (O)2CH2CFThree
CH2CH (OMe)2 CH (Me) SMe
CH2CH (OMe)2 CH (Me) SEt
CH2CH (OMe)2 CH (Me) SCFThree
CH2CH (OMe)2 CH (Me) SCH2CFThree
CH2CH (OMe)2 CH (Me) S (O) Me
CH2CH (OMe)2 CH (Me) S (O) Et
CH2CH (OMe)2 CH (Me) S (O) CFThree
CH2CH (OMe)2 CH (Me) S (O) CH2CFThree
CH2CH (OMe)2 CH (Me) S (O)2Me
CH2CH (OMe)2 CH (Me) S (O)2Et
CH2CH (OMe)2 CH (Me) S (O)2CFThree
CH2CH (OMe)2 CH (Me) S (O)2CH2CFThree
CH2CH (OMe)2 CH (Et) SMe
CH2CH (OMe)2 CH (Et) SEt
CH2CH (OMe)2 CH (Et) SCFThree
CH2CH (OMe)2 CH (Et) SCH2CFThree
CH2CH (OMe)2 CH (Et) S (O) Me
CH2CH (OMe)2 CH (Et) S (O) Et
CH2CH (OMe)2 CH (Et) S (O) CFThree
CH2CH (OMe)2 CH (Et) S (O) CH2CFThree
CH2CH (OMe)2 CH (Et) S (O)2Me
CH2CH (OMe)2 CH (Et) S (O)2Et
CH2CH (OMe)2 CH (Et) S (O)2CFThree
CH2CH (OMe)2 CH (Et) S (O)2CH2CFThree
CH2CH (OMe)2 CH (n-Pr) SMe
CH2CH (OMe)2 CH (n-Pr) SEt
CH2CH (OMe)2 CH (n-Pr) SCFThree
CH2CH (OMe)2 CH (n-Pr) SCH2CFThree
CH2CH (OMe)2 CH (n-Pr) S (O) Me
CH2CH (OMe)2 CH (n-Pr) S (O) Et
CH2CH (OMe)2 CH (n-Pr) S (O) CFThree
CH2CH (OMe)2 CH (n-Pr) S (O) CH2CFThree
CH2CH (OMe)2 CH (n-Pr) S (O)2Me
CH2CH (OMe)2 CH (n-Pr) S (O)2Et
CH2CH (OMe)2 CH (n-Pr) S (O)2CFThree
CH2CH (OMe)2 CH (n-Pr) S (O)2CH2CFThree
CH2CH (OMe)2 CH (i-Pr) SMe
CH2CH (OMe)2 CH (i-Pr) SEt
CH2CH (OMe)2 CH (i-Pr) SCFThree
CH2CH (OMe)2 CH (i-Pr) SCH2CFThree
CH2CH (OMe)2 CH (i-Pr) S (O) Me
CH2CH (OMe)2 CH (i-Pr) S (O) Et
CH2CH (OMe)2 CH (i-Pr) S (O) CFThree
CH2CH (OMe)2 CH (i-Pr) S (O) CH2CFThree
CH2CH (OMe)2 CH (i-Pr) S (O)2Me
CH2CH (OMe)2 CH (i-Pr) S (O)2Et
CH2CH (OMe)2 CH (i-Pr) S (O)2CFThree
CH2CH (OMe)2 CH (i-Pr) S (O)2CH2CFThree
CH2CH (OMe)2 CH (n-Bu) SMe
CH2CH (OMe)2 CH (n-Bu) SEt
CH2CH (OMe)2 CH (n-Bu) SCFThree
CH2CH (OMe)2 CH (n-Bu) SCH2CFThree
CH2CH (OMe)2 CH (n-Bu) S (O) Me
CH2CH (OMe)2 CH (n-Bu) S (O) Et
CH2CH (OMe)2 CH (n-Bu) S (O) CFThree
CH2CH (OMe)2 CH (n-Bu) S (O) CH2CFThree
CH2CH (OMe)2 CH (n-Bu) S (O)2Me
CH2CH (OMe)2 CH (n-Bu) S (O)2Et
CH2CH (OMe)2 CH (n-Bu) S (O)2CFThree
CH2CH (OMe)2 CH (n-Bu) S (O)2CH2CFThree
CH2CH (OMe)2 CH (i-Bu) SMe
CH2CH (OMe)2 CH (i-Bu) SEt
CH2CH (OMe)2 CH (i-Bu) SCFThree
CH2CH (OMe)2 CH (i-Bu) SCH2CFThree
CH2CH (OMe)2 CH (i-Bu) S (O) Me
CH2CH (OMe)2 CH (i-Bu) S (O) Et
CH2CH (OMe)2 CH (i-Bu) S (O) CFThree
CH2CH (OMe)2 CH (i-Bu) S (O) CH2CFThree
CH2CH (OMe)2 CH (i-Bu) S (O)2Me
CH2CH (OMe)2 CH (i-Bu) S (O)2Et
CH2CH (OMe)2 CH (i-Bu) S (O)2CFThree
CH2CH (OMe)2 CH (i-Bu) S (O)2CH2CFThree
CH2CH (OMe)2 CH (s-Bu) SMe
CH2CH (OMe)2 CH (s-Bu) SEt
CH2CH (OMe)2 CH (s-Bu) SCFThree
CH2CH (OMe)2 CH (s-Bu) SCH2CFThree
CH2CH (OMe)2 CH (s-Bu) S (O) Me
CH2CH (OMe)2 CH (s-Bu) S (O) Et
CH2CH (OMe)2 CH (s-Bu) S (O) CFThree
CH2CH (OMe)2 CH (s-Bu) S (O) CH2CFThree
CH2CH (OMe)2 CH (s-Bu) S (O)2Me
CH2CH (OMe)2 CH (s-Bu) S (O)2Et
CH2CH (OMe)2 CH (s-Bu) S (O)2CFThree
CH2CH (OMe)2 CH (s-Bu) S (O)2CH2CFThree
CH2CH (OMe)2 CH (t-Bu) SMe
CH2CH (OMe)2 CH (t-Bu) SEt
CH2CH (OMe)2 CH (t-Bu) SCFThree
CH2CH (OMe)2 CH (t-Bu) SCH2CFThree
CH2CH (OMe)2 CH (t-Bu) S (O) Me
CH2CH (OMe)2 CH (t-Bu) S (O) Et
CH2CH (OMe)2 CH (t-Bu) S (O) CFThree
CH2CH (OMe)2 CH (t-Bu) S (O) CH2CFThree
CH2CH (OMe)2 CH (t-Bu) S (O)2Me
CH2CH (OMe)2 CH (t-Bu) S (O)2Et
CH2CH (OMe)2 CH (t-Bu) S (O)2CFThree
CH2CH (OMe)2 CH (t-Bu) S (O)2CH2CFThree
CH2CH (OMe)2 CH (CFThreeSMe
CH2CH (OMe)2 CH (CFThree) SEt
CH2CH (OMe)2 CH (CFThree) SCFThree
CH2CH (OMe)2 CH (CFThree) SCH2CFThree
CH2CH (OMe)2 CH (CFThree) S (O) Me
CH2CH (OMe)2 CH (CFThree) S (O) Et
CH2CH (OMe)2 CH (CFThree) S (O) CFThree
CH2CH (OMe)2 CH (CFThree) S (O) CH2CFThree
CH2CH (OMe)2 CH (CFThree) S (O)2Me
CH2CH (OMe)2 CH (CFThree) S (O)2Et
CH2CH (OMe)2 CH (CFThree) S (O)2CFThree
CH2CH (OMe)2 CH (CFThree) S (O)2CH2CFThree
CH2CH (OMe)2 CH2CH2SMe
CH2CH (OMe)2 CH2CH2SEt
CH2CH (OMe)2 CH2CH2SCFThree
CH2CH (OMe)2 CH2CH2SCH2CFThree
CH2CH (OMe)2 CH2CH2S (O) Me
CH2CH (OMe)2 CH2CH2S (O) Et
CH2CH (OMe)2 CH2CH2S (O) CFThree
CH2CH (OMe)2 CH2CH2S (O) CH2CFThree
CH2CH (OMe)2 CH2CH2S (O)2Me
CH2CH (OMe)2 CH2CH2S (O)2Et
CH2CH (OMe)2 CH2CH2S (O)2CFThree
CH2CH (OMe)2 CH2CH2S (O)2CH2CFThree
CH2CH (OMe)2 CH (Me) CH2SMe
CH2CH (OMe)2 CH (Me) CH2SEt
CH2CH (OMe)2 CH (Me) CH2SCFThree
CH2CH (OMe)2 CH (Me) CH2SCH2CFThree
CH2CH (OMe)2 CH (Me) CH2S (O) Me
CH2CH (OMe)2 CH (Me) CH2S (O) Et
CH2CH (OMe)2 CH (Me) CH2S (O) CFThree
CH2CH (OMe)2 CH (Me) CH2S (O) CH2CFThree
CH2CH (OMe)2 CH (Me) CH2S (O)2Me
CH2CH (OMe)2 CH (Me) CH2S (O)2Et
CH2CH (OMe)2 CH (Me) CH2S (O)2CFThree
CH2CH (OMe)2 CH (Me) CH2S (O)2CH2CFThree
CH2CH (OMe)2 CH (Et) CH2SMe
CH2CH (OMe)2 CH (Et) CH2SEt
CH2CH (OMe)2 CH (Et) CH2SCFThree
CH2CH (OMe)2 CH (Et) CH2SCH2CFThree
CH2CH (OMe)2 CH (Et) CH2S (O) Me
CH2CH (OMe)2 CH (Et) CH2S (O) Et
CH2CH (OMe)2 CH (Et) CH2S (O) CFThree
CH2CH (OMe)2 CH (Et) CH2S (O) CH2CFThree
CH2CH (OMe)2 CH (Et) CH2S (O)2Me
CH2CH (OMe)2 CH (Et) CH2S (O)2Et
CH2CH (OMe)2 CH (Et) CH2S (O)2CFThree
CH2CH (OMe)2 CH (Et) CH2S (O)2CH2CFThree
CH2CH (OMe)2 C (Me)2CH2SMe
CH2CH (OMe)2 C (Me)2CH2SEt
CH2CH (OMe)2 C (Me)2CH2SCFThree
CH2CH (OMe)2 C (Me)2CH2SCH2CFThree
CH2CH (OMe)2 C (Me)2CH2S (O) Me
CH2CH (OMe)2 C (Me)2CH2S (O) Et
CH2CH (OMe)2 C (Me)2CH2S (O) CFThree
CH2CH (OMe)2 C (Me)2CH2S (O) CH2CFThree
CH2CH (OMe)2 C (Me)2CH2S (O)2Me
CH2CH (OMe)2 C (Me)2CH2S (O)2Et
CH2CH (OMe)2 C (Me)2CH2S (O)2CFThree
CH2CH (OMe)2 C (Me)2CH2S (O)2CH2CFThree
CH2CH (OMe)2 CH2CH (Me) SMe
CH2CH (OMe)2 CH2CH (Me) SEt
CH2CH (OMe)2 CH2CH (Me) SCFThree
CH2CH (OMe)2 CH2CH (Me) SCH2CFThree
CH2CH (OMe)2 CH2CH (Me) S (O) Me
CH2CH (OMe)2 CH2CH (Me) S (O) Et
CH2CH (OMe)2 CH2CH (Me) S (O) CFThree
CH2CH (OMe)2 CH2CH (Me) S (O) CH2CFThree
CH2CH (OMe)2 CH2CH (Me) S (O)2Me
CH2CH (OMe)2 CH2CH (Me) S (O)2Et
CH2CH (OMe)2 CH2CH (Me) S (O)2CFThree
CH2CH (OMe)2 CH2CH (Me) S (O)2CH2CFThree
CH2CH (OMe)2 CH2CH (Et) SMe
CH2CH (OMe)2 CH2CH (Et) SEt
CH2CH (OMe)2 CH2CH (Et) SCFThree
CH2CH (OMe)2 CH2CH (Et) SCH2CFThree
CH2CH (OMe)2 CH2CH (Et) S (O) Me
CH2CH (OMe)2 CH2CH (Et) S (O) Et
CH2CH (OMe)2 CH2CH (Et) S (O) CFThree
CH2CH (OMe)2 CH2CH (Et) S (O) CH2CFThree
CH2CH (OMe)2 CH2CH (Et) S (O)2Me
CH2CH (OMe)2 CH2CH (Et) S (O)2Et
CH2CH (OMe)2 CH2CH (Et) S (O)2CFThree
CH2CH (OMe)2 CH2CH (Et) S (O)2CH2CFThree
CH2CH (OMe)2 CH (Me) CH (Me) SMe
CH2CH (OMe)2 CH (Me) CH (Me) SEt
CH2CH (OMe)2 CH (Me) CH (Me) SCFThree
CH2CH (OMe)2 CH (Me) CH (Me) SCH2CFThree
CH2CH (OMe)2 CH (Me) CH (Me) S (O) Me
CH2CH (OMe)2 CH (Me) CH (Me) S (O) Et
CH2CH (OMe)2 CH (Me) CH (Me) S (O) CFThree
CH2CH (OMe)2 CH (Me) CH (Me) S (O) CH2CFThree
CH2CH (OMe)2 CH (Me) CH (Me) S (O)2Me
CH2CH (OMe)2 CH (Me) CH (Me) S (O)2Et
CH2CH (OMe)2 CH (Me) CH (Me) S (O)2CFThree
CH2CH (OMe)2 CH (Me) CH (Me) S (O)2CH2CFThree
CH (Me) OEt CH2SMe
CH (Me) OEt CH2SEt
CH (Me) OEt CH2SCFThree
CH (Me) OEt CH2SCH2CFThree
CH (Me) OEt CH2S (O) Me
CH (Me) OEt CH2S (O) Et
CH (Me) OEt CH2S (O) CFThree
CH (Me) OEt CH2S (O) CH2CFThree
CH (Me) OEt CH2S (O)2Me
CH (Me) OEt CH2S (O)2Et
CH (Me) OEt CH2S (O)2CFThree
CH (Me) OEt CH2S (O)2CH2CFThree
CH (Me) OEt CH (Me) SMe
CH (Me) OEt CH (Me) SEt
CH (Me) OEt CH (Me) SCFThree
CH (Me) OEt CH (Me) SCH2CFThree
CH (Me) OEt CH (Me) S (O) Me
CH (Me) OEt CH (Me) S (O) Et
CH (Me) OEt CH (Me) S (O) CFThree
CH (Me) OEt CH (Me) S (O) CH2CFThree
CH (Me) OEt CH (Me) S (O)2Me
CH (Me) OEt CH (Me) S (O)2Et
CH (Me) OEt CH (Me) S (O)2CFThree
CH (Me) OEt CH (Me) S (O)2CH2CFThree
CH (Me) OEt CH (Et) SMe
CH (Me) OEt CH (Et) SEt
CH (Me) OEt CH (Et) SCFThree
CH (Me) OEt CH (Et) SCH2CFThree
CH (Me) OEt CH (Et) S (O) Me
CH (Me) OEt CH (Et) S (O) Et
CH (Me) OEt CH (Et) S (O) CFThree
CH (Me) OEt CH (Et) S (O) CH2CFThree
CH (Me) OEt CH (Et) S (O)2Me
CH (Me) OEt CH (Et) S (O)2Et
CH (Me) OEt CH (Et) S (O)2CFThree
CH (Me) OEt CH (Et) S (O)2CH2CFThree
CH (Me) OEt CH (n-Pr) SMe
CH (Me) OEt CH (n-Pr) SEt
CH (Me) OEt CH (n-Pr) SCFThree
CH (Me) OEt CH (n-Pr) SCH2CFThree
CH (Me) OEt CH (n-Pr) S (O) Me
CH (Me) OEt CH (n-Pr) S (O) Et
CH (Me) OEt CH (n-Pr) S (O) CFThree
CH (Me) OEt CH (n-Pr) S (O) CH2CFThree
CH (Me) OEt CH (n-Pr) S (O)2Me
CH (Me) OEt CH (n-Pr) S (O)2Et
CH (Me) OEt CH (n-Pr) S (O)2CFThree
CH (Me) OEt CH (n-Pr) S (O)2CH2CFThree
CH (Me) OEt CH (i-Pr) SMe
CH (Me) OEt CH (i-Pr) SEt
CH (Me) OEt CH (i-Pr) SCFThree
CH (Me) OEt CH (i-Pr) SCH2CFThree
CH (Me) OEt CH (i-Pr) S (O) Me
CH (Me) OEt CH (i-Pr) S (O) Et
CH (Me) OEt CH (i-Pr) S (O) CFThree
CH (Me) OEt CH (i-Pr) S (O) CH2CFThree
CH (Me) OEt CH (i-Pr) S (O)2Me
CH (Me) OEt CH (i-Pr) S (O)2Et
CH (Me) OEt CH (i-Pr) S (O)2CFThree
CH (Me) OEt CH (i-Pr) S (O)2CH2CFThree
CH (Me) OEt CH (n-Bu) SMe
CH (Me) OEt CH (n-Bu) SEt
CH (Me) OEt CH (n-Bu) SCFThree
CH (Me) OEt CH (n-Bu) SCH2CFThree
CH (Me) OEt CH (n-Bu) S (O) Me
CH (Me) OEt CH (n-Bu) S (O) Et
CH (Me) OEt CH (n-Bu) S (O) CFThree
CH (Me) OEt CH (n-Bu) S (O) CH2CFThree
CH (Me) OEt CH (n-Bu) S (O)2Me
CH (Me) OEt CH (n-Bu) S (O)2Et
CH (Me) OEt CH (n-Bu) S (O)2CFThree
CH (Me) OEt CH (n-Bu) S (O)2CH2CFThree
CH (Me) OEt CH (i-Bu) SMe
CH (Me) OEt CH (i-Bu) SEt
CH (Me) OEt CH (i-Bu) SCFThree
CH (Me) OEt CH (i-Bu) SCH2CFThree
CH (Me) OEt CH (i-Bu) S (O) Me
CH (Me) OEt CH (i-Bu) S (O) Et
CH (Me) OEt CH (i-Bu) S (O) CFThree
CH (Me) OEt CH (i-Bu) S (O) CH2CFThree
CH (Me) OEt CH (i-Bu) S (O)2Me
CH (Me) OEt CH (i-Bu) S (O)2Et
CH (Me) OEt CH (i-Bu) S (O)2CFThree
CH (Me) OEt CH (i-Bu) S (O)2CH2CFThree
CH (Me) OEt CH (s-Bu) SMe
CH (Me) OEt CH (s-Bu) SEt
CH (Me) OEt CH (s-Bu) SCFThree
CH (Me) OEt CH (s-Bu) SCH2CFThree
CH (Me) OEt CH (s-Bu) S (O) Me
CH (Me) OEt CH (s-Bu) S (O) Et
CH (Me) OEt CH (s-Bu) S (O) CFThree
CH (Me) OEt CH (s-Bu) S (O) CH2CFThree
CH (Me) OEt CH (s-Bu) S (O)2Me
CH (Me) OEt CH (s-Bu) S (O)2Et
CH (Me) OEt CH (s-Bu) S (O)2CFThree
CH (Me) OEt CH (s-Bu) S (O)2CH2CFThree
CH (Me) OEt CH (t-Bu) SMe
CH (Me) OEt CH (t-Bu) SEt
CH (Me) OEt CH (t-Bu) SCFThree
CH (Me) OEt CH (t-Bu) SCH2CFThree
CH (Me) OEt CH (t-Bu) S (O) Me
CH (Me) OEt CH (t-Bu) S (O) Et
CH (Me) OEt CH (t-Bu) S (O) CFThree
CH (Me) OEt CH (t-Bu) S (O) CH2CFThree
CH (Me) OEt CH (t-Bu) S (O)2Me
CH (Me) OEt CH (t-Bu) S (O)2Et
CH (Me) OEt CH (t-Bu) S (O)2CFThree
CH (Me) OEt CH (t-Bu) S (O)2CH2CFThree
CH (Me) OEt CH (CFThreeSMe
CH (Me) OEt CH (CFThree) SEt
CH (Me) OEt CH (CFThree) SCFThree
CH (Me) OEt CH (CFThree) SCH2CFThree
CH (Me) OEt CH (CFThree) S (O) Me
CH (Me) OEt CH (CFThree) S (O) Et
CH (Me) OEt CH (CFThree) S (O) CFThree
CH (Me) OEt CH (CFThree) S (O) CH2CFThree
CH (Me) OEt CH (CFThree) S (O)2Me
CH (Me) OEt CH (CFThree) S (O)2Et
CH (Me) OEt CH (CFThree) S (O)2CFThree
CH (Me) OEt CH (CFThree) S (O)2CH2CFThree
CH (Me) OEt CH2CH2SMe
CH (Me) OEt CH2CH2SEt
CH (Me) OEt CH2CH2SCFThree
CH (Me) OEt CH2CH2SCH2CFThree
CH (Me) OEt CH2CH2S (O) Me
CH (Me) OEt CH2CH2S (O) Et
CH (Me) OEt CH2CH2S (O) CFThree
CH (Me) OEt CH2CH2S (O) CH2CFThree
CH (Me) OEt CH2CH2S (O)2Me
CH (Me) OEt CH2CH2S (O)2Et
CH (Me) OEt CH2CH2S (O)2CFThree
CH (Me) OEt CH2CH2S (O)2CH2CFThree
CH (Me) OEt CH (Me) CH2SMe
CH (Me) OEt CH (Me) CH2SEt
CH (Me) OEt CH (Me) CH2SCFThree
CH (Me) OEt CH (Me) CH2SCH2CFThree
CH (Me) OEt CH (Me) CH2S (O) Me
CH (Me) OEt CH (Me) CH2S (O) Et
CH (Me) OEt CH (Me) CH2S (O) CFThree
CH (Me) OEt CH (Me) CH2S (O) CH2CFThree
CH (Me) OEt CH (Me) CH2S (O)2Me
CH (Me) OEt CH (Me) CH2S (O)2Et
CH (Me) OEt CH (Me) CH2S (O)2CFThree
CH (Me) OEt CH (Me) CH2S (O)2CH2CFThree
CH (Me) OEt CH (Et) CH2SMe
CH (Me) OEt CH (Et) CH2SEt
CH (Me) OEt CH (Et) CH2SCFThree
CH (Me) OEt CH (Et) CH2SCH2CFThree
CH (Me) OEt CH (Et) CH2S (O) Me
CH (Me) OEt CH (Et) CH2S (O) Et
CH (Me) OEt CH (Et) CH2S (O) CFThree
CH (Me) OEt CH (Et) CH2S (O) CH2CFThree
CH (Me) OEt CH (Et) CH2S (O)2Me
CH (Me) OEt CH (Et) CH2S (O)2Et
CH (Me) OEt CH (Et) CH2S (O)2CFThree
CH (Me) OEt CH (Et) CH2S (O)2CH2CFThree
CH (Me) OEt C (Me)2CH2SMe
CH (Me) OEt C (Me)2CH2SEt
CH (Me) OEt C (Me)2CH2SCFThree
CH (Me) OEt C (Me)2CH2SCH2CFThree
CH (Me) OEt C (Me)2CH2S (O) Me
CH (Me) OEt C (Me)2CH2S (O) Et
CH (Me) OEt C (Me)2CH2S (O) CFThree
CH (Me) OEt C (Me)2CH2S (O) CH2CFThree
CH (Me) OEt C (Me)2CH2S (O)2Me
CH (Me) OEt C (Me)2CH2S (O)2Et
CH (Me) OEt C (Me)2CH2S (O)2CFThree
CH (Me) OEt C (Me)2CH2S (O)2CH2CFThree
CH (Me) OEt CH2CH (Me) SMe
CH (Me) OEt CH2CH (Me) SEt
CH (Me) OEt CH2CH (Me) SCFThree
CH (Me) OEt CH2CH (Me) SCH2CFThree
CH (Me) OEt CH2CH (Me) S (O) Me
CH (Me) OEt CH2CH (Me) S (O) Et
CH (Me) OEt CH2CH (Me) S (O) CFThree
CH (Me) OEt CH2CH (Me) S (O) CH2CFThree
CH (Me) OEt CH2CH (Me) S (O)2Me
CH (Me) OEt CH2CH (Me) S (O)2Et
CH (Me) OEt CH2CH (Me) S (O)2CFThree
CH (Me) OEt CH2CH (Me) S (O)2CH2CFThree
CH (Me) OEt CH2CH (Et) SMe
CH (Me) OEt CH2CH (Et) SEt
CH (Me) OEt CH2CH (Et) SCFThree
CH (Me) OEt CH2CH (Et) SCH2CFThree
CH (Me) OEt CH2CH (Et) S (O) Me
CH (Me) OEt CH2CH (Et) S (O) Et
CH (Me) OEt CH2CH (Et) S (O) CFThree
CH (Me) OEt CH2CH (Et) S (O) CH2CFThree
CH (Me) OEt CH2CH (Et) S (O)2Me
CH (Me) OEt CH2CH (Et) S (O)2Et
CH (Me) OEt CH2CH (Et) S (O)2CFThree
CH (Me) OEt CH2CH (Et) S (O)2CH2CFThree
CH (Me) OEt CH (Me) CH (Me) SMe
CH (Me) OEt CH (Me) CH (Me) SEt
CH (Me) OEt CH (Me) CH (Me) SCFThree
CH (Me) OEt CH (Me) CH (Me) SCH2CFThree
CH (Me) OEt CH (Me) CH (Me) S (O) Me
CH (Me) OEt CH (Me) CH (Me) S (O) Et
CH (Me) OEt CH (Me) CH (Me) S (O) CFThree
CH (Me) OEt CH (Me) CH (Me) S (O) CH2CFThree
CH (Me) OEt CH (Me) CH (Me) S (O)2Me
CH (Me) OEt CH (Me) CH (Me) S (O)2Et
CH (Me) OEt CH (Me) CH (Me) S (O)2CFThree
CH (Me) OEt CH (Me) CH (Me) S (O)2CH2CFThree
S (O)2Me CH2SMe
S (O)2Me CH2SEt
S (O)2Me CH2SCFThree
S (O)2Me CH2SCH2CFThree
S (O)2Me CH2S (O) Me
S (O)2Me CH2S (O) Et
S (O)2Me CH2S (O) CFThree
S (O)2Me CH2S (O) CH2CFThree
S (O)2Me CH2S (O)2Me
S (O)2Me CH2S (O)2Et
S (O)2Me CH2S (O)2CFThree
S (O)2Me CH2S (O)2CH2CFThree
S (O)2Me CH (Me) SMe
S (O)2Me CH (Me) SEt
S (O)2Me CH (Me) SCFThree
S (O)2Me CH (Me) SCH2CFThree
S (O)2Me CH (Me) S (O) Me
S (O)2Me CH (Me) S (O) Et
S (O)2Me CH (Me) S (O) CFThree
S (O)2Me CH (Me) S (O) CH2CFThree
S (O)2Me CH (Me) S (O)2Me
S (O)2Me CH (Me) S (O)2Et
S (O)2Me CH (Me) S (O)2CFThree
S (O)2Me CH (Me) S (O)2CH2CFThree
S (O)2Me CH (Et) SMe
S (O)2Me CH (Et) SEt
S (O)2Me CH (Et) SCFThree
S (O)2Me CH (Et) SCH2CFThree
S (O)2Me CH (Et) S (O) Me
S (O)2Me CH (Et) S (O) Et
S (O)2Me CH (Et) S (O) CFThree
S (O)2Me CH (Et) S (O) CH2CFThree
S (O)2Me CH (Et) S (O)2Me
S (O)2Me CH (Et) S (O)2Et
S (O)2Me CH (Et) S (O)2CFThree
S (O)2Me CH (Et) S (O)2CH2CFThree
S (O)2Me CH (n-Pr) SMe
S (O)2Me CH (n-Pr) SEt
S (O)2Me CH (n-Pr) SCFThree
S (O)2Me CH (n-Pr) SCH2CFThree
S (O)2Me CH (n-Pr) S (O) Me
S (O)2Me CH (n-Pr) S (O) Et
S (O)2Me CH (n-Pr) S (O) CFThree
S (O)2Me CH (n-Pr) S (O) CH2CFThree
S (O)2Me CH (n-Pr) S (O)2Me
S (O)2Me CH (n-Pr) S (O)2Et
S (O)2Me CH (n-Pr) S (O)2CFThree
S (O)2Me CH (n-Pr) S (O)2CH2CFThree
S (O)2Me CH (i-Pr) SMe
S (O)2Me CH (i-Pr) SEt
S (O)2Me CH (i-Pr) SCFThree
S (O)2Me CH (i-Pr) SCH2CFThree
S (O)2Me CH (i-Pr) S (O) Me
S (O)2Me CH (i-Pr) S (O) Et
S (O)2Me CH (i-Pr) S (O) CFThree
S (O)2Me CH (i-Pr) S (O) CH2CFThree
S (O)2Me CH (i-Pr) S (O)2Me
S (O)2Me CH (i-Pr) S (O)2Et
S (O)2Me CH (i-Pr) S (O)2CFThree
S (O)2Me CH (i-Pr) S (O)2CH2CFThree
S (O)2Me CH (n-Bu) SMe
S (O)2Me CH (n-Bu) SEt
S (O)2Me CH (n-Bu) SCFThree
S (O)2Me CH (n-Bu) SCH2CFThree
S (O)2Me CH (n-Bu) S (O) Me
S (O)2Me CH (n-Bu) S (O) Et
S (O)2Me CH (n-Bu) S (O) CFThree
S (O)2Me CH (n-Bu) S (O) CH2CFThree
S (O)2Me CH (n-Bu) S (O)2Me
S (O)2Me CH (n-Bu) S (O)2Et
S (O)2Me CH (n-Bu) S (O)2CFThree
S (O)2Me CH (n-Bu) S (O)2CH2CFThree
S (O)2Me CH (i-Bu) SMe
S (O)2Me CH (i-Bu) SEt
S (O)2Me CH (i-Bu) SCFThree
S (O)2Me CH (i-Bu) SCH2CFThree
S (O)2Me CH (i-Bu) S (O) Me
S (O)2Me CH (i-Bu) S (O) Et
S (O)2Me CH (i-Bu) S (O) CFThree
S (O)2Me CH (i-Bu) S (O) CH2CFThree
S (O)2Me CH (i-Bu) S (O)2Me
S (O)2Me CH (i-Bu) S (O)2Et
S (O)2Me CH (i-Bu) S (O)2CFThree
S (O)2Me CH (i-Bu) S (O)2CH2CFThree
S (O)2Me CH (s-Bu) SMe
S (O)2Me CH (s-Bu) SEt
S (O)2Me CH (s-Bu) SCFThree
S (O)2Me CH (s-Bu) SCH2CFThree
S (O)2Me CH (s-Bu) S (O) Me
S (O)2Me CH (s-Bu) S (O) Et
S (O)2Me CH (s-Bu) S (O) CFThree
S (O)2Me CH (s-Bu) S (O) CH2CFThree
S (O)2Me CH (s-Bu) S (O)2Me
S (O)2Me CH (s-Bu) S (O)2Et
S (O)2Me CH (s-Bu) S (O)2CFThree
S (O)2Me CH (s-Bu) S (O)2CH2CFThree
S (O)2Me CH (t-Bu) SMe
S (O)2Me CH (t-Bu) SEt
S (O)2Me CH (t-Bu) SCFThree
S (O)2Me CH (t-Bu) SCH2CFThree
S (O)2Me CH (t-Bu) S (O) Me
S (O)2Me CH (t-Bu) S (O) Et
S (O)2Me CH (t-Bu) S (O) CFThree
S (O)2Me CH (t-Bu) S (O) CH2CFThree
S (O)2Me CH (t-Bu) S (O)2Me
S (O)2Me CH (t-Bu) S (O)2Et
S (O)2Me CH (t-Bu) S (O)2CFThree
S (O)2Me CH (t-Bu) S (O)2CH2CFThree
S (O)2Me CH (CFThreeSMe
S (O)2Me CH (CFThree) SEt
S (O)2Me CH (CFThree) SCFThree
S (O)2Me CH (CFThree) SCH2CFThree
S (O)2Me CH (CFThree) S (O) Me
S (O)2Me CH (CFThree) S (O) Et
S (O)2Me CH (CFThree) S (O) CFThree
S (O)2Me CH (CFThree) S (O) CH2CFThree
S (O)2Me CH (CFThree) S (O)2Me
S (O)2Me CH (CFThree) S (O)2Et
S (O)2Me CH (CFThree) S (O)2CFThree
S (O)2Me CH (CFThree) S (O)2CH2CFThree
S (O)2Me CH2CH2SMe
S (O)2Me CH2CH2SEt
S (O)2Me CH2CH2SCFThree
S (O)2Me CH2CH2SCH2CFThree
S (O)2Me CH2CH2S (O) Me
S (O)2Me CH2CH2S (O) Et
S (O)2Me CH2CH2S (O) CFThree
S (O)2Me CH2CH2S (O) CH2CFThree
S (O)2Me CH2CH2S (O)2Me
S (O)2Me CH2CH2S (O)2Et
S (O)2Me CH2CH2S (O)2CFThree
S (O)2Me CH2CH2S (O)2CH2CFThree
S (O)2Me CH (Me) CH2SMe
S (O)2Me CH (Me) CH2SEt
S (O)2Me CH (Me) CH2SCFThree
S (O)2Me CH (Me) CH2SCH2CFThree
S (O)2Me CH (Me) CH2S (O) Me
S (O)2Me CH (Me) CH2S (O) Et
S (O)2Me CH (Me) CH2S (O) CFThree
S (O)2Me CH (Me) CH2S (O) CH2CFThree
S (O)2Me CH (Me) CH2S (O)2Me
S (O)2Me CH (Me) CH2S (O)2Et
S (O)2Me CH (Me) CH2S (O)2CFThree
S (O)2Me CH (Me) CH2S (O)2CH2CFThree
S (O)2Me CH (Et) CH2SMe
S (O)2Me CH (Et) CH2SEt
S (O)2Me CH (Et) CH2SCFThree
S (O)2Me CH (Et) CH2SCH2CFThree
S (O)2Me CH (Et) CH2S (O) Me
S (O)2Me CH (Et) CH2S (O) Et
S (O)2Me CH (Et) CH2S (O) CFThree
S (O)2Me CH (Et) CH2S (O) CH2CFThree
S (O)2Me CH (Et) CH2S (O)2Me
S (O)2Me CH (Et) CH2S (O)2Et
S (O)2Me CH (Et) CH2S (O)2CFThree
S (O)2Me CH (Et) CH2S (O)2CH2CFThree
S (O)2Me C (Me)2CH2SMe
S (O)2Me C (Me)2CH2SEt
S (O)2Me C (Me)2CH2SCFThree
S (O)2Me C (Me)2CH2SCH2CFThree
S (O)2Me C (Me)2CH2S (O) Me
S (O)2Me C (Me)2CH2S (O) Et
S (O)2Me C (Me)2CH2S (O) CFThree
S (O)2Me C (Me)2CH2S (O) CH2CFThree
S (O)2Me C (Me)2CH2S (O)2Me
S (O)2Me C (Me)2CH2S (O)2Et
S (O)2Me C (Me)2CH2S (O)2CFThree
S (O)2Me C (Me)2CH2S (O)2CH2CFThree
S (O)2Me CH2CH (Me) SMe
S (O)2Me CH2CH (Me) SEt
S (O)2Me CH2CH (Me) SCFThree
S (O)2Me CH2CH (Me) SCH2CFThree
S (O)2Me CH2CH (Me) S (O) Me
S (O)2Me CH2CH (Me) S (O) Et
S (O)2Me CH2CH (Me) S (O) CFThree
S (O)2Me CH2CH (Me) S (O) CH2CFThree
S (O)2Me CH2CH (Me) S (O)2Me
S (O)2Me CH2CH (Me) S (O)2Et
S (O)2Me CH2CH (Me) S (O)2CFThree
S (O)2Me CH2CH (Me) S (O)2CH2CFThree
S (O)2Me CH2CH (Et) SMe
S (O)2Me CH2CH (Et) SEt
S (O)2Me CH2CH (Et) SCFThree
S (O)2Me CH2CH (Et) SCH2CFThree
S (O)2Me CH2CH (Et) S (O) Me
S (O)2Me CH2CH (Et) S (O) Et
S (O)2Me CH2CH (Et) S (O) CFThree
S (O)2Me CH2CH (Et) S (O) CH2CFThree
S (O)2Me CH2CH (Et) S (O)2Me
S (O)2Me CH2CH (Et) S (O)2Et
S (O)2Me CH2CH (Et) S (O)2CFThree
S (O)2Me CH2CH (Et) S (O)2CH2CFThree
S (O)2Me CH (Me) CH (Me) SMe
S (O)2Me CH (Me) CH (Me) SEt
S (O)2Me CH (Me) CH (Me) SCFThree
S (O)2Me CH (Me) CH (Me) SCH2CFThree
S (O)2Me CH (Me) CH (Me) S (O) Me
S (O)2Me CH (Me) CH (Me) S (O) Et
S (O)2Me CH (Me) CH (Me) S (O) CFThree
S (O)2Me CH (Me) CH (Me) S (O) CH2CFThree
S (O)2Me CH (Me) CH (Me) S (O)2Me
S (O)2Me CH (Me) CH (Me) S (O)2Et
S (O)2Me CH (Me) CH (Me) S (O)2CFThree
S (O)2Me CH (Me) CH (Me) S (O)2CH2CFThree
D2-32a CH2SMe
D2-32a CH2SEt
D2-32a CH2SCFThree
D2-32a CH2SCH2CFThree
D2-32a CH2S (O) Me
D2-32a CH2S (O) Et
D2-32a CH2S (O) CFThree
D2-32a CH2S (O) CH2CFThree
D2-32a CH2S (O)2Me
D2-32a CH2S (O)2Et
D2-32a CH2S (O)2CFThree
D2-32a CH2S (O)2CH2CFThree
D2-32a CH (Me) SMe
D2-32a CH (Me) SEt
D2-32a CH (Me) SCFThree
D2-32a CH (Me) SCH2CFThree
D2-32a CH (Me) S (O) Me
D2-32a CH (Me) S (O) Et
D2-32a CH (Me) S (O) CFThree
D2-32a CH (Me) S (O) CH2CFThree
D2-32a CH (Me) S (O)2Me
D2-32a CH (Me) S (O)2Et
D2-32a CH (Me) S (O)2CFThree
D2-32a CH (Me) S (O)2CH2CFThree
D2-32a CH (Et) SMe
D2-32a CH (Et) SEt
D2-32a CH (Et) SCFThree
D2-32a CH (Et) SCH2CFThree
D2-32a CH (Et) S (O) Me
D2-32a CH (Et) S (O) Et
D2-32a CH (Et) S (O) CFThree
D2-32a CH (Et) S (O) CH2CFThree
D2-32a CH (Et) S (O)2Me
D2-32a CH (Et) S (O)2Et
D2-32a CH (Et) S (O)2CFThree
D2-32a CH (Et) S (O)2CH2CFThree
D2-32a CH (n-Pr) SMe
D2-32a CH (n-Pr) SEt
D2-32a CH (n-Pr) SCFThree
D2-32a CH (n-Pr) SCH2CFThree
D2-32a CH (n-Pr) S (O) Me
D2-32a CH (n-Pr) S (O) Et
D2-32a CH (n-Pr) S (O) CFThree
D2-32a CH (n-Pr) S (O) CH2CFThree
D2-32a CH (n-Pr) S (O)2Me
D2-32a CH (n-Pr) S (O)2Et
D2-32a CH (n-Pr) S (O)2CFThree
D2-32a CH (n-Pr) S (O)2CH2CFThree
D2-32a CH (i-Pr) SMe
D2-32a CH (i-Pr) SEt
D2-32a CH (i-Pr) SCFThree
D2-32a CH (i-Pr) SCH2CFThree
D2-32a CH (i-Pr) S (O) Me
D2-32a CH (i-Pr) S (O) Et
D2-32a CH (i-Pr) S (O) CFThree
D2-32a CH (i-Pr) S (O) CH2CFThree
D2-32a CH (i-Pr) S (O)2Me
D2-32a CH (i-Pr) S (O)2Et
D2-32a CH (i-Pr) S (O)2CFThree
D2-32a CH (i-Pr) S (O)2CH2CFThree
D2-32a CH (n-Bu) SMe
D2-32a CH (n-Bu) SEt
D2-32a CH (n-Bu) SCFThree
D2-32a CH (n-Bu) SCH2CFThree
D2-32a CH (n-Bu) S (O) Me
D2-32a CH (n-Bu) S (O) Et
D2-32a CH (n-Bu) S (O) CFThree
D2-32a CH (n-Bu) S (O) CH2CFThree
D2-32a CH (n-Bu) S (O)2Me
D2-32a CH (n-Bu) S (O)2Et
D2-32a CH (n-Bu) S (O)2CFThree
D2-32a CH (n-Bu) S (O)2CH2CFThree
D2-32a CH (i-Bu) SMe
D2-32a CH (i-Bu) SEt
D2-32a CH (i-Bu) SCFThree
D2-32a CH (i-Bu) SCH2CFThree
D2-32a CH (i-Bu) S (O) Me
D2-32a CH (i-Bu) S (O) Et
D2-32a CH (i-Bu) S (O) CFThree
D2-32a CH (i-Bu) S (O) CH2CFThree
D2-32a CH (i-Bu) S (O)2Me
D2-32a CH (i-Bu) S (O)2Et
D2-32a CH (i-Bu) S (O)2CFThree
D2-32a CH (i-Bu) S (O)2CH2CFThree
D2-32a CH (s-Bu) SMe
D2-32a CH (s-Bu) SEt
D2-32a CH (s-Bu) SCFThree
D2-32a CH (s-Bu) SCH2CFThree
D2-32a CH (s-Bu) S (O) Me
D2-32a CH (s-Bu) S (O) Et
D2-32a CH (s-Bu) S (O) CFThree
D2-32a CH (s-Bu) S (O) CH2CFThree
D2-32a CH (s-Bu) S (O)2Me
D2-32a CH (s-Bu) S (O)2Et
D2-32a CH (s-Bu) S (O)2CFThree
D2-32a CH (s-Bu) S (O)2CH2CFThree
D2-32a CH (t-Bu) SMe
D2-32a CH (t-Bu) SEt
D2-32a CH (t-Bu) SCFThree
D2-32a CH (t-Bu) SCH2CFThree
D2-32a CH (t-Bu) S (O) Me
D2-32a CH (t-Bu) S (O) Et
D2-32a CH (t-Bu) S (O) CFThree
D2-32a CH (t-Bu) S (O) CH2CFThree
D2-32a CH (t-Bu) S (O)2Me
D2-32a CH (t-Bu) S (O)2Et
D2-32a CH (t-Bu) S (O)2CFThree
D2-32a CH (t-Bu) S (O)2CH2CFThree
D2-32a CH (CFThreeSMe
D2-32a CH (CFThree) SEt
D2-32a CH (CFThree) SCFThree
D2-32a CH (CFThree) SCH2CFThree
D2-32a CH (CFThree) S (O) Me
D2-32a CH (CFThree) S (O) Et
D2-32a CH (CFThree) S (O) CFThree
D2-32a CH (CFThree) S (O) CH2CFThree
D2-32a CH (CFThree) S (O)2Me
D2-32a CH (CFThree) S (O)2Et
D2-32a CH (CFThree) S (O)2CFThree
D2-32a CH (CFThree) S (O)2CH2CFThree
D2-32a CH2CH2SMe
D2-32a CH2CH2SEt
D2-32a CH2CH2SCFThree
D2-32a CH2CH2SCH2CFThree
D2-32a CH2CH2S (O) Me
D2-32a CH2CH2S (O) Et
D2-32a CH2CH2S (O) CFThree
D2-32a CH2CH2S (O) CH2CFThree
D2-32a CH2CH2S (O)2Me
D2-32a CH2CH2S (O)2Et
D2-32a CH2CH2S (O)2CFThree
D2-32a CH2CH2S (O)2CH2CFThree
D2-32a CH (Me) CH2SMe
D2-32a CH (Me) CH2SEt
D2-32a CH (Me) CH2SCFThree
D2-32a CH (Me) CH2SCH2CFThree
D2-32a CH (Me) CH2S (O) Me
D2-32a CH (Me) CH2S (O) Et
D2-32a CH (Me) CH2S (O) CFThree
D2-32a CH (Me) CH2S (O) CH2CFThree
D2-32a CH (Me) CH2S (O)2Me
D2-32a CH (Me) CH2S (O)2Et
D2-32a CH (Me) CH2S (O)2CFThree
D2-32a CH (Me) CH2S (O)2CH2CFThree
D2-32a CH (Et) CH2SMe
D2-32a CH (Et) CH2SEt
D2-32a CH (Et) CH2SCFThree
D2-32a CH (Et) CH2SCH2CFThree
D2-32a CH (Et) CH2S (O) Me
D2-32a CH (Et) CH2S (O) Et
D2-32a CH (Et) CH2S (O) CFThree
D2-32a CH (Et) CH2S (O) CH2CFThree
D2-32a CH (Et) CH2S (O)2Me
D2-32a CH (Et) CH2S (O)2Et
D2-32a CH (Et) CH2S (O)2CFThree
D2-32a CH (Et) CH2S (O)2CH2CFThree
D2-32a C (Me)2CH2SMe
D2-32a C (Me)2CH2SEt
D2-32a C (Me)2CH2SCFThree
D2-32a C (Me)2CH2SCH2CFThree
D2-32a C (Me)2CH2S (O) Me
D2-32a C (Me)2CH2S (O) Et
D2-32a C (Me)2CH2S (O) CFThree
D2-32a C (Me)2CH2S (O) CH2CFThree
D2-32a C (Me)2CH2S (O)2Me
D2-32a C (Me)2CH2S (O)2Et
D2-32a C (Me)2CH2S (O)2CFThree
D2-32a C (Me)2CH2S (O)2CH2CFThree
D2-32a CH2CH (Me) SMe
D2-32a CH2CH (Me) SEt
D2-32a CH2CH (Me) SCFThree
D2-32a CH2CH (Me) SCH2CFThree
D2-32a CH2CH (Me) S (O) Me
D2-32a CH2CH (Me) S (O) Et
D2-32a CH2CH (Me) S (O) CFThree
D2-32a CH2CH (Me) S (O) CH2CFThree
D2-32a CH2CH (Me) S (O)2Me
D2-32a CH2CH (Me) S (O)2Et
D2-32a CH2CH (Me) S (O)2CFThree
D2-32a CH2CH (Me) S (O)2CH2CFThree
D2-32a CH2CH (Et) SMe
D2-32a CH2CH (Et) SEt
D2-32a CH2CH (Et) SCFThree
D2-32a CH2CH (Et) SCH2CFThree
D2-32a CH2CH (Et) S (O) Me
D2-32a CH2CH (Et) S (O) Et
D2-32a CH2CH (Et) S (O) CFThree
D2-32a CH2CH (Et) S (O) CH2CFThree
D2-32a CH2CH (Et) S (O)2Me
D2-32a CH2CH (Et) S (O)2Et
D2-32a CH2CH (Et) S (O)2CFThree
D2-32a CH2CH (Et) S (O)2CH2CFThree
D2-32a CH (Me) CH (Me) SMe
D2-32a CH (Me) CH (Me) SEt
D2-32a CH (Me) CH (Me) SCFThree
D2-32a CH (Me) CH (Me) SCH2CFThree
D2-32a CH (Me) CH (Me) S (O) Me
D2-32a CH (Me) CH (Me) S (O) Et
D2-32a CH (Me) CH (Me) S (O) CFThree
D2-32a CH (Me) CH (Me) S (O) CH2CFThree
D2-32a CH (Me) CH (Me) S (O)2Me
D2-32a CH (Me) CH (Me) S (O)2Et
D2-32a CH (Me) CH (Me) S (O)2CFThree
D2-32a CH (Me) CH (Me) S (O)2CH2CFThree
D2-33a CH2SMe
D2-33a CH2SEt
D2-33a CH2SCFThree
D2-33a CH2SCH2CFThree
D2-33a CH2S (O) Me
D2-33a CH2S (O) Et
D2-33a CH2S (O) CFThree
D2-33a CH2S (O) CH2CFThree
D2-33a CH2S (O)2Me
D2-33a CH2S (O)2Et
D2-33a CH2S (O)2CFThree
D2-33a CH2S (O)2CH2CFThree
D2-33a CH (Me) SMe
D2-33a CH (Me) SEt
D2-33a CH (Me) SCFThree
D2-33a CH (Me) SCH2CFThree
D2-33a CH (Me) S (O) Me
D2-33a CH (Me) S (O) Et
D2-33a CH (Me) S (O) CFThree
D2-33a CH (Me) S (O) CH2CFThree
D2-33a CH (Me) S (O)2Me
D2-33a CH (Me) S (O)2Et
D2-33a CH (Me) S (O)2CFThree
D2-33a CH (Me) S (O)2CH2CFThree
D2-33a CH (Et) SMe
D2-33a CH (Et) SEt
D2-33a CH (Et) SCFThree
D2-33a CH (Et) SCH2CFThree
D2-33a CH (Et) S (O) Me
D2-33a CH (Et) S (O) Et
D2-33a CH (Et) S (O) CFThree
D2-33a CH (Et) S (O) CH2CFThree
D2-33a CH (Et) S (O)2Me
D2-33a CH (Et) S (O)2Et
D2-33a CH (Et) S (O)2CFThree
D2-33a CH (Et) S (O)2CH2CFThree
D2-33a CH (n-Pr) SMe
D2-33a CH (n-Pr) SEt
D2-33a CH (n-Pr) SCFThree
D2-33a CH (n-Pr) SCH2CFThree
D2-33a CH (n-Pr) S (O) Me
D2-33a CH (n-Pr) S (O) Et
D2-33a CH (n-Pr) S (O) CFThree
D2-33a CH (n-Pr) S (O) CH2CFThree
D2-33a CH (n-Pr) S (O)2Me
D2-33a CH (n-Pr) S (O)2Et
D2-33a CH (n-Pr) S (O)2CFThree
D2-33a CH (n-Pr) S (O)2CH2CFThree
D2-33a CH (i-Pr) SMe
D2-33a CH (i-Pr) SEt
D2-33a CH (i-Pr) SCFThree
D2-33a CH (i-Pr) SCH2CFThree
D2-33a CH (i-Pr) S (O) Me
D2-33a CH (i-Pr) S (O) Et
D2-33a CH (i-Pr) S (O) CFThree
D2-33a CH (i-Pr) S (O) CH2CFThree
D2-33a CH (i-Pr) S (O)2Me
D2-33a CH (i-Pr) S (O)2Et
D2-33a CH (i-Pr) S (O)2CFThree
D2-33a CH (i-Pr) S (O)2CH2CFThree
D2-33a CH (n-Bu) SMe
D2-33a CH (n-Bu) SEt
D2-33a CH (n-Bu) SCFThree
D2-33a CH (n-Bu) SCH2CFThree
D2-33a CH (n-Bu) S (O) Me
D2-33a CH (n-Bu) S (O) Et
D2-33a CH (n-Bu) S (O) CFThree
D2-33a CH (n-Bu) S (O) CH2CFThree
D2-33a CH (n-Bu) S (O)2Me
D2-33a CH (n-Bu) S (O)2Et
D2-33a CH (n-Bu) S (O)2CFThree
D2-33a CH (n-Bu) S (O)2CH2CFThree
D2-33a CH (i-Bu) SMe
D2-33a CH (i-Bu) SEt
D2-33a CH (i-Bu) SCFThree
D2-33a CH (i-Bu) SCH2CFThree
D2-33a CH (i-Bu) S (O) Me
D2-33a CH (i-Bu) S (O) Et
D2-33a CH (i-Bu) S (O) CFThree
D2-33a CH (i-Bu) S (O) CH2CFThree
D2-33a CH (i-Bu) S (O)2Me
D2-33a CH (i-Bu) S (O)2Et
D2-33a CH (i-Bu) S (O)2CFThree
D2-33a CH (i-Bu) S (O)2CH2CFThree
D2-33a CH (s-Bu) SMe
D2-33a CH (s-Bu) SEt
D2-33a CH (s-Bu) SCFThree
D2-33a CH (s-Bu) SCH2CFThree
D2-33a CH (s-Bu) S (O) Me
D2-33a CH (s-Bu) S (O) Et
D2-33a CH (s-Bu) S (O) CFThree
D2-33a CH (s-Bu) S (O) CH2CFThree
D2-33a CH (s-Bu) S (O)2Me
D2-33a CH (s-Bu) S (O)2Et
D2-33a CH (s-Bu) S (O)2CFThree
D2-33a CH (s-Bu) S (O)2CH2CFThree
D2-33a CH (t-Bu) SMe
D2-33a CH (t-Bu) SEt
D2-33a CH (t-Bu) SCFThree
D2-33a CH (t-Bu) SCH2CFThree
D2-33a CH (t-Bu) S (O) Me
D2-33a CH (t-Bu) S (O) Et
D2-33a CH (t-Bu) S (O) CFThree
D2-33a CH (t-Bu) S (O) CH2CFThree
D2-33a CH (t-Bu) S (O)2Me
D2-33a CH (t-Bu) S (O)2Et
D2-33a CH (t-Bu) S (O)2CFThree
D2-33a CH (t-Bu) S (O)2CH2CFThree
D2-33a CH (CFThreeSMe
D2-33a CH (CFThree) SEt
D2-33a CH (CFThree) SCFThree
D2-33a CH (CFThree) SCH2CFThree
D2-33a CH (CFThree) S (O) Me
D2-33a CH (CFThree) S (O) Et
D2-33a CH (CFThree) S (O) CFThree
D2-33a CH (CFThree) S (O) CH2CFThree
D2-33a CH (CFThree) S (O)2Me
D2-33a CH (CFThree) S (O)2Et
D2-33a CH (CFThree) S (O)2CFThree
D2-33a CH (CFThree) S (O)2CH2CFThree
D2-33a CH2CH2SMe
D2-33a CH2CH2SEt
D2-33a CH2CH2SCFThree
D2-33a CH2CH2SCH2CFThree
D2-33a CH2CH2S (O) Me
D2-33a CH2CH2S (O) Et
D2-33a CH2CH2S (O) CFThree
D2-33a CH2CH2S (O) CH2CFThree
D2-33a CH2CH2S (O)2Me
D2-33a CH2CH2S (O)2Et
D2-33a CH2CH2S (O)2CFThree
D2-33a CH2CH2S (O)2CH2CFThree
D2-33a CH (Me) CH2SMe
D2-33a CH (Me) CH2SEt
D2-33a CH (Me) CH2SCFThree
D2-33a CH (Me) CH2SCH2CFThree
D2-33a CH (Me) CH2S (O) Me
D2-33a CH (Me) CH2S (O) Et
D2-33a CH (Me) CH2S (O) CFThree
D2-33a CH (Me) CH2S (O) CH2CFThree
D2-33a CH (Me) CH2S (O)2Me
D2-33a CH (Me) CH2S (O)2Et
D2-33a CH (Me) CH2S (O)2CFThree
D2-33a CH (Me) CH2S (O)2CH2CFThree
D2-33a CH (Et) CH2SMe
D2-33a CH (Et) CH2SEt
D2-33a CH (Et) CH2SCFThree
D2-33a CH (Et) CH2SCH2CFThree
D2-33a CH (Et) CH2S (O) Me
D2-33a CH (Et) CH2S (O) Et
D2-33a CH (Et) CH2S (O) CFThree
D2-33a CH (Et) CH2S (O) CH2CFThree
D2-33a CH (Et) CH2S (O)2Me
D2-33a CH (Et) CH2S (O)2Et
D2-33a CH (Et) CH2S (O)2CFThree
D2-33a CH (Et) CH2S (O)2CH2CFThree
D2-33a C (Me)2CH2SMe
D2-33a C (Me)2CH2SEt
D2-33a C (Me)2CH2SCFThree
D2-33a C (Me)2CH2SCH2CFThree
D2-33a C (Me)2CH2S (O) Me
D2-33a C (Me)2CH2S (O) Et
D2-33a C (Me)2CH2S (O) CFThree
D2-33a C (Me)2CH2S (O) CH2CFThree
D2-33a C (Me)2CH2S (O)2Me
D2-33a C (Me)2CH2S (O)2Et
D2-33a C (Me)2CH2S (O)2CFThree
D2-33a C (Me)2CH2S (O)2CH2CFThree
D2-33a CH2CH (Me) SMe
D2-33a CH2CH (Me) SEt
D2-33a CH2CH (Me) SCFThree
D2-33a CH2CH (Me) SCH2CFThree
D2-33a CH2CH (Me) S (O) Me
D2-33a CH2CH (Me) S (O) Et
D2-33a CH2CH (Me) S (O) CFThree
D2-33a CH2CH (Me) S (O) CH2CFThree
D2-33a CH2CH (Me) S (O)2Me
D2-33a CH2CH (Me) S (O)2Et
D2-33a CH2CH (Me) S (O)2CFThree
D2-33a CH2CH (Me) S (O)2CH2CFThree
D2-33a CH2CH (Et) SMe
D2-33a CH2CH (Et) SEt
D2-33a CH2CH (Et) SCFThree
D2-33a CH2CH (Et) SCH2CFThree
D2-33a CH2CH (Et) S (O) Me
D2-33a CH2CH (Et) S (O) Et
D2-33a CH2CH (Et) S (O) CFThree
D2-33a CH2CH (Et) S (O) CH2CFThree
D2-33a CH2CH (Et) S (O)2Me
D2-33a CH2CH (Et) S (O)2Et
D2-33a CH2CH (Et) S (O)2CFThree
D2-33a CH2CH (Et) S (O)2CH2CFThree
D2-33a CH (Me) CH (Me) SMe
D2-33a CH (Me) CH (Me) SEt
D2-33a CH (Me) CH (Me) SCFThree
D2-33a CH (Me) CH (Me) SCH2CFThree
D2-33a CH (Me) CH (Me) S (O) Me
D2-33a CH (Me) CH (Me) S (O) Et
D2-33a CH (Me) CH (Me) S (O) CFThree
D2-33a CH (Me) CH (Me) S (O) CH2CFThree
D2-33a CH (Me) CH (Me) S (O)2Me
D2-33a CH (Me) CH (Me) S (O)2Et
D2-33a CH (Me) CH (Me) S (O)2CFThree
D2-33a CH (Me) CH (Me) S (O)2CH2CFThree
D2-34a CH2SMe
D2-34a CH2SEt
D2-34a CH2SCFThree
D2-34a CH2SCH2CFThree
D2-34a CH2S (O) Me
D2-34a CH2S (O) Et
D2-34a CH2S (O) CFThree
D2-34a CH2S (O) CH2CFThree
D2-34a CH2S (O)2Me
D2-34a CH2S (O)2Et
D2-34a CH2S (O)2CFThree
D2-34a CH2S (O)2CH2CFThree
D2-34a CH (Me) SMe
D2-34a CH (Me) SEt
D2-34a CH (Me) SCFThree
D2-34a CH (Me) SCH2CFThree
D2-34a CH (Me) S (O) Me
D2-34a CH (Me) S (O) Et
D2-34a CH (Me) S (O) CFThree
D2-34a CH (Me) S (O) CH2CFThree
D2-34a CH (Me) S (O)2Me
D2-34a CH (Me) S (O)2Et
D2-34a CH (Me) S (O)2CFThree
D2-34a CH (Me) S (O)2CH2CFThree
D2-34a CH (Et) SMe
D2-34a CH (Et) SEt
D2-34a CH (Et) SCFThree
D2-34a CH (Et) SCH2CFThree
D2-34a CH (Et) S (O) Me
D2-34a CH (Et) S (O) Et
D2-34a CH (Et) S (O) CFThree
D2-34a CH (Et) S (O) CH2CFThree
D2-34a CH (Et) S (O)2Me
D2-34a CH (Et) S (O)2Et
D2-34a CH (Et) S (O)2CFThree
D2-34a CH (Et) S (O)2CH2CFThree
D2-34a CH (n-Pr) SMe
D2-34a CH (n-Pr) SEt
D2-34a CH (n-Pr) SCFThree
D2-34a CH (n-Pr) SCH2CFThree
D2-34a CH (n-Pr) S (O) Me
D2-34a CH (n-Pr) S (O) Et
D2-34a CH (n-Pr) S (O) CFThree
D2-34a CH (n-Pr) S (O) CH2CFThree
D2-34a CH (n-Pr) S (O)2Me
D2-34a CH (n-Pr) S (O)2Et
D2-34a CH (n-Pr) S (O)2CFThree
D2-34a CH (n-Pr) S (O)2CH2CFThree
D2-34a CH (i-Pr) SMe
D2-34a CH (i-Pr) SEt
D2-34a CH (i-Pr) SCFThree
D2-34a CH (i-Pr) SCH2CFThree
D2-34a CH (i-Pr) S (O) Me
D2-34a CH (i-Pr) S (O) Et
D2-34a CH (i-Pr) S (O) CFThree
D2-34a CH (i-Pr) S (O) CH2CFThree
D2-34a CH (i-Pr) S (O)2Me
D2-34a CH (i-Pr) S (O)2Et
D2-34a CH (i-Pr) S (O)2CFThree
D2-34a CH (i-Pr) S (O)2CH2CFThree
D2-34a CH (n-Bu) SMe
D2-34a CH (n-Bu) SEt
D2-34a CH (n-Bu) SCFThree
D2-34a CH (n-Bu) SCH2CFThree
D2-34a CH (n-Bu) S (O) Me
D2-34a CH (n-Bu) S (O) Et
D2-34a CH (n-Bu) S (O) CFThree
D2-34a CH (n-Bu) S (O) CH2CFThree
D2-34a CH (n-Bu) S (O)2Me
D2-34a CH (n-Bu) S (O)2Et
D2-34a CH (n-Bu) S (O)2CFThree
D2-34a CH (n-Bu) S (O)2CH2CFThree
D2-34a CH (i-Bu) SMe
D2-34a CH (i-Bu) SEt
D2-34a CH (i-Bu) SCFThree
D2-34a CH (i-Bu) SCH2CFThree
D2-34a CH (i-Bu) S (O) Me
D2-34a CH (i-Bu) S (O) Et
D2-34a CH (i-Bu) S (O) CFThree
D2-34a CH (i-Bu) S (O) CH2CFThree
D2-34a CH (i-Bu) S (O)2Me
D2-34a CH (i-Bu) S (O)2Et
D2-34a CH (i-Bu) S (O)2CFThree
D2-34a CH (i-Bu) S (O)2CH2CFThree
D2-34a CH (s-Bu) SMe
D2-34a CH (s-Bu) SEt
D2-34a CH (s-Bu) SCFThree
D2-34a CH (s-Bu) SCH2CFThree
D2-34a CH (s-Bu) S (O) Me
D2-34a CH (s-Bu) S (O) Et
D2-34a CH (s-Bu) S (O) CFThree
D2-34a CH (s-Bu) S (O) CH2CFThree
D2-34a CH (s-Bu) S (O)2Me
D2-34a CH (s-Bu) S (O)2Et
D2-34a CH (s-Bu) S (O)2CFThree
D2-34a CH (s-Bu) S (O)2CH2CFThree
D2-34a CH (t-Bu) SMe
D2-34a CH (t-Bu) SEt
D2-34a CH (t-Bu) SCFThree
D2-34a CH (t-Bu) SCH2CFThree
D2-34a CH (t-Bu) S (O) Me
D2-34a CH (t-Bu) S (O) Et
D2-34a CH (t-Bu) S (O) CFThree
D2-34a CH (t-Bu) S (O) CH2CFThree
D2-34a CH (t-Bu) S (O)2Me
D2-34a CH (t-Bu) S (O)2Et
D2-34a CH (t-Bu) S (O)2CFThree
D2-34a CH (t-Bu) S (O)2CH2CFThree
D2-34a CH (CFThreeSMe
D2-34a CH (CFThree) SEt
D2-34a CH (CFThree) SCFThree
D2-34a CH (CFThree) SCH2CFThree
D2-34a CH (CFThree) S (O) Me
D2-34a CH (CFThree) S (O) Et
D2-34a CH (CFThree) S (O) CFThree
D2-34a CH (CFThree) S (O) CH2CFThree
D2-34a CH (CFThree) S (O)2Me
D2-34a CH (CFThree) S (O)2Et
D2-34a CH (CFThree) S (O)2CFThree
D2-34a CH (CFThree) S (O)2CH2CFThree
D2-34a CH2CH2SMe
D2-34a CH2CH2SEt
D2-34a CH2CH2SCFThree
D2-34a CH2CH2SCH2CFThree
D2-34a CH2CH2S (O) Me
D2-34a CH2CH2S (O) Et
D2-34a CH2CH2S (O) CFThree
D2-34a CH2CH2S (O) CH2CFThree
D2-34a CH2CH2S (O)2Me
D2-34a CH2CH2S (O)2Et
D2-34a CH2CH2S (O)2CFThree
D2-34a CH2CH2S (O)2CH2CFThree
D2-34a CH (Me) CH2SMe
D2-34a CH (Me) CH2SEt
D2-34a CH (Me) CH2SCFThree
D2-34a CH (Me) CH2SCH2CFThree
D2-34a CH (Me) CH2S (O) Me
D2-34a CH (Me) CH2S (O) Et
D2-34a CH (Me) CH2S (O) CFThree
D2-34a CH (Me) CH2S (O) CH2CFThree
D2-34a CH (Me) CH2S (O)2Me
D2-34a CH (Me) CH2S (O)2Et
D2-34a CH (Me) CH2S (O)2CFThree
D2-34a CH (Me) CH2S (O)2CH2CFThree
D2-34a CH (Et) CH2SMe
D2-34a CH (Et) CH2SEt
D2-34a CH (Et) CH2SCFThree
D2-34a CH (Et) CH2SCH2CFThree
D2-34a CH (Et) CH2S (O) Me
D2-34a CH (Et) CH2S (O) Et
D2-34a CH (Et) CH2S (O) CFThree
D2-34a CH (Et) CH2S (O) CH2CFThree
D2-34a CH (Et) CH2S (O)2Me
D2-34a CH (Et) CH2S (O)2Et
D2-34a CH (Et) CH2S (O)2CFThree
D2-34a CH (Et) CH2S (O)2CH2CFThree
D2-34a C (Me)2CH2SMe
D2-34a C (Me)2CH2SEt
D2-34a C (Me)2CH2SCFThree
D2-34a C (Me)2CH2SCH2CFThree
D2-34a C (Me)2CH2S (O) Me
D2-34a C (Me)2CH2S (O) Et
D2-34a C (Me)2CH2S (O) CFThree
D2-34a C (Me)2CH2S (O) CH2CFThree
D2-34a C (Me)2CH2S (O)2Me
D2-34a C (Me)2CH2S (O)2Et
D2-34a C (Me)2CH2S (O)2CFThree
D2-34a C (Me)2CH2S (O)2CH2CFThree
D2-34a CH2CH (Me) SMe
D2-34a CH2CH (Me) SEt
D2-34a CH2CH (Me) SCFThree
D2-34a CH2CH (Me) SCH2CFThree
D2-34a CH2CH (Me) S (O) Me
D2-34a CH2CH (Me) S (O) Et
D2-34a CH2CH (Me) S (O) CFThree
D2-34a CH2CH (Me) S (O) CH2CFThree
D2-34a CH2CH (Me) S (O)2Me
D2-34a CH2CH (Me) S (O)2Et
D2-34a CH2CH (Me) S (O)2CFThree
D2-34a CH2CH (Me) S (O)2CH2CFThree
D2-34a CH2CH (Et) SMe
D2-34a CH2CH (Et) SEt
D2-34a CH2CH (Et) SCFThree
D2-34a CH2CH (Et) SCH2CFThree
D2-34a CH2CH (Et) S (O) Me
D2-34a CH2CH (Et) S (O) Et
D2-34a CH2CH (Et) S (O) CFThree
D2-34a CH2CH (Et) S (O) CH2CFThree
D2-34a CH2CH (Et) S (O)2Me
D2-34a CH2CH (Et) S (O)2Et
D2-34a CH2CH (Et) S (O)2CFThree
D2-34a CH2CH (Et) S (O)2CH2CFThree
D2-34a CH (Me) CH (Me) SMe
D2-34a CH (Me) CH (Me) SEt
D2-34a CH (Me) CH (Me) SCFThree
D2-34a CH (Me) CH (Me) SCH2CFThree
D2-34a CH (Me) CH (Me) S (O) Me
D2-34a CH (Me) CH (Me) S (O) Et
D2-34a CH (Me) CH (Me) S (O) CFThree
D2-34a CH (Me) CH (Me) S (O) CH2CFThree
D2-34a CH (Me) CH (Me) S (O)2Me
D2-34a CH (Me) CH (Me) S (O)2Et
D2-34a CH (Me) CH (Me) S (O)2CFThree
D2-34a CH (Me) CH (Me) S (O)2CH2CFThree
D2-36a CH2SMe
D2-36a CH2SEt
D2-36a CH2SCFThree
D2-36a CH2SCH2CFThree
D2-36a CH2S (O) Me
D2-36a CH2S (O) Et
D2-36a CH2S (O) CFThree
D2-36a CH2S (O) CH2CFThree
D2-36a CH2S (O)2Me
D2-36a CH2S (O)2Et
D2-36a CH2S (O)2CFThree
D2-36a CH2S (O)2CH2CFThree
D2-36a CH (Me) SMe
D2-36a CH (Me) SEt
D2-36a CH (Me) SCFThree
D2-36a CH (Me) SCH2CFThree
D2-36a CH (Me) S (O) Me
D2-36a CH (Me) S (O) Et
D2-36a CH (Me) S (O) CFThree
D2-36a CH (Me) S (O) CH2CFThree
D2-36a CH (Me) S (O)2Me
D2-36a CH (Me) S (O)2Et
D2-36a CH (Me) S (O)2CFThree
D2-36a CH (Me) S (O)2CH2CFThree
D2-36a CH (Et) SMe
D2-36a CH (Et) SEt
D2-36a CH (Et) SCFThree
D2-36a CH (Et) SCH2CFThree
D2-36a CH (Et) S (O) Me
D2-36a CH (Et) S (O) Et
D2-36a CH (Et) S (O) CFThree
D2-36a CH (Et) S (O) CH2CFThree
D2-36a CH (Et) S (O)2Me
D2-36a CH (Et) S (O)2Et
D2-36a CH (Et) S (O)2CFThree
D2-36a CH (Et) S (O)2CH2CFThree
D2-36a CH (n-Pr) SMe
D2-36a CH (n-Pr) SEt
D2-36a CH (n-Pr) SCFThree
D2-36a CH (n-Pr) SCH2CFThree
D2-36a CH (n-Pr) S (O) Me
D2-36a CH (n-Pr) S (O) Et
D2-36a CH (n-Pr) S (O) CFThree
D2-36a CH (n-Pr) S (O) CH2CFThree
D2-36a CH (n-Pr) S (O)2Me
D2-36a CH (n-Pr) S (O)2Et
D2-36a CH (n-Pr) S (O)2CFThree
D2-36a CH (n-Pr) S (O)2CH2CFThree
D2-36a CH (i-Pr) SMe
D2-36a CH (i-Pr) SEt
D2-36a CH (i-Pr) SCFThree
D2-36a CH (i-Pr) SCH2CFThree
D2-36a CH (i-Pr) S (O) Me
D2-36a CH (i-Pr) S (O) Et
D2-36a CH (i-Pr) S (O) CFThree
D2-36a CH (i-Pr) S (O) CH2CFThree
D2-36a CH (i-Pr) S (O)2Me
D2-36a CH (i-Pr) S (O)2Et
D2-36a CH (i-Pr) S (O)2CFThree
D2-36a CH (i-Pr) S (O)2CH2CFThree
D2-36a CH (n-Bu) SMe
D2-36a CH (n-Bu) SEt
D2-36a CH (n-Bu) SCFThree
D2-36a CH (n-Bu) SCH2CFThree
D2-36a CH (n-Bu) S (O) Me
D2-36a CH (n-Bu) S (O) Et
D2-36a CH (n-Bu) S (O) CFThree
D2-36a CH (n-Bu) S (O) CH2CFThree
D2-36a CH (n-Bu) S (O)2Me
D2-36a CH (n-Bu) S (O)2Et
D2-36a CH (n-Bu) S (O)2CFThree
D2-36a CH (n-Bu) S (O)2CH2CFThree
D2-36a CH (i-Bu) SMe
D2-36a CH (i-Bu) SEt
D2-36a CH (i-Bu) SCFThree
D2-36a CH (i-Bu) SCH2CFThree
D2-36a CH (i-Bu) S (O) Me
D2-36a CH (i-Bu) S (O) Et
D2-36a CH (i-Bu) S (O) CFThree
D2-36a CH (i-Bu) S (O) CH2CFThree
D2-36a CH (i-Bu) S (O)2Me
D2-36a CH (i-Bu) S (O)2Et
D2-36a CH (i-Bu) S (O)2CFThree
D2-36a CH (i-Bu) S (O)2CH2CFThree
D2-36a CH (s-Bu) SMe
D2-36a CH (s-Bu) SEt
D2-36a CH (s-Bu) SCFThree
D2-36a CH (s-Bu) SCH2CFThree
D2-36a CH (s-Bu) S (O) Me
D2-36a CH (s-Bu) S (O) Et
D2-36a CH (s-Bu) S (O) CFThree
D2-36a CH (s-Bu) S (O) CH2CFThree
D2-36a CH (s-Bu) S (O)2Me
D2-36a CH (s-Bu) S (O)2Et
D2-36a CH (s-Bu) S (O)2CFThree
D2-36a CH (s-Bu) S (O)2CH2CFThree
D2-36a CH (t-Bu) SMe
D2-36a CH (t-Bu) SEt
D2-36a CH (t-Bu) SCFThree
D2-36a CH (t-Bu) SCH2CFThree
D2-36a CH (t-Bu) S (O) Me
D2-36a CH (t-Bu) S (O) Et
D2-36a CH (t-Bu) S (O) CFThree
D2-36a CH (t-Bu) S (O) CH2CFThree
D2-36a CH (t-Bu) S (O)2Me
D2-36a CH (t-Bu) S (O)2Et
D2-36a CH (t-Bu) S (O)2CFThree
D2-36a CH (t-Bu) S (O)2CH2CFThree
D2-36a CH (CFThreeSMe
D2-36a CH (CFThree) SEt
D2-36a CH (CFThree) SCFThree
D2-36a CH (CFThree) SCH2CFThree
D2-36a CH (CFThree) S (O) Me
D2-36a CH (CFThree) S (O) Et
D2-36a CH (CFThree) S (O) CFThree
D2-36a CH (CFThree) S (O) CH2CFThree
D2-36a CH (CFThree) S (O)2Me
D2-36a CH (CFThree) S (O)2Et
D2-36a CH (CFThree) S (O)2CFThree
D2-36a CH (CFThree) S (O)2CH2CFThree
D2-36a CH2CH2SMe
D2-36a CH2CH2SEt
D2-36a CH2CH2SCFThree
D2-36a CH2CH2SCH2CFThree
D2-36a CH2CH2S (O) Me
D2-36a CH2CH2S (O) Et
D2-36a CH2CH2S (O) CFThree
D2-36a CH2CH2S (O) CH2CFThree
D2-36a CH2CH2S (O)2Me
D2-36a CH2CH2S (O)2Et
D2-36a CH2CH2S (O)2CFThree
D2-36a CH2CH2S (O)2CH2CFThree
D2-36a CH (Me) CH2SMe
D2-36a CH (Me) CH2SEt
D2-36a CH (Me) CH2SCFThree
D2-36a CH (Me) CH2SCH2CFThree
D2-36a CH (Me) CH2S (O) Me
D2-36a CH (Me) CH2S (O) Et
D2-36a CH (Me) CH2S (O) CFThree
D2-36a CH (Me) CH2S (O) CH2CFThree
D2-36a CH (Me) CH2S (O)2Me
D2-36a CH (Me) CH2S (O)2Et
D2-36a CH (Me) CH2S (O)2CFThree
D2-36a CH (Me) CH2S (O)2CH2CFThree
D2-36a CH (Et) CH2SMe
D2-36a CH (Et) CH2SEt
D2-36a CH (Et) CH2SCFThree
D2-36a CH (Et) CH2SCH2CFThree
D2-36a CH (Et) CH2S (O) Me
D2-36a CH (Et) CH2S (O) Et
D2-36a CH (Et) CH2S (O) CFThree
D2-36a CH (Et) CH2S (O) CH2CFThree
D2-36a CH (Et) CH2S (O)2Me
D2-36a CH (Et) CH2S (O)2Et
D2-36a CH (Et) CH2S (O)2CFThree
D2-36a CH (Et) CH2S (O)2CH2CFThree
D2-36a C (Me)2CH2SMe
D2-36a C (Me)2CH2SEt
D2-36a C (Me)2CH2SCFThree
D2-36a C (Me)2CH2SCH2CFThree
D2-36a C (Me)2CH2S (O) Me
D2-36a C (Me)2CH2S (O) Et
D2-36a C (Me)2CH2S (O) CFThree
D2-36a C (Me)2CH2S (O) CH2CFThree
D2-36a C (Me)2CH2S (O)2Me
D2-36a C (Me)2CH2S (O)2Et
D2-36a C (Me)2CH2S (O)2CFThree
D2-36a C (Me)2CH2S (O)2CH2CFThree
D2-36a CH2CH (Me) SMe
D2-36a CH2CH (Me) SEt
D2-36a CH2CH (Me) SCFThree
D2-36a CH2CH (Me) SCH2CFThree
D2-36a CH2CH (Me) S (O) Me
D2-36a CH2CH (Me) S (O) Et
D2-36a CH2CH (Me) S (O) CFThree
D2-36a CH2CH (Me) S (O) CH2CFThree
D2-36a CH2CH (Me) S (O)2Me
D2-36a CH2CH (Me) S (O)2Et
D2-36a CH2CH (Me) S (O)2CFThree
D2-36a CH2CH (Me) S (O)2CH2CFThree
D2-36a CH2CH (Et) SMe
D2-36a CH2CH (Et) SEt
D2-36a CH2CH (Et) SCFThree
D2-36a CH2CH (Et) SCH2CFThree
D2-36a CH2CH (Et) S (O) Me
D2-36a CH2CH (Et) S (O) Et
D2-36a CH2CH (Et) S (O) CFThree
D2-36a CH2CH (Et) S (O) CH2CFThree
D2-36a CH2CH (Et) S (O)2Me
D2-36a CH2CH (Et) S (O)2Et
D2-36a CH2CH (Et) S (O)2CFThree
D2-36a CH2CH (Et) S (O)2CH2CFThree
D2-36a CH (Me) CH (Me) SMe
D2-36a CH (Me) CH (Me) SEt
D2-36a CH (Me) CH (Me) SCFThree
D2-36a CH (Me) CH (Me) SCH2CFThree
D2-36a CH (Me) CH (Me) S (O) Me
D2-36a CH (Me) CH (Me) S (O) Et
D2-36a CH (Me) CH (Me) S (O) CFThree
D2-36a CH (Me) CH (Me) S (O) CH2CFThree
D2-36a CH (Me) CH (Me) S (O)2Me
D2-36a CH (Me) CH (Me) S (O)2Et
D2-36a CH (Me) CH (Me) S (O)2CFThree
D2-36a CH (Me) CH (Me) S (O)2CH2CFThree
D2-37a CH2SMe
D2-37a CH2SEt
D2-37a CH2SCFThree
D2-37a CH2SCH2CFThree
D2-37a CH2S (O) Me
D2-37a CH2S (O) Et
D2-37a CH2S (O) CFThree
D2-37a CH2S (O) CH2CFThree
D2-37a CH2S (O)2Me
D2-37a CH2S (O)2Et
D2-37a CH2S (O)2CFThree
D2-37a CH2S (O)2CH2CFThree
D2-37a CH (Me) SMe
D2-37a CH (Me) SEt
D2-37a CH (Me) SCFThree
D2-37a CH (Me) SCH2CFThree
D2-37a CH (Me) S (O) Me
D2-37a CH (Me) S (O) Et
D2-37a CH (Me) S (O) CFThree
D2-37a CH (Me) S (O) CH2CFThree
D2-37a CH (Me) S (O)2Me
D2-37a CH (Me) S (O)2Et
D2-37a CH (Me) S (O)2CFThree
D2-37a CH (Me) S (O)2CH2CFThree
D2-37a CH (Et) SMe
D2-37a CH (Et) SEt
D2-37a CH (Et) SCFThree
D2-37a CH (Et) SCH2CFThree
D2-37a CH (Et) S (O) Me
D2-37a CH (Et) S (O) Et
D2-37a CH (Et) S (O) CFThree
D2-37a CH (Et) S (O) CH2CFThree
D2-37a CH (Et) S (O)2Me
D2-37a CH (Et) S (O)2Et
D2-37a CH (Et) S (O)2CFThree
D2-37a CH (Et) S (O)2CH2CFThree
D2-37a CH (n-Pr) SMe
D2-37a CH (n-Pr) SEt
D2-37a CH (n-Pr) SCFThree
D2-37a CH (n-Pr) SCH2CFThree
D2-37a CH (n-Pr) S (O) Me
D2-37a CH (n-Pr) S (O) Et
D2-37a CH (n-Pr) S (O) CFThree
D2-37a CH (n-Pr) S (O) CH2CFThree
D2-37a CH (n-Pr) S (O)2Me
D2-37a CH (n-Pr) S (O)2Et
D2-37a CH (n-Pr) S (O)2CFThree
D2-37a CH (n-Pr) S (O)2CH2CFThree
D2-37a CH (i-Pr) SMe
D2-37a CH (i-Pr) SEt
D2-37a CH (i-Pr) SCFThree
D2-37a CH (i-Pr) SCH2CFThree
D2-37a CH (i-Pr) S (O) Me
D2-37a CH (i-Pr) S (O) Et
D2-37a CH (i-Pr) S (O) CFThree
D2-37a CH (i-Pr) S (O) CH2CFThree
D2-37a CH (i-Pr) S (O)2Me
D2-37a CH (i-Pr) S (O)2Et
D2-37a CH (i-Pr) S (O)2CFThree
D2-37a CH (i-Pr) S (O)2CH2CFThree
D2-37a CH (n-Bu) SMe
D2-37a CH (n-Bu) SEt
D2-37a CH (n-Bu) SCFThree
D2-37a CH (n-Bu) SCH2CFThree
D2-37a CH (n-Bu) S (O) Me
D2-37a CH (n-Bu) S (O) Et
D2-37a CH (n-Bu) S (O) CFThree
D2-37a CH (n-Bu) S (O) CH2CFThree
D2-37a CH (n-Bu) S (O)2Me
D2-37a CH (n-Bu) S (O)2Et
D2-37a CH (n-Bu) S (O)2CFThree
D2-37a CH (n-Bu) S (O)2CH2CFThree
D2-37a CH (i-Bu) SMe
D2-37a CH (i-Bu) SEt
D2-37a CH (i-Bu) SCFThree
D2-37a CH (i-Bu) SCH2CFThree
D2-37a CH (i-Bu) S (O) Me
D2-37a CH (i-Bu) S (O) Et
D2-37a CH (i-Bu) S (O) CFThree
D2-37a CH (i-Bu) S (O) CH2CFThree
D2-37a CH (i-Bu) S (O)2Me
D2-37a CH (i-Bu) S (O)2Et
D2-37a CH (i-Bu) S (O)2CFThree
D2-37a CH (i-Bu) S (O)2CH2CFThree
D2-37a CH (s-Bu) SMe
D2-37a CH (s-Bu) SEt
D2-37a CH (s-Bu) SCFThree
D2-37a CH (s-Bu) SCH2CFThree
D2-37a CH (s-Bu) S (O) Me
D2-37a CH (s-Bu) S (O) Et
D2-37a CH (s-Bu) S (O) CFThree
D2-37a CH (s-Bu) S (O) CH2CFThree
D2-37a CH (s-Bu) S (O)2Me
D2-37a CH (s-Bu) S (O)2Et
D2-37a CH (s-Bu) S (O)2CFThree
D2-37a CH (s-Bu) S (O)2CH2CFThree
D2-37a CH (t-Bu) SMe
D2-37a CH (t-Bu) SEt
D2-37a CH (t-Bu) SCFThree
D2-37a CH (t-Bu) SCH2CFThree
D2-37a CH (t-Bu) S (O) Me
D2-37a CH (t-Bu) S (O) Et
D2-37a CH (t-Bu) S (O) CFThree
D2-37a CH (t-Bu) S (O) CH2CFThree
D2-37a CH (t-Bu) S (O)2Me
D2-37a CH (t-Bu) S (O)2Et
D2-37a CH (t-Bu) S (O)2CFThree
D2-37a CH (t-Bu) S (O)2CH2CFThree
D2-37a CH (CFThreeSMe
D2-37a CH (CFThree) SEt
D2-37a CH (CFThree) SCFThree
D2-37a CH (CFThree) SCH2CFThree
D2-37a CH (CFThree) S (O) Me
D2-37a CH (CFThree) S (O) Et
D2-37a CH (CFThree) S (O) CFThree
D2-37a CH (CFThree) S (O) CH2CFThree
D2-37a CH (CFThree) S (O)2Me
D2-37a CH (CFThree) S (O)2Et
D2-37a CH (CFThree) S (O)2CFThree
D2-37a CH (CFThree) S (O)2CH2CFThree
D2-37a CH2CH2SMe
D2-37a CH2CH2SEt
D2-37a CH2CH2SCFThree
D2-37a CH2CH2SCH2CFThree
D2-37a CH2CH2S (O) Me
D2-37a CH2CH2S (O) Et
D2-37a CH2CH2S (O) CFThree
D2-37a CH2CH2S (O) CH2CFThree
D2-37a CH2CH2S (O)2Me
D2-37a CH2CH2S (O)2Et
D2-37a CH2CH2S (O)2CFThree
D2-37a CH2CH2S (O)2CH2CFThree
D2-37a CH (Me) CH2SMe
D2-37a CH (Me) CH2SEt
D2-37a CH (Me) CH2SCFThree
D2-37a CH (Me) CH2SCH2CFThree
D2-37a CH (Me) CH2S (O) Me
D2-37a CH (Me) CH2S (O) Et
D2-37a CH (Me) CH2S (O) CFThree
D2-37a CH (Me) CH2S (O) CH2CFThree
D2-37a CH (Me) CH2S (O)2Me
D2-37a CH (Me) CH2S (O)2Et
D2-37a CH (Me) CH2S (O)2CFThree
D2-37a CH (Me) CH2S (O)2CH2CFThree
D2-37a CH (Et) CH2SMe
D2-37a CH (Et) CH2SEt
D2-37a CH (Et) CH2SCFThree
D2-37a CH (Et) CH2SCH2CFThree
D2-37a CH (Et) CH2S (O) Me
D2-37a CH (Et) CH2S (O) Et
D2-37a CH (Et) CH2S (O) CFThree
D2-37a CH (Et) CH2S (O) CH2CFThree
D2-37a CH (Et) CH2S (O)2Me
D2-37a CH (Et) CH2S (O)2Et
D2-37a CH (Et) CH2S (O)2CFThree
D2-37a CH (Et) CH2S (O)2CH2CFThree
D2-37a C (Me)2CH2SMe
D2-37a C (Me)2CH2SEt
D2-37a C (Me)2CH2SCFThree
D2-37a C (Me)2CH2SCH2CFThree
D2-37a C (Me)2CH2S (O) Me
D2-37a C (Me)2CH2S (O) Et
D2-37a C (Me)2CH2S (O) CFThree
D2-37a C (Me)2CH2S (O) CH2CFThree
D2-37a C (Me)2CH2S (O)2Me
D2-37a C (Me)2CH2S (O)2Et
D2-37a C (Me)2CH2S (O)2CFThree
D2-37a C (Me)2CH2S (O)2CH2CFThree
D2-37a CH2CH (Me) SMe
D2-37a CH2CH (Me) SEt
D2-37a CH2CH (Me) SCFThree
D2-37a CH2CH (Me) SCH2CFThree
D2-37a CH2CH (Me) S (O) Me
D2-37a CH2CH (Me) S (O) Et
D2-37a CH2CH (Me) S (O) CFThree
D2-37a CH2CH (Me) S (O) CH2CFThree
D2-37a CH2CH (Me) S (O)2Me
D2-37a CH2CH (Me) S (O)2Et
D2-37a CH2CH (Me) S (O)2CFThree
D2-37a CH2CH (Me) S (O)2CH2CFThree
D2-37a CH2CH (Et) SMe
D2-37a CH2CH (Et) SEt
D2-37a CH2CH (Et) SCFThree
D2-37a CH2CH (Et) SCH2CFThree
D2-37a CH2CH (Et) S (O) Me
D2-37a CH2CH (Et) S (O) Et
D2-37a CH2CH (Et) S (O) CFThree
D2-37a CH2CH (Et) S (O) CH2CFThree
D2-37a CH2CH (Et) S (O)2Me
D2-37a CH2CH (Et) S (O)2Et
D2-37a CH2CH (Et) S (O)2CFThree
D2-37a CH2CH (Et) S (O)2CH2CFThree
D2-37a CH (Me) CH (Me) SMe
D2-37a CH (Me) CH (Me) SEt
D2-37a CH (Me) CH (Me) SCFThree
D2-37a CH (Me) CH (Me) SCH2CFThree
D2-37a CH (Me) CH (Me) S (O) Me
D2-37a CH (Me) CH (Me) S (O) Et
D2-37a CH (Me) CH (Me) S (O) CFThree
D2-37a CH (Me) CH (Me) S (O) CH2CFThree
D2-37a CH (Me) CH (Me) S (O)2Me
D2-37a CH (Me) CH (Me) S (O)2Et
D2-37a CH (Me) CH (Me) S (O)2CFThree
D2-37a CH (Me) CH (Me) S (O)2CH2CFThree
D2-38a CH2SMe
D2-38a CH2SEt
D2-38a CH2SCFThree
D2-38a CH2SCH2CFThree
D2-38a CH2S (O) Me
D2-38a CH2S (O) Et
D2-38a CH2S (O) CFThree
D2-38a CH2S (O) CH2CFThree
D2-38a CH2S (O)2Me
D2-38a CH2S (O)2Et
D2-38a CH2S (O)2CFThree
D2-38a CH2S (O)2CH2CFThree
D2-38a CH (Me) SMe
D2-38a CH (Me) SEt
D2-38a CH (Me) SCFThree
D2-38a CH (Me) SCH2CFThree
D2-38a CH (Me) S (O) Me
D2-38a CH (Me) S (O) Et
D2-38a CH (Me) S (O) CFThree
D2-38a CH (Me) S (O) CH2CFThree
D2-38a CH (Me) S (O)2Me
D2-38a CH (Me) S (O)2Et
D2-38a CH (Me) S (O)2CFThree
D2-38a CH (Me) S (O)2CH2CFThree
D2-38a CH (Et) SMe
D2-38a CH (Et) SEt
D2-38a CH (Et) SCFThree
D2-38a CH (Et) SCH2CFThree
D2-38a CH (Et) S (O) Me
D2-38a CH (Et) S (O) Et
D2-38a CH (Et) S (O) CFThree
D2-38a CH (Et) S (O) CH2CFThree
D2-38a CH (Et) S (O)2Me
D2-38a CH (Et) S (O)2Et
D2-38a CH (Et) S (O)2CFThree
D2-38a CH (Et) S (O)2CH2CFThree
D2-38a CH (n-Pr) SMe
D2-38a CH (n-Pr) SEt
D2-38a CH (n-Pr) SCFThree
D2-38a CH (n-Pr) SCH2CFThree
D2-38a CH (n-Pr) S (O) Me
D2-38a CH (n-Pr) S (O) Et
D2-38a CH (n-Pr) S (O) CFThree
D2-38a CH (n-Pr) S (O) CH2CFThree
D2-38a CH (n-Pr) S (O)2Me
D2-38a CH (n-Pr) S (O)2Et
D2-38a CH (n-Pr) S (O)2CFThree
D2-38a CH (n-Pr) S (O)2CH2CFThree
D2-38a CH (i-Pr) SMe
D2-38a CH (i-Pr) SEt
D2-38a CH (i-Pr) SCFThree
D2-38a CH (i-Pr) SCH2CFThree
D2-38a CH (i-Pr) S (O) Me
D2-38a CH (i-Pr) S (O) Et
D2-38a CH (i-Pr) S (O) CFThree
D2-38a CH (i-Pr) S (O) CH2CFThree
D2-38a CH (i-Pr) S (O)2Me
D2-38a CH (i-Pr) S (O)2Et
D2-38a CH (i-Pr) S (O)2CFThree
D2-38a CH (i-Pr) S (O)2CH2CFThree
D2-38a CH (n-Bu) SMe
D2-38a CH (n-Bu) SEt
D2-38a CH (n-Bu) SCFThree
D2-38a CH (n-Bu) SCH2CFThree
D2-38a CH (n-Bu) S (O) Me
D2-38a CH (n-Bu) S (O) Et
D2-38a CH (n-Bu) S (O) CFThree
D2-38a CH (n-Bu) S (O) CH2CFThree
D2-38a CH (n-Bu) S (O)2Me
D2-38a CH (n-Bu) S (O)2Et
D2-38a CH (n-Bu) S (O)2CFThree
D2-38a CH (n-Bu) S (O)2CH2CFThree
D2-38a CH (i-Bu) SMe
D2-38a CH (i-Bu) SEt
D2-38a CH (i-Bu) SCFThree
D2-38a CH (i-Bu) SCH2CFThree
D2-38a CH (i-Bu) S (O) Me
D2-38a CH (i-Bu) S (O) Et
D2-38a CH (i-Bu) S (O) CFThree
D2-38a CH (i-Bu) S (O) CH2CFThree
D2-38a CH (i-Bu) S (O)2Me
D2-38a CH (i-Bu) S (O)2Et
D2-38a CH (i-Bu) S (O)2CFThree
D2-38a CH (i-Bu) S (O)2CH2CFThree
D2-38a CH (s-Bu) SMe
D2-38a CH (s-Bu) SEt
D2-38a CH (s-Bu) SCFThree
D2-38a CH (s-Bu) SCH2CFThree
D2-38a CH (s-Bu) S (O) Me
D2-38a CH (s-Bu) S (O) Et
D2-38a CH (s-Bu) S (O) CFThree
D2-38a CH (s-Bu) S (O) CH2CFThree
D2-38a CH (s-Bu) S (O)2Me
D2-38a CH (s-Bu) S (O)2Et
D2-38a CH (s-Bu) S (O)2CFThree
D2-38a CH (s-Bu) S (O)2CH2CFThree
D2-38a CH (t-Bu) SMe
D2-38a CH (t-Bu) SEt
D2-38a CH (t-Bu) SCFThree
D2-38a CH (t-Bu) SCH2CFThree
D2-38a CH (t-Bu) S (O) Me
D2-38a CH (t-Bu) S (O) Et
D2-38a CH (t-Bu) S (O) CFThree
D2-38a CH (t-Bu) S (O) CH2CFThree
D2-38a CH (t-Bu) S (O)2Me
D2-38a CH (t-Bu) S (O)2Et
D2-38a CH (t-Bu) S (O)2CFThree
D2-38a CH (t-Bu) S (O)2CH2CFThree
D2-38a CH (CFThreeSMe
D2-38a CH (CFThree) SEt
D2-38a CH (CFThree) SCFThree
D2-38a CH (CFThree) SCH2CFThree
D2-38a CH (CFThree) S (O) Me
D2-38a CH (CFThree) S (O) Et
D2-38a CH (CFThree) S (O) CFThree
D2-38a CH (CFThree) S (O) CH2CFThree
D2-38a CH (CFThree) S (O)2Me
D2-38a CH (CFThree) S (O)2Et
D2-38a CH (CFThree) S (O)2CFThree
D2-38a CH (CFThree) S (O)2CH2CFThree
D2-38a CH2CH2SMe
D2-38a CH2CH2SEt
D2-38a CH2CH2SCFThree
D2-38a CH2CH2SCH2CFThree
D2-38a CH2CH2S (O) Me
D2-38a CH2CH2S (O) Et
D2-38a CH2CH2S (O) CFThree
D2-38a CH2CH2S (O) CH2CFThree
D2-38a CH2CH2S (O)2Me
D2-38a CH2CH2S (O)2Et
D2-38a CH2CH2S (O)2CFThree
D2-38a CH2CH2S (O)2CH2CFThree
D2-38a CH (Me) CH2SMe
D2-38a CH (Me) CH2SEt
D2-38a CH (Me) CH2SCFThree
D2-38a CH (Me) CH2SCH2CFThree
D2-38a CH (Me) CH2S (O) Me
D2-38a CH (Me) CH2S (O) Et
D2-38a CH (Me) CH2S (O) CFThree
D2-38a CH (Me) CH2S (O) CH2CFThree
D2-38a CH (Me) CH2S (O)2Me
D2-38a CH (Me) CH2S (O)2Et
D2-38a CH (Me) CH2S (O)2CFThree
D2-38a CH (Me) CH2S (O)2CH2CFThree
D2-38a CH (Et) CH2SMe
D2-38a CH (Et) CH2SEt
D2-38a CH (Et) CH2SCFThree
D2-38a CH (Et) CH2SCH2CFThree
D2-38a CH (Et) CH2S (O) Me
D2-38a CH (Et) CH2S (O) Et
D2-38a CH (Et) CH2S (O) CFThree
D2-38a CH (Et) CH2S (O) CH2CFThree
D2-38a CH (Et) CH2S (O)2Me
D2-38a CH (Et) CH2S (O)2Et
D2-38a CH (Et) CH2S (O)2CFThree
D2-38a CH (Et) CH2S (O)2CH2CFThree
D2-38a C (Me)2CH2SMe
D2-38a C (Me)2CH2SEt
D2-38a C (Me)2CH2SCFThree
D2-38a C (Me)2CH2SCH2CFThree
D2-38a C (Me)2CH2S (O) Me
D2-38a C (Me)2CH2S (O) Et
D2-38a C (Me)2CH2S (O) CFThree
D2-38a C (Me)2CH2S (O) CH2CFThree
D2-38a C (Me)2CH2S (O)2Me
D2-38a C (Me)2CH2S (O)2Et
D2-38a C (Me)2CH2S (O)2CFThree
D2-38a C (Me)2CH2S (O)2CH2CFThree
D2-38a CH2CH (Me) SMe
D2-38a CH2CH (Me) SEt
D2-38a CH2CH (Me) SCFThree
D2-38a CH2CH (Me) SCH2CFThree
D2-38a CH2CH (Me) S (O) Me
D2-38a CH2CH (Me) S (O) Et
D2-38a CH2CH (Me) S (O) CFThree
D2-38a CH2CH (Me) S (O) CH2CFThree
D2-38a CH2CH (Me) S (O)2Me
D2-38a CH2CH (Me) S (O)2Et
D2-38a CH2CH (Me) S (O)2CFThree
D2-38a CH2CH (Me) S (O)2CH2CFThree
D2-38a CH2CH (Et) SMe
D2-38a CH2CH (Et) SEt
D2-38a CH2CH (Et) SCFThree
D2-38a CH2CH (Et) SCH2CFThree
D2-38a CH2CH (Et) S (O) Me
D2-38a CH2CH (Et) S (O) Et
D2-38a CH2CH (Et) S (O) CFThree
D2-38a CH2CH (Et) S (O) CH2CFThree
D2-38a CH2CH (Et) S (O)2Me
D2-38a CH2CH (Et) S (O)2Et
D2-38a CH2CH (Et) S (O)2CFThree
D2-38a CH2CH (Et) S (O)2CH2CFThree
D2-38a CH (Me) CH (Me) SMe
D2-38a CH (Me) CH (Me) SEt
D2-38a CH (Me) CH (Me) SCFThree
D2-38a CH (Me) CH (Me) SCH2CFThree
D2-38a CH (Me) CH (Me) S (O) Me
D2-38a CH (Me) CH (Me) S (O) Et
D2-38a CH (Me) CH (Me) S (O) CFThree
D2-38a CH (Me) CH (Me) S (O) CH2CFThree
D2-38a CH (Me) CH (Me) S (O)2Me
D2-38a CH (Me) CH (Me) S (O)2Et
D2-38a CH (Me) CH (Me) S (O)2CFThree
D2-38a CH (Me) CH (Me) S (O)2CH2CFThree
D2-92a CH2SMe
D2-92a CH2SEt
D2-92a CH2SCFThree
D2-92a CH2SCH2CFThree
D2-92a CH2S (O) Me
D2-92a CH2S (O) Et
D2-92a CH2S (O) CFThree
D2-92a CH2S (O) CH2CFThree
D2-92a CH2S (O)2Me
D2-92a CH2S (O)2Et
D2-92a CH2S (O)2CFThree
D2-92a CH2S (O)2CH2CFThree
D2-92a CH (Me) SMe
D2-92a CH (Me) SEt
D2-92a CH (Me) SCFThree
D2-92a CH (Me) SCH2CFThree
D2-92a CH (Me) S (O) Me
D2-92a CH (Me) S (O) Et
D2-92a CH (Me) S (O) CFThree
D2-92a CH (Me) S (O) CH2CFThree
D2-92a CH (Me) S (O)2Me
D2-92a CH (Me) S (O)2Et
D2-92a CH (Me) S (O)2CFThree
D2-92a CH (Me) S (O)2CH2CFThree
D2-92a CH (Et) SMe
D2-92a CH (Et) SEt
D2-92a CH (Et) SCFThree
D2-92a CH (Et) SCH2CFThree
D2-92a CH (Et) S (O) Me
D2-92a CH (Et) S (O) Et
D2-92a CH (Et) S (O) CFThree
D2-92a CH (Et) S (O) CH2CFThree
D2-92a CH (Et) S (O)2Me
D2-92a CH (Et) S (O)2Et
D2-92a CH (Et) S (O)2CFThree
D2-92a CH (Et) S (O)2CH2CFThree
D2-92a CH (n-Pr) SMe
D2-92a CH (n-Pr) SEt
D2-92a CH (n-Pr) SCFThree
D2-92a CH (n-Pr) SCH2CFThree
D2-92a CH (n-Pr) S (O) Me
D2-92a CH (n-Pr) S (O) Et
D2-92a CH (n-Pr) S (O) CFThree
D2-92a CH (n-Pr) S (O) CH2CFThree
D2-92a CH (n-Pr) S (O)2Me
D2-92a CH (n-Pr) S (O)2Et
D2-92a CH (n-Pr) S (O)2CFThree
D2-92a CH (n-Pr) S (O)2CH2CFThree
D2-92a CH (i-Pr) SMe
D2-92a CH (i-Pr) SEt
D2-92a CH (i-Pr) SCFThree
D2-92a CH (i-Pr) SCH2CFThree
D2-92a CH (i-Pr) S (O) Me
D2-92a CH (i-Pr) S (O) Et
D2-92a CH (i-Pr) S (O) CFThree
D2-92a CH (i-Pr) S (O) CH2CFThree
D2-92a CH (i-Pr) S (O)2Me
D2-92a CH (i-Pr) S (O)2Et
D2-92a CH (i-Pr) S (O)2CFThree
D2-92a CH (i-Pr) S (O)2CH2CFThree
D2-92a CH (n-Bu) SMe
D2-92a CH (n-Bu) SEt
D2-92a CH (n-Bu) SCFThree
D2-92a CH (n-Bu) SCH2CFThree
D2-92a CH (n-Bu) S (O) Me
D2-92a CH (n-Bu) S (O) Et
D2-92a CH (n-Bu) S (O) CFThree
D2-92a CH (n-Bu) S (O) CH2CFThree
D2-92a CH (n-Bu) S (O)2Me
D2-92a CH (n-Bu) S (O)2Et
D2-92a CH (n-Bu) S (O)2CFThree
D2-92a CH (n-Bu) S (O)2CH2CFThree
D2-92a CH (i-Bu) SMe
D2-92a CH (i-Bu) SEt
D2-92a CH (i-Bu) SCFThree
D2-92a CH (i-Bu) SCH2CFThree
D2-92a CH (i-Bu) S (O) Me
D2-92a CH (i-Bu) S (O) Et
D2-92a CH (i-Bu) S (O) CFThree
D2-92a CH (i-Bu) S (O) CH2CFThree
D2-92a CH (i-Bu) S (O)2Me
D2-92a CH (i-Bu) S (O)2Et
D2-92a CH (i-Bu) S (O)2CFThree
D2-92a CH (i-Bu) S (O)2CH2CFThree
D2-92a CH (s-Bu) SMe
D2-92a CH (s-Bu) SEt
D2-92a CH (s-Bu) SCFThree
D2-92a CH (s-Bu) SCH2CFThree
D2-92a CH (s-Bu) S (O) Me
D2-92a CH (s-Bu) S (O) Et
D2-92a CH (s-Bu) S (O) CFThree
D2-92a CH (s-Bu) S (O) CH2CFThree
D2-92a CH (s-Bu) S (O)2Me
D2-92a CH (s-Bu) S (O)2Et
D2-92a CH (s-Bu) S (O)2CFThree
D2-92a CH (s-Bu) S (O)2CH2CFThree
D2-92a CH (t-Bu) SMe
D2-92a CH (t-Bu) SEt
D2-92a CH (t-Bu) SCFThree
D2-92a CH (t-Bu) SCH2CFThree
D2-92a CH (t-Bu) S (O) Me
D2-92a CH (t-Bu) S (O) Et
D2-92a CH (t-Bu) S (O) CFThree
D2-92a CH (t-Bu) S (O) CH2CFThree
D2-92a CH (t-Bu) S (O)2Me
D2-92a CH (t-Bu) S (O)2Et
D2-92a CH (t-Bu) S (O)2CFThree
D2-92a CH (t-Bu) S (O)2CH2CFThree
D2-92a CH (CFThreeSMe
D2-92a CH (CFThree) SEt
D2-92a CH (CFThree) SCFThree
D2-92a CH (CFThree) SCH2CFThree
D2-92a CH (CFThree) S (O) Me
D2-92a CH (CFThree) S (O) Et
D2-92a CH (CFThree) S (O) CFThree
D2-92a CH (CFThree) S (O) CH2CFThree
D2-92a CH (CFThree) S (O)2Me
D2-92a CH (CFThree) S (O)2Et
D2-92a CH (CFThree) S (O)2CFThree
D2-92a CH (CFThree) S (O)2CH2CFThree
D2-92a CH2CH2SMe
D2-92a CH2CH2SEt
D2-92a CH2CH2SCFThree
D2-92a CH2CH2SCH2CFThree
D2-92a CH2CH2S (O) Me
D2-92a CH2CH2S (O) Et
D2-92a CH2CH2S (O) CFThree
D2-92a CH2CH2S (O) CH2CFThree
D2-92a CH2CH2S (O)2Me
D2-92a CH2CH2S (O)2Et
D2-92a CH2CH2S (O)2CFThree
D2-92a CH2CH2S (O)2CH2CFThree
D2-92a CH (Me) CH2SMe
D2-92a CH (Me) CH2SEt
D2-92a CH (Me) CH2SCFThree
D2-92a CH (Me) CH2SCH2CFThree
D2-92a CH (Me) CH2S (O) Me
D2-92a CH (Me) CH2S (O) Et
D2-92a CH (Me) CH2S (O) CFThree
D2-92a CH (Me) CH2S (O) CH2CFThree
D2-92a CH (Me) CH2S (O)2Me
D2-92a CH (Me) CH2S (O)2Et
D2-92a CH (Me) CH2S (O)2CFThree
D2-92a CH (Me) CH2S (O)2CH2CFThree
D2-92a CH (Et) CH2SMe
D2-92a CH (Et) CH2SEt
D2-92a CH (Et) CH2SCFThree
D2-92a CH (Et) CH2SCH2CFThree
D2-92a CH (Et) CH2S (O) Me
D2-92a CH (Et) CH2S (O) Et
D2-92a CH (Et) CH2S (O) CFThree
D2-92a CH (Et) CH2S (O) CH2CFThree
D2-92a CH (Et) CH2S (O)2Me
D2-92a CH (Et) CH2S (O)2Et
D2-92a CH (Et) CH2S (O)2CFThree
D2-92a CH (Et) CH2S (O)2CH2CFThree
D2-92a C (Me)2CH2SMe
D2-92a C (Me)2CH2SEt
D2-92a C (Me)2CH2SCFThree
D2-92a C (Me)2CH2SCH2CFThree
D2-92a C (Me)2CH2S (O) Me
D2-92a C (Me)2CH2S (O) Et
D2-92a C (Me)2CH2S (O) CFThree
D2-92a C (Me)2CH2S (O) CH2CFThree
D2-92a C (Me)2CH2S (O)2Me
D2-92a C (Me)2CH2S (O)2Et
D2-92a C (Me)2CH2S (O)2CFThree
D2-92a C (Me)2CH2S (O)2CH2CFThree
D2-92a CH2CH (Me) SMe
D2-92a CH2CH (Me) SEt
D2-92a CH2CH (Me) SCFThree
D2-92a CH2CH (Me) SCH2CFThree
D2-92a CH2CH (Me) S (O) Me
D2-92a CH2CH (Me) S (O) Et
D2-92a CH2CH (Me) S (O) CFThree
D2-92a CH2CH (Me) S (O) CH2CFThree
D2-92a CH2CH (Me) S (O)2Me
D2-92a CH2CH (Me) S (O)2Et
D2-92a CH2CH (Me) S (O)2CFThree
D2-92a CH2CH (Me) S (O)2CH2CFThree
D2-92a CH2CH (Et) SMe
D2-92a CH2CH (Et) SEt
D2-92a CH2CH (Et) SCFThree
D2-92a CH2CH (Et) SCH2CFThree
D2-92a CH2CH (Et) S (O) Me
D2-92a CH2CH (Et) S (O) Et
D2-92a CH2CH (Et) S (O) CFThree
D2-92a CH2CH (Et) S (O) CH2CFThree
D2-92a CH2CH (Et) S (O)2Me
D2-92a CH2CH (Et) S (O)2Et
D2-92a CH2CH (Et) S (O)2CFThree
D2-92a CH2CH (Et) S (O)2CH2CFThree
D2-92a CH (Me) CH (Me) SMe
D2-92a CH (Me) CH (Me) SEt
D2-92a CH (Me) CH (Me) SCFThree
D2-92a CH (Me) CH (Me) SCH2CFThree
D2-92a CH (Me) CH (Me) S (O) Me
D2-92a CH (Me) CH (Me) S (O) Et
D2-92a CH (Me) CH (Me) S (O) CFThree
D2-92a CH (Me) CH (Me) S (O) CH2CFThree
D2-92a CH (Me) CH (Me) S (O)2Me
D2-92a CH (Me) CH (Me) S (O)2Et
D2-92a CH (Me) CH (Me) S (O)2CFThree
D2-92a CH (Me) CH (Me) S (O)2CH2CFThree
CH (Me) SMe CH2SMe
CH (Me) SMe CH2SEt
CH (Me) SMe CH2SCFThree
CH (Me) SMe CH2SCH2CFThree
CH (Me) SMe CH2S (O) Me
CH (Me) SMe CH2S (O) Et
CH (Me) SMe CH2S (O) CFThree
CH (Me) SMe CH2S (O) CH2CFThree
CH (Me) SMe CH2S (O)2Me
CH (Me) SMe CH2S (O)2Et
CH (Me) SMe CH2S (O)2CFThree
CH (Me) SMe CH2S (O)2CH2CFThree
CH (Me) SMe CH (Me) SMe
CH (Me) SMe CH (Me) SEt
CH (Me) SMe CH (Me) SCFThree
CH (Me) SMe CH (Me) SCH2CFThree
CH (Me) SMe CH (Me) S (O) Me
CH (Me) SMe CH (Me) S (O) Et
CH (Me) SMe CH (Me) S (O) CFThree
CH (Me) SMe CH (Me) S (O) CH2CFThree
CH (Me) SMe CH (Me) S (O)2Me
CH (Me) SMe CH (Me) S (O)2Et
CH (Me) SMe CH (Me) S (O)2CFThree
CH (Me) SMe CH (Me) S (O)2CH2CFThree
CH (Me) SMe CH (Et) SMe
CH (Me) SMe CH (Et) SEt
CH (Me) SMe CH (Et) SCFThree
CH (Me) SMe CH (Et) SCH2CFThree
CH (Me) SMe CH (Et) S (O) Me
CH (Me) SMe CH (Et) S (O) Et
CH (Me) SMe CH (Et) S (O) CFThree
CH (Me) SMe CH (Et) S (O) CH2CFThree
CH (Me) SMe CH (Et) S (O)2Me
CH (Me) SMe CH (Et) S (O)2Et
CH (Me) SMe CH (Et) S (O)2CFThree
CH (Me) SMe CH (Et) S (O)2CH2CFThree
CH (Me) SMe CH (n-Pr) SMe
CH (Me) SMe CH (n-Pr) SEt
CH (Me) SMe CH (n-Pr) SCFThree
CH (Me) SMe CH (n-Pr) SCH2CFThree
CH (Me) SMe CH (n-Pr) S (O) Me
CH (Me) SMe CH (n-Pr) S (O) Et
CH (Me) SMe CH (n-Pr) S (O) CFThree
CH (Me) SMe CH (n-Pr) S (O) CH2CFThree
CH (Me) SMe CH (n-Pr) S (O)2Me
CH (Me) SMe CH (n-Pr) S (O)2Et
CH (Me) SMe CH (n-Pr) S (O)2CFThree
CH (Me) SMe CH (n-Pr) S (O)2CH2CFThree
CH (Me) SMe CH (i-Pr) SMe
CH (Me) SMe CH (i-Pr) SEt
CH (Me) SMe CH (i-Pr) SCFThree
CH (Me) SMe CH (i-Pr) SCH2CFThree
CH (Me) SMe CH (i-Pr) S (O) Me
CH (Me) SMe CH (i-Pr) S (O) Et
CH (Me) SMe CH (i-Pr) S (O) CFThree
CH (Me) SMe CH (i-Pr) S (O) CH2CFThree
CH (Me) SMe CH (i-Pr) S (O)2Me
CH (Me) SMe CH (i-Pr) S (O)2Et
CH (Me) SMe CH (i-Pr) S (O)2CFThree
CH (Me) SMe CH (i-Pr) S (O)2CH2CFThree
CH (Me) SMe CH (n-Bu) SMe
CH (Me) SMe CH (n-Bu) SEt
CH (Me) SMe CH (n-Bu) SCFThree
CH (Me) SMe CH (n-Bu) SCH2CFThree
CH (Me) SMe CH (n-Bu) S (O) Me
CH (Me) SMe CH (n-Bu) S (O) Et
CH (Me) SMe CH (n-Bu) S (O) CFThree
CH (Me) SMe CH (n-Bu) S (O) CH2CFThree
CH (Me) SMe CH (n-Bu) S (O)2Me
CH (Me) SMe CH (n-Bu) S (O)2Et
CH (Me) SMe CH (n-Bu) S (O)2CFThree
CH (Me) SMe CH (n-Bu) S (O)2CH2CFThree
CH (Me) SMe CH (i-Bu) SMe
CH (Me) SMe CH (i-Bu) SEt
CH (Me) SMe CH (i-Bu) SCFThree
CH (Me) SMe CH (i-Bu) SCH2CFThree
CH (Me) SMe CH (i-Bu) S (O) Me
CH (Me) SMe CH (i-Bu) S (O) Et
CH (Me) SMe CH (i-Bu) S (O) CFThree
CH (Me) SMe CH (i-Bu) S (O) CH2CFThree
CH (Me) SMe CH (i-Bu) S (O)2Me
CH (Me) SMe CH (i-Bu) S (O)2Et
CH (Me) SMe CH (i-Bu) S (O)2CFThree
CH (Me) SMe CH (i-Bu) S (O)2CH2CFThree
CH (Me) SMe CH (s-Bu) SMe
CH (Me) SMe CH (s-Bu) SEt
CH (Me) SMe CH (s-Bu) SCFThree
CH (Me) SMe CH (s-Bu) SCH2CFThree
CH (Me) SMe CH (s-Bu) S (O) Me
CH (Me) SMe CH (s-Bu) S (O) Et
CH (Me) SMe CH (s-Bu) S (O) CFThree
CH (Me) SMe CH (s-Bu) S (O) CH2CFThree
CH (Me) SMe CH (s-Bu) S (O)2Me
CH (Me) SMe CH (s-Bu) S (O)2Et
CH (Me) SMe CH (s-Bu) S (O)2CFThree
CH (Me) SMe CH (s-Bu) S (O)2CH2CFThree
CH (Me) SMe CH (t-Bu) SMe
CH (Me) SMe CH (t-Bu) SEt
CH (Me) SMe CH (t-Bu) SCFThree
CH (Me) SMe CH (t-Bu) SCH2CFThree
CH (Me) SMe CH (t-Bu) S (O) Me
CH (Me) SMe CH (t-Bu) S (O) Et
CH (Me) SMe CH (t-Bu) S (O) CFThree
CH (Me) SMe CH (t-Bu) S (O) CH2CFThree
CH (Me) SMe CH (t-Bu) S (O)2Me
CH (Me) SMe CH (t-Bu) S (O)2Et
CH (Me) SMe CH (t-Bu) S (O)2CFThree
CH (Me) SMe CH (t-Bu) S (O)2CH2CFThree
CH (Me) SMe CH (CFThreeSMe
CH (Me) SMe CH (CFThree) SEt
CH (Me) SMe CH (CFThree) SCFThree
CH (Me) SMe CH (CFThree) SCH2CFThree
CH (Me) SMe CH (CFThree) S (O) Me
CH (Me) SMe CH (CFThree) S (O) Et
CH (Me) SMe CH (CFThree) S (O) CFThree
CH (Me) SMe CH (CFThree) S (O) CH2CFThree
CH (Me) SMe CH (CFThree) S (O)2Me
CH (Me) SMe CH (CFThree) S (O)2Et
CH (Me) SMe CH (CFThree) S (O)2CFThree
CH (Me) SMe CH (CFThree) S (O)2CH2CFThree
CH (Me) SMe CH2CH2SMe
CH (Me) SMe CH2CH2SEt
CH (Me) SMe CH2CH2SCFThree
CH (Me) SMe CH2CH2SCH2CFThree
CH (Me) SMe CH2CH2S (O) Me
CH (Me) SMe CH2CH2S (O) Et
CH (Me) SMe CH2CH2S (O) CFThree
CH (Me) SMe CH2CH2S (O) CH2CFThree
CH (Me) SMe CH2CH2S (O)2Me
CH (Me) SMe CH2CH2S (O)2Et
CH (Me) SMe CH2CH2S (O)2CFThree
CH (Me) SMe CH2CH2S (O)2CH2CFThree
CH (Me) SMe CH (Me) CH2SMe
CH (Me) SMe CH (Me) CH2SEt
CH (Me) SMe CH (Me) CH2SCFThree
CH (Me) SMe CH (Me) CH2SCH2CFThree
CH (Me) SMe CH (Me) CH2S (O) Me
CH (Me) SMe CH (Me) CH2S (O) Et
CH (Me) SMe CH (Me) CH2S (O) CFThree
CH (Me) SMe CH (Me) CH2S (O) CH2CFThree
CH (Me) SMe CH (Me) CH2S (O)2Me
CH (Me) SMe CH (Me) CH2S (O)2Et
CH (Me) SMe CH (Me) CH2S (O)2CFThree
CH (Me) SMe CH (Me) CH2S (O)2CH2CFThree
CH (Me) SMe CH (Et) CH2SMe
CH (Me) SMe CH (Et) CH2SEt
CH (Me) SMe CH (Et) CH2SCFThree
CH (Me) SMe CH (Et) CH2SCH2CFThree
CH (Me) SMe CH (Et) CH2S (O) Me
CH (Me) SMe CH (Et) CH2S (O) Et
CH (Me) SMe CH (Et) CH2S (O) CFThree
CH (Me) SMe CH (Et) CH2S (O) CH2CFThree
CH (Me) SMe CH (Et) CH2S (O)2Me
CH (Me) SMe CH (Et) CH2S (O)2Et
CH (Me) SMe CH (Et) CH2S (O)2CFThree
CH (Me) SMe CH (Et) CH2S (O)2CH2CFThree
CH (Me) SMe C (Me)2CH2SMe
CH (Me) SMe C (Me)2CH2SEt
CH (Me) SMe C (Me)2CH2SCFThree
CH (Me) SMe C (Me)2CH2SCH2CFThree
CH (Me) SMe C (Me)2CH2S (O) Me
CH (Me) SMe C (Me)2CH2S (O) Et
CH (Me) SMe C (Me)2CH2S (O) CFThree
CH (Me) SMe C (Me)2CH2S (O) CH2CFThree
CH (Me) SMe C (Me)2CH2S (O)2Me
CH (Me) SMe C (Me)2CH2S (O)2Et
CH (Me) SMe C (Me)2CH2S (O)2CFThree
CH (Me) SMe C (Me)2CH2S (O)2CH2CFThree
CH (Me) SMe CH2CH (Me) SMe
CH (Me) SMe CH2CH (Me) SEt
CH (Me) SMe CH2CH (Me) SCFThree
CH (Me) SMe CH2CH (Me) SCH2CFThree
CH (Me) SMe CH2CH (Me) S (O) Me
CH (Me) SMe CH2CH (Me) S (O) Et
CH (Me) SMe CH2CH (Me) S (O) CFThree
CH (Me) SMe CH2CH (Me) S (O) CH2CFThree
CH (Me) SMe CH2CH (Me) S (O)2Me
CH (Me) SMe CH2CH (Me) S (O)2Et
CH (Me) SMe CH2CH (Me) S (O)2CFThree
CH (Me) SMe CH2CH (Me) S (O)2CH2CFThree
CH (Me) SMe CH2CH (Et) SMe
CH (Me) SMe CH2CH (Et) SEt
CH (Me) SMe CH2CH (Et) SCFThree
CH (Me) SMe CH2CH (Et) SCH2CFThree
CH (Me) SMe CH2CH (Et) S (O) Me
CH (Me) SMe CH2CH (Et) S (O) Et
CH (Me) SMe CH2CH (Et) S (O) CFThree
CH (Me) SMe CH2CH (Et) S (O) CH2CFThree
CH (Me) SMe CH2CH (Et) S (O)2Me
CH (Me) SMe CH2CH (Et) S (O)2Et
CH (Me) SMe CH2CH (Et) S (O)2CFThree
CH (Me) SMe CH2CH (Et) S (O)2CH2CFThree
CH (Me) SMe CH (Me) CH (Me) SMe
CH (Me) SMe CH (Me) CH (Me) SEt
CH (Me) SMe CH (Me) CH (Me) SCFThree
CH (Me) SMe CH (Me) CH (Me) SCH2CFThree
CH (Me) SMe CH (Me) CH (Me) S (O) Me
CH (Me) SMe CH (Me) CH (Me) S (O) Et
CH (Me) SMe CH (Me) CH (Me) S (O) CFThree
CH (Me) SMe CH (Me) CH (Me) S (O) CH2CFThree
CH (Me) SMe CH (Me) CH (Me) S (O)2Me
CH (Me) SMe CH (Me) CH (Me) S (O)2Et
CH (Me) SMe CH (Me) CH (Me) S (O)2CFThree
CH (Me) SMe CH (Me) CH (Me) S (O)2CH2CFThree
C (O) Me CH2SMe
C (O) Me CH2SEt
C (O) Me CH2SCFThree
C (O) Me CH2SCH2CFThree
C (O) Me CH2S (O) Me
C (O) Me CH2S (O) Et
C (O) Me CH2S (O) CFThree
C (O) Me CH2S (O) CH2CFThree
C (O) Me CH2S (O)2Me
C (O) Me CH2S (O)2Et
C (O) Me CH2S (O)2CFThree
C (O) Me CH2S (O)2CH2CFThree
C (O) Me CH (Me) SMe
C (O) Me CH (Me) SEt
C (O) Me CH (Me) SCFThree
C (O) Me CH (Me) SCH2CFThree
C (O) Me CH (Me) S (O) Me
C (O) Me CH (Me) S (O) Et
C (O) Me CH (Me) S (O) CFThree
C (O) Me CH (Me) S (O) CH2CFThree
C (O) Me CH (Me) S (O)2Me
C (O) Me CH (Me) S (O)2Et
C (O) Me CH (Me) S (O)2CFThree
C (O) Me CH (Me) S (O)2CH2CFThree
C (O) Me CH (Et) SMe
C (O) Me CH (Et) SEt
C (O) Me CH (Et) SCFThree
C (O) Me CH (Et) SCH2CFThree
C (O) Me CH (Et) S (O) Me
C (O) Me CH (Et) S (O) Et
C (O) Me CH (Et) S (O) CFThree
C (O) Me CH (Et) S (O) CH2CFThree
C (O) Me CH (Et) S (O)2Me
C (O) Me CH (Et) S (O)2Et
C (O) Me CH (Et) S (O)2CFThree
C (O) Me CH (Et) S (O)2CH2CFThree
C (O) Me CH (n-Pr) SMe
C (O) Me CH (n-Pr) SEt
C (O) Me CH (n-Pr) SCFThree
C (O) Me CH (n-Pr) SCH2CFThree
C (O) Me CH (n-Pr) S (O) Me
C (O) Me CH (n-Pr) S (O) Et
C (O) Me CH (n-Pr) S (O) CFThree
C (O) Me CH (n-Pr) S (O) CH2CFThree
C (O) Me CH (n-Pr) S (O)2Me
C (O) Me CH (n-Pr) S (O)2Et
C (O) Me CH (n-Pr) S (O)2CFThree
C (O) Me CH (n-Pr) S (O)2CH2CFThree
C (O) Me CH (i-Pr) SMe
C (O) Me CH (i-Pr) SEt
C (O) Me CH (i-Pr) SCFThree
C (O) Me CH (i-Pr) SCH2CFThree
C (O) Me CH (i-Pr) S (O) Me
C (O) Me CH (i-Pr) S (O) Et
C (O) Me CH (i-Pr) S (O) CFThree
C (O) Me CH (i-Pr) S (O) CH2CFThree
C (O) Me CH (i-Pr) S (O)2Me
C (O) Me CH (i-Pr) S (O)2Et
C (O) Me CH (i-Pr) S (O)2CFThree
C (O) Me CH (i-Pr) S (O)2CH2CFThree
C (O) Me CH (n-Bu) SMe
C (O) Me CH (n-Bu) SEt
C (O) Me CH (n-Bu) SCFThree
C (O) Me CH (n-Bu) SCH2CFThree
C (O) Me CH (n-Bu) S (O) Me
C (O) Me CH (n-Bu) S (O) Et
C (O) Me CH (n-Bu) S (O) CFThree
C (O) Me CH (n-Bu) S (O) CH2CFThree
C (O) Me CH (n-Bu) S (O)2Me
C (O) Me CH (n-Bu) S (O)2Et
C (O) Me CH (n-Bu) S (O)2CFThree
C (O) Me CH (n-Bu) S (O)2CH2CFThree
C (O) Me CH (i-Bu) SMe
C (O) Me CH (i-Bu) SEt
C (O) Me CH (i-Bu) SCFThree
C (O) Me CH (i-Bu) SCH2CFThree
C (O) Me CH (i-Bu) S (O) Me
C (O) Me CH (i-Bu) S (O) Et
C (O) Me CH (i-Bu) S (O) CFThree
C (O) Me CH (i-Bu) S (O) CH2CFThree
C (O) Me CH (i-Bu) S (O)2Me
C (O) Me CH (i-Bu) S (O)2Et
C (O) Me CH (i-Bu) S (O)2CFThree
C (O) Me CH (i-Bu) S (O)2CH2CFThree
C (O) Me CH (s-Bu) SMe
C (O) Me CH (s-Bu) SEt
C (O) Me CH (s-Bu) SCFThree
C (O) Me CH (s-Bu) SCH2CFThree
C (O) Me CH (s-Bu) S (O) Me
C (O) Me CH (s-Bu) S (O) Et
C (O) Me CH (s-Bu) S (O) CFThree
C (O) Me CH (s-Bu) S (O) CH2CFThree
C (O) Me CH (s-Bu) S (O)2Me
C (O) Me CH (s-Bu) S (O)2Et
C (O) Me CH (s-Bu) S (O)2CFThree
C (O) Me CH (s-Bu) S (O)2CH2CFThree
C (O) Me CH (t-Bu) SMe
C (O) Me CH (t-Bu) SEt
C (O) Me CH (t-Bu) SCFThree
C (O) Me CH (t-Bu) SCH2CFThree
C (O) Me CH (t-Bu) S (O) Me
C (O) Me CH (t-Bu) S (O) Et
C (O) Me CH (t-Bu) S (O) CFThree
C (O) Me CH (t-Bu) S (O) CH2CFThree
C (O) Me CH (t-Bu) S (O)2Me
C (O) Me CH (t-Bu) S (O)2Et
C (O) Me CH (t-Bu) S (O)2CFThree
C (O) Me CH (t-Bu) S (O)2CH2CFThree
C (O) Me CH (CFThreeSMe
C (O) Me CH (CFThree) SEt
C (O) Me CH (CFThree) SCFThree
C (O) Me CH (CFThree) SCH2CFThree
C (O) Me CH (CFThree) S (O) Me
C (O) Me CH (CFThree) S (O) Et
C (O) Me CH (CFThree) S (O) CFThree
C (O) Me CH (CFThree) S (O) CH2CFThree
C (O) Me CH (CFThree) S (O)2Me
C (O) Me CH (CFThree) S (O)2Et
C (O) Me CH (CFThree) S (O)2CFThree
C (O) Me CH (CFThree) S (O)2CH2CFThree
C (O) Me CH2CH2SMe
C (O) Me CH2CH2SEt
C (O) Me CH2CH2SCFThree
C (O) Me CH2CH2SCH2CFThree
C (O) Me CH2CH2S (O) Me
C (O) Me CH2CH2S (O) Et
C (O) Me CH2CH2S (O) CFThree
C (O) Me CH2CH2S (O) CH2CFThree
C (O) Me CH2CH2S (O)2Me
C (O) Me CH2CH2S (O)2Et
C (O) Me CH2CH2S (O)2CFThree
C (O) Me CH2CH2S (O)2CH2CFThree
C (O) Me CH (Me) CH2SMe
C (O) Me CH (Me) CH2SEt
C (O) Me CH (Me) CH2SCFThree
C (O) Me CH (Me) CH2SCH2CFThree
C (O) Me CH (Me) CH2S (O) Me
C (O) Me CH (Me) CH2S (O) Et
C (O) Me CH (Me) CH2S (O) CFThree
C (O) Me CH (Me) CH2S (O) CH2CFThree
C (O) Me CH (Me) CH2S (O)2Me
C (O) Me CH (Me) CH2S (O)2Et
C (O) Me CH (Me) CH2S (O)2CFThree
C (O) Me CH (Me) CH2S (O)2CH2CFThree
C (O) Me CH (Et) CH2SMe
C (O) Me CH (Et) CH2SEt
C (O) Me CH (Et) CH2SCFThree
C (O) Me CH (Et) CH2SCH2CFThree
C (O) Me CH (Et) CH2S (O) Me
C (O) Me CH (Et) CH2S (O) Et
C (O) Me CH (Et) CH2S (O) CFThree
C (O) Me CH (Et) CH2S (O) CH2CFThree
C (O) Me CH (Et) CH2S (O)2Me
C (O) Me CH (Et) CH2S (O)2Et
C (O) Me CH (Et) CH2S (O)2CFThree
C (O) Me CH (Et) CH2S (O)2CH2CFThree
C (O) Me C (Me)2CH2SMe
C (O) Me C (Me)2CH2SEt
C (O) Me C (Me)2CH2SCFThree
C (O) Me C (Me)2CH2SCH2CFThree
C (O) Me C (Me)2CH2S (O) Me
C (O) Me C (Me)2CH2S (O) Et
C (O) Me C (Me)2CH2S (O) CFThree
C (O) Me C (Me)2CH2S (O) CH2CFThree
C (O) Me C (Me)2CH2S (O)2Me
C (O) Me C (Me)2CH2S (O)2Et
C (O) Me C (Me)2CH2S (O)2CFThree
C (O) Me C (Me)2CH2S (O)2CH2CFThree
C (O) Me CH2CH (Me) SMe
C (O) Me CH2CH (Me) SEt
C (O) Me CH2CH (Me) SCFThree
C (O) Me CH2CH (Me) SCH2CFThree
C (O) Me CH2CH (Me) S (O) Me
C (O) Me CH2CH (Me) S (O) Et
C (O) Me CH2CH (Me) S (O) CFThree
C (O) Me CH2CH (Me) S (O) CH2CFThree
C (O) Me CH2CH (Me) S (O)2Me
C (O) Me CH2CH (Me) S (O)2Et
C (O) Me CH2CH (Me) S (O)2CFThree
C (O) Me CH2CH (Me) S (O)2CH2CFThree
C (O) Me CH2CH (Et) SMe
C (O) Me CH2CH (Et) SEt
C (O) Me CH2CH (Et) SCFThree
C (O) Me CH2CH (Et) SCH2CFThree
C (O) Me CH2CH (Et) S (O) Me
C (O) Me CH2CH (Et) S (O) Et
C (O) Me CH2CH (Et) S (O) CFThree
C (O) Me CH2CH (Et) S (O) CH2CFThree
C (O) Me CH2CH (Et) S (O)2Me
C (O) Me CH2CH (Et) S (O)2Et
C (O) Me CH2CH (Et) S (O)2CFThree
C (O) Me CH2CH (Et) S (O)2CH2CFThree
C (O) Me CH (Me) CH (Me) SMe
C (O) Me CH (Me) CH (Me) SEt
C (O) Me CH (Me) CH (Me) SCFThree
C (O) Me CH (Me) CH (Me) SCH2CFThree
C (O) Me CH (Me) CH (Me) S (O) Me
C (O) Me CH (Me) CH (Me) S (O) Et
C (O) Me CH (Me) CH (Me) S (O) CFThree
C (O) Me CH (Me) CH (Me) S (O) CH2CFThree
C (O) Me CH (Me) CH (Me) S (O)2Me
C (O) Me CH (Me) CH (Me) S (O)2Et
C (O) Me CH (Me) CH (Me) S (O)2CFThree
C (O) Me CH (Me) CH (Me) S (O)2CH2CFThree
C (O) OMe CH2SMe
C (O) OMe CH2SEt
C (O) OMe CH2SCFThree
C (O) OMe CH2SCH2CFThree
C (O) OMe CH2S (O) Me
C (O) OMe CH2S (O) Et
C (O) OMe CH2S (O) CFThree
C (O) OMe CH2S (O) CH2CFThree
C (O) OMe CH2S (O)2Me
C (O) OMe CH2S (O)2Et
C (O) OMe CH2S (O)2CFThree
C (O) OMe CH2S (O)2CH2CFThree
C (O) OMe CH (Me) SMe
C (O) OMe CH (Me) SEt
C (O) OMe CH (Me) SCFThree
C (O) OMe CH (Me) SCH2CFThree
C (O) OMe CH (Me) S (O) Me
C (O) OMe CH (Me) S (O) Et
C (O) OMe CH (Me) S (O) CFThree
C (O) OMe CH (Me) S (O) CH2CFThree
C (O) OMe CH (Me) S (O)2Me
C (O) OMe CH (Me) S (O)2Et
C (O) OMe CH (Me) S (O)2CFThree
C (O) OMe CH (Me) S (O)2CH2CFThree
C (O) OMe CH (Et) SMe
C (O) OMe CH (Et) SEt
C (O) OMe CH (Et) SCFThree
C (O) OMe CH (Et) SCH2CFThree
C (O) OMe CH (Et) S (O) Me
C (O) OMe CH (Et) S (O) Et
C (O) OMe CH (Et) S (O) CFThree
C (O) OMe CH (Et) S (O) CH2CFThree
C (O) OMe CH (Et) S (O)2Me
C (O) OMe CH (Et) S (O)2Et
C (O) OMe CH (Et) S (O)2CFThree
C (O) OMe CH (Et) S (O)2CH2CFThree
C (O) OMe CH (n-Pr) SMe
C (O) OMe CH (n-Pr) SEt
C (O) OMe CH (n-Pr) SCFThree
C (O) OMe CH (n-Pr) SCH2CFThree
C (O) OMe CH (n-Pr) S (O) Me
C (O) OMe CH (n-Pr) S (O) Et
C (O) OMe CH (n-Pr) S (O) CFThree
C (O) OMe CH (n-Pr) S (O) CH2CFThree
C (O) OMe CH (n-Pr) S (O)2Me
C (O) OMe CH (n-Pr) S (O)2Et
C (O) OMe CH (n-Pr) S (O)2CFThree
C (O) OMe CH (n-Pr) S (O)2CH2CFThree
C (O) OMe CH (i-Pr) SMe
C (O) OMe CH (i-Pr) SEt
C (O) OMe CH (i-Pr) SCFThree
C (O) OMe CH (i-Pr) SCH2CFThree
C (O) OMe CH (i-Pr) S (O) Me
C (O) OMe CH (i-Pr) S (O) Et
C (O) OMe CH (i-Pr) S (O) CFThree
C (O) OMe CH (i-Pr) S (O) CH2CFThree
C (O) OMe CH (i-Pr) S (O)2Me
C (O) OMe CH (i-Pr) S (O)2Et
C (O) OMe CH (i-Pr) S (O)2CFThree
C (O) OMe CH (i-Pr) S (O)2CH2CFThree
C (O) OMe CH (n-Bu) SMe
C (O) OMe CH (n-Bu) SEt
C (O) OMe CH (n-Bu) SCFThree
C (O) OMe CH (n-Bu) SCH2CFThree
C (O) OMe CH (n-Bu) S (O) Me
C (O) OMe CH (n-Bu) S (O) Et
C (O) OMe CH (n-Bu) S (O) CFThree
C (O) OMe CH (n-Bu) S (O) CH2CFThree
C (O) OMe CH (n-Bu) S (O)2Me
C (O) OMe CH (n-Bu) S (O)2Et
C (O) OMe CH (n-Bu) S (O)2CFThree
C (O) OMe CH (n-Bu) S (O)2CH2CFThree
C (O) OMe CH (i-Bu) SMe
C (O) OMe CH (i-Bu) SEt
C (O) OMe CH (i-Bu) SCFThree
C (O) OMe CH (i-Bu) SCH2CFThree
C (O) OMe CH (i-Bu) S (O) Me
C (O) OMe CH (i-Bu) S (O) Et
C (O) OMe CH (i-Bu) S (O) CFThree
C (O) OMe CH (i-Bu) S (O) CH2CFThree
C (O) OMe CH (i-Bu) S (O)2Me
C (O) OMe CH (i-Bu) S (O)2Et
C (O) OMe CH (i-Bu) S (O)2CFThree
C (O) OMe CH (i-Bu) S (O)2CH2CFThree
C (O) OMe CH (s-Bu) SMe
C (O) OMe CH (s-Bu) SEt
C (O) OMe CH (s-Bu) SCFThree
C (O) OMe CH (s-Bu) SCH2CFThree
C (O) OMe CH (s-Bu) S (O) Me
C (O) OMe CH (s-Bu) S (O) Et
C (O) OMe CH (s-Bu) S (O) CFThree
C (O) OMe CH (s-Bu) S (O) CH2CFThree
C (O) OMe CH (s-Bu) S (O)2Me
C (O) OMe CH (s-Bu) S (O)2Et
C (O) OMe CH (s-Bu) S (O)2CFThree
C (O) OMe CH (s-Bu) S (O)2CH2CFThree
C (O) OMe CH (t-Bu) SMe
C (O) OMe CH (t-Bu) SEt
C (O) OMe CH (t-Bu) SCFThree
C (O) OMe CH (t-Bu) SCH2CFThree
C (O) OMe CH (t-Bu) S (O) Me
C (O) OMe CH (t-Bu) S (O) Et
C (O) OMe CH (t-Bu) S (O) CFThree
C (O) OMe CH (t-Bu) S (O) CH2CFThree
C (O) OMe CH (t-Bu) S (O)2Me
C (O) OMe CH (t-Bu) S (O)2Et
C (O) OMe CH (t-Bu) S (O)2CFThree
C (O) OMe CH (t-Bu) S (O)2CH2CFThree
C (O) OMe CH (CFThreeSMe
C (O) OMe CH (CFThree) SEt
C (O) OMe CH (CFThree) SCFThree
C (O) OMe CH (CFThree) SCH2CFThree
C (O) OMe CH (CFThree) S (O) Me
C (O) OMe CH (CFThree) S (O) Et
C (O) OMe CH (CFThree) S (O) CFThree
C (O) OMe CH (CFThree) S (O) CH2CFThree
C (O) OMe CH (CFThree) S (O)2Me
C (O) OMe CH (CFThree) S (O)2Et
C (O) OMe CH (CFThree) S (O)2CFThree
C (O) OMe CH (CFThree) S (O)2CH2CFThree
C (O) OMe CH2CH2SMe
C (O) OMe CH2CH2SEt
C (O) OMe CH2CH2SCFThree
C (O) OMe CH2CH2SCH2CFThree
C (O) OMe CH2CH2S (O) Me
C (O) OMe CH2CH2S (O) Et
C (O) OMe CH2CH2S (O) CFThree
C (O) OMe CH2CH2S (O) CH2CFThree
C (O) OMe CH2CH2S (O)2Me
C (O) OMe CH2CH2S (O)2Et
C (O) OMe CH2CH2S (O)2CFThree
C (O) OMe CH2CH2S (O)2CH2CFThree
C (O) OMe CH (Me) CH2SMe
C (O) OMe CH (Me) CH2SEt
C (O) OMe CH (Me) CH2SCFThree
C (O) OMe CH (Me) CH2SCH2CFThree
C (O) OMe CH (Me) CH2S (O) Me
C (O) OMe CH (Me) CH2S (O) Et
C (O) OMe CH (Me) CH2S (O) CFThree
C (O) OMe CH (Me) CH2S (O) CH2CFThree
C (O) OMe CH (Me) CH2S (O)2Me
C (O) OMe CH (Me) CH2S (O)2Et
C (O) OMe CH (Me) CH2S (O)2CFThree
C (O) OMe CH (Me) CH2S (O)2CH2CFThree
C (O) OMe CH (Et) CH2SMe
C (O) OMe CH (Et) CH2SEt
C (O) OMe CH (Et) CH2SCFThree
C (O) OMe CH (Et) CH2SCH2CFThree
C (O) OMe CH (Et) CH2S (O) Me
C (O) OMe CH (Et) CH2S (O) Et
C (O) OMe CH (Et) CH2S (O) CFThree
C (O) OMe CH (Et) CH2S (O) CH2CFThree
C (O) OMe CH (Et) CH2S (O)2Me
C (O) OMe CH (Et) CH2S (O)2Et
C (O) OMe CH (Et) CH2S (O)2CFThree
C (O) OMe CH (Et) CH2S (O)2CH2CFThree
C (O) OMe C (Me)2CH2SMe
C (O) OMe C (Me)2CH2SEt
C (O) OMe C (Me)2CH2SCFThree
C (O) OMe C (Me)2CH2SCH2CFThree
C (O) OMe C (Me)2CH2S (O) Me
C (O) OMe C (Me)2CH2S (O) Et
C (O) OMe C (Me)2CH2S (O) CFThree
C (O) OMe C (Me)2CH2S (O) CH2CFThree
C (O) OMe C (Me)2CH2S (O)2Me
C (O) OMe C (Me)2CH2S (O)2Et
C (O) OMe C (Me)2CH2S (O)2CFThree
C (O) OMe C (Me)2CH2S (O)2CH2CFThree
C (O) OMe CH2CH (Me) SMe
C (O) OMe CH2CH (Me) SEt
C (O) OMe CH2CH (Me) SCFThree
C (O) OMe CH2CH (Me) SCH2CFThree
C (O) OMe CH2CH (Me) S (O) Me
C (O) OMe CH2CH (Me) S (O) Et
C (O) OMe CH2CH (Me) S (O) CFThree
C (O) OMe CH2CH (Me) S (O) CH2CFThree
C (O) OMe CH2CH (Me) S (O)2Me
C (O) OMe CH2CH (Me) S (O)2Et
C (O) OMe CH2CH (Me) S (O)2CFThree
C (O) OMe CH2CH (Me) S (O)2CH2CFThree
C (O) OMe CH2CH (Et) SMe
C (O) OMe CH2CH (Et) SEt
C (O) OMe CH2CH (Et) SCFThree
C (O) OMe CH2CH (Et) SCH2CFThree
C (O) OMe CH2CH (Et) S (O) Me
C (O) OMe CH2CH (Et) S (O) Et
C (O) OMe CH2CH (Et) S (O) CFThree
C (O) OMe CH2CH (Et) S (O) CH2CFThree
C (O) OMe CH2CH (Et) S (O)2Me
C (O) OMe CH2CH (Et) S (O)2Et
C (O) OMe CH2CH (Et) S (O)2CFThree
C (O) OMe CH2CH (Et) S (O)2CH2CFThree
C (O) OMe CH (Me) CH (Me) SMe
C (O) OMe CH (Me) CH (Me) SEt
C (O) OMe CH (Me) CH (Me) SCFThree
C (O) OMe CH (Me) CH (Me) SCH2CFThree
C (O) OMe CH (Me) CH (Me) S (O) Me
C (O) OMe CH (Me) CH (Me) S (O) Et
C (O) OMe CH (Me) CH (Me) S (O) CFThree
C (O) OMe CH (Me) CH (Me) S (O) CH2CFThree
C (O) OMe CH (Me) CH (Me) S (O)2Me
C (O) OMe CH (Me) CH (Me) S (O)2Et
C (O) OMe CH (Me) CH (Me) S (O)2CFThree
C (O) OMe CH (Me) CH (Me) S (O)2CH2CFThree
CH2OMe CH2SMe
CH2OMe CH2SEt
CH2OMe CH2SCFThree
CH2OMe CH2SCH2CFThree
CH2OMe CH2S (O) Me
CH2OMe CH2S (O) Et
CH2OMe CH2S (O) CFThree
CH2OMe CH2S (O) CH2CFThree
CH2OMe CH2S (O)2Me
CH2OMe CH2S (O)2Et
CH2OMe CH2S (O)2CFThree
CH2OMe CH2S (O)2CH2CFThree
CH2OMe CH (Me) SMe
CH2OMe CH (Me) SEt
CH2OMe CH (Me) SCFThree
CH2OMe CH (Me) SCH2CFThree
CH2OMe CH (Me) S (O) Me
CH2OMe CH (Me) S (O) Et
CH2OMe CH (Me) S (O) CFThree
CH2OMe CH (Me) S (O) CH2CFThree
CH2OMe CH (Me) S (O)2Me
CH2OMe CH (Me) S (O)2Et
CH2OMe CH (Me) S (O)2CFThree
CH2OMe CH (Me) S (O)2CH2CFThree
CH2OMe CH (Et) SMe
CH2OMe CH (Et) SEt
CH2OMe CH (Et) SCFThree
CH2OMe CH (Et) SCH2CFThree
CH2OMe CH (Et) S (O) Me
CH2OMe CH (Et) S (O) Et
CH2OMe CH (Et) S (O) CFThree
CH2OMe CH (Et) S (O) CH2CFThree
CH2OMe CH (Et) S (O)2Me
CH2OMe CH (Et) S (O)2Et
CH2OMe CH (Et) S (O)2CFThree
CH2OMe CH (Et) S (O)2CH2CFThree
CH2OMe CH (n-Pr) SMe
CH2OMe CH (n-Pr) SEt
CH2OMe CH (n-Pr) SCFThree
CH2OMe CH (n-Pr) SCH2CFThree
CH2OMe CH (n-Pr) S (O) Me
CH2OMe CH (n-Pr) S (O) Et
CH2OMe CH (n-Pr) S (O) CFThree
CH2OMe CH (n-Pr) S (O) CH2CFThree
CH2OMe CH (n-Pr) S (O)2Me
CH2OMe CH (n-Pr) S (O)2Et
CH2OMe CH (n-Pr) S (O)2CFThree
CH2OMe CH (n-Pr) S (O)2CH2CFThree
CH2OMe CH (i-Pr) SMe
CH2OMe CH (i-Pr) SEt
CH2OMe CH (i-Pr) SCFThree
CH2OMe CH (i-Pr) SCH2CFThree
CH2OMe CH (i-Pr) S (O) Me
CH2OMe CH (i-Pr) S (O) Et
CH2OMe CH (i-Pr) S (O) CFThree
CH2OMe CH (i-Pr) S (O) CH2CFThree
CH2OMe CH (i-Pr) S (O)2Me
CH2OMe CH (i-Pr) S (O)2Et
CH2OMe CH (i-Pr) S (O)2CFThree
CH2OMe CH (i-Pr) S (O)2CH2CFThree
CH2OMe CH (n-Bu) SMe
CH2OMe CH (n-Bu) SEt
CH2OMe CH (n-Bu) SCFThree
CH2OMe CH (n-Bu) SCH2CFThree
CH2OMe CH (n-Bu) S (O) Me
CH2OMe CH (n-Bu) S (O) Et
CH2OMe CH (n-Bu) S (O) CFThree
CH2OMe CH (n-Bu) S (O) CH2CFThree
CH2OMe CH (n-Bu) S (O)2Me
CH2OMe CH (n-Bu) S (O)2Et
CH2OMe CH (n-Bu) S (O)2CFThree
CH2OMe CH (n-Bu) S (O)2CH2CFThree
CH2OMe CH (i-Bu) SMe
CH2OMe CH (i-Bu) SEt
CH2OMe CH (i-Bu) SCFThree
CH2OMe CH (i-Bu) SCH2CFThree
CH2OMe CH (i-Bu) S (O) Me
CH2OMe CH (i-Bu) S (O) Et
CH2OMe CH (i-Bu) S (O) CFThree
CH2OMe CH (i-Bu) S (O) CH2CFThree
CH2OMe CH (i-Bu) S (O)2Me
CH2OMe CH (i-Bu) S (O)2Et
CH2OMe CH (i-Bu) S (O)2CFThree
CH2OMe CH (i-Bu) S (O)2CH2CFThree
CH2OMe CH (s-Bu) SMe
CH2OMe CH (s-Bu) SEt
CH2OMe CH (s-Bu) SCFThree
CH2OMe CH (s-Bu) SCH2CFThree
CH2OMe CH (s-Bu) S (O) Me
CH2OMe CH (s-Bu) S (O) Et
CH2OMe CH (s-Bu) S (O) CFThree
CH2OMe CH (s-Bu) S (O) CH2CFThree
CH2OMe CH (s-Bu) S (O)2Me
CH2OMe CH (s-Bu) S (O)2Et
CH2OMe CH (s-Bu) S (O)2CFThree
CH2OMe CH (s-Bu) S (O)2CH2CFThree
CH2OMe CH (t-Bu) SMe
CH2OMe CH (t-Bu) SEt
CH2OMe CH (t-Bu) SCFThree
CH2OMe CH (t-Bu) SCH2CFThree
CH2OMe CH (t-Bu) S (O) Me
CH2OMe CH (t-Bu) S (O) Et
CH2OMe CH (t-Bu) S (O) CFThree
CH2OMe CH (t-Bu) S (O) CH2CFThree
CH2OMe CH (t-Bu) S (O)2Me
CH2OMe CH (t-Bu) S (O)2Et
CH2OMe CH (t-Bu) S (O)2CFThree
CH2OMe CH (t-Bu) S (O)2CH2CFThree
CH2OMe CH (CFThreeSMe
CH2OMe CH (CFThree) SEt
CH2OMe CH (CFThree) SCFThree
CH2OMe CH (CFThree) SCH2CFThree
CH2OMe CH (CFThree) S (O) Me
CH2OMe CH (CFThree) S (O) Et
CH2OMe CH (CFThree) S (O) CFThree
CH2OMe CH (CFThree) S (O) CH2CFThree
CH2OMe CH (CFThree) S (O)2Me
CH2OMe CH (CFThree) S (O)2Et
CH2OMe CH (CFThree) S (O)2CFThree
CH2OMe CH (CFThree) S (O)2CH2CFThree
CH2OMe CH2CH2SMe
CH2OMe CH2CH2SEt
CH2OMe CH2CH2SCFThree
CH2OMe CH2CH2SCH2CFThree
CH2OMe CH2CH2S (O) Me
CH2OMe CH2CH2S (O) Et
CH2OMe CH2CH2S (O) CFThree
CH2OMe CH2CH2S (O) CH2CFThree
CH2OMe CH2CH2S (O)2Me
CH2OMe CH2CH2S (O)2Et
CH2OMe CH2CH2S (O)2CFThree
CH2OMe CH2CH2S (O)2CH2CFThree
CH2OMe CH (Me) CH2SMe
CH2OMe CH (Me) CH2SEt
CH2OMe CH (Me) CH2SCFThree
CH2OMe CH (Me) CH2SCH2CFThree
CH2OMe CH (Me) CH2S (O) Me
CH2OMe CH (Me) CH2S (O) Et
CH2OMe CH (Me) CH2S (O) CFThree
CH2OMe CH (Me) CH2S (O) CH2CFThree
CH2OMe CH (Me) CH2S (O)2Me
CH2OMe CH (Me) CH2S (O)2Et
CH2OMe CH (Me) CH2S (O)2CFThree
CH2OMe CH (Me) CH2S (O)2CH2CFThree
CH2OMe CH (Et) CH2SMe
CH2OMe CH (Et) CH2SEt
CH2OMe CH (Et) CH2SCFThree
CH2OMe CH (Et) CH2SCH2CFThree
CH2OMe CH (Et) CH2S (O) Me
CH2OMe CH (Et) CH2S (O) Et
CH2OMe CH (Et) CH2S (O) CFThree
CH2OMe CH (Et) CH2S (O) CH2CFThree
CH2OMe CH (Et) CH2S (O)2Me
CH2OMe CH (Et) CH2S (O)2Et
CH2OMe CH (Et) CH2S (O)2CFThree
CH2OMe CH (Et) CH2S (O)2CH2CFThree
CH2OMe C (Me)2CH2SMe
CH2OMe C (Me)2CH2SEt
CH2OMe C (Me)2CH2SCFThree
CH2OMe C (Me)2CH2SCH2CFThree
CH2OMe C (Me)2CH2S (O) Me
CH2OMe C (Me)2CH2S (O) Et
CH2OMe C (Me)2CH2S (O) CFThree
CH2OMe C (Me)2CH2S (O) CH2CFThree
CH2OMe C (Me)2CH2S (O)2Me
CH2OMe C (Me)2CH2S (O)2Et
CH2OMe C (Me)2CH2S (O)2CFThree
CH2OMe C (Me)2CH2S (O)2CH2CFThree
CH2OMe CH2CH (Me) SMe
CH2OMe CH2CH (Me) SEt
CH2OMe CH2CH (Me) SCFThree
CH2OMe CH2CH (Me) SCH2CFThree
CH2OMe CH2CH (Me) S (O) Me
CH2OMe CH2CH (Me) S (O) Et
CH2OMe CH2CH (Me) S (O) CFThree
CH2OMe CH2CH (Me) S (O) CH2CFThree
CH2OMe CH2CH (Me) S (O)2Me
CH2OMe CH2CH (Me) S (O)2Et
CH2OMe CH2CH (Me) S (O)2CFThree
CH2OMe CH2CH (Me) S (O)2CH2CFThree
CH2OMe CH2CH (Et) SMe
CH2OMe CH2CH (Et) SEt
CH2OMe CH2CH (Et) SCFThree
CH2OMe CH2CH (Et) SCH2CFThree
CH2OMe CH2CH (Et) S (O) Me
CH2OMe CH2CH (Et) S (O) Et
CH2OMe CH2CH (Et) S (O) CFThree
CH2OMe CH2CH (Et) S (O) CH2CFThree
CH2OMe CH2CH (Et) S (O)2Me
CH2OMe CH2CH (Et) S (O)2Et
CH2OMe CH2CH (Et) S (O)2CFThree
CH2OMe CH2CH (Et) S (O)2CH2CFThree
CH2OMe CH (Me) CH (Me) SMe
CH2OMe CH (Me) CH (Me) SEt
CH2OMe CH (Me) CH (Me) SCFThree
CH2OMe CH (Me) CH (Me) SCH2CFThree
CH2OMe CH (Me) CH (Me) S (O) Me
CH2OMe CH (Me) CH (Me) S (O) Et
CH2OMe CH (Me) CH (Me) S (O) CFThree
CH2OMe CH (Me) CH (Me) S (O) CH2CFThree
CH2OMe CH (Me) CH (Me) S (O)2Me
CH2OMe CH (Me) CH (Me) S (O)2Et
CH2OMe CH (Me) CH (Me) S (O)2CFThree
CH2OMe CH (Me) CH (Me) S (O)2CH2CFThree
CH2SMe CH2SMe
CH2SEt CH2SMe
CH2S (O) Me CH2SMe
CH2S (O) Et CH2SMe
CH2S (O)2Me CH2SMe
CH2S (O)2Et CH2SMe
CH (Me) SMe CH2SMe
CH (Me) SEt CH2SMe
CH (Me) S (O) Me CH2SMe
CH (Me) S (O) Et CH2SMe
CH (Me) S (O)2Me CH2SMe
CH (Me) S (O)2Et CH2SMe
CH (Et) SMe CH2SMe
CH (Et) SEt CH2SMe
CH (Et) S (O) Me CH2SMe
CH (Et) S (O) Et CH2SMe
CH (Et) S (O)2Me CH2SMe
CH (Et) S (O)2Et CH2SMe
CH (n-Pr) SMe CH2SMe
CH (n-Pr) SEt CH2SMe
CH (n-Pr) S (O) Me CH2SMe
CH (n-Pr) S (O) Et CH2SMe
CH (n-Pr) S (O)2Me CH2SMe
CH (n-Pr) S (O)2Et CH2SMe
CH (i-Pr) SMe CH2SMe
CH (i-Pr) SEt CH2SMe
CH (i-Pr) S (O) Me CH2SMe
CH (i-Pr) S (O) Et CH2SMe
CH (i-Pr) S (O)2Me CH2SMe
CH (i-Pr) S (O)2Et CH2SMe
CH (n-Bu) SMe CH2SMe
CH (n-Bu) SEt CH2SMe
CH (n-Bu) S (O) Me CH2SMe
CH (n-Bu) S (O) Et CH2SMe
CH (n-Bu) S (O)2Me CH2SMe
CH (n-Bu) S (O)2Et CH2SMe
CH (i-Bu) SMe CH2SMe
CH (i-Bu) SEt CH2SMe
CH (i-Bu) S (O) Me CH2SMe
CH (i-Bu) S (O) Et CH2SMe
CH (i-Bu) S (O)2Me CH2SMe
CH (i-Bu) S (O)2Et CH2SMe
CH (s-Bu) SMe CH2SMe
CH (s-Bu) SEt CH2SMe
CH (s-Bu) S (O) Me CH2SMe
CH (s-Bu) S (O) Et CH2SMe
CH (s-Bu) S (O)2Me CH2SMe
CH (s-Bu) S (O)2Et CH2SMe
CH (t-Bu) SMe CH2SMe
CH (t-Bu) SEt CH2SMe
CH (t-Bu) S (O) Me CH2SMe
CH (t-Bu) S (O) Et CH2SMe
CH (t-Bu) S (O)2Me CH2SMe
CH (t-Bu) S (O)2Et CH2SMe
CH2CH2SMe CH2SMe
CH2CH2SEt CH2SMe
CH2CH2S (O)2Me CH2SMe
CH2CH2S (O)2Et CH2SMe
CH (Me) CH2SMe CH2SMe
CH (Me) CH2SEt CH2SMe
CH (Me) CH2S (O) Me CH2SMe
CH (Me) CH2S (O) Et CH2SMe
CH (Me) CH2S (O)2Me CH2SMe
CH (Me) CH2S (O)2Et CH2SMe
CH (Et) CH2SMe CH2SMe
CH (Et) CH2SEt CH2SMe
CH (Et) CH2S (O) Me CH2SMe
CH (Et) CH2S (O) Et CH2SMe
CH (Et) CH2S (O)2Me CH2SMe
CH (Et) CH2S (O)2Et CH2SMe
C (Me)2CH2SMe CH2SMe
C (Me)2CH2SEt CH2SMe
C (Me)2CH2S (O) Me CH2SMe
C (Me)2CH2S (O) Et CH2SMe
C (Me)2CH2S (O)2Me CH2SMe
C (Me)2CH2S (O)2Et CH2SMe
CH2CH (Me) SMe CH2SMe
CH2CH (Me) SEt CH2SMe
CH2CH (Me) S (O) Me CH2SMe
CH2CH (Me) S (O) Et CH2SMe
CH2CH (Me) S (O)2Me CH2SMe
CH2CH (Me) S (O)2Et CH2SMe
CH2CH (Et) SMe CH2SMe
CH2CH (Et) SEt CH2SMe
CH2CH (Et) S (O) Me CH2SMe
CH2CH (Et) S (O) Et CH2SMe
CH2CH (Et) S (O)2Me CH2SMe
CH2CH (Et) S (O)2Et CH2SMe
CH (Me) CH (Me) SMe CH2SMe
CH (Me) CH (Me) SEt CH2SMe
CH (Me) CH (Me) S (O) Me CH2SMe
CH (Me) CH (Me) S (O) Et CH2SMe
CH (Me) CH (Me) S (O)2Me CH2SMe
CH (Me) CH (Me) S (O)2Et CH2SMe
CH2SMe CH2S (O) Me
CH2SEt CH2S (O) Me
CH2S (O) Me CH2S (O) Me
CH2S (O) Et CH2S (O) Me
CH2S (O)2Me CH2S (O) Me
CH2S (O)2Et CH2S (O) Me
CH (Me) SMe CH2S (O) Me
CH (Me) SEt CH2S (O) Me
CH (Me) S (O) Me CH2S (O) Me
CH (Me) S (O) Et CH2S (O) Me
CH (Me) S (O)2Me CH2S (O) Me
CH (Me) S (O)2Et CH2S (O) Me
CH (Et) SMe CH2S (O) Me
CH (Et) SEt CH2S (O) Me
CH (Et) S (O) Me CH2S (O) Me
CH (Et) S (O) Et CH2S (O) Me
CH (Et) S (O)2Me CH2S (O) Me
CH (Et) S (O)2Et CH2S (O) Me
CH (n-Pr) SMe CH2S (O) Me
CH (n-Pr) SEt CH2S (O) Me
CH (n-Pr) S (O) Me CH2S (O) Me
CH (n-Pr) S (O) Et CH2S (O) Me
CH (n-Pr) S (O)2Me CH2S (O) Me
CH (n-Pr) S (O)2Et CH2S (O) Me
CH (i-Pr) SMe CH2S (O) Me
CH (i-Pr) SEt CH2S (O) Me
CH (i-Pr) S (O) Me CH2S (O) Me
CH (i-Pr) S (O) Et CH2S (O) Me
CH (i-Pr) S (O)2Me CH2S (O) Me
CH (i-Pr) S (O)2Et CH2S (O) Me
CH (n-Bu) SMe CH2S (O) Me
CH (n-Bu) SEt CH2S (O) Me
CH (n-Bu) S (O) Me CH2S (O) Me
CH (n-Bu) S (O) Et CH2S (O) Me
CH (n-Bu) S (O)2Me CH2S (O) Me
CH (n-Bu) S (O)2Et CH2S (O) Me
CH (i-Bu) SMe CH2S (O) Me
CH (i-Bu) SEt CH2S (O) Me
CH (i-Bu) S (O) Me CH2S (O) Me
CH (i-Bu) S (O) Et CH2S (O) Me
CH (i-Bu) S (O)2Me CH2S (O) Me
CH (i-Bu) S (O)2Et CH2S (O) Me
CH (s-Bu) SMe CH2S (O) Me
CH (s-Bu) SEt CH2S (O) Me
CH (s-Bu) S (O) Me CH2S (O) Me
CH (s-Bu) S (O) Et CH2S (O) Me
CH (s-Bu) S (O)2Me CH2S (O) Me
CH (s-Bu) S (O)2Et CH2S (O) Me
CH (t-Bu) SMe CH2S (O) Me
CH (t-Bu) SEt CH2S (O) Me
CH (t-Bu) S (O) Me CH2S (O) Me
CH (t-Bu) S (O) Et CH2S (O) Me
CH (t-Bu) S (O)2Me CH2S (O) Me
CH (t-Bu) S (O)2Et CH2S (O) Me
CH2CH2SMe CH2S (O) Me
CH2CH2SEt CH2S (O) Me
CH2CH2S (O)2Me CH2S (O) Me
CH2CH2S (O)2Et CH2S (O) Me
CH (Me) CH2SMe CH2S (O) Me
CH (Me) CH2SEt CH2S (O) Me
CH (Me) CH2S (O) Me CH2S (O) Me
CH (Me) CH2S (O) Et CH2S (O) Me
CH (Me) CH2S (O)2Me CH2S (O) Me
CH (Me) CH2S (O)2Et CH2S (O) Me
CH (Et) CH2SMe CH2S (O) Me
CH (Et) CH2SEt CH2S (O) Me
CH (Et) CH2S (O) Me CH2S (O) Me
CH (Et) CH2S (O) Et CH2S (O) Me
CH (Et) CH2S (O)2Me CH2S (O) Me
CH (Et) CH2S (O)2Et CH2S (O) Me
C (Me)2CH2SMe CH2S (O) Me
C (Me)2CH2SEt CH2S (O) Me
C (Me)2CH2S (O) Me CH2S (O) Me
C (Me)2CH2S (O) Et CH2S (O) Me
C (Me)2CH2S (O)2Me CH2S (O) Me
C (Me)2CH2S (O)2Et CH2S (O) Me
CH2CH (Me) SMe CH2S (O) Me
CH2CH (Me) SEt CH2S (O) Me
CH2CH (Me) S (O) Me CH2S (O) Me
CH2CH (Me) S (O) Et CH2S (O) Me
CH2CH (Me) S (O)2Me CH2S (O) Me
CH2CH (Me) S (O)2Et CH2S (O) Me
CH2CH (Et) SMe CH2S (O) Me
CH2CH (Et) SEt CH2S (O) Me
CH2CH (Et) S (O) Me CH2S (O) Me
CH2CH (Et) S (O) Et CH2S (O) Me
CH2CH (Et) S (O)2Me CH2S (O) Me
CH2CH (Et) S (O)2Et CH2S (O) Me
CH (Me) CH (Me) SMe CH2S (O) Me
CH (Me) CH (Me) SEt CH2S (O) Me
CH (Me) CH (Me) S (O) Me CH2S (O) Me
CH (Me) CH (Me) S (O) Et CH2S (O) Me
CH (Me) CH (Me) S (O)2Me CH2S (O) Me
CH (Me) CH (Me) S (O)2Et CH2S (O) Me
CH2SMe CH2S (O)2Me
CH2SEt CH2S (O)2Me
CH2S (O) Me CH2S (O)2Me
CH2S (O) Et CH2S (O)2Me
CH2S (O)2Me CH2S (O)2Me
CH2S (O)2Et CH2S (O)2Me
CH (Me) SMe CH2S (O)2Me
CH (Me) SEt CH2S (O)2Me
CH (Me) S (O) Me CH2S (O)2Me
CH (Me) S (O) Et CH2S (O)2Me
CH (Me) S (O)2Me CH2S (O)2Me
CH (Me) S (O)2Et CH2S (O)2Me
CH (Et) SMe CH2S (O)2Me
CH (Et) SEt CH2S (O)2Me
CH (Et) S (O) Me CH2S (O)2Me
CH (Et) S (O) Et CH2S (O)2Me
CH (Et) S (O)2Me CH2S (O)2Me
CH (Et) S (O)2Et CH2S (O)2Me
CH (n-Pr) SMe CH2S (O)2Me
CH (n-Pr) SEt CH2S (O)2Me
CH (n-Pr) S (O) Me CH2S (O)2Me
CH (n-Pr) S (O) Et CH2S (O)2Me
CH (n-Pr) S (O)2Me CH2S (O)2Me
CH (n-Pr) S (O)2Et CH2S (O)2Me
CH (i-Pr) SMe CH2S (O)2Me
CH (i-Pr) SEt CH2S (O)2Me
CH (i-Pr) S (O) Me CH2S (O)2Me
CH (i-Pr) S (O) Et CH2S (O)2Me
CH (i-Pr) S (O)2Me CH2S (O)2Me
CH (i-Pr) S (O)2Et CH2S (O)2Me
CH (n-Bu) SMe CH2S (O)2Me
CH (n-Bu) SEt CH2S (O)2Me
CH (n-Bu) S (O) Me CH2S (O)2Me
CH (n-Bu) S (O) Et CH2S (O)2Me
CH (n-Bu) S (O)2Me CH2S (O)2Me
CH (n-Bu) S (O)2Et CH2S (O)2Me
CH (i-Bu) SMe CH2S (O)2Me
CH (i-Bu) SEt CH2S (O)2Me
CH (i-Bu) S (O) Me CH2S (O)2Me
CH (i-Bu) S (O) Et CH2S (O)2Me
CH (i-Bu) S (O)2Me CH2S (O)2Me
CH (i-Bu) S (O)2Et CH2S (O)2Me
CH (s-Bu) SMe CH2S (O)2Me
CH (s-Bu) SEt CH2S (O)2Me
CH (s-Bu) S (O) Me CH2S (O)2Me
CH (s-Bu) S (O) Et CH2S (O)2Me
CH (s-Bu) S (O)2Me CH2S (O)2Me
CH (s-Bu) S (O)2Et CH2S (O)2Me
CH (t-Bu) SMe CH2S (O)2Me
CH (t-Bu) SEt CH2S (O)2Me
CH (t-Bu) S (O) Me CH2S (O)2Me
CH (t-Bu) S (O) Et CH2S (O)2Me
CH (t-Bu) S (O)2Me CH2S (O)2Me
CH (t-Bu) S (O)2Et CH2S (O)2Me
CH2CH2SMe CH2S (O)2Me
CH2CH2SEt CH2S (O)2Me
CH2CH2S (O)2Me CH2S (O)2Me
CH2CH2S (O)2Et CH2S (O)2Me
CH (Me) CH2SMe CH2S (O)2Me
CH (Me) CH2SEt CH2S (O)2Me
CH (Me) CH2S (O) Me CH2S (O)2Me
CH (Me) CH2S (O) Et CH2S (O)2Me
CH (Me) CH2S (O)2Me CH2S (O)2Me
CH (Me) CH2S (O)2Et CH2S (O)2Me
CH (Et) CH2SMe CH2S (O)2Me
CH (Et) CH2SEt CH2S (O)2Me
CH (Et) CH2S (O) Me CH2S (O)2Me
CH (Et) CH2S (O) Et CH2S (O)2Me
CH (Et) CH2S (O)2Me CH2S (O)2Me
CH (Et) CH2S (O)2Et CH2S (O)2Me
C (Me)2CH2SMe CH2S (O)2Me
C (Me)2CH2SEt CH2S (O)2Me
C (Me)2CH2S (O) Me CH2S (O)2Me
C (Me)2CH2S (O) Et CH2S (O)2Me
C (Me)2CH2S (O)2Me CH2S (O)2Me
C (Me)2CH2S (O)2Et CH2S (O)2Me
CH2CH (Me) SMe CH2S (O)2Me
CH2CH (Me) SEt CH2S (O)2Me
CH2CH (Me) S (O) Me CH2S (O)2Me
CH2CH (Me) S (O) Et CH2S (O)2Me
CH2CH (Me) S (O)2Me CH2S (O)2Me
CH2CH (Me) S (O)2Et CH2S (O)2Me
CH2CH (Et) SMe CH2S (O)2Me
CH2CH (Et) SEt CH2S (O)2Me
CH2CH (Et) S (O) Me CH2S (O)2Me
CH2CH (Et) S (O) Et CH2S (O)2Me
CH2CH (Et) S (O)2Me CH2S (O)2Me
CH2CH (Et) S (O)2Et CH2S (O)2Me
CH (Me) CH (Me) SMe CH2S (O)2Me
CH (Me) CH (Me) SEt CH2S (O)2Me
CH (Me) CH (Me) S (O) Me CH2S (O)2Me
CH (Me) CH (Me) S (O) Et CH2S (O)2Me
CH (Me) CH (Me) S (O)2Me CH2S (O)2Me
CH (Me) CH (Me) S (O)2Et CH2S (O)2Me
CH2SMe SMe
CH2SEt SMe
CH2S (O) Me SMe
CH2S (O) Et SMe
CH2S (O)2Me SMe
CH2S (O)2Et SMe
CH (Me) SMe SMe
CH (Me) SEt SMe
CH (Me) S (O) Me SMe
CH (Me) S (O) Et SMe
CH (Me) S (O)2Me SMe
CH (Me) S (O)2Et SMe
CH (Et) SMe SMe
CH (Et) SEt SMe
CH (Et) S (O) Me SMe
CH (Et) S (O) Et SMe
CH (Et) S (O)2Me SMe
CH (Et) S (O)2Et SMe
CH (n-Pr) SMe SMe
CH (n-Pr) SEt SMe
CH (n-Pr) S (O) Me SMe
CH (n-Pr) S (O) Et SMe
CH (n-Pr) S (O)2Me SMe
CH (n-Pr) S (O)2Et SMe
CH (i-Pr) SMe SMe
CH (i-Pr) SEt SMe
CH (i-Pr) S (O) Me SMe
CH (i-Pr) S (O) Et SMe
CH (i-Pr) S (O)2Me SMe
CH (i-Pr) S (O)2Et SMe
CH (n-Bu) SMe SMe
CH (n-Bu) SEt SMe
CH (n-Bu) S (O) Me SMe
CH (n-Bu) S (O) Et SMe
CH (n-Bu) S (O)2Me SMe
CH (n-Bu) S (O)2Et SMe
CH (i-Bu) SMe SMe
CH (i-Bu) SEt SMe
CH (i-Bu) S (O) Me SMe
CH (i-Bu) S (O) Et SMe
CH (i-Bu) S (O)2Me SMe
CH (i-Bu) S (O)2Et SMe
CH (s-Bu) SMe SMe
CH (s-Bu) SEt SMe
CH (s-Bu) S (O) Me SMe
CH (s-Bu) S (O) Et SMe
CH (s-Bu) S (O)2Me SMe
CH (s-Bu) S (O)2Et SMe
CH (t-Bu) SMe SMe
CH (t-Bu) SEt SMe
CH (t-Bu) S (O) Me SMe
CH (t-Bu) S (O) Et SMe
CH (t-Bu) S (O)2Me SMe
CH (t-Bu) S (O)2Et SMe
CH2CH2SMe SMe
CH2CH2SEt SMe
CH2CH2S (O)2Me SMe
CH2CH2S (O)2Et SMe
CH (Me) CH2SMe SMe
CH (Me) CH2SEt SMe
CH (Me) CH2S (O) Me SMe
CH (Me) CH2S (O) Et SMe
CH (Me) CH2S (O)2Me SMe
CH (Me) CH2S (O)2Et SMe
CH (Et) CH2SMe SMe
CH (Et) CH2SEt SMe
CH (Et) CH2S (O) Me SMe
CH (Et) CH2S (O) Et SMe
CH (Et) CH2S (O)2Me SMe
CH (Et) CH2S (O)2Et SMe
C (Me)2CH2SMe SMe
C (Me)2CH2SEt SMe
C (Me)2CH2S (O) Me SMe
C (Me)2CH2S (O) Et SMe
C (Me)2CH2S (O)2Me SMe
C (Me)2CH2S (O)2Et SMe
CH2CH (Me) SMe SMe
CH2CH (Me) SEt SMe
CH2CH (Me) S (O) Me SMe
CH2CH (Me) S (O) Et SMe
CH2CH (Me) S (O)2Me SMe
CH2CH (Me) S (O)2Et SMe
CH2CH (Et) SMe SMe
CH2CH (Et) SEt SMe
CH2CH (Et) S (O) Me SMe
CH2CH (Et) S (O) Et SMe
CH2CH (Et) S (O)2Me SMe
CH2CH (Et) S (O)2Et SMe
CH (Me) CH (Me) SMe SMe
CH (Me) CH (Me) SEt SMe
CH (Me) CH (Me) S (O) Me SMe
CH (Me) CH (Me) S (O) Et SMe
CH (Me) CH (Me) S (O)2Me SMe
CH (Me) CH (Me) S (O)2Et SMe
CH2SMe S (O) Me
CH2SEt S (O) Me
CH2S (O) Me S (O) Me
CH2S (O) Et S (O) Me
CH2S (O)2Me S (O) Me
CH2S (O)2Et S (O) Me
CH (Me) SMe S (O) Me
CH (Me) SEt S (O) Me
CH (Me) S (O) Me S (O) Me
CH (Me) S (O) Et S (O) Me
CH (Me) S (O)2Me S (O) Me
CH (Me) S (O)2Et S (O) Me
CH (Et) SMe S (O) Me
CH (Et) SEt S (O) Me
CH (Et) S (O) Me S (O) Me
CH (Et) S (O) Et S (O) Me
CH (Et) S (O)2Me S (O) Me
CH (Et) S (O)2Et S (O) Me
CH (n-Pr) SMe S (O) Me
CH (n-Pr) SEt S (O) Me
CH (n-Pr) S (O) Me S (O) Me
CH (n-Pr) S (O) Et S (O) Me
CH (n-Pr) S (O)2Me S (O) Me
CH (n-Pr) S (O)2Et S (O) Me
CH (i-Pr) SMe S (O) Me
CH (i-Pr) SEt S (O) Me
CH (i-Pr) S (O) Me S (O) Me
CH (i-Pr) S (O) Et S (O) Me
CH (i-Pr) S (O)2Me S (O) Me
CH (i-Pr) S (O)2Et S (O) Me
CH (n-Bu) SMe S (O) Me
CH (n-Bu) SEt S (O) Me
CH (n-Bu) S (O) Me S (O) Me
CH (n-Bu) S (O) Et S (O) Me
CH (n-Bu) S (O)2Me S (O) Me
CH (n-Bu) S (O)2Et S (O) Me
CH (i-Bu) SMe S (O) Me
CH (i-Bu) SEt S (O) Me
CH (i-Bu) S (O) Me S (O) Me
CH (i-Bu) S (O) Et S (O) Me
CH (i-Bu) S (O)2Me S (O) Me
CH (i-Bu) S (O)2Et S (O) Me
CH (s-Bu) SMe S (O) Me
CH (s-Bu) SEt S (O) Me
CH (s-Bu) S (O) Me S (O) Me
CH (s-Bu) S (O) Et S (O) Me
CH (s-Bu) S (O)2Me S (O) Me
CH (s-Bu) S (O)2Et S (O) Me
CH (t-Bu) SMe S (O) Me
CH (t-Bu) SEt S (O) Me
CH (t-Bu) S (O) Me S (O) Me
CH (t-Bu) S (O) Et S (O) Me
CH (t-Bu) S (O)2Me S (O) Me
CH (t-Bu) S (O)2Et S (O) Me
CH2CH2SMe S (O) Me
CH2CH2SEt S (O) Me
CH2CH2S (O)2Me S (O) Me
CH2CH2S (O)2Et S (O) Me
CH (Me) CH2SMe S (O) Me
CH (Me) CH2SEt S (O) Me
CH (Me) CH2S (O) Me S (O) Me
CH (Me) CH2S (O) Et S (O) Me
CH (Me) CH2S (O)2Me S (O) Me
CH (Me) CH2S (O)2Et S (O) Me
CH (Et) CH2SMe S (O) Me
CH (Et) CH2SEt S (O) Me
CH (Et) CH2S (O) Me S (O) Me
CH (Et) CH2S (O) Et S (O) Me
CH (Et) CH2S (O)2Me S (O) Me
CH (Et) CH2S (O)2Et S (O) Me
C (Me)2CH2SMe S (O) Me
C (Me)2CH2SEt S (O) Me
C (Me)2CH2S (O) Me S (O) Me
C (Me)2CH2S (O) Et S (O) Me
C (Me)2CH2S (O)2Me S (O) Me
C (Me)2CH2S (O)2Et S (O) Me
CH2CH (Me) SMe S (O) Me
CH2CH (Me) SEt S (O) Me
CH2CH (Me) S (O) Me S (O) Me
CH2CH (Me) S (O) Et S (O) Me
CH2CH (Me) S (O)2Me S (O) Me
CH2CH (Me) S (O)2Et S (O) Me
CH2CH (Et) SMe S (O) Me
CH2CH (Et) SEt S (O) Me
CH2CH (Et) S (O) Me S (O) Me
CH2CH (Et) S (O) Et S (O) Me
CH2CH (Et) S (O)2Me S (O) Me
CH2CH (Et) S (O)2Et S (O) Me
CH (Me) CH (Me) SMe S (O) Me
CH (Me) CH (Me) SEt S (O) Me
CH (Me) CH (Me) S (O) Me S (O) Me
CH (Me) CH (Me) S (O) Et S (O) Me
CH (Me) CH (Me) S (O)2Me S (O) Me
CH (Me) CH (Me) S (O)2Et S (O) Me
CH2SMe S (O)2Me
CH2SEt S (O)2Me
CH2S (O) Me S (O)2Me
CH2S (O) Et S (O)2Me
CH2S (O)2Me S (O)2Me
CH2S (O)2Et S (O)2Me
CH (Me) SMe S (O)2Me
CH (Me) SEt S (O)2Me
CH (Me) S (O) Me S (O)2Me
CH (Me) S (O) Et S (O)2Me
CH (Me) S (O)2Me S (O)2Me
CH (Me) S (O)2Et S (O)2Me
CH (Et) SMe S (O)2Me
CH (Et) SEt S (O)2Me
CH (Et) S (O) Me S (O)2Me
CH (Et) S (O) Et S (O)2Me
CH (Et) S (O)2Me S (O)2Me
CH (Et) S (O)2Et S (O)2Me
CH (n-Pr) SMe S (O)2Me
CH (n-Pr) SEt S (O)2Me
CH (n-Pr) S (O) Me S (O)2Me
CH (n-Pr) S (O) Et S (O)2Me
CH (n-Pr) S (O)2Me S (O)2Me
CH (n-Pr) S (O)2Et S (O)2Me
CH (i-Pr) SMe S (O)2Me
CH (i-Pr) SEt S (O)2Me
CH (i-Pr) S (O) Me S (O)2Me
CH (i-Pr) S (O) Et S (O)2Me
CH (i-Pr) S (O)2Me S (O)2Me
CH (i-Pr) S (O)2Et S (O)2Me
CH (n-Bu) SMe S (O)2Me
CH (n-Bu) SEt S (O)2Me
CH (n-Bu) S (O) Me S (O)2Me
CH (n-Bu) S (O) Et S (O)2Me
CH (n-Bu) S (O)2Me S (O)2Me
CH (n-Bu) S (O)2Et S (O)2Me
CH (i-Bu) SMe S (O)2Me
CH (i-Bu) SEt S (O)2Me
CH (i-Bu) S (O) Me S (O)2Me
CH (i-Bu) S (O) Et S (O)2Me
CH (i-Bu) S (O)2Me S (O)2Me
CH (i-Bu) S (O)2Et S (O)2Me
CH (s-Bu) SMe S (O)2Me
CH (s-Bu) SEt S (O)2Me
CH (s-Bu) S (O) Me S (O)2Me
CH (s-Bu) S (O) Et S (O)2Me
CH (s-Bu) S (O)2Me S (O)2Me
CH (s-Bu) S (O)2Et S (O)2Me
CH (t-Bu) SMe S (O)2Me
CH (t-Bu) SEt S (O)2Me
CH (t-Bu) S (O) Me S (O)2Me
CH (t-Bu) S (O) Et S (O)2Me
CH (t-Bu) S (O)2Me S (O)2Me
CH (t-Bu) S (O)2Et S (O)2Me
CH2CH2SMe S (O)2Me
CH2CH2SEt S (O)2Me
CH2CH2S (O)2Me S (O)2Me
CH2CH2S (O)2Et S (O)2Me
CH (Me) CH2SMe S (O)2Me
CH (Me) CH2SEt S (O)2Me
CH (Me) CH2S (O) Me S (O)2Me
CH (Me) CH2S (O) Et S (O)2Me
CH (Me) CH2S (O)2Me S (O)2Me
CH (Me) CH2S (O)2Et S (O)2Me
CH (Et) CH2SMe S (O)2Me
CH (Et) CH2SEt S (O)2Me
CH (Et) CH2S (O) Me S (O)2Me
CH (Et) CH2S (O) Et S (O)2Me
CH (Et) CH2S (O)2Me S (O)2Me
CH (Et) CH2S (O)2Et S (O)2Me
C (Me)2CH2SMe S (O)2Me
C (Me)2CH2SEt S (O)2Me
C (Me)2CH2S (O) Me S (O)2Me
C (Me)2CH2S (O) Et S (O)2Me
C (Me)2CH2S (O)2Me S (O)2Me
C (Me)2CH2S (O)2Et S (O)2Me
CH2CH (Me) SMe S (O)2Me
CH2CH (Me) SEt S (O)2Me
CH2CH (Me) S (O) Me S (O)2Me
CH2CH (Me) S (O) Et S (O)2Me
CH2CH (Me) S (O)2Me S (O)2Me
CH2CH (Me) S (O)2Et S (O)2Me
CH2CH (Et) SMe S (O)2Me
CH2CH (Et) SEt S (O)2Me
CH2CH (Et) S (O) Me S (O)2Me
CH2CH (Et) S (O) Et S (O)2Me
CH2CH (Et) S (O)2Me S (O)2Me
CH2CH (Et) S (O)2Et S (O)2Me
CH (Me) CH (Me) SMe S (O)2Me
CH (Me) CH (Me) SEt S (O)2Me
CH (Me) CH (Me) S (O) Me S (O)2Me
CH (Me) CH (Me) S (O) Et S (O)2Me
CH (Me) CH (Me) S (O)2Me S (O)2Me
CH (Me) CH (Me) S (O)2Et S (O)2Me
CH2SMe H
CH2SEt H
CH2S (O) Me H
CH2S (O) Et H
CH2S (O)2Me H
CH2S (O)2Et H
CH (Me) SMe H
CH (Me) SEt H
CH (Me) S (O) Me H
CH (Me) S (O) Et H
CH (Me) S (O)2Me H
CH (Me) S (O)2Et H
CH (Et) SMe H
CH (Et) SEt H
CH (Et) S (O) Me H
CH (Et) S (O) Et H
CH (Et) S (O)2Me H
CH (Et) S (O)2Et H
CH (n-Pr) SMe H
CH (n-Pr) SEt H
CH (n-Pr) S (O) Me H
CH (n-Pr) S (O) Et H
CH (n-Pr) S (O)2Me H
CH (n-Pr) S (O)2Et H
CH (i-Pr) SMe H
CH (i-Pr) SEt H
CH (i-Pr) S (O) Me H
CH (i-Pr) S (O) Et H
CH (i-Pr) S (O)2Me H
CH (i-Pr) S (O)2Et H
CH (n-Bu) SMe H
CH (n-Bu) SEt H
CH (n-Bu) S (O) Me H
CH (n-Bu) S (O) Et H
CH (n-Bu) S (O)2Me H
CH (n-Bu) S (O)2Et H
CH (i-Bu) SMe H
CH (i-Bu) SEt H
CH (i-Bu) S (O) Me H
CH (i-Bu) S (O) Et H
CH (i-Bu) S (O)2Me H
CH (i-Bu) S (O)2Et H
CH (s-Bu) SMe H
CH (s-Bu) SEt H
CH (s-Bu) S (O) Me H
CH (s-Bu) S (O) Et H
CH (s-Bu) S (O)2Me H
CH (s-Bu) S (O)2Et H
CH (t-Bu) SMe H
CH (t-Bu) SEt H
CH (t-Bu) S (O) Me H
CH (t-Bu) S (O) Et H
CH (t-Bu) S (O)2Me H
CH (t-Bu) S (O)2Et H
CH2CH2SMe H
CH2CH2SEt H
CH2CH2S (O)2Me H
CH2CH2S (O)2Et H
CH (Me) CH2SMe H
CH (Me) CH2SEt H
CH (Me) CH2S (O) Me H
CH (Me) CH2S (O) Et H
CH (Me) CH2S (O)2Me H
CH (Me) CH2S (O)2Et H
CH (Et) CH2SMe H
CH (Et) CH2SEt H
CH (Et) CH2S (O) Me H
CH (Et) CH2S (O) Et H
CH (Et) CH2S (O)2Me H
CH (Et) CH2S (O)2Et H
C (Me)2CH2SMe H
C (Me)2CH2SEt H
C (Me)2CH2S (O) Me H
C (Me)2CH2S (O) Et H
C (Me)2CH2S (O)2Me H
C (Me)2CH2S (O)2Et H
CH2CH (Me) SMe H
CH2CH (Me) SEt H
CH2CH (Me) S (O) Me H
CH2CH (Me) S (O) Et H
CH2CH (Me) S (O)2Me H
CH2CH (Me) S (O)2Et H
CH2CH (Et) SMe H
CH2CH (Et) SEt H
CH2CH (Et) S (O) Me H
CH2CH (Et) S (O) Et H
CH2CH (Et) S (O)2Me H
CH2CH (Et) S (O)2Et H
CH (Me) CH (Me) SMe H
CH (Me) CH (Me) SEt H
CH (Me) CH (Me) S (O) Me H
CH (Me) CH (Me) S (O) Et H
CH (Me) CH (Me) S (O)2Me H
CH (Me) CH (Me) S (O)2Et H
CH2SMe Me
CH2SEt Me
CH2S (O) Me Me
CH2S (O) Et Me
CH2S (O)2Me Me
CH2S (O)2Et Me
CH (Me) SMe Me
CH (Me) SEt Me
CH (Me) S (O) Me Me
CH (Me) S (O) Et Me
CH (Me) S (O)2Me Me
CH (Me) S (O)2Et Me
CH (Et) SMe Me
CH (Et) SEt Me
CH (Et) S (O) Me Me
CH (Et) S (O) Et Me
CH (Et) S (O)2Me Me
CH (Et) S (O)2Et Me
CH (n-Pr) SMe Me
CH (n-Pr) SEt Me
CH (n-Pr) S (O) Me Me
CH (n-Pr) S (O) Et Me
CH (n-Pr) S (O)2Me Me
CH (n-Pr) S (O)2Et Me
CH (i-Pr) SMe Me
CH (i-Pr) SEt Me
CH (i-Pr) S (O) Me Me
CH (i-Pr) S (O) Et Me
CH (i-Pr) S (O)2Me Me
CH (i-Pr) S (O)2Et Me
CH (n-Bu) SMe Me
CH (n-Bu) SEt Me
CH (n-Bu) S (O) Me Me
CH (n-Bu) S (O) Et Me
CH (n-Bu) S (O)2Me Me
CH (n-Bu) S (O)2Et Me
CH (i-Bu) SMe Me
CH (i-Bu) SEt Me
CH (i-Bu) S (O) Me Me
CH (i-Bu) S (O) Et Me
CH (i-Bu) S (O)2Me Me
CH (i-Bu) S (O)2Et Me
CH (s-Bu) SMe Me
CH (s-Bu) SEt Me
CH (s-Bu) S (O) Me Me
CH (s-Bu) S (O) Et Me
CH (s-Bu) S (O)2Me Me
CH (s-Bu) S (O)2Et Me
CH (t-Bu) SMe Me
CH (t-Bu) SEt Me
CH (t-Bu) S (O) Me Me
CH (t-Bu) S (O) Et Me
CH (t-Bu) S (O)2Me Me
CH (t-Bu) S (O)2Et Me
CH2CH2SMe Me
CH2CH2SEt Me
CH2CH2S (O)2Me Me
CH2CH2S (O)2Et Me
CH (Me) CH2SMe Me
CH (Me) CH2SEt Me
CH (Me) CH2S (O) Me Me
CH (Me) CH2S (O) Et Me
CH (Me) CH2S (O)2Me Me
CH (Me) CH2S (O)2Et Me
CH (Et) CH2SMe Me
CH (Et) CH2SEt Me
CH (Et) CH2S (O) Me Me
CH (Et) CH2S (O) Et Me
CH (Et) CH2S (O)2Me Me
CH (Et) CH2S (O)2Et Me
C (Me)2CH2SMe Me
C (Me)2CH2SEt Me
C (Me)2CH2S (O) Me Me
C (Me)2CH2S (O) Et Me
C (Me)2CH2S (O)2Me Me
C (Me)2CH2S (O)2Et Me
CH2CH (Me) SMe Me
CH2CH (Me) SEt Me
CH2CH (Me) S (O) Me Me
CH2CH (Me) S (O) Et Me
CH2CH (Me) S (O)2Me Me
CH2CH (Me) S (O)2Et Me
CH2CH (Et) SMe Me
CH2CH (Et) SEt Me
CH2CH (Et) S (O) Me Me
CH2CH (Et) S (O) Et Me
CH2CH (Et) S (O)2Me Me
CH2CH (Et) S (O)2Et Me
CH (Me) CH (Me) SMe Me
CH (Me) CH (Me) SEt Me
CH (Me) CH (Me) S (O) Me Me
CH (Me) CH (Me) S (O) Et Me
CH (Me) CH (Me) S (O)2Me Me
CH (Me) CH (Me) S (O)2Et Me
CH2SMe CFThree
CH2SEt CFThree
CH2S (O) Me CFThree
CH2S (O) Et CFThree
CH2S (O)2Me CFThree
CH2S (O)2Et CFThree
CH (Me) SMe CFThree
CH (Me) SEt CFThree
CH (Me) S (O) Me CFThree
CH (Me) S (O) Et CFThree
CH (Me) S (O)2Me CFThree
CH (Me) S (O)2Et CFThree
CH (Et) SMe CFThree
CH (Et) SEt CFThree
CH (Et) S (O) Me CFThree
CH (Et) S (O) Et CFThree
CH (Et) S (O)2Me CFThree
CH (Et) S (O)2Et CFThree
CH (n-Pr) SMe CFThree
CH (n-Pr) SEt CFThree
CH (n-Pr) S (O) Me CFThree
CH (n-Pr) S (O) Et CFThree
CH (n-Pr) S (O)2Me CFThree
CH (n-Pr) S (O)2Et CFThree
CH (i-Pr) SMe CFThree
CH (i-Pr) SEt CFThree
CH (i-Pr) S (O) Me CFThree
CH (i-Pr) S (O) Et CFThree
CH (i-Pr) S (O)2Me CFThree
CH (i-Pr) S (O)2Et CFThree
CH (n-Bu) SMe CFThree
CH (n-Bu) SEt CFThree
CH (n-Bu) S (O) Me CFThree
CH (n-Bu) S (O) Et CFThree
CH (n-Bu) S (O)2Me CFThree
CH (n-Bu) S (O)2Et CFThree
CH (i-Bu) SMe CFThree
CH (i-Bu) SEt CFThree
CH (i-Bu) S (O) Me CFThree
CH (i-Bu) S (O) Et CFThree
CH (i-Bu) S (O)2Me CFThree
CH (i-Bu) S (O)2Et CFThree
CH (s-Bu) SMe CFThree
CH (s-Bu) SEt CFThree
CH (s-Bu) S (O) Me CFThree
CH (s-Bu) S (O) Et CFThree
CH (s-Bu) S (O)2Me CFThree
CH (s-Bu) S (O)2Et CFThree
CH (t-Bu) SMe CFThree
CH (t-Bu) SEt CFThree
CH (t-Bu) S (O) Me CFThree
CH (t-Bu) S (O) Et CFThree
CH (t-Bu) S (O)2Me CFThree
CH (t-Bu) S (O)2Et CFThree
CH2CH2SMe CFThree
CH2CH2SEt CFThree
CH2CH2S (O)2Me CFThree
CH2CH2S (O)2Et CFThree
CH (Me) CH2SMe CFThree
CH (Me) CH2SEt CFThree
CH (Me) CH2S (O) Me CFThree
CH (Me) CH2S (O) Et CFThree
CH (Me) CH2S (O)2Me CFThree
CH (Me) CH2S (O)2Et CFThree
CH (Et) CH2SMe CFThree
CH (Et) CH2SEt CFThree
CH (Et) CH2S (O) Me CFThree
CH (Et) CH2S (O) Et CFThree
CH (Et) CH2S (O)2Me CFThree
CH (Et) CH2S (O)2Et CFThree
C (Me)2CH2SMe CFThree
C (Me)2CH2SEt CFThree
C (Me)2CH2S (O) Me CFThree
C (Me)2CH2S (O) Et CFThree
C (Me)2CH2S (O)2Me CFThree
C (Me)2CH2S (O)2Et CFThree
CH2CH (Me) SMe CFThree
CH2CH (Me) SEt CFThree
CH2CH (Me) S (O) Me CFThree
CH2CH (Me) S (O) Et CFThree
CH2CH (Me) S (O)2Me CFThree
CH2CH (Me) S (O)2Et CFThree
CH2CH (Et) SMe CFThree
CH2CH (Et) SEt CFThree
CH2CH (Et) S (O) Me CFThree
CH2CH (Et) S (O) Et CFThree
CH2CH (Et) S (O)2Me CFThree
CH2CH (Et) S (O)2Et CFThree
CH (Me) CH (Me) SMe CFThree
CH (Me) CH (Me) SEt CFThree
CH (Me) CH (Me) S (O) Me CFThree
CH (Me) CH (Me) S (O) Et CFThree
CH (Me) CH (Me) S (O)2Me CFThree
CH (Me) CH (Me) S (O)2Et CFThree
CH2SMe CN
CH2SEt CN
CH2S (O) Me CN
CH2S (O) Et CN
CH2S (O)2Me CN
CH2S (O)2Et CN
CH (Me) SMe CN
CH (Me) SEt CN
CH (Me) S (O) Me CN
CH (Me) S (O) Et CN
CH (Me) S (O)2Me CN
CH (Me) S (O)2Et CN
CH (Et) SMe CN
CH (Et) SEt CN
CH (Et) S (O) Me CN
CH (Et) S (O) Et CN
CH (Et) S (O)2Me CN
CH (Et) S (O)2Et CN
CH (n-Pr) SMe CN
CH (n-Pr) SEt CN
CH (n-Pr) S (O) Me CN
CH (n-Pr) S (O) Et CN
CH (n-Pr) S (O)2Me CN
CH (n-Pr) S (O)2Et CN
CH (i-Pr) SMe CN
CH (i-Pr) SEt CN
CH (i-Pr) S (O) Me CN
CH (i-Pr) S (O) Et CN
CH (i-Pr) S (O)2Me CN
CH (i-Pr) S (O)2Et CN
CH (n-Bu) SMe CN
CH (n-Bu) SEt CN
CH (n-Bu) S (O) Me CN
CH (n-Bu) S (O) Et CN
CH (n-Bu) S (O)2Me CN
CH (n-Bu) S (O)2Et CN
CH (i-Bu) SMe CN
CH (i-Bu) SEt CN
CH (i-Bu) S (O) Me CN
CH (i-Bu) S (O) Et CN
CH (i-Bu) S (O)2Me CN
CH (i-Bu) S (O)2Et CN
CH (s-Bu) SMe CN
CH (s-Bu) SEt CN
CH (s-Bu) S (O) Me CN
CH (s-Bu) S (O) Et CN
CH (s-Bu) S (O)2Me CN
CH (s-Bu) S (O)2Et CN
CH (t-Bu) SMe CN
CH (t-Bu) SEt CN
CH (t-Bu) S (O) Me CN
CH (t-Bu) S (O) Et CN
CH (t-Bu) S (O)2Me CN
CH (t-Bu) S (O)2Et CN
CH2CH2SMe CN
CH2CH2SEt CN
CH2CH2S (O)2Me CN
CH2CH2S (O)2Et CN
CH (Me) CH2SMe CN
CH (Me) CH2SEt CN
CH (Me) CH2S (O) Me CN
CH (Me) CH2S (O) Et CN
CH (Me) CH2S (O)2Me CN
CH (Me) CH2S (O)2Et CN
CH (Et) CH2SMe CN
CH (Et) CH2SEt CN
CH (Et) CH2S (O) Me CN
CH (Et) CH2S (O) Et CN
CH (Et) CH2S (O)2Me CN
CH (Et) CH2S (O)2Et CN
C (Me)2CH2SMe CN
C (Me)2CH2SEt CN
C (Me)2CH2S (O) Me CN
C (Me)2CH2S (O) Et CN
C (Me)2CH2S (O)2Me CN
C (Me)2CH2S (O)2Et CN
CH2CH (Me) SMe CN
CH2CH (Me) SEt CN
CH2CH (Me) S (O) Me CN
CH2CH (Me) S (O) Et CN
CH2CH (Me) S (O)2Me CN
CH2CH (Me) S (O)2Et CN
CH2CH (Et) SMe CN
CH2CH (Et) SEt CN
CH2CH (Et) S (O) Me CN
CH2CH (Et) S (O) Et CN
CH2CH (Et) S (O)2Me CN
CH2CH (Et) S (O)2Et CN
CH (Me) CH (Me) SMe CN
CH (Me) CH (Me) SEt CN
CH (Me) CH (Me) S (O) Me CN
CH (Me) CH (Me) S (O) Et CN
CH (Me) CH (Me) S (O)2Me CN
CH (Me) CH (Me) S (O)2Et CN
CH2SMe Cl
CH2SEt Cl
CH2S (O) Me Cl
CH2S (O) Et Cl
CH2S (O)2Me Cl
CH2S (O)2Et Cl
CH (Me) SMe Cl
CH (Me) SEt Cl
CH (Me) S (O) Me Cl
CH (Me) S (O) Et Cl
CH (Me) S (O)2Me Cl
CH (Me) S (O)2Et Cl
CH (Et) SMe Cl
CH (Et) SEt Cl
CH (Et) S (O) Me Cl
CH (Et) S (O) Et Cl
CH (Et) S (O)2Me Cl
CH (Et) S (O)2Et Cl
CH (n-Pr) SMe Cl
CH (n-Pr) SEt Cl
CH (n-Pr) S (O) Me Cl
CH (n-Pr) S (O) Et Cl
CH (n-Pr) S (O)2Me Cl
CH (n-Pr) S (O)2Et Cl
CH (i-Pr) SMe Cl
CH (i-Pr) SEt Cl
CH (i-Pr) S (O) Me Cl
CH (i-Pr) S (O) Et Cl
CH (i-Pr) S (O)2Me Cl
CH (i-Pr) S (O)2Et Cl
CH (n-Bu) SMe Cl
CH (n-Bu) SEt Cl
CH (n-Bu) S (O) Me Cl
CH (n-Bu) S (O) Et Cl
CH (n-Bu) S (O)2Me Cl
CH (n-Bu) S (O)2Et Cl
CH (i-Bu) SMe Cl
CH (i-Bu) SEt Cl
CH (i-Bu) S (O) Me Cl
CH (i-Bu) S (O) Et Cl
CH (i-Bu) S (O)2Me Cl
CH (i-Bu) S (O)2Et Cl
CH (s-Bu) SMe Cl
CH (s-Bu) SEt Cl
CH (s-Bu) S (O) Me Cl
CH (s-Bu) S (O) Et Cl
CH (s-Bu) S (O)2Me Cl
CH (s-Bu) S (O)2Et Cl
CH (t-Bu) SMe Cl
CH (t-Bu) SEt Cl
CH (t-Bu) S (O) Me Cl
CH (t-Bu) S (O) Et Cl
CH (t-Bu) S (O)2Me Cl
CH (t-Bu) S (O)2Et Cl
CH2CH2SMe Cl
CH2CH2SEt Cl
CH2CH2S (O)2Me Cl
CH2CH2S (O)2Et Cl
CH (Me) CH2SMe Cl
CH (Me) CH2SEt Cl
CH (Me) CH2S (O) Me Cl
CH (Me) CH2S (O) Et Cl
CH (Me) CH2S (O)2Me Cl
CH (Me) CH2S (O)2Et Cl
CH (Et) CH2SMe Cl
CH (Et) CH2SEt Cl
CH (Et) CH2S (O) Me Cl
CH (Et) CH2S (O) Et Cl
CH (Et) CH2S (O)2Me Cl
CH (Et) CH2S (O)2Et Cl
C (Me)2CH2SMe Cl
C (Me)2CH2SEt Cl
C (Me)2CH2S (O) Me Cl
C (Me)2CH2S (O) Et Cl
C (Me)2CH2S (O)2Me Cl
C (Me)2CH2S (O)2Et Cl
CH2CH (Me) SMe Cl
CH2CH (Me) SEt Cl
CH2CH (Me) S (O) Me Cl
CH2CH (Me) S (O) Et Cl
CH2CH (Me) S (O)2Me Cl
CH2CH (Me) S (O)2Et Cl
CH2CH (Et) SMe Cl
CH2CH (Et) SEt Cl
CH2CH (Et) S (O) Me Cl
CH2CH (Et) S (O) Et Cl
CH2CH (Et) S (O)2Me Cl
CH2CH (Et) S (O)2Et Cl
CH (Me) CH (Me) SMe Cl
CH (Me) CH (Me) SEt Cl
CH (Me) CH (Me) S (O) Me Cl
CH (Me) CH (Me) S (O) Et Cl
CH (Me) CH (Me) S (O)2Me Cl
CH (Me) CH (Me) S (O)2Et Cl
CH2SMe C (O) OMe
CH2SEt C (O) OMe
CH2S (O) Me C (O) OMe
CH2S (O) Et C (O) OMe
CH2S (O)2Me C (O) OMe
CH2S (O)2Et C (O) OMe
CH (Me) SMe C (O) OMe
CH (Me) SEt C (O) OMe
CH (Me) S (O) Me C (O) OMe
CH (Me) S (O) Et C (O) OMe
CH (Me) S (O)2Me C (O) OMe
CH (Me) S (O)2Et C (O) OMe
CH (Et) SMe C (O) OMe
CH (Et) SEt C (O) OMe
CH (Et) S (O) Me C (O) OMe
CH (Et) S (O) Et C (O) OMe
CH (Et) S (O)2Me C (O) OMe
CH (Et) S (O)2Et C (O) OMe
CH (n-Pr) SMe C (O) OMe
CH (n-Pr) SEt C (O) OMe
CH (n-Pr) S (O) Me C (O) OMe
CH (n-Pr) S (O) Et C (O) OMe
CH (n-Pr) S (O)2Me C (O) OMe
CH (n-Pr) S (O)2Et C (O) OMe
CH (i-Pr) SMe C (O) OMe
CH (i-Pr) SEt C (O) OMe
CH (i-Pr) S (O) Me C (O) OMe
CH (i-Pr) S (O) Et C (O) OMe
CH (i-Pr) S (O)2Me C (O) OMe
CH (i-Pr) S (O)2Et C (O) OMe
CH (n-Bu) SMe C (O) OMe
CH (n-Bu) SEt C (O) OMe
CH (n-Bu) S (O) Me C (O) OMe
CH (n-Bu) S (O) Et C (O) OMe
CH (n-Bu) S (O)2Me C (O) OMe
CH (n-Bu) S (O)2Et C (O) OMe
CH (i-Bu) SMe C (O) OMe
CH (i-Bu) SEt C (O) OMe
CH (i-Bu) S (O) Me C (O) OMe
CH (i-Bu) S (O) Et C (O) OMe
CH (i-Bu) S (O)2Me C (O) OMe
CH (i-Bu) S (O)2Et C (O) OMe
CH (s-Bu) SMe C (O) OMe
CH (s-Bu) SEt C (O) OMe
CH (s-Bu) S (O) Me C (O) OMe
CH (s-Bu) S (O) Et C (O) OMe
CH (s-Bu) S (O)2Me C (O) OMe
CH (s-Bu) S (O)2Et C (O) OMe
CH (t-Bu) SMe C (O) OMe
CH (t-Bu) SEt C (O) OMe
CH (t-Bu) S (O) Me C (O) OMe
CH (t-Bu) S (O) Et C (O) OMe
CH (t-Bu) S (O)2Me C (O) OMe
CH (t-Bu) S (O)2Et C (O) OMe
CH2CH2SMe C (O) OMe
CH2CH2SEt C (O) OMe
CH2CH2S (O)2Me C (O) OMe
CH2CH2S (O)2Et C (O) OMe
CH (Me) CH2SMe C (O) OMe
CH (Me) CH2SEt C (O) OMe
CH (Me) CH2S (O) Me C (O) OMe
CH (Me) CH2S (O) Et C (O) OMe
CH (Me) CH2S (O)2Me C (O) OMe
CH (Me) CH2S (O)2Et C (O) OMe
CH (Et) CH2SMe C (O) OMe
CH (Et) CH2SEt C (O) OMe
CH (Et) CH2S (O) Me C (O) OMe
CH (Et) CH2S (O) Et C (O) OMe
CH (Et) CH2S (O)2Me C (O) OMe
CH (Et) CH2S (O)2Et C (O) OMe
C (Me)2CH2SMe C (O) OMe
C (Me)2CH2SEt C (O) OMe
C (Me)2CH2S (O) Me C (O) OMe
C (Me)2CH2S (O) Et C (O) OMe
C (Me)2CH2S (O)2Me C (O) OMe
C (Me)2CH2S (O)2Et C (O) OMe
CH2CH (Me) SMe C (O) OMe
CH2CH (Me) SEt C (O) OMe
CH2CH (Me) S (O) Me C (O) OMe
CH2CH (Me) S (O) Et C (O) OMe
CH2CH (Me) S (O)2Me C (O) OMe
CH2CH (Me) S (O)2Et C (O) OMe
CH2CH (Et) SMe C (O) OMe
CH2CH (Et) SEt C (O) OMe
CH2CH (Et) S (O) Me C (O) OMe
CH2CH (Et) S (O) Et C (O) OMe
CH2CH (Et) S (O)2Me C (O) OMe
CH2CH (Et) S (O)2Et C (O) OMe
CH (Me) CH (Me) SMe C (O) OMe
CH (Me) CH (Me) SEt C (O) OMe
CH (Me) CH (Me) S (O) Me C (O) OMe
CH (Me) CH (Me) S (O) Et C (O) OMe
CH (Me) CH (Me) S (O)2Me C (O) OMe
CH (Me) CH (Me) S (O)2Et C (O) OMe
CH2OMe CH2SMe
CH2OMe CH2SEt
CH2OMe CH2SCFThree
CH2OMe CH2SCH2CFThree
CH2OMe CH2S (O) Me
CH2OMe CH2S (O) Et
CH2OMe CH2S (O) CFThree
CH2OMe CH2S (O) CH2CFThree
CH2OMe CH2S (O)2Me
CH2OMe CH2S (O)2Et
CH2OMe CH2S (O)2CFThree
CH2OMe CH2S (O)2CH2CFThree
CH2OMe CH (Me) SMe
CH2OMe CH (Me) SEt
CH2OMe CH (Me) SCFThree
CH2OMe CH (Me) SCH2CFThree
CH2OMe CH (Me) S (O) Me
CH2OMe CH (Me) S (O) Et
CH2OMe CH (Me) S (O) CFThree
CH2OMe CH (Me) S (O) CH2CFThree
CH2OMe CH (Me) S (O)2Me
CH2OMe CH (Me) S (O)2Et
CH2OMe CH (Me) S (O)2CFThree
CH2OMe CH (Me) S (O)2CH2CFThree
CH2OMe CH (Et) SMe
CH2OMe CH (Et) SEt
CH2OMe CH (Et) SCFThree
CH2OMe CH (Et) SCH2CFThree
CH2OMe CH (Et) S (O) Me
CH2OMe CH (Et) S (O) Et
CH2OMe CH (Et) S (O) CFThree
CH2OMe CH (Et) S (O) CH2CFThree
CH2OMe CH (Et) S (O)2Me
CH2OMe CH (Et) S (O)2Et
CH2OMe CH (Et) S (O)2CFThree
CH2OMe CH (Et) S (O)2CH2CFThree
CH2OMe CH (n-Pr) SMe
CH2OMe CH (n-Pr) SEt
CH2OMe CH (n-Pr) SCFThree
CH2OMe CH (n-Pr) SCH2CFThree
CH2OMe CH (n-Pr) S (O) Me
CH2OMe CH (n-Pr) S (O) Et
CH2OMe CH (n-Pr) S (O) CFThree
CH2OMe CH (n-Pr) S (O) CH2CFThree
CH2OMe CH (n-Pr) S (O)2Me
CH2OMe CH (n-Pr) S (O)2Et
CH2OMe CH (n-Pr) S (O)2CFThree
CH2OMe CH (n-Pr) S (O)2CH2CFThree
CH2OMe CH (i-Pr) SMe
CH2OMe CH (i-Pr) SEt
CH2OMe CH (i-Pr) SCFThree
CH2OMe CH (i-Pr) SCH2CFThree
CH2OMe CH (i-Pr) S (O) Me
CH2OMe CH (i-Pr) S (O) Et
CH2OMe CH (i-Pr) S (O) CFThree
CH2OMe CH (i-Pr) S (O) CH2CFThree
CH2OMe CH (i-Pr) S (O)2Me
CH2OMe CH (i-Pr) S (O)2Et
CH2OMe CH (i-Pr) S (O)2CFThree
CH2OMe CH (i-Pr) S (O)2CH2CFThree
CH2OMe CH (n-Bu) SMe
CH2OMe CH (n-Bu) SEt
CH2OMe CH (n-Bu) SCFThree
CH2OMe CH (n-Bu) SCH2CFThree
CH2OMe CH (n-Bu) S (O) Me
CH2OMe CH (n-Bu) S (O) Et
CH2OMe CH (n-Bu) S (O) CFThree
CH2OMe CH (n-Bu) S (O) CH2CFThree
CH2OMe CH (n-Bu) S (O)2Me
CH2OMe CH (n-Bu) S (O)2Et
CH2OMe CH (n-Bu) S (O)2CFThree
CH2OMe CH (n-Bu) S (O)2CH2CFThree
CH2OMe CH (i-Bu) SMe
CH2OMe CH (i-Bu) SEt
CH2OMe CH (i-Bu) SCFThree
CH2OMe CH (i-Bu) SCH2CFThree
CH2OMe CH (i-Bu) S (O) Me
CH2OMe CH (i-Bu) S (O) Et
CH2OMe CH (i-Bu) S (O) CFThree
CH2OMe CH (i-Bu) S (O) CH2CFThree
CH2OMe CH (i-Bu) S (O)2Me
CH2OMe CH (i-Bu) S (O)2Et
CH2OMe CH (i-Bu) S (O)2CFThree
CH2OMe CH (i-Bu) S (O)2CH2CFThree
CH2OMe CH (s-Bu) SMe
CH2OMe CH (s-Bu) SEt
CH2OMe CH (s-Bu) SCFThree
CH2OMe CH (s-Bu) SCH2CFThree
CH2OMe CH (s-Bu) S (O) Me
CH2OMe CH (s-Bu) S (O) Et
CH2OMe CH (s-Bu) S (O) CFThree
CH2OMe CH (s-Bu) S (O) CH2CFThree
CH2OMe CH (s-Bu) S (O)2Me
CH2OMe CH (s-Bu) S (O)2Et
CH2OMe CH (s-Bu) S (O)2CFThree
CH2OMe CH (s-Bu) S (O)2CH2CFThree
CH2OMe CH (t-Bu) SMe
CH2OMe CH (t-Bu) SEt
CH2OMe CH (t-Bu) SCFThree
CH2OMe CH (t-Bu) SCH2CFThree
CH2OMe CH (t-Bu) S (O) Me
CH2OMe CH (t-Bu) S (O) Et
CH2OMe CH (t-Bu) S (O) CFThree
CH2OMe CH (t-Bu) S (O) CH2CFThree
CH2OMe CH (t-Bu) S (O)2Me
CH2OMe CH (t-Bu) S (O)2Et
CH2OMe CH (t-Bu) S (O)2CFThree
CH2OMe CH (t-Bu) S (O)2CH2CFThree
CH2OMe CH (CFThreeSMe
CH2OMe CH (CFThree) SEt
CH2OMe CH (CFThree) SCFThree
CH2OMe CH (CFThree) SCH2CFThree
CH2OMe CH (CFThree) S (O) Me
CH2OMe CH (CFThree) S (O) Et
CH2OMe CH (CFThree) S (O) CFThree
CH2OMe CH (CFThree) S (O) CH2CFThree
CH2OMe CH (CFThree) S (O)2Me
CH2OMe CH (CFThree) S (O)2Et
CH2OMe CH (CFThree) S (O)2CFThree
CH2OMe CH (CFThree) S (O)2CH2CFThree
CH2OMe CH2CH2SMe
CH2OMe CH2CH2SEt
CH2OMe CH2CH2SCFThree
CH2OMe CH2CH2SCH2CFThree
CH2OMe CH2CH2S (O) Me
CH2OMe CH2CH2S (O) Et
CH2OMe CH2CH2S (O) CFThree
CH2OMe CH2CH2S (O) CH2CFThree
CH2OMe CH2CH2S (O)2Me
CH2OMe CH2CH2S (O)2Et
CH2OMe CH2CH2S (O)2CFThree
CH2OMe CH2CH2S (O)2CH2CFThree
CH2OMe CH (Me) CH2SMe
CH2OMe CH (Me) CH2SEt
CH2OMe CH (Me) CH2SCFThree
CH2OMe CH (Me) CH2SCH2CFThree
CH2OMe CH (Me) CH2S (O) Me
CH2OMe CH (Me) CH2S (O) Et
CH2OMe CH (Me) CH2S (O) CFThree
CH2OMe CH (Me) CH2S (O) CH2CFThree
CH2OMe CH (Me) CH2S (O)2Me
CH2OMe CH (Me) CH2S (O)2Et
CH2OMe CH (Me) CH2S (O)2CFThree
CH2OMe CH (Me) CH2S (O)2CH2CFThree
CH2OMe CH (Et) CH2SMe
CH2OMe CH (Et) CH2SEt
CH2OMe CH (Et) CH2SCFThree
CH2OMe CH (Et) CH2SCH2CFThree
CH2OMe CH (Et) CH2S (O) Me
CH2OMe CH (Et) CH2S (O) Et
CH2OMe CH (Et) CH2S (O) CFThree
CH2OMe CH (Et) CH2S (O) CH2CFThree
CH2OMe CH (Et) CH2S (O)2Me
CH2OMe CH (Et) CH2S (O)2Et
CH2OMe CH (Et) CH2S (O)2CFThree
CH2OMe CH (Et) CH2S (O)2CH2CFThree
CH2OMe C (Me)2CH2SMe
CH2OMe C (Me)2CH2SEt
CH2OMe C (Me)2CH2SCFThree
CH2OMe C (Me)2CH2SCH2CFThree
CH2OMe C (Me)2CH2S (O) Me
CH2OMe C (Me)2CH2S (O) Et
CH2OMe C (Me)2CH2S (O) CFThree
CH2OMe C (Me)2CH2S (O) CH2CFThree
CH2OMe C (Me)2CH2S (O)2Me
CH2OMe C (Me)2CH2S (O)2Et
CH2OMe C (Me)2CH2S (O)2CFThree
CH2OMe C (Me)2CH2S (O)2CH2CFThree
CH2OMe CH2CH (Me) SMe
CH2OMe CH2CH (Me) SEt
CH2OMe CH2CH (Me) SCFThree
CH2OMe CH2CH (Me) SCH2CFThree
CH2OMe CH2CH (Me) S (O) Me
CH2OMe CH2CH (Me) S (O) Et
CH2OMe CH2CH (Me) S (O) CFThree
CH2OMe CH2CH (Me) S (O) CH2CFThree
CH2OMe CH2CH (Me) S (O)2Me
CH2OMe CH2CH (Me) S (O)2Et
CH2OMe CH2CH (Me) S (O)2CFThree
CH2OMe CH2CH (Me) S (O)2CH2CFThree
CH2OMe CH2CH (Et) SMe
CH2OMe CH2CH (Et) SEt
CH2OMe CH2CH (Et) SCFThree
CH2OMe CH2CH (Et) SCH2CFThree
CH2OMe CH2CH (Et) S (O) Me
CH2OMe CH2CH (Et) S (O) Et
CH2OMe CH2CH (Et) S (O) CFThree
CH2OMe CH2CH (Et) S (O) CH2CFThree
CH2OMe CH2CH (Et) S (O)2Me
CH2OMe CH2CH (Et) S (O)2Et
CH2OMe CH2CH (Et) S (O)2CFThree
CH2OMe CH2CH (Et) S (O)2CH2CFThree
CH2OMe CH (Me) CH (Me) SMe
CH2OMe CH (Me) CH (Me) SEt
CH2OMe CH (Me) CH (Me) SCFThree
CH2OMe CH (Me) CH (Me) SCH2CFThree
CH2OMe CH (Me) CH (Me) S (O) Me
CH2OMe CH (Me) CH (Me) S (O) Et
CH2OMe CH (Me) CH (Me) S (O) CFThree
CH2OMe CH (Me) CH (Me) S (O) CH2CFThree
CH2OMe CH (Me) CH (Me) S (O)2Me
CH2OMe CH (Me) CH (Me) S (O)2Et
CH2OMe CH (Me) CH (Me) S (O)2CFThree
CH2OMe CH (Me) CH (Me) S (O)2CH2CFThree
CH2C (= NOMe) Me CH2SMe
CH2C (= NOMe) Me CH2SEt
CH2C (= NOMe) Me CH2SCFThree
CH2C (= NOMe) Me CH2SCH2CFThree
CH2C (= NOMe) Me CH2S (O) Me
CH2C (= NOMe) Me CH2S (O) Et
CH2C (= NOMe) Me CH2S (O) CFThree
CH2C (= NOMe) Me CH2S (O) CH2CFThree
CH2C (= NOMe) Me CH2S (O)2Me
CH2C (= NOMe) Me CH2S (O)2Et
CH2C (= NOMe) Me CH2S (O)2CFThree
CH2C (= NOMe) Me CH2S (O)2CH2CFThree
CH2C (= NOMe) Me CH (Me) SMe
CH2C (= NOMe) Me CH (Me) SEt
CH2C (= NOMe) Me CH (Me) SCFThree
CH2C (= NOMe) Me CH (Me) SCH2CFThree
CH2C (= NOMe) Me CH (Me) S (O) Me
CH2C (= NOMe) Me CH (Me) S (O) Et
CH2C (= NOMe) Me CH (Me) S (O) CFThree
CH2C (= NOMe) Me CH (Me) S (O) CH2CFThree
CH2C (= NOMe) Me CH (Me) S (O)2Me
CH2C (= NOMe) Me CH (Me) S (O)2Et
CH2C (= NOMe) Me CH (Me) S (O)2CFThree
CH2C (= NOMe) Me CH (Me) S (O)2CH2CFThree
CH2C (= NOMe) Me CH (Et) SMe
CH2C (= NOMe) Me CH (Et) SEt
CH2C (= NOMe) Me CH (Et) SCFThree
CH2C (= NOMe) Me CH (Et) SCH2CFThree
CH2C (= NOMe) Me CH (Et) S (O) Me
CH2C (= NOMe) Me CH (Et) S (O) Et
CH2C (= NOMe) Me CH (Et) S (O) CFThree
CH2C (= NOMe) Me CH (Et) S (O) CH2CFThree
CH2C (= NOMe) Me CH (Et) S (O)2Me
CH2C (= NOMe) Me CH (Et) S (O)2Et
CH2C (= NOMe) Me CH (Et) S (O)2CFThree
CH2C (= NOMe) Me CH (Et) S (O)2CH2CFThree
CH2C (= NOMe) Me CH (n-Pr) SMe
CH2C (= NOMe) Me CH (n-Pr) SEt
CH2C (= NOMe) Me CH (n-Pr) SCFThree
CH2C (= NOMe) Me CH (n-Pr) SCH2CFThree
CH2C (= NOMe) Me CH (n-Pr) S (O) Me
CH2C (= NOMe) Me CH (n-Pr) S (O) Et
CH2C (= NOMe) Me CH (n-Pr) S (O) CFThree
CH2C (= NOMe) Me CH (n-Pr) S (O) CH2CFThree
CH2C (= NOMe) Me CH (n-Pr) S (O)2Me
CH2C (= NOMe) Me CH (n-Pr) S (O)2Et
CH2C (= NOMe) Me CH (n-Pr) S (O)2CFThree
CH2C (= NOMe) Me CH (n-Pr) S (O)2CH2CFThree
CH2C (= NOMe) Me CH (i-Pr) SMe
CH2C (= NOMe) Me CH (i-Pr) SEt
CH2C (= NOMe) Me CH (i-Pr) SCFThree
CH2C (= NOMe) Me CH (i-Pr) SCH2CFThree
CH2C (= NOMe) Me CH (i-Pr) S (O) Me
CH2C (= NOMe) Me CH (i-Pr) S (O) Et
CH2C (= NOMe) Me CH (i-Pr) S (O) CFThree
CH2C (= NOMe) Me CH (i-Pr) S (O) CH2CFThree
CH2C (= NOMe) Me CH (i-Pr) S (O)2Me
CH2C (= NOMe) Me CH (i-Pr) S (O)2Et
CH2C (= NOMe) Me CH (i-Pr) S (O)2CFThree
CH2C (= NOMe) Me CH (i-Pr) S (O)2CH2CFThree
CH2C (= NOMe) Me CH (n-Bu) SMe
CH2C (= NOMe) Me CH (n-Bu) SEt
CH2C (= NOMe) Me CH (n-Bu) SCFThree
CH2C (= NOMe) Me CH (n-Bu) SCH2CFThree
CH2C (= NOMe) Me CH (n-Bu) S (O) Me
CH2C (= NOMe) Me CH (n-Bu) S (O) Et
CH2C (= NOMe) Me CH (n-Bu) S (O) CFThree
CH2C (= NOMe) Me CH (n-Bu) S (O) CH2CFThree
CH2C (= NOMe) Me CH (n-Bu) S (O)2Me
CH2C (= NOMe) Me CH (n-Bu) S (O)2Et
CH2C (= NOMe) Me CH (n-Bu) S (O)2CFThree
CH2C (= NOMe) Me CH (n-Bu) S (O)2CH2CFThree
CH2C (= NOMe) Me CH (i-Bu) SMe
CH2C (= NOMe) Me CH (i-Bu) SEt
CH2C (= NOMe) Me CH (i-Bu) SCFThree
CH2C (= NOMe) Me CH (i-Bu) SCH2CFThree
CH2C (= NOMe) Me CH (i-Bu) S (O) Me
CH2C (= NOMe) Me CH (i-Bu) S (O) Et
CH2C (= NOMe) Me CH (i-Bu) S (O) CFThree
CH2C (= NOMe) Me CH (i-Bu) S (O) CH2CFThree
CH2C (= NOMe) Me CH (i-Bu) S (O)2Me
CH2C (= NOMe) Me CH (i-Bu) S (O)2Et
CH2C (= NOMe) Me CH (i-Bu) S (O)2CFThree
CH2C (= NOMe) Me CH (i-Bu) S (O)2CH2CFThree
CH2C (= NOMe) Me CH (s-Bu) SMe
CH2C (= NOMe) Me CH (s-Bu) SEt
CH2C (= NOMe) Me CH (s-Bu) SCFThree
CH2C (= NOMe) Me CH (s-Bu) SCH2CFThree
CH2C (= NOMe) Me CH (s-Bu) S (O) Me
CH2C (= NOMe) Me CH (s-Bu) S (O) Et
CH2C (= NOMe) Me CH (s-Bu) S (O) CFThree
CH2C (= NOMe) Me CH (s-Bu) S (O) CH2CFThree
CH2C (= NOMe) Me CH (s-Bu) S (O)2Me
CH2C (= NOMe) Me CH (s-Bu) S (O)2Et
CH2C (= NOMe) Me CH (s-Bu) S (O)2CFThree
CH2C (= NOMe) Me CH (s-Bu) S (O)2CH2CFThree
CH2C (= NOMe) Me CH (t-Bu) SMe
CH2C (= NOMe) Me CH (t-Bu) SEt
CH2C (= NOMe) Me CH (t-Bu) SCFThree
CH2C (= NOMe) Me CH (t-Bu) SCH2CFThree
CH2C (= NOMe) Me CH (t-Bu) S (O) Me
CH2C (= NOMe) Me CH (t-Bu) S (O) Et
CH2C (= NOMe) Me CH (t-Bu) S (O) CFThree
CH2C (= NOMe) Me CH (t-Bu) S (O) CH2CFThree
CH2C (= NOMe) Me CH (t-Bu) S (O)2Me
CH2C (= NOMe) Me CH (t-Bu) S (O)2Et
CH2C (= NOMe) Me CH (t-Bu) S (O)2CFThree
CH2C (= NOMe) Me CH (t-Bu) S (O)2CH2CFThree
CH2C (= NOMe) Me CH (CFThreeSMe
CH2C (= NOMe) Me CH (CFThree) SEt
CH2C (= NOMe) Me CH (CFThree) SCFThree
CH2C (= NOMe) Me CH (CFThree) SCH2CFThree
CH2C (= NOMe) Me CH (CFThree) S (O) Me
CH2C (= NOMe) Me CH (CFThree) S (O) Et
CH2C (= NOMe) Me CH (CFThree) S (O) CFThree
CH2C (= NOMe) Me CH (CFThree) S (O) CH2CFThree
CH2C (= NOMe) Me CH (CFThree) S (O)2Me
CH2C (= NOMe) Me CH (CFThree) S (O)2Et
CH2C (= NOMe) Me CH (CFThree) S (O)2CFThree
CH2C (= NOMe) Me CH (CFThree) S (O)2CH2CFThree
CH2C (= NOMe) Me CH2CH2SMe
CH2C (= NOMe) Me CH2CH2SEt
CH2C (= NOMe) Me CH2CH2SCFThree
CH2C (= NOMe) Me CH2CH2SCH2CFThree
CH2C (= NOMe) Me CH2CH2S (O) Me
CH2C (= NOMe) Me CH2CH2S (O) Et
CH2C (= NOMe) Me CH2CH2S (O) CFThree
CH2C (= NOMe) Me CH2CH2S (O) CH2CFThree
CH2C (= NOMe) Me CH2CH2S (O)2Me
CH2C (= NOMe) Me CH2CH2S (O)2Et
CH2C (= NOMe) Me CH2CH2S (O)2CFThree
CH2C (= NOMe) Me CH2CH2S (O)2CH2CFThree
CH2C (= NOMe) Me CH (Me) CH2SMe
CH2C (= NOMe) Me CH (Me) CH2SEt
CH2C (= NOMe) Me CH (Me) CH2SCFThree
CH2C (= NOMe) Me CH (Me) CH2SCH2CFThree
CH2C (= NOMe) Me CH (Me) CH2S (O) Me
CH2C (= NOMe) Me CH (Me) CH2S (O) Et
CH2C (= NOMe) Me CH (Me) CH2S (O) CFThree
CH2C (= NOMe) Me CH (Me) CH2S (O) CH2CFThree
CH2C (= NOMe) Me CH (Me) CH2S (O)2Me
CH2C (= NOMe) Me CH (Me) CH2S (O)2Et
CH2C (= NOMe) Me CH (Me) CH2S (O)2CFThree
CH2C (= NOMe) Me CH (Me) CH2S (O)2CH2CFThree
CH2C (= NOMe) Me CH (Et) CH2SMe
CH2C (= NOMe) Me CH (Et) CH2SEt
CH2C (= NOMe) Me CH (Et) CH2SCFThree
CH2C (= NOMe) Me CH (Et) CH2SCH2CFThree
CH2C (= NOMe) Me CH (Et) CH2S (O) Me
CH2C (= NOMe) Me CH (Et) CH2S (O) Et
CH2C (= NOMe) Me CH (Et) CH2S (O) CFThree
CH2C (= NOMe) Me CH (Et) CH2S (O) CH2CFThree
CH2C (= NOMe) Me CH (Et) CH2S (O)2Me
CH2C (= NOMe) Me CH (Et) CH2S (O)2Et
CH2C (= NOMe) Me CH (Et) CH2S (O)2CFThree
CH2C (= NOMe) Me CH (Et) CH2S (O)2CH2CFThree
CH2C (= NOMe) Me C (Me)2CH2SMe
CH2C (= NOMe) Me C (Me)2CH2SEt
CH2C (= NOMe) Me C (Me)2CH2SCFThree
CH2C (= NOMe) Me C (Me)2CH2SCH2CFThree
CH2C (= NOMe) Me C (Me)2CH2S (O) Me
CH2C (= NOMe) Me C (Me)2CH2S (O) Et
CH2C (= NOMe) Me C (Me)2CH2S (O) CFThree
CH2C (= NOMe) Me C (Me)2CH2S (O) CH2CFThree
CH2C (= NOMe) Me C (Me)2CH2S (O)2Me
CH2C (= NOMe) Me C (Me)2CH2S (O)2Et
CH2C (= NOMe) Me C (Me)2CH2S (O)2CFThree
CH2C (= NOMe) Me C (Me)2CH2S (O)2CH2CFThree
CH2C (= NOMe) Me CH2CH (Me) SMe
CH2C (= NOMe) Me CH2CH (Me) SEt
CH2C (= NOMe) Me CH2CH (Me) SCFThree
CH2C (= NOMe) Me CH2CH (Me) SCH2CFThree
CH2C (= NOMe) Me CH2CH (Me) S (O) Me
CH2C (= NOMe) Me CH2CH (Me) S (O) Et
CH2C (= NOMe) Me CH2CH (Me) S (O) CFThree
CH2C (= NOMe) Me CH2CH (Me) S (O) CH2CFThree
CH2C (= NOMe) Me CH2CH (Me) S (O)2Me
CH2C (= NOMe) Me CH2CH (Me) S (O)2Et
CH2C (= NOMe) Me CH2CH (Me) S (O)2CFThree
CH2C (= NOMe) Me CH2CH (Me) S (O)2CH2CFThree
CH2C (= NOMe) Me CH2CH (Et) SMe
CH2C (= NOMe) Me CH2CH (Et) SEt
CH2C (= NOMe) Me CH2CH (Et) SCFThree
CH2C (= NOMe) Me CH2CH (Et) SCH2CFThree
CH2C (= NOMe) Me CH2CH (Et) S (O) Me
CH2C (= NOMe) Me CH2CH (Et) S (O) Et
CH2C (= NOMe) Me CH2CH (Et) S (O) CFThree
CH2C (= NOMe) Me CH2CH (Et) S (O) CH2CFThree
CH2C (= NOMe) Me CH2CH (Et) S (O)2Me
CH2C (= NOMe) Me CH2CH (Et) S (O)2Et
CH2C (= NOMe) Me CH2CH (Et) S (O)2CFThree
CH2C (= NOMe) Me CH2CH (Et) S (O)2CH2CFThree
CH2C (= NOMe) Me CH (Me) CH (Me) SMe
CH2C (= NOMe) Me CH (Me) CH (Me) SEt
CH2C (= NOMe) Me CH (Me) CH (Me) SCFThree
CH2C (= NOMe) Me CH (Me) CH (Me) SCH2CFThree
CH2C (= NOMe) Me CH (Me) CH (Me) S (O) Me
CH2C (= NOMe) Me CH (Me) CH (Me) S (O) Et
CH2C (= NOMe) Me CH (Me) CH (Me) S (O) CFThree
CH2C (= NOMe) Me CH (Me) CH (Me) S (O) CH2CFThree
CH2C (= NOMe) Me CH (Me) CH (Me) S (O)2Me
CH2C (= NOMe) Me CH (Me) CH (Me) S (O)2Et
CH2C (= NOMe) Me CH (Me) CH (Me) S (O)2CFThree
CH2C (= NOMe) Me CH (Me) CH (Me) S (O)2CH2CFThree
――――――――――――――――――
[Table 2]
――――――――――――――――――
X1
――――――――――――――――――
C(=NOMe)Me
CH2C(=NOMe)Me
H
Me
Et
CF3
CH2CF3
CH2CN
CH2CH=CH2
CH2CH(OMe)2
CH(Me)OEt
S(O)2Me
D2-32a
D2-33a
D2-34a
D2-36a
D2-37a
D2-38a
D2-92a
CH(Me)SMe
C(O)Me
C(O)OH
C(O)OMe
C(O)OEt
CH2OMe
CH2SMe
CH2SEt
CH2SCF3
CH2SCH2CF3
CH2S(O)Me
CH2S(O)Et
CH2S(O)CF3
CH2S(O)CH2CF3
CH2S(O)2Me
CH2S(O)2Et
CH2S(O)2CF3
CH2S(O)2CH2CF3
CH(Me)SMe
CH(Me)SEt
CH(Me)SCF3
CH(Me)SCH2CF3
CH(Me)S(O)Me
CH(Me)S(O)Et
CH(Me)S(O)CF3
CH(Me)S(O)CH2CF3
CH(Me)S(O)2Me
CH(Me)S(O)2Et
CH(Me)S(O)2CF3
CH(Me)S(O)2CH2CF3
CH(Et)SMe
CH(Et)SEt
CH(Et)SCF3
CH(Et)SCH2CF3
CH(Et)S(O)Me
CH(Et)S(O)Et
CH(Et)S(O)CF3
CH(Et)S(O)CH2CF3
CH(Et)S(O)2Me
CH(Et)S(O)2Et
CH(Et)S(O)2CF3
CH(Et)S(O)2CH2CF3
CH(n-Pr)SMe
CH(n-Pr)SEt
CH(n-Pr)SCF3
CH(n-Pr)SCH2CF3
CH(n-Pr)S(O)Me
CH(n-Pr)S(O)Et
CH(n-Pr)S(O)CF3
CH(n-Pr)S(O)CH2CF3
CH(n-Pr)S(O)2Me
CH(n-Pr)S(O)2Et
CH(n-Pr)S(O)2CF3
CH(n-Pr)S(O)2CH2CF3
CH(i-Pr)SMe
CH(i-Pr)SEt
CH(i-Pr)SCF3
CH(i-Pr)SCH2CF3
CH(i-Pr)S(O)Me
CH(i-Pr)S(O)Et
CH(i-Pr)S(O)CF3
CH(i-Pr)S(O)CH2CF3
CH(i-Pr)S(O)2Me
CH(i-Pr)S(O)2Et
CH(i-Pr)S(O)2CF3
CH(i-Pr)S(O)2CH2CF3
CH(n-Bu)SMe
CH(n-Bu)SEt
CH(n-Bu)SCF3
CH(n-Bu)SCH2CF3
CH(n-Bu)S(O)Me
CH(n-Bu)S(O)Et
CH(n-Bu)S(O)CF3
CH(n-Bu)S(O)CH2CF3
CH(n-Bu)S(O)2Me
CH(n-Bu)S(O)2Et
CH(n-Bu)S(O)2CF3
CH(n-Bu)S(O)2CH2CF3
CH(i-Bu)SMe
CH(i-Bu)SEt
CH(i-Bu)SCF3
CH(i-Bu)SCH2CF3
CH(i-Bu)S(O)Me
CH(i-Bu)S(O)Et
CH(i-Bu)S(O)CF3
CH(i-Bu)S(O)CH2CF3
CH(i-Bu)S(O)2Me
CH(i-Bu)S(O)2Et
CH(i-Bu)S(O)2CF3
CH(i-Bu)S(O)2CH2CF3
CH(s-Bu)SMe
CH(s-Bu)SEt
CH(s-Bu)SCF3
CH(s-Bu)SCH2CF3
CH(s-Bu)S(O)Me
CH(s-Bu)S(O)Et
CH(s-Bu)S(O)CF3
CH(s-Bu)S(O)CH2CF3
CH(s-Bu)S(O)2Me
CH(s-Bu)S(O)2Et
CH(s-Bu)S(O)2CF3
CH(s-Bu)S(O)2CH2CF3
CH(t-Bu)SMe
CH(t-Bu)SEt
CH(t-Bu)SCF3
CH(t-Bu)SCH2CF3
CH(t-Bu)S(O)Me
CH(t-Bu)S(O)Et
CH(t-Bu)S(O)CF3
CH(t-Bu)S(O)CH2CF3
CH(t-Bu)S(O)2Me
CH(t-Bu)S(O)2Et
CH(t-Bu)S(O)2CF3
CH(t-Bu)S(O)2CH2CF3
CH(CF3)SMe
CH(CF3)SEt
CH(CF3)SCF3
CH(CF3)SCH2CF3
CH(CF3)S(O)Me
CH(CF3)S(O)Et
CH(CF3)S(O)CF3
CH(CF3)S(O)CH2CF3
CH(CF3)S(O)2Me
CH(CF3)S(O)2Et
CH(CF3)S(O)2CF3
CH(CF3)S(O)2CH2CF3
CH2CH2SMe
CH2CH2SEt
CH2CH2SCF3
CH2CH2SCH2CF3
CH2CH2S(O)Me
CH2CH2S(O)Et
CH2CH2S(O)CF3
CH2CH2S(O)CH2CF3
CH2CH2S(O)2Me
CH2CH2S(O)2Et
CH2CH2S(O)2CF3
CH2CH2S(O)2CH2CF3
CH(Me)CH2SMe
CH(Me)CH2SEt
CH(Me)CH2SCF3
CH(Me)CH2SCH2CF3
CH(Me)CH2S(O)Me
CH(Me)CH2S(O)Et
CH(Me)CH2S(O)CF3
CH(Me)CH2S(O)CH2CF3
CH(Me)CH2S(O)2Me
CH(Me)CH2S(O)2Et
CH(Me)CH2S(O)2CF3
CH(Me)CH2S(O)2CH2CF3
CH(Et)CH2SMe
CH(Et)CH2SEt
CH(Et)CH2SCF3
CH(Et)CH2SCH2CF3
CH(Et)CH2S(O)Me
CH(Et)CH2S(O)Et
CH(Et)CH2S(O)CF3
CH(Et)CH2S(O)CH2CF3
CH(Et)CH2S(O)2Me
CH(Et)CH2S(O)2Et
CH(Et)CH2S(O)2CF3
CH(Et)CH2S(O)2CH2CF3
C(Me)2CH2SMe
C(Me)2CH2SEt
C(Me)2CH2SCF3
C(Me)2CH2SCH2CF3
C(Me)2CH2S(O)Me
C(Me)2CH2S(O)Et
C(Me)2CH2S(O)CF3
C(Me)2CH2S(O)CH2CF3
C(Me)2CH2S(O)2Me
C(Me)2CH2S(O)2Et
C(Me)2CH2S(O)2CF3
C(Me)2CH2S(O)2CH2CF3
CH2CH(Me)SMe
CH2CH(Me)SEt
CH2CH(Me)SCF3
CH2CH(Me)SCH2CF3
CH2CH(Me)S(O)Me
CH2CH(Me)S(O)Et
CH2CH(Me)S(O)CF3
CH2CH(Me)S(O)CH2CF3
CH2CH(Me)S(O)2Me
CH2CH(Me)S(O)2Et
CH2CH(Me)S(O)2CF3
CH2CH(Me)S(O)2CH2CF3
CH2CH(Et)SMe
CH2CH(Et)SEt
CH2CH(Et)SCF3
CH2CH(Et)SCH2CF3
CH2CH(Et)S(O)Me
CH2CH(Et)S(O)Et
CH2CH(Et)S(O)CF3
CH2CH(Et)S(O)CH2CF3
CH2CH(Et)S(O)2Me
CH2CH(Et)S(O)2Et
CH2CH(Et)S(O)2CF3
CH2CH(Et)S(O)2CH2CF3
CH(Me)CH(Me)SMe
CH(Me)CH(Me)SEt
CH(Me)CH(Me)SCF3
CH(Me)CH(Me)SCH2CF3
CH(Me)CH(Me)S(O)Me
CH(Me)CH(Me)S(O)Et
CH(Me)CH(Me)S(O)CF3
CH(Me)CH(Me)S(O)CH2CF3
CH(Me)CH(Me)S(O)2Me
CH(Me)CH(Me)S(O)2Et
CH(Me)CH(Me)S(O)2CF3
CH(Me)CH(Me)S(O)2CH2CF3
CH2SMe
CH2SEt
CH2SCF3
CH2SCH2CF3
CH2S(O)Me
CH2S(O)Et
CH2S(O)CF3
CH2S(O)CH2CF3
CH2S(O)2Me
CH2S(O)2Et
CH2S(O)2CF3
CH2S(O)2CH2CF3
CH(Me)SMe
CH(Me)SEt
CH(Me)SCF3
CH(Me)SCH2CF3
CH(Me)S(O)Me
CH(Me)S(O)Et
CH(Me)S(O)CF3
CH(Me)S(O)CH2CF3
CH(Me)S(O)2Me
CH(Me)S(O)2Et
CH(Me)S(O)2CF3
CH(Me)S(O)2CH2CF3
CH(Et)SMe
CH(Et)SEt
CH(Et)SCF3
CH(Et)SCH2CF3
――――――――――――――――――
〔第3表〕
――――――――――――――――――
X 1
――――――――――――――――――
C (= NOMe) Me
CH 2 C (= NOMe) Me
H
Me
Et
CF 3
CH 2 CF 3
CH 2 CN
CH 2 CH = CH 2
CH 2 CH (OMe) 2
CH (Me) OEt
S (O) 2 Me
D2-32a
D2-33a
D2-34a
D2-36a
D2-37a
D2-38a
D2-92a
CH (Me) SMe
C (O) Me
C (O) OH
C (O) OMe
C (O) OEt
CH 2 OMe
CH 2 SMe
CH 2 SEt
CH 2 SCF 3
CH 2 SCH 2 CF 3
CH 2 S (O) Me
CH 2 S (O) Et
CH 2 S (O) CF 3
CH 2 S (O) CH 2 CF 3
CH 2 S (O) 2 Me
CH 2 S (O) 2 Et
CH 2 S (O) 2 CF 3
CH 2 S (O) 2 CH 2 CF 3
CH (Me) SMe
CH (Me) SEt
CH (Me) SCF 3
CH (Me) SCH 2 CF 3
CH (Me) S (O) Me
CH (Me) S (O) Et
CH (Me) S (O) CF 3
CH (Me) S (O) CH 2 CF 3
CH (Me) S (O) 2 Me
CH (Me) S (O) 2 Et
CH (Me) S (O) 2 CF 3
CH (Me) S (O) 2 CH 2 CF 3
CH (Et) SMe
CH (Et) SEt
CH (Et) SCF 3
CH (Et) SCH 2 CF 3
CH (Et) S (O) Me
CH (Et) S (O) Et
CH (Et) S (O) CF 3
CH (Et) S (O) CH 2 CF 3
CH (Et) S (O) 2 Me
CH (Et) S (O) 2 Et
CH (Et) S (O) 2 CF 3
CH (Et) S (O) 2 CH 2 CF 3
CH (n-Pr) SMe
CH (n-Pr) SEt
CH (n-Pr) SCF 3
CH (n-Pr) SCH 2 CF 3
CH (n-Pr) S (O) Me
CH (n-Pr) S (O) Et
CH (n-Pr) S (O) CF 3
CH (n-Pr) S (O) CH 2 CF 3
CH (n-Pr) S (O) 2 Me
CH (n-Pr) S (O) 2 Et
CH (n-Pr) S (O) 2 CF 3
CH (n-Pr) S (O) 2 CH 2 CF 3
CH (i-Pr) SMe
CH (i-Pr) SEt
CH (i-Pr) SCF 3
CH (i-Pr) SCH 2 CF 3
CH (i-Pr) S (O) Me
CH (i-Pr) S (O) Et
CH (i-Pr) S (O) CF 3
CH (i-Pr) S (O) CH 2 CF 3
CH (i-Pr) S (O) 2 Me
CH (i-Pr) S (O) 2 Et
CH (i-Pr) S (O) 2 CF 3
CH (i-Pr) S (O) 2 CH 2 CF 3
CH (n-Bu) SMe
CH (n-Bu) SEt
CH (n-Bu) SCF 3
CH (n-Bu) SCH 2 CF 3
CH (n-Bu) S (O) Me
CH (n-Bu) S (O) Et
CH (n-Bu) S (O) CF 3
CH (n-Bu) S (O) CH 2 CF 3
CH (n-Bu) S (O) 2 Me
CH (n-Bu) S (O) 2 Et
CH (n-Bu) S (O) 2 CF 3
CH (n-Bu) S (O) 2 CH 2 CF 3
CH (i-Bu) SMe
CH (i-Bu) SEt
CH (i-Bu) SCF 3
CH (i-Bu) SCH 2 CF 3
CH (i-Bu) S (O) Me
CH (i-Bu) S (O) Et
CH (i-Bu) S (O) CF 3
CH (i-Bu) S (O) CH 2 CF 3
CH (i-Bu) S (O) 2 Me
CH (i-Bu) S (O) 2 Et
CH (i-Bu) S (O) 2 CF 3
CH (i-Bu) S (O) 2 CH 2 CF 3
CH (s-Bu) SMe
CH (s-Bu) SEt
CH (s-Bu) SCF 3
CH (s-Bu) SCH 2 CF 3
CH (s-Bu) S (O) Me
CH (s-Bu) S (O) Et
CH (s-Bu) S (O) CF 3
CH (s-Bu) S (O) CH 2 CF 3
CH (s-Bu) S (O) 2 Me
CH (s-Bu) S (O) 2 Et
CH (s-Bu) S (O) 2 CF 3
CH (s-Bu) S (O) 2 CH 2 CF 3
CH (t-Bu) SMe
CH (t-Bu) SEt
CH (t-Bu) SCF 3
CH (t-Bu) SCH 2 CF 3
CH (t-Bu) S (O) Me
CH (t-Bu) S (O) Et
CH (t-Bu) S (O) CF 3
CH (t-Bu) S (O) CH 2 CF 3
CH (t-Bu) S (O) 2 Me
CH (t-Bu) S (O) 2 Et
CH (t-Bu) S (O) 2 CF 3
CH (t-Bu) S (O) 2 CH 2 CF 3
CH (CF 3 ) SMe
CH (CF 3 ) SEt
CH (CF 3 ) SCF 3
CH (CF 3 ) SCH 2 CF 3
CH (CF 3 ) S (O) Me
CH (CF 3 ) S (O) Et
CH (CF 3 ) S (O) CF 3
CH (CF 3 ) S (O) CH 2 CF 3
CH (CF 3 ) S (O) 2 Me
CH (CF 3 ) S (O) 2 Et
CH (CF 3 ) S (O) 2 CF 3
CH (CF 3 ) S (O) 2 CH 2 CF 3
CH 2 CH 2 SMe
CH 2 CH 2 SEt
CH 2 CH 2 SCF 3
CH 2 CH 2 SCH 2 CF 3
CH 2 CH 2 S (O) Me
CH 2 CH 2 S (O) Et
CH 2 CH 2 S (O) CF 3
CH 2 CH 2 S (O) CH 2 CF 3
CH 2 CH 2 S (O) 2 Me
CH 2 CH 2 S (O) 2 Et
CH 2 CH 2 S (O) 2 CF 3
CH 2 CH 2 S (O) 2 CH 2 CF 3
CH (Me) CH 2 SMe
CH (Me) CH 2 SEt
CH (Me) CH 2 SCF 3
CH (Me) CH 2 SCH 2 CF 3
CH (Me) CH 2 S (O) Me
CH (Me) CH 2 S (O) Et
CH (Me) CH 2 S (O) CF 3
CH (Me) CH 2 S (O) CH 2 CF 3
CH (Me) CH 2 S (O) 2 Me
CH (Me) CH 2 S (O) 2 Et
CH (Me) CH 2 S (O) 2 CF 3
CH (Me) CH 2 S (O) 2 CH 2 CF 3
CH (Et) CH 2 SMe
CH (Et) CH 2 SEt
CH (Et) CH 2 SCF 3
CH (Et) CH 2 SCH 2 CF 3
CH (Et) CH 2 S (O) Me
CH (Et) CH 2 S (O) Et
CH (Et) CH 2 S (O) CF 3
CH (Et) CH 2 S (O) CH 2 CF 3
CH (Et) CH 2 S (O) 2 Me
CH (Et) CH 2 S (O) 2 Et
CH (Et) CH 2 S (O) 2 CF 3
CH (Et) CH 2 S (O) 2 CH 2 CF 3
C (Me) 2 CH 2 SMe
C (Me) 2 CH 2 SEt
C (Me) 2 CH 2 SCF 3
C (Me) 2 CH 2 SCH 2 CF 3
C (Me) 2 CH 2 S (O) Me
C (Me) 2 CH 2 S (O) Et
C (Me) 2 CH 2 S (O) CF 3
C (Me) 2 CH 2 S (O) CH 2 CF 3
C (Me) 2 CH 2 S (O) 2 Me
C (Me) 2 CH 2 S (O) 2 Et
C (Me) 2 CH 2 S (O) 2 CF 3
C (Me) 2 CH 2 S (O) 2 CH 2 CF 3
CH 2 CH (Me) SMe
CH 2 CH (Me) SEt
CH 2 CH (Me) SCF 3
CH 2 CH (Me) SCH 2 CF 3
CH 2 CH (Me) S (O) Me
CH 2 CH (Me) S (O) Et
CH 2 CH (Me) S (O) CF 3
CH 2 CH (Me) S (O) CH 2 CF 3
CH 2 CH (Me) S (O) 2 Me
CH 2 CH (Me) S (O) 2 Et
CH 2 CH (Me) S (O) 2 CF 3
CH 2 CH (Me) S (O) 2 CH 2 CF 3
CH 2 CH (Et) SMe
CH 2 CH (Et) SEt
CH 2 CH (Et) SCF 3
CH 2 CH (Et) SCH 2 CF 3
CH 2 CH (Et) S (O) Me
CH 2 CH (Et) S (O) Et
CH 2 CH (Et) S (O) CF 3
CH 2 CH (Et) S (O) CH 2 CF 3
CH 2 CH (Et) S (O) 2 Me
CH 2 CH (Et) S (O) 2 Et
CH 2 CH (Et) S (O) 2 CF 3
CH 2 CH (Et) S (O) 2 CH 2 CF 3
CH (Me) CH (Me) SMe
CH (Me) CH (Me) SEt
CH (Me) CH (Me) SCF 3
CH (Me) CH (Me) SCH 2 CF 3
CH (Me) CH (Me) S (O) Me
CH (Me) CH (Me) S (O) Et
CH (Me) CH (Me) S (O) CF 3
CH (Me) CH (Me) S (O) CH 2 CF 3
CH (Me) CH (Me) S (O) 2 Me
CH (Me) CH (Me) S (O) 2 Et
CH (Me) CH (Me) S (O) 2 CF 3
CH (Me) CH (Me) S (O) 2 CH 2 CF 3
CH 2 SMe
CH 2 SEt
CH 2 SCF 3
CH 2 SCH 2 CF 3
CH 2 S (O) Me
CH 2 S (O) Et
CH 2 S (O) CF 3
CH 2 S (O) CH 2 CF 3
CH 2 S (O) 2 Me
CH 2 S (O) 2 Et
CH 2 S (O) 2 CF 3
CH 2 S (O) 2 CH 2 CF 3
CH (Me) SMe
CH (Me) SEt
CH (Me) SCF 3
CH (Me) SCH 2 CF 3
CH (Me) S (O) Me
CH (Me) S (O) Et
CH (Me) S (O) CF 3
CH (Me) S (O) CH 2 CF 3
CH (Me) S (O) 2 Me
CH (Me) S (O) 2 Et
CH (Me) S (O) 2 CF 3
CH (Me) S (O) 2 CH 2 CF 3
CH (Et) SMe
CH (Et) SEt
CH (Et) SCF 3
CH (Et) SCH 2 CF 3
――――――――――――――――――
[Table 3]
――――――――――――――――――
X1-2 X1-1
――――――――――――――――――
H CH2SMe
H CH2SEt
H CH2SCF3
H CH2SCH2CF3
H CH2S(O)Me
H CH2S(O)Et
H CH2S(O)CF3
H CH2S(O)CH2CF3
H CH2S(O)2Me
H CH2S(O)2Et
H CH2S(O)2CF3
H CH2S(O)2CH2CF3
H CH(Me)SMe
H CH(Me)SEt
H CH(Me)SCF3
H CH(Me)SCH2CF3
H CH(Me)S(O)Me
H CH(Me)S(O)Et
H CH(Me)S(O)CF3
H CH(Me)S(O)CH2CF3
H CH(Me)S(O)2Me
H CH(Me)S(O)2Et
H CH(Me)S(O)2CF3
H CH(Me)S(O)2CH2CF3
H CH(Et)SMe
H CH(Et)SEt
H CH(Et)SCF3
H CH(Et)SCH2CF3
H CH(Et)S(O)Me
H CH(Et)S(O)Et
H CH(Et)S(O)CF3
H CH(Et)S(O)CH2CF3
H CH(Et)S(O)2Me
H CH(Et)S(O)2Et
H CH(Et)S(O)2CF3
H CH(Et)S(O)2CH2CF3
H CH(n-Pr)SMe
H CH(n-Pr)SEt
H CH(n-Pr)SCF3
H CH(n-Pr)SCH2CF3
H CH(n-Pr)S(O)Me
H CH(n-Pr)S(O)Et
H CH(n-Pr)S(O)CF3
H CH(n-Pr)S(O)CH2CF3
H CH(n-Pr)S(O)2Me
H CH(n-Pr)S(O)2Et
H CH(n-Pr)S(O)2CF3
H CH(n-Pr)S(O)2CH2CF3
H CH(i-Pr)SMe
H CH(i-Pr)SEt
H CH(i-Pr)SCF3
H CH(i-Pr)SCH2CF3
H CH(i-Pr)S(O)Me
H CH(i-Pr)S(O)Et
H CH(i-Pr)S(O)CF3
H CH(i-Pr)S(O)CH2CF3
H CH(i-Pr)S(O)2Me
H CH(i-Pr)S(O)2Et
H CH(i-Pr)S(O)2CF3
H CH(i-Pr)S(O)2CH2CF3
H CH(n-Bu)SMe
H CH(n-Bu)SEt
H CH(n-Bu)SCF3
H CH(n-Bu)SCH2CF3
H CH(n-Bu)S(O)Me
H CH(n-Bu)S(O)Et
H CH(n-Bu)S(O)CF3
H CH(n-Bu)S(O)CH2CF3
H CH(n-Bu)S(O)2Me
H CH(n-Bu)S(O)2Et
H CH(n-Bu)S(O)2CF3
H CH(n-Bu)S(O)2CH2CF3
H CH(i-Bu)SMe
H CH(i-Bu)SEt
H CH(i-Bu)SCF3
H CH(i-Bu)SCH2CF3
H CH(i-Bu)S(O)Me
H CH(i-Bu)S(O)Et
H CH(i-Bu)S(O)CF3
H CH(i-Bu)S(O)CH2CF3
H CH(i-Bu)S(O)2Me
H CH(i-Bu)S(O)2Et
H CH(i-Bu)S(O)2CF3
H CH(i-Bu)S(O)2CH2CF3
H CH(s-Bu)SMe
H CH(s-Bu)SEt
H CH(s-Bu)SCF3
H CH(s-Bu)SCH2CF3
H CH(s-Bu)S(O)Me
H CH(s-Bu)S(O)Et
H CH(s-Bu)S(O)CF3
H CH(s-Bu)S(O)CH2CF3
H CH(s-Bu)S(O)2Me
H CH(s-Bu)S(O)2Et
H CH(s-Bu)S(O)2CF3
H CH(s-Bu)S(O)2CH2CF3
H CH(t-Bu)SMe
H CH(t-Bu)SEt
H CH(t-Bu)SCF3
H CH(t-Bu)SCH2CF3
H CH(t-Bu)S(O)Me
H CH(t-Bu)S(O)Et
H CH(t-Bu)S(O)CF3
H CH(t-Bu)S(O)CH2CF3
H CH(t-Bu)S(O)2Me
H CH(t-Bu)S(O)2Et
H CH(t-Bu)S(O)2CF3
H CH(t-Bu)S(O)2CH2CF3
H CH(CF3)SMe
H CH(CF3)SEt
H CH(CF3)SCF3
H CH(CF3)SCH2CF3
H CH(CF3)S(O)Me
H CH(CF3)S(O)Et
H CH(CF3)S(O)CF3
H CH(CF3)S(O)CH2CF3
H CH(CF3)S(O)2Me
H CH(CF3)S(O)2Et
H CH(CF3)S(O)2CF3
H CH(CF3)S(O)2CH2CF3
H CH2CH2SMe
H CH2CH2SEt
H CH2CH2SCF3
H CH2CH2SCH2CF3
H CH2CH2S(O)Me
H CH2CH2S(O)Et
H CH2CH2S(O)CF3
H CH2CH2S(O)CH2CF3
H CH2CH2S(O)2Me
H CH2CH2S(O)2Et
H CH2CH2S(O)2CF3
H CH2CH2S(O)2CH2CF3
H CH(Me)CH2SMe
H CH(Me)CH2SEt
H CH(Me)CH2SCF3
H CH(Me)CH2SCH2CF3
H CH(Me)CH2S(O)Me
H CH(Me)CH2S(O)Et
H CH(Me)CH2S(O)CF3
H CH(Me)CH2S(O)CH2CF3
H CH(Me)CH2S(O)2Me
H CH(Me)CH2S(O)2Et
H CH(Me)CH2S(O)2CF3
H CH(Me)CH2S(O)2CH2CF3
H CH(Et)CH2SMe
H CH(Et)CH2SEt
H CH(Et)CH2SCF3
H CH(Et)CH2SCH2CF3
H CH(Et)CH2S(O)Me
H CH(Et)CH2S(O)Et
H CH(Et)CH2S(O)CF3
H CH(Et)CH2S(O)CH2CF3
H CH(Et)CH2S(O)2Me
H CH(Et)CH2S(O)2Et
H CH(Et)CH2S(O)2CF3
H CH(Et)CH2S(O)2CH2CF3
H C(Me)2CH2SMe
H C(Me)2CH2SEt
H C(Me)2CH2SCF3
H C(Me)2CH2SCH2CF3
H C(Me)2CH2S(O)Me
H C(Me)2CH2S(O)Et
H C(Me)2CH2S(O)CF3
H C(Me)2CH2S(O)CH2CF3
H C(Me)2CH2S(O)2Me
H C(Me)2CH2S(O)2Et
H C(Me)2CH2S(O)2CF3
H C(Me)2CH2S(O)2CH2CF3
H CH2CH(Me)SMe
H CH2CH(Me)SEt
H CH2CH(Me)SCF3
H CH2CH(Me)SCH2CF3
H CH2CH(Me)S(O)Me
H CH2CH(Me)S(O)Et
H CH2CH(Me)S(O)CF3
H CH2CH(Me)S(O)CH2CF3
H CH2CH(Me)S(O)2Me
H CH2CH(Me)S(O)2Et
H CH2CH(Me)S(O)2CF3
H CH2CH(Me)S(O)2CH2CF3
H CH2CH(Et)SMe
H CH2CH(Et)SEt
H CH2CH(Et)SCF3
H CH2CH(Et)SCH2CF3
H CH2CH(Et)S(O)Me
H CH2CH(Et)S(O)Et
H CH2CH(Et)S(O)CF3
H CH2CH(Et)S(O)CH2CF3
H CH2CH(Et)S(O)2Me
H CH2CH(Et)S(O)2Et
H CH2CH(Et)S(O)2CF3
H CH2CH(Et)S(O)2CH2CF3
H CH(Me)CH(Me)SMe
H CH(Me)CH(Me)SEt
H CH(Me)CH(Me)SCF3
H CH(Me)CH(Me)SCH2CF3
H CH(Me)CH(Me)S(O)Me
H CH(Me)CH(Me)S(O)Et
H CH(Me)CH(Me)S(O)CF3
H CH(Me)CH(Me)S(O)CH2CF3
H CH(Me)CH(Me)S(O)2Me
H CH(Me)CH(Me)S(O)2Et
H CH(Me)CH(Me)S(O)2CF3
H CH(Me)CH(Me)S(O)2CH2CF3
Me CH2SMe
Me CH2SEt
Me CH2SCF3
Me CH2SCH2CF3
Me CH2S(O)Me
Me CH2S(O)Et
Me CH2S(O)CF3
Me CH2S(O)CH2CF3
Me CH2S(O)2Me
Me CH2S(O)2Et
Me CH2S(O)2CF3
Me CH2S(O)2CH2CF3
Me CH(Me)SMe
Me CH(Me)SEt
Me CH(Me)SCF3
Me CH(Me)SCH2CF3
Me CH(Me)S(O)Me
Me CH(Me)S(O)Et
Me CH(Me)S(O)CF3
Me CH(Me)S(O)CH2CF3
Me CH(Me)S(O)2Me
Me CH(Me)S(O)2Et
Me CH(Me)S(O)2CF3
Me CH(Me)S(O)2CH2CF3
Me CH(Et)SMe
Me CH(Et)SEt
Me CH(Et)SCF3
Me CH(Et)SCH2CF3
Me CH(Et)S(O)Me
Me CH(Et)S(O)Et
Me CH(Et)S(O)CF3
Me CH(Et)S(O)CH2CF3
Me CH(Et)S(O)2Me
Me CH(Et)S(O)2Et
Me CH(Et)S(O)2CF3
Me CH(Et)S(O)2CH2CF3
Me CH(n-Pr)SMe
Me CH(n-Pr)SEt
Me CH(n-Pr)SCF3
Me CH(n-Pr)SCH2CF3
Me CH(n-Pr)S(O)Me
Me CH(n-Pr)S(O)Et
Me CH(n-Pr)S(O)CF3
Me CH(n-Pr)S(O)CH2CF3
Me CH(n-Pr)S(O)2Me
Me CH(n-Pr)S(O)2Et
Me CH(n-Pr)S(O)2CF3
Me CH(n-Pr)S(O)2CH2CF3
Me CH(i-Pr)SMe
Me CH(i-Pr)SEt
Me CH(i-Pr)SCF3
Me CH(i-Pr)SCH2CF3
Me CH(i-Pr)S(O)Me
Me CH(i-Pr)S(O)Et
Me CH(i-Pr)S(O)CF3
Me CH(i-Pr)S(O)CH2CF3
Me CH(i-Pr)S(O)2Me
Me CH(i-Pr)S(O)2Et
Me CH(i-Pr)S(O)2CF3
Me CH(i-Pr)S(O)2CH2CF3
Me CH(n-Bu)SMe
Me CH(n-Bu)SEt
Me CH(n-Bu)SCF3
Me CH(n-Bu)SCH2CF3
Me CH(n-Bu)S(O)Me
Me CH(n-Bu)S(O)Et
Me CH(n-Bu)S(O)CF3
Me CH(n-Bu)S(O)CH2CF3
Me CH(n-Bu)S(O)2Me
Me CH(n-Bu)S(O)2Et
Me CH(n-Bu)S(O)2CF3
Me CH(n-Bu)S(O)2CH2CF3
Me CH(i-Bu)SMe
Me CH(i-Bu)SEt
Me CH(i-Bu)SCF3
Me CH(i-Bu)SCH2CF3
Me CH(i-Bu)S(O)Me
Me CH(i-Bu)S(O)Et
Me CH(i-Bu)S(O)CF3
Me CH(i-Bu)S(O)CH2CF3
Me CH(i-Bu)S(O)2Me
Me CH(i-Bu)S(O)2Et
Me CH(i-Bu)S(O)2CF3
Me CH(i-Bu)S(O)2CH2CF3
Me CH(s-Bu)SMe
Me CH(s-Bu)SEt
Me CH(s-Bu)SCF3
Me CH(s-Bu)SCH2CF3
Me CH(s-Bu)S(O)Me
Me CH(s-Bu)S(O)Et
Me CH(s-Bu)S(O)CF3
Me CH(s-Bu)S(O)CH2CF3
Me CH(s-Bu)S(O)2Me
Me CH(s-Bu)S(O)2Et
Me CH(s-Bu)S(O)2CF3
Me CH(s-Bu)S(O)2CH2CF3
Me CH(t-Bu)SMe
Me CH(t-Bu)SEt
Me CH(t-Bu)SCF3
Me CH(t-Bu)SCH2CF3
Me CH(t-Bu)S(O)Me
Me CH(t-Bu)S(O)Et
Me CH(t-Bu)S(O)CF3
Me CH(t-Bu)S(O)CH2CF3
Me CH(t-Bu)S(O)2Me
Me CH(t-Bu)S(O)2Et
Me CH(t-Bu)S(O)2CF3
Me CH(t-Bu)S(O)2CH2CF3
Me CH(CF3)SMe
Me CH(CF3)SEt
Me CH(CF3)SCF3
Me CH(CF3)SCH2CF3
Me CH(CF3)S(O)Me
Me CH(CF3)S(O)Et
Me CH(CF3)S(O)CF3
Me CH(CF3)S(O)CH2CF3
Me CH(CF3)S(O)2Me
Me CH(CF3)S(O)2Et
Me CH(CF3)S(O)2CF3
Me CH(CF3)S(O)2CH2CF3
Me CH2CH2SMe
Me CH2CH2SEt
Me CH2CH2SCF3
Me CH2CH2SCH2CF3
Me CH2CH2S(O)Me
Me CH2CH2S(O)Et
Me CH2CH2S(O)CF3
Me CH2CH2S(O)CH2CF3
Me CH2CH2S(O)2Me
Me CH2CH2S(O)2Et
Me CH2CH2S(O)2CF3
Me CH2CH2S(O)2CH2CF3
Me CH(Me)CH2SMe
Me CH(Me)CH2SEt
Me CH(Me)CH2SCF3
Me CH(Me)CH2SCH2CF3
Me CH(Me)CH2S(O)Me
Me CH(Me)CH2S(O)Et
Me CH(Me)CH2S(O)CF3
Me CH(Me)CH2S(O)CH2CF3
Me CH(Me)CH2S(O)2Me
Me CH(Me)CH2S(O)2Et
Me CH(Me)CH2S(O)2CF3
Me CH(Me)CH2S(O)2CH2CF3
Me CH(Et)CH2SMe
Me CH(Et)CH2SEt
Me CH(Et)CH2SCF3
Me CH(Et)CH2SCH2CF3
Me CH(Et)CH2S(O)Me
Me CH(Et)CH2S(O)Et
Me CH(Et)CH2S(O)CF3
Me CH(Et)CH2S(O)CH2CF3
Me CH(Et)CH2S(O)2Me
Me CH(Et)CH2S(O)2Et
Me CH(Et)CH2S(O)2CF3
Me CH(Et)CH2S(O)2CH2CF3
Me C(Me)2CH2SMe
Me C(Me)2CH2SEt
Me C(Me)2CH2SCF3
Me C(Me)2CH2SCH2CF3
Me C(Me)2CH2S(O)Me
Me C(Me)2CH2S(O)Et
Me C(Me)2CH2S(O)CF3
Me C(Me)2CH2S(O)CH2CF3
Me C(Me)2CH2S(O)2Me
Me C(Me)2CH2S(O)2Et
Me C(Me)2CH2S(O)2CF3
Me C(Me)2CH2S(O)2CH2CF3
Me CH2CH(Me)SMe
Me CH2CH(Me)SEt
Me CH2CH(Me)SCF3
Me CH2CH(Me)SCH2CF3
Me CH2CH(Me)S(O)Me
Me CH2CH(Me)S(O)Et
Me CH2CH(Me)S(O)CF3
Me CH2CH(Me)S(O)CH2CF3
Me CH2CH(Me)S(O)2Me
Me CH2CH(Me)S(O)2Et
Me CH2CH(Me)S(O)2CF3
Me CH2CH(Me)S(O)2CH2CF3
Me CH2CH(Et)SMe
Me CH2CH(Et)SEt
Me CH2CH(Et)SCF3
Me CH2CH(Et)SCH2CF3
Me CH2CH(Et)S(O)Me
Me CH2CH(Et)S(O)Et
Me CH2CH(Et)S(O)CF3
Me CH2CH(Et)S(O)CH2CF3
Me CH2CH(Et)S(O)2Me
Me CH2CH(Et)S(O)2Et
Me CH2CH(Et)S(O)2CF3
Me CH2CH(Et)S(O)2CH2CF3
Me CH(Me)CH(Me)SMe
Me CH(Me)CH(Me)SEt
Me CH(Me)CH(Me)SCF3
Me CH(Me)CH(Me)SCH2CF3
Me CH(Me)CH(Me)S(O)Me
Me CH(Me)CH(Me)S(O)Et
Me CH(Me)CH(Me)S(O)CF3
Me CH(Me)CH(Me)S(O)CH2CF3
Me CH(Me)CH(Me)S(O)2Me
Me CH(Me)CH(Me)S(O)2Et
Me CH(Me)CH(Me)S(O)2CF3
Me CH(Me)CH(Me)S(O)2CH2CF3
CH2CF3 CH2SMe
CH2CF3 CH2SEt
CH2CF3 CH2SCF3
CH2CF3 CH2SCH2CF3
CH2CF3 CH2S(O)Me
CH2CF3 CH2S(O)Et
CH2CF3 CH2S(O)CF3
CH2CF3 CH2S(O)CH2CF3
CH2CF3 CH2S(O)2Me
CH2CF3 CH2S(O)2Et
CH2CF3 CH2S(O)2CF3
CH2CF3 CH2S(O)2CH2CF3
CH2CF3 CH(Me)SMe
CH2CF3 CH(Me)SEt
CH2CF3 CH(Me)SCF3
CH2CF3 CH(Me)SCH2CF3
CH2CF3 CH(Me)S(O)Me
CH2CF3 CH(Me)S(O)Et
CH2CF3 CH(Me)S(O)CF3
CH2CF3 CH(Me)S(O)CH2CF3
CH2CF3 CH(Me)S(O)2Me
CH2CF3 CH(Me)S(O)2Et
CH2CF3 CH(Me)S(O)2CF3
CH2CF3 CH(Me)S(O)2CH2CF3
CH2CF3 CH(Et)SMe
CH2CF3 CH(Et)SEt
CH2CF3 CH(Et)SCF3
CH2CF3 CH(Et)SCH2CF3
CH2CF3 CH(Et)S(O)Me
CH2CF3 CH(Et)S(O)Et
CH2CF3 CH(Et)S(O)CF3
CH2CF3 CH(Et)S(O)CH2CF3
CH2CF3 CH(Et)S(O)2Me
CH2CF3 CH(Et)S(O)2Et
CH2CF3 CH(Et)S(O)2CF3
CH2CF3 CH(Et)S(O)2CH2CF3
CH2CF3 CH(n-Pr)SMe
CH2CF3 CH(n-Pr)SEt
CH2CF3 CH(n-Pr)SCF3
CH2CF3 CH(n-Pr)SCH2CF3
CH2CF3 CH(n-Pr)S(O)Me
CH2CF3 CH(n-Pr)S(O)Et
CH2CF3 CH(n-Pr)S(O)CF3
CH2CF3 CH(n-Pr)S(O)CH2CF3
CH2CF3 CH(n-Pr)S(O)2Me
CH2CF3 CH(n-Pr)S(O)2Et
CH2CF3 CH(n-Pr)S(O)2CF3
CH2CF3 CH(n-Pr)S(O)2CH2CF3
CH2CF3 CH(i-Pr)SMe
CH2CF3 CH(i-Pr)SEt
CH2CF3 CH(i-Pr)SCF3
CH2CF3 CH(i-Pr)SCH2CF3
CH2CF3 CH(i-Pr)S(O)Me
CH2CF3 CH(i-Pr)S(O)Et
CH2CF3 CH(i-Pr)S(O)CF3
CH2CF3 CH(i-Pr)S(O)CH2CF3
CH2CF3 CH(i-Pr)S(O)2Me
CH2CF3 CH(i-Pr)S(O)2Et
CH2CF3 CH(i-Pr)S(O)2CF3
CH2CF3 CH(i-Pr)S(O)2CH2CF3
CH2CF3 CH(n-Bu)SMe
CH2CF3 CH(n-Bu)SEt
CH2CF3 CH(n-Bu)SCF3
CH2CF3 CH(n-Bu)SCH2CF3
CH2CF3 CH(n-Bu)S(O)Me
CH2CF3 CH(n-Bu)S(O)Et
CH2CF3 CH(n-Bu)S(O)CF3
CH2CF3 CH(n-Bu)S(O)CH2CF3
CH2CF3 CH(n-Bu)S(O)2Me
CH2CF3 CH(n-Bu)S(O)2Et
CH2CF3 CH(n-Bu)S(O)2CF3
CH2CF3 CH(n-Bu)S(O)2CH2CF3
CH2CF3 CH(i-Bu)SMe
CH2CF3 CH(i-Bu)SEt
CH2CF3 CH(i-Bu)SCF3
CH2CF3 CH(i-Bu)SCH2CF3
CH2CF3 CH(i-Bu)S(O)Me
CH2CF3 CH(i-Bu)S(O)Et
CH2CF3 CH(i-Bu)S(O)CF3
CH2CF3 CH(i-Bu)S(O)CH2CF3
CH2CF3 CH(i-Bu)S(O)2Me
CH2CF3 CH(i-Bu)S(O)2Et
CH2CF3 CH(i-Bu)S(O)2CF3
CH2CF3 CH(i-Bu)S(O)2CH2CF3
CH2CF3 CH(s-Bu)SMe
CH2CF3 CH(s-Bu)SEt
CH2CF3 CH(s-Bu)SCF3
CH2CF3 CH(s-Bu)SCH2CF3
CH2CF3 CH(s-Bu)S(O)Me
CH2CF3 CH(s-Bu)S(O)Et
CH2CF3 CH(s-Bu)S(O)CF3
CH2CF3 CH(s-Bu)S(O)CH2CF3
CH2CF3 CH(s-Bu)S(O)2Me
CH2CF3 CH(s-Bu)S(O)2Et
CH2CF3 CH(s-Bu)S(O)2CF3
CH2CF3 CH(s-Bu)S(O)2CH2CF3
CH2CF3 CH(t-Bu)SMe
CH2CF3 CH(t-Bu)SEt
CH2CF3 CH(t-Bu)SCF3
CH2CF3 CH(t-Bu)SCH2CF3
CH2CF3 CH(t-Bu)S(O)Me
CH2CF3 CH(t-Bu)S(O)Et
CH2CF3 CH(t-Bu)S(O)CF3
CH2CF3 CH(t-Bu)S(O)CH2CF3
CH2CF3 CH(t-Bu)S(O)2Me
CH2CF3 CH(t-Bu)S(O)2Et
CH2CF3 CH(t-Bu)S(O)2CF3
CH2CF3 CH(t-Bu)S(O)2CH2CF3
CH2CF3 CH(CF3)SMe
CH2CF3 CH(CF3)SEt
CH2CF3 CH(CF3)SCF3
CH2CF3 CH(CF3)SCH2CF3
CH2CF3 CH(CF3)S(O)Me
CH2CF3 CH(CF3)S(O)Et
CH2CF3 CH(CF3)S(O)CF3
CH2CF3 CH(CF3)S(O)CH2CF3
CH2CF3 CH(CF3)S(O)2Me
CH2CF3 CH(CF3)S(O)2Et
CH2CF3 CH(CF3)S(O)2CF3
CH2CF3 CH(CF3)S(O)2CH2CF3
CH2CF3 CH2CH2SMe
CH2CF3 CH2CH2SEt
CH2CF3 CH2CH2SCF3
CH2CF3 CH2CH2SCH2CF3
CH2CF3 CH2CH2S(O)Me
CH2CF3 CH2CH2S(O)Et
CH2CF3 CH2CH2S(O)CF3
CH2CF3 CH2CH2S(O)CH2CF3
CH2CF3 CH2CH2S(O)2Me
CH2CF3 CH2CH2S(O)2Et
CH2CF3 CH2CH2S(O)2CF3
CH2CF3 CH2CH2S(O)2CH2CF3
CH2CF3 CH(Me)CH2SMe
CH2CF3 CH(Me)CH2SEt
CH2CF3 CH(Me)CH2SCF3
CH2CF3 CH(Me)CH2SCH2CF3
CH2CF3 CH(Me)CH2S(O)Me
CH2CF3 CH(Me)CH2S(O)Et
CH2CF3 CH(Me)CH2S(O)CF3
CH2CF3 CH(Me)CH2S(O)CH2CF3
CH2CF3 CH(Me)CH2S(O)2Me
CH2CF3 CH(Me)CH2S(O)2Et
CH2CF3 CH(Me)CH2S(O)2CF3
CH2CF3 CH(Me)CH2S(O)2CH2CF3
CH2CF3 CH(Et)CH2SMe
CH2CF3 CH(Et)CH2SEt
CH2CF3 CH(Et)CH2SCF3
CH2CF3 CH(Et)CH2SCH2CF3
CH2CF3 CH(Et)CH2S(O)Me
CH2CF3 CH(Et)CH2S(O)Et
CH2CF3 CH(Et)CH2S(O)CF3
CH2CF3 CH(Et)CH2S(O)CH2CF3
CH2CF3 CH(Et)CH2S(O)2Me
CH2CF3 CH(Et)CH2S(O)2Et
CH2CF3 CH(Et)CH2S(O)2CF3
CH2CF3 CH(Et)CH2S(O)2CH2CF3
CH2CF3 C(Me)2CH2SMe
CH2CF3 C(Me)2CH2SEt
CH2CF3 C(Me)2CH2SCF3
CH2CF3 C(Me)2CH2SCH2CF3
CH2CF3 C(Me)2CH2S(O)Me
CH2CF3 C(Me)2CH2S(O)Et
CH2CF3 C(Me)2CH2S(O)CF3
CH2CF3 C(Me)2CH2S(O)CH2CF3
CH2CF3 C(Me)2CH2S(O)2Me
CH2CF3 C(Me)2CH2S(O)2Et
CH2CF3 C(Me)2CH2S(O)2CF3
CH2CF3 C(Me)2CH2S(O)2CH2CF3
CH2CF3 CH2CH(Me)SMe
CH2CF3 CH2CH(Me)SEt
CH2CF3 CH2CH(Me)SCF3
CH2CF3 CH2CH(Me)SCH2CF3
CH2CF3 CH2CH(Me)S(O)Me
CH2CF3 CH2CH(Me)S(O)Et
CH2CF3 CH2CH(Me)S(O)CF3
CH2CF3 CH2CH(Me)S(O)CH2CF3
CH2CF3 CH2CH(Me)S(O)2Me
CH2CF3 CH2CH(Me)S(O)2Et
CH2CF3 CH2CH(Me)S(O)2CF3
CH2CF3 CH2CH(Me)S(O)2CH2CF3
CH2CF3 CH2CH(Et)SMe
CH2CF3 CH2CH(Et)SEt
CH2CF3 CH2CH(Et)SCF3
CH2CF3 CH2CH(Et)SCH2CF3
CH2CF3 CH2CH(Et)S(O)Me
CH2CF3 CH2CH(Et)S(O)Et
CH2CF3 CH2CH(Et)S(O)CF3
CH2CF3 CH2CH(Et)S(O)CH2CF3
CH2CF3 CH2CH(Et)S(O)2Me
CH2CF3 CH2CH(Et)S(O)2Et
CH2CF3 CH2CH(Et)S(O)2CF3
CH2CF3 CH2CH(Et)S(O)2CH2CF3
CH2CF3 CH(Me)CH(Me)SMe
CH2CF3 CH(Me)CH(Me)SEt
CH2CF3 CH(Me)CH(Me)SCF3
CH2CF3 CH(Me)CH(Me)SCH2CF3
CH2CF3 CH(Me)CH(Me)S(O)Me
CH2CF3 CH(Me)CH(Me)S(O)Et
CH2CF3 CH(Me)CH(Me)S(O)CF3
CH2CF3 CH(Me)CH(Me)S(O)CH2CF3
CH2CF3 CH(Me)CH(Me)S(O)2Me
CH2CF3 CH(Me)CH(Me)S(O)2Et
CH2CF3 CH(Me)CH(Me)S(O)2CF3
CH2CF3 CH(Me)CH(Me)S(O)2CH2CF3
CH2CN CH2SMe
CH2CN CH2SEt
CH2CN CH2SCF3
CH2CN CH2SCH2CF3
CH2CN CH2S(O)Me
CH2CN CH2S(O)Et
CH2CN CH2S(O)CF3
CH2CN CH2S(O)CH2CF3
CH2CN CH2S(O)2Me
CH2CN CH2S(O)2Et
CH2CN CH2S(O)2CF3
CH2CN CH2S(O)2CH2CF3
CH2CN CH(Me)SMe
CH2CN CH(Me)SEt
CH2CN CH(Me)SCF3
CH2CN CH(Me)SCH2CF3
CH2CN CH(Me)S(O)Me
CH2CN CH(Me)S(O)Et
CH2CN CH(Me)S(O)CF3
CH2CN CH(Me)S(O)CH2CF3
CH2CN CH(Me)S(O)2Me
CH2CN CH(Me)S(O)2Et
CH2CN CH(Me)S(O)2CF3
CH2CN CH(Me)S(O)2CH2CF3
CH2CN CH(Et)SMe
CH2CN CH(Et)SEt
CH2CN CH(Et)SCF3
CH2CN CH(Et)SCH2CF3
CH2CN CH(Et)S(O)Me
CH2CN CH(Et)S(O)Et
CH2CN CH(Et)S(O)CF3
CH2CN CH(Et)S(O)CH2CF3
CH2CN CH(Et)S(O)2Me
CH2CN CH(Et)S(O)2Et
CH2CN CH(Et)S(O)2CF3
CH2CN CH(Et)S(O)2CH2CF3
CH2CN CH(n-Pr)SMe
CH2CN CH(n-Pr)SEt
CH2CN CH(n-Pr)SCF3
CH2CN CH(n-Pr)SCH2CF3
CH2CN CH(n-Pr)S(O)Me
CH2CN CH(n-Pr)S(O)Et
CH2CN CH(n-Pr)S(O)CF3
CH2CN CH(n-Pr)S(O)CH2CF3
CH2CN CH(n-Pr)S(O)2Me
CH2CN CH(n-Pr)S(O)2Et
CH2CN CH(n-Pr)S(O)2CF3
CH2CN CH(n-Pr)S(O)2CH2CF3
CH2CN CH(i-Pr)SMe
CH2CN CH(i-Pr)SEt
CH2CN CH(i-Pr)SCF3
CH2CN CH(i-Pr)SCH2CF3
CH2CN CH(i-Pr)S(O)Me
CH2CN CH(i-Pr)S(O)Et
CH2CN CH(i-Pr)S(O)CF3
CH2CN CH(i-Pr)S(O)CH2CF3
CH2CN CH(i-Pr)S(O)2Me
CH2CN CH(i-Pr)S(O)2Et
CH2CN CH(i-Pr)S(O)2CF3
CH2CN CH(i-Pr)S(O)2CH2CF3
CH2CN CH(n-Bu)SMe
CH2CN CH(n-Bu)SEt
CH2CN CH(n-Bu)SCF3
CH2CN CH(n-Bu)SCH2CF3
CH2CN CH(n-Bu)S(O)Me
CH2CN CH(n-Bu)S(O)Et
CH2CN CH(n-Bu)S(O)CF3
CH2CN CH(n-Bu)S(O)CH2CF3
CH2CN CH(n-Bu)S(O)2Me
CH2CN CH(n-Bu)S(O)2Et
CH2CN CH(n-Bu)S(O)2CF3
CH2CN CH(n-Bu)S(O)2CH2CF3
CH2CN CH(i-Bu)SMe
CH2CN CH(i-Bu)SEt
CH2CN CH(i-Bu)SCF3
CH2CN CH(i-Bu)SCH2CF3
CH2CN CH(i-Bu)S(O)Me
CH2CN CH(i-Bu)S(O)Et
CH2CN CH(i-Bu)S(O)CF3
CH2CN CH(i-Bu)S(O)CH2CF3
CH2CN CH(i-Bu)S(O)2Me
CH2CN CH(i-Bu)S(O)2Et
CH2CN CH(i-Bu)S(O)2CF3
CH2CN CH(i-Bu)S(O)2CH2CF3
CH2CN CH(s-Bu)SMe
CH2CN CH(s-Bu)SEt
CH2CN CH(s-Bu)SCF3
CH2CN CH(s-Bu)SCH2CF3
CH2CN CH(s-Bu)S(O)Me
CH2CN CH(s-Bu)S(O)Et
CH2CN CH(s-Bu)S(O)CF3
CH2CN CH(s-Bu)S(O)CH2CF3
CH2CN CH(s-Bu)S(O)2Me
CH2CN CH(s-Bu)S(O)2Et
CH2CN CH(s-Bu)S(O)2CF3
CH2CN CH(s-Bu)S(O)2CH2CF3
CH2CN CH(t-Bu)SMe
CH2CN CH(t-Bu)SEt
CH2CN CH(t-Bu)SCF3
CH2CN CH(t-Bu)SCH2CF3
CH2CN CH(t-Bu)S(O)Me
CH2CN CH(t-Bu)S(O)Et
CH2CN CH(t-Bu)S(O)CF3
CH2CN CH(t-Bu)S(O)CH2CF3
CH2CN CH(t-Bu)S(O)2Me
CH2CN CH(t-Bu)S(O)2Et
CH2CN CH(t-Bu)S(O)2CF3
CH2CN CH(t-Bu)S(O)2CH2CF3
CH2CN CH(CF3)SMe
CH2CN CH(CF3)SEt
CH2CN CH(CF3)SCF3
CH2CN CH(CF3)SCH2CF3
CH2CN CH(CF3)S(O)Me
CH2CN CH(CF3)S(O)Et
CH2CN CH(CF3)S(O)CF3
CH2CN CH(CF3)S(O)CH2CF3
CH2CN CH(CF3)S(O)2Me
CH2CN CH(CF3)S(O)2Et
CH2CN CH(CF3)S(O)2CF3
CH2CN CH(CF3)S(O)2CH2CF3
CH2CN CH2CH2SMe
CH2CN CH2CH2SEt
CH2CN CH2CH2SCF3
CH2CN CH2CH2SCH2CF3
CH2CN CH2CH2S(O)Me
CH2CN CH2CH2S(O)Et
CH2CN CH2CH2S(O)CF3
CH2CN CH2CH2S(O)CH2CF3
CH2CN CH2CH2S(O)2Me
CH2CN CH2CH2S(O)2Et
CH2CN CH2CH2S(O)2CF3
CH2CN CH2CH2S(O)2CH2CF3
CH2CN CH(Me)CH2SMe
CH2CN CH(Me)CH2SEt
CH2CN CH(Me)CH2SCF3
CH2CN CH(Me)CH2SCH2CF3
CH2CN CH(Me)CH2S(O)Me
CH2CN CH(Me)CH2S(O)Et
CH2CN CH(Me)CH2S(O)CF3
CH2CN CH(Me)CH2S(O)CH2CF3
CH2CN CH(Me)CH2S(O)2Me
CH2CN CH(Me)CH2S(O)2Et
CH2CN CH(Me)CH2S(O)2CF3
CH2CN CH(Me)CH2S(O)2CH2CF3
CH2CN CH(Et)CH2SMe
CH2CN CH(Et)CH2SEt
CH2CN CH(Et)CH2SCF3
CH2CN CH(Et)CH2SCH2CF3
CH2CN CH(Et)CH2S(O)Me
CH2CN CH(Et)CH2S(O)Et
CH2CN CH(Et)CH2S(O)CF3
CH2CN CH(Et)CH2S(O)CH2CF3
CH2CN CH(Et)CH2S(O)2Me
CH2CN CH(Et)CH2S(O)2Et
CH2CN CH(Et)CH2S(O)2CF3
CH2CN CH(Et)CH2S(O)2CH2CF3
CH2CN C(Me)2CH2SMe
CH2CN C(Me)2CH2SEt
CH2CN C(Me)2CH2SCF3
CH2CN C(Me)2CH2SCH2CF3
CH2CN C(Me)2CH2S(O)Me
CH2CN C(Me)2CH2S(O)Et
CH2CN C(Me)2CH2S(O)CF3
CH2CN C(Me)2CH2S(O)CH2CF3
CH2CN C(Me)2CH2S(O)2Me
CH2CN C(Me)2CH2S(O)2Et
CH2CN C(Me)2CH2S(O)2CF3
CH2CN C(Me)2CH2S(O)2CH2CF3
CH2CN CH2CH(Me)SMe
CH2CN CH2CH(Me)SEt
CH2CN CH2CH(Me)SCF3
CH2CN CH2CH(Me)SCH2CF3
CH2CN CH2CH(Me)S(O)Me
CH2CN CH2CH(Me)S(O)Et
CH2CN CH2CH(Me)S(O)CF3
CH2CN CH2CH(Me)S(O)CH2CF3
CH2CN CH2CH(Me)S(O)2Me
CH2CN CH2CH(Me)S(O)2Et
CH2CN CH2CH(Me)S(O)2CF3
CH2CN CH2CH(Me)S(O)2CH2CF3
CH2CN CH2CH(Et)SMe
CH2CN CH2CH(Et)SEt
CH2CN CH2CH(Et)SCF3
CH2CN CH2CH(Et)SCH2CF3
CH2CN CH2CH(Et)S(O)Me
CH2CN CH2CH(Et)S(O)Et
CH2CN CH2CH(Et)S(O)CF3
CH2CN CH2CH(Et)S(O)CH2CF3
CH2CN CH2CH(Et)S(O)2Me
CH2CN CH2CH(Et)S(O)2Et
CH2CN CH2CH(Et)S(O)2CF3
CH2CN CH2CH(Et)S(O)2CH2CF3
CH2CN CH(Me)CH(Me)SMe
CH2CN CH(Me)CH(Me)SEt
CH2CN CH(Me)CH(Me)SCF3
CH2CN CH(Me)CH(Me)SCH2CF3
CH2CN CH(Me)CH(Me)S(O)Me
CH2CN CH(Me)CH(Me)S(O)Et
CH2CN CH(Me)CH(Me)S(O)CF3
CH2CN CH(Me)CH(Me)S(O)CH2CF3
CH2CN CH(Me)CH(Me)S(O)2Me
CH2CN CH(Me)CH(Me)S(O)2Et
CH2CN CH(Me)CH(Me)S(O)2CF3
CH2CN CH(Me)CH(Me)S(O)2CH2CF3
CH2CH=CH2 CH2SMe
CH2CH=CH2 CH2SEt
CH2CH=CH2 CH2SCF3
CH2CH=CH2 CH2SCH2CF3
CH2CH=CH2 CH2S(O)Me
CH2CH=CH2 CH2S(O)Et
CH2CH=CH2 CH2S(O)CF3
CH2CH=CH2 CH2S(O)CH2CF3
CH2CH=CH2 CH2S(O)2Me
CH2CH=CH2 CH2S(O)2Et
CH2CH=CH2 CH2S(O)2CF3
CH2CH=CH2 CH2S(O)2CH2CF3
CH2CH=CH2 CH(Me)SMe
CH2CH=CH2 CH(Me)SEt
CH2CH=CH2 CH(Me)SCF3
CH2CH=CH2 CH(Me)SCH2CF3
CH2CH=CH2 CH(Me)S(O)Me
CH2CH=CH2 CH(Me)S(O)Et
CH2CH=CH2 CH(Me)S(O)CF3
CH2CH=CH2 CH(Me)S(O)CH2CF3
CH2CH=CH2 CH(Me)S(O)2Me
CH2CH=CH2 CH(Me)S(O)2Et
CH2CH=CH2 CH(Me)S(O)2CF3
CH2CH=CH2 CH(Me)S(O)2CH2CF3
CH2CH=CH2 CH(Et)SMe
CH2CH=CH2 CH(Et)SEt
CH2CH=CH2 CH(Et)SCF3
CH2CH=CH2 CH(Et)SCH2CF3
CH2CH=CH2 CH(Et)S(O)Me
CH2CH=CH2 CH(Et)S(O)Et
CH2CH=CH2 CH(Et)S(O)CF3
CH2CH=CH2 CH(Et)S(O)CH2CF3
CH2CH=CH2 CH(Et)S(O)2Me
CH2CH=CH2 CH(Et)S(O)2Et
CH2CH=CH2 CH(Et)S(O)2CF3
CH2CH=CH2 CH(Et)S(O)2CH2CF3
CH2CH=CH2 CH(n-Pr)SMe
CH2CH=CH2 CH(n-Pr)SEt
CH2CH=CH2 CH(n-Pr)SCF3
CH2CH=CH2 CH(n-Pr)SCH2CF3
CH2CH=CH2 CH(n-Pr)S(O)Me
CH2CH=CH2 CH(n-Pr)S(O)Et
CH2CH=CH2 CH(n-Pr)S(O)CF3
CH2CH=CH2 CH(n-Pr)S(O)CH2CF3
CH2CH=CH2 CH(n-Pr)S(O)2Me
CH2CH=CH2 CH(n-Pr)S(O)2Et
CH2CH=CH2 CH(n-Pr)S(O)2CF3
CH2CH=CH2 CH(n-Pr)S(O)2CH2CF3
CH2CH=CH2 CH(i-Pr)SMe
CH2CH=CH2 CH(i-Pr)SEt
CH2CH=CH2 CH(i-Pr)SCF3
CH2CH=CH2 CH(i-Pr)SCH2CF3
CH2CH=CH2 CH(i-Pr)S(O)Me
CH2CH=CH2 CH(i-Pr)S(O)Et
CH2CH=CH2 CH(i-Pr)S(O)CF3
CH2CH=CH2 CH(i-Pr)S(O)CH2CF3
CH2CH=CH2 CH(i-Pr)S(O)2Me
CH2CH=CH2 CH(i-Pr)S(O)2Et
CH2CH=CH2 CH(i-Pr)S(O)2CF3
CH2CH=CH2 CH(i-Pr)S(O)2CH2CF3
CH2CH=CH2 CH(n-Bu)SMe
CH2CH=CH2 CH(n-Bu)SEt
CH2CH=CH2 CH(n-Bu)SCF3
CH2CH=CH2 CH(n-Bu)SCH2CF3
CH2CH=CH2 CH(n-Bu)S(O)Me
CH2CH=CH2 CH(n-Bu)S(O)Et
CH2CH=CH2 CH(n-Bu)S(O)CF3
CH2CH=CH2 CH(n-Bu)S(O)CH2CF3
CH2CH=CH2 CH(n-Bu)S(O)2Me
CH2CH=CH2 CH(n-Bu)S(O)2Et
CH2CH=CH2 CH(n-Bu)S(O)2CF3
CH2CH=CH2 CH(n-Bu)S(O)2CH2CF3
CH2CH=CH2 CH(i-Bu)SMe
CH2CH=CH2 CH(i-Bu)SEt
CH2CH=CH2 CH(i-Bu)SCF3
CH2CH=CH2 CH(i-Bu)SCH2CF3
CH2CH=CH2 CH(i-Bu)S(O)Me
CH2CH=CH2 CH(i-Bu)S(O)Et
CH2CH=CH2 CH(i-Bu)S(O)CF3
CH2CH=CH2 CH(i-Bu)S(O)CH2CF3
CH2CH=CH2 CH(i-Bu)S(O)2Me
CH2CH=CH2 CH(i-Bu)S(O)2Et
CH2CH=CH2 CH(i-Bu)S(O)2CF3
CH2CH=CH2 CH(i-Bu)S(O)2CH2CF3
CH2CH=CH2 CH(s-Bu)SMe
CH2CH=CH2 CH(s-Bu)SEt
CH2CH=CH2 CH(s-Bu)SCF3
CH2CH=CH2 CH(s-Bu)SCH2CF3
CH2CH=CH2 CH(s-Bu)S(O)Me
CH2CH=CH2 CH(s-Bu)S(O)Et
CH2CH=CH2 CH(s-Bu)S(O)CF3
CH2CH=CH2 CH(s-Bu)S(O)CH2CF3
CH2CH=CH2 CH(s-Bu)S(O)2Me
CH2CH=CH2 CH(s-Bu)S(O)2Et
CH2CH=CH2 CH(s-Bu)S(O)2CF3
CH2CH=CH2 CH(s-Bu)S(O)2CH2CF3
CH2CH=CH2 CH(t-Bu)SMe
CH2CH=CH2 CH(t-Bu)SEt
CH2CH=CH2 CH(t-Bu)SCF3
CH2CH=CH2 CH(t-Bu)SCH2CF3
CH2CH=CH2 CH(t-Bu)S(O)Me
CH2CH=CH2 CH(t-Bu)S(O)Et
CH2CH=CH2 CH(t-Bu)S(O)CF3
CH2CH=CH2 CH(t-Bu)S(O)CH2CF3
CH2CH=CH2 CH(t-Bu)S(O)2Me
CH2CH=CH2 CH(t-Bu)S(O)2Et
CH2CH=CH2 CH(t-Bu)S(O)2CF3
CH2CH=CH2 CH(t-Bu)S(O)2CH2CF3
CH2CH=CH2 CH(CF3)SMe
CH2CH=CH2 CH(CF3)SEt
CH2CH=CH2 CH(CF3)SCF3
CH2CH=CH2 CH(CF3)SCH2CF3
CH2CH=CH2 CH(CF3)S(O)Me
CH2CH=CH2 CH(CF3)S(O)Et
CH2CH=CH2 CH(CF3)S(O)CF3
CH2CH=CH2 CH(CF3)S(O)CH2CF3
CH2CH=CH2 CH(CF3)S(O)2Me
CH2CH=CH2 CH(CF3)S(O)2Et
CH2CH=CH2 CH(CF3)S(O)2CF3
CH2CH=CH2 CH(CF3)S(O)2CH2CF3
CH2CH=CH2 CH2CH2SMe
CH2CH=CH2 CH2CH2SEt
CH2CH=CH2 CH2CH2SCF3
CH2CH=CH2 CH2CH2SCH2CF3
CH2CH=CH2 CH2CH2S(O)Me
CH2CH=CH2 CH2CH2S(O)Et
CH2CH=CH2 CH2CH2S(O)CF3
CH2CH=CH2 CH2CH2S(O)CH2CF3
CH2CH=CH2 CH2CH2S(O)2Me
CH2CH=CH2 CH2CH2S(O)2Et
CH2CH=CH2 CH2CH2S(O)2CF3
CH2CH=CH2 CH2CH2S(O)2CH2CF3
CH2CH=CH2 CH(Me)CH2SMe
CH2CH=CH2 CH(Me)CH2SEt
CH2CH=CH2 CH(Me)CH2SCF3
CH2CH=CH2 CH(Me)CH2SCH2CF3
CH2CH=CH2 CH(Me)CH2S(O)Me
CH2CH=CH2 CH(Me)CH2S(O)Et
CH2CH=CH2 CH(Me)CH2S(O)CF3
CH2CH=CH2 CH(Me)CH2S(O)CH2CF3
CH2CH=CH2 CH(Me)CH2S(O)2Me
CH2CH=CH2 CH(Me)CH2S(O)2Et
CH2CH=CH2 CH(Me)CH2S(O)2CF3
CH2CH=CH2 CH(Me)CH2S(O)2CH2CF3
CH2CH=CH2 CH(Et)CH2SMe
CH2CH=CH2 CH(Et)CH2SEt
CH2CH=CH2 CH(Et)CH2SCF3
CH2CH=CH2 CH(Et)CH2SCH2CF3
CH2CH=CH2 CH(Et)CH2S(O)Me
CH2CH=CH2 CH(Et)CH2S(O)Et
CH2CH=CH2 CH(Et)CH2S(O)CF3
CH2CH=CH2 CH(Et)CH2S(O)CH2CF3
CH2CH=CH2 CH(Et)CH2S(O)2Me
CH2CH=CH2 CH(Et)CH2S(O)2Et
CH2CH=CH2 CH(Et)CH2S(O)2CF3
CH2CH=CH2 CH(Et)CH2S(O)2CH2CF3
CH2CH=CH2 C(Me)2CH2SMe
CH2CH=CH2 C(Me)2CH2SEt
CH2CH=CH2 C(Me)2CH2SCF3
CH2CH=CH2 C(Me)2CH2SCH2CF3
CH2CH=CH2 C(Me)2CH2S(O)Me
CH2CH=CH2 C(Me)2CH2S(O)Et
CH2CH=CH2 C(Me)2CH2S(O)CF3
CH2CH=CH2 C(Me)2CH2S(O)CH2CF3
CH2CH=CH2 C(Me)2CH2S(O)2Me
CH2CH=CH2 C(Me)2CH2S(O)2Et
CH2CH=CH2 C(Me)2CH2S(O)2CF3
CH2CH=CH2 C(Me)2CH2S(O)2CH2CF3
CH2CH=CH2 CH2CH(Me)SMe
CH2CH=CH2 CH2CH(Me)SEt
CH2CH=CH2 CH2CH(Me)SCF3
CH2CH=CH2 CH2CH(Me)SCH2CF3
CH2CH=CH2 CH2CH(Me)S(O)Me
CH2CH=CH2 CH2CH(Me)S(O)Et
CH2CH=CH2 CH2CH(Me)S(O)CF3
CH2CH=CH2 CH2CH(Me)S(O)CH2CF3
CH2CH=CH2 CH2CH(Me)S(O)2Me
CH2CH=CH2 CH2CH(Me)S(O)2Et
CH2CH=CH2 CH2CH(Me)S(O)2CF3
CH2CH=CH2 CH2CH(Me)S(O)2CH2CF3
CH2CH=CH2 CH2CH(Et)SMe
CH2CH=CH2 CH2CH(Et)SEt
CH2CH=CH2 CH2CH(Et)SCF3
CH2CH=CH2 CH2CH(Et)SCH2CF3
CH2CH=CH2 CH2CH(Et)S(O)Me
CH2CH=CH2 CH2CH(Et)S(O)Et
CH2CH=CH2 CH2CH(Et)S(O)CF3
CH2CH=CH2 CH2CH(Et)S(O)CH2CF3
CH2CH=CH2 CH2CH(Et)S(O)2Me
CH2CH=CH2 CH2CH(Et)S(O)2Et
CH2CH=CH2 CH2CH(Et)S(O)2CF3
CH2CH=CH2 CH2CH(Et)S(O)2CH2CF3
CH2CH=CH2 CH(Me)CH(Me)SMe
CH2CH=CH2 CH(Me)CH(Me)SEt
CH2CH=CH2 CH(Me)CH(Me)SCF3
CH2CH=CH2 CH(Me)CH(Me)SCH2CF3
CH2CH=CH2 CH(Me)CH(Me)S(O)Me
CH2CH=CH2 CH(Me)CH(Me)S(O)Et
CH2CH=CH2 CH(Me)CH(Me)S(O)CF3
CH2CH=CH2 CH(Me)CH(Me)S(O)CH2CF3
CH2CH=CH2 CH(Me)CH(Me)S(O)2Me
CH2CH=CH2 CH(Me)CH(Me)S(O)2Et
CH2CH=CH2 CH(Me)CH(Me)S(O)2CF3
CH2CH=CH2 CH(Me)CH(Me)S(O)2CH2CF3
CH2CH(OMe)2 CH2SMe
CH2CH(OMe)2 CH2SEt
CH2CH(OMe)2 CH2SCF3
CH2CH(OMe)2 CH2SCH2CF3
CH2CH(OMe)2 CH2S(O)Me
CH2CH(OMe)2 CH2S(O)Et
CH2CH(OMe)2 CH2S(O)CF3
CH2CH(OMe)2 CH2S(O)CH2CF3
CH2CH(OMe)2 CH2S(O)2Me
CH2CH(OMe)2 CH2S(O)2Et
CH2CH(OMe)2 CH2S(O)2CF3
CH2CH(OMe)2 CH2S(O)2CH2CF3
CH2CH(OMe)2 CH(Me)SMe
CH2CH(OMe)2 CH(Me)SEt
CH2CH(OMe)2 CH(Me)SCF3
CH2CH(OMe)2 CH(Me)SCH2CF3
CH2CH(OMe)2 CH(Me)S(O)Me
CH2CH(OMe)2 CH(Me)S(O)Et
CH2CH(OMe)2 CH(Me)S(O)CF3
CH2CH(OMe)2 CH(Me)S(O)CH2CF3
CH2CH(OMe)2 CH(Me)S(O)2Me
CH2CH(OMe)2 CH(Me)S(O)2Et
CH2CH(OMe)2 CH(Me)S(O)2CF3
CH2CH(OMe)2 CH(Me)S(O)2CH2CF3
CH2CH(OMe)2 CH(Et)SMe
CH2CH(OMe)2 CH(Et)SEt
CH2CH(OMe)2 CH(Et)SCF3
CH2CH(OMe)2 CH(Et)SCH2CF3
CH2CH(OMe)2 CH(Et)S(O)Me
CH2CH(OMe)2 CH(Et)S(O)Et
CH2CH(OMe)2 CH(Et)S(O)CF3
CH2CH(OMe)2 CH(Et)S(O)CH2CF3
CH2CH(OMe)2 CH(Et)S(O)2Me
CH2CH(OMe)2 CH(Et)S(O)2Et
CH2CH(OMe)2 CH(Et)S(O)2CF3
CH2CH(OMe)2 CH(Et)S(O)2CH2CF3
CH2CH(OMe)2 CH(n-Pr)SMe
CH2CH(OMe)2 CH(n-Pr)SEt
CH2CH(OMe)2 CH(n-Pr)SCF3
CH2CH(OMe)2 CH(n-Pr)SCH2CF3
CH2CH(OMe)2 CH(n-Pr)S(O)Me
CH2CH(OMe)2 CH(n-Pr)S(O)Et
CH2CH(OMe)2 CH(n-Pr)S(O)CF3
CH2CH(OMe)2 CH(n-Pr)S(O)CH2CF3
CH2CH(OMe)2 CH(n-Pr)S(O)2Me
CH2CH(OMe)2 CH(n-Pr)S(O)2Et
CH2CH(OMe)2 CH(n-Pr)S(O)2CF3
CH2CH(OMe)2 CH(n-Pr)S(O)2CH2CF3
CH2CH(OMe)2 CH(i-Pr)SMe
CH2CH(OMe)2 CH(i-Pr)SEt
CH2CH(OMe)2 CH(i-Pr)SCF3
CH2CH(OMe)2 CH(i-Pr)SCH2CF3
CH2CH(OMe)2 CH(i-Pr)S(O)Me
CH2CH(OMe)2 CH(i-Pr)S(O)Et
CH2CH(OMe)2 CH(i-Pr)S(O)CF3
CH2CH(OMe)2 CH(i-Pr)S(O)CH2CF3
CH2CH(OMe)2 CH(i-Pr)S(O)2Me
CH2CH(OMe)2 CH(i-Pr)S(O)2Et
CH2CH(OMe)2 CH(i-Pr)S(O)2CF3
CH2CH(OMe)2 CH(i-Pr)S(O)2CH2CF3
CH2CH(OMe)2 CH(n-Bu)SMe
CH2CH(OMe)2 CH(n-Bu)SEt
CH2CH(OMe)2 CH(n-Bu)SCF3
CH2CH(OMe)2 CH(n-Bu)SCH2CF3
CH2CH(OMe)2 CH(n-Bu)S(O)Me
CH2CH(OMe)2 CH(n-Bu)S(O)Et
CH2CH(OMe)2 CH(n-Bu)S(O)CF3
CH2CH(OMe)2 CH(n-Bu)S(O)CH2CF3
CH2CH(OMe)2 CH(n-Bu)S(O)2Me
CH2CH(OMe)2 CH(n-Bu)S(O)2Et
CH2CH(OMe)2 CH(n-Bu)S(O)2CF3
CH2CH(OMe)2 CH(n-Bu)S(O)2CH2CF3
CH2CH(OMe)2 CH(i-Bu)SMe
CH2CH(OMe)2 CH(i-Bu)SEt
CH2CH(OMe)2 CH(i-Bu)SCF3
CH2CH(OMe)2 CH(i-Bu)SCH2CF3
CH2CH(OMe)2 CH(i-Bu)S(O)Me
CH2CH(OMe)2 CH(i-Bu)S(O)Et
CH2CH(OMe)2 CH(i-Bu)S(O)CF3
CH2CH(OMe)2 CH(i-Bu)S(O)CH2CF3
CH2CH(OMe)2 CH(i-Bu)S(O)2Me
CH2CH(OMe)2 CH(i-Bu)S(O)2Et
CH2CH(OMe)2 CH(i-Bu)S(O)2CF3
CH2CH(OMe)2 CH(i-Bu)S(O)2CH2CF3
CH2CH(OMe)2 CH(s-Bu)SMe
CH2CH(OMe)2 CH(s-Bu)SEt
CH2CH(OMe)2 CH(s-Bu)SCF3
CH2CH(OMe)2 CH(s-Bu)SCH2CF3
CH2CH(OMe)2 CH(s-Bu)S(O)Me
CH2CH(OMe)2 CH(s-Bu)S(O)Et
CH2CH(OMe)2 CH(s-Bu)S(O)CF3
CH2CH(OMe)2 CH(s-Bu)S(O)CH2CF3
CH2CH(OMe)2 CH(s-Bu)S(O)2Me
CH2CH(OMe)2 CH(s-Bu)S(O)2Et
CH2CH(OMe)2 CH(s-Bu)S(O)2CF3
CH2CH(OMe)2 CH(s-Bu)S(O)2CH2CF3
CH2CH(OMe)2 CH(t-Bu)SMe
CH2CH(OMe)2 CH(t-Bu)SEt
CH2CH(OMe)2 CH(t-Bu)SCF3
CH2CH(OMe)2 CH(t-Bu)SCH2CF3
CH2CH(OMe)2 CH(t-Bu)S(O)Me
CH2CH(OMe)2 CH(t-Bu)S(O)Et
CH2CH(OMe)2 CH(t-Bu)S(O)CF3
CH2CH(OMe)2 CH(t-Bu)S(O)CH2CF3
CH2CH(OMe)2 CH(t-Bu)S(O)2Me
CH2CH(OMe)2 CH(t-Bu)S(O)2Et
CH2CH(OMe)2 CH(t-Bu)S(O)2CF3
CH2CH(OMe)2 CH(t-Bu)S(O)2CH2CF3
CH2CH(OMe)2 CH(CF3)SMe
CH2CH(OMe)2 CH(CF3)SEt
CH2CH(OMe)2 CH(CF3)SCF3
CH2CH(OMe)2 CH(CF3)SCH2CF3
CH2CH(OMe)2 CH(CF3)S(O)Me
CH2CH(OMe)2 CH(CF3)S(O)Et
CH2CH(OMe)2 CH(CF3)S(O)CF3
CH2CH(OMe)2 CH(CF3)S(O)CH2CF3
CH2CH(OMe)2 CH(CF3)S(O)2Me
CH2CH(OMe)2 CH(CF3)S(O)2Et
CH2CH(OMe)2 CH(CF3)S(O)2CF3
CH2CH(OMe)2 CH(CF3)S(O)2CH2CF3
CH2CH(OMe)2 CH2CH2SMe
CH2CH(OMe)2 CH2CH2SEt
CH2CH(OMe)2 CH2CH2SCF3
CH2CH(OMe)2 CH2CH2SCH2CF3
CH2CH(OMe)2 CH2CH2S(O)Me
CH2CH(OMe)2 CH2CH2S(O)Et
CH2CH(OMe)2 CH2CH2S(O)CF3
CH2CH(OMe)2 CH2CH2S(O)CH2CF3
CH2CH(OMe)2 CH2CH2S(O)2Me
CH2CH(OMe)2 CH2CH2S(O)2Et
CH2CH(OMe)2 CH2CH2S(O)2CF3
CH2CH(OMe)2 CH2CH2S(O)2CH2CF3
CH2CH(OMe)2 CH(Me)CH2SMe
CH2CH(OMe)2 CH(Me)CH2SEt
CH2CH(OMe)2 CH(Me)CH2SCF3
CH2CH(OMe)2 CH(Me)CH2SCH2CF3
CH2CH(OMe)2 CH(Me)CH2S(O)Me
CH2CH(OMe)2 CH(Me)CH2S(O)Et
CH2CH(OMe)2 CH(Me)CH2S(O)CF3
CH2CH(OMe)2 CH(Me)CH2S(O)CH2CF3
CH2CH(OMe)2 CH(Me)CH2S(O)2Me
CH2CH(OMe)2 CH(Me)CH2S(O)2Et
CH2CH(OMe)2 CH(Me)CH2S(O)2CF3
CH2CH(OMe)2 CH(Me)CH2S(O)2CH2CF3
CH2CH(OMe)2 CH(Et)CH2SMe
CH2CH(OMe)2 CH(Et)CH2SEt
CH2CH(OMe)2 CH(Et)CH2SCF3
CH2CH(OMe)2 CH(Et)CH2SCH2CF3
CH2CH(OMe)2 CH(Et)CH2S(O)Me
CH2CH(OMe)2 CH(Et)CH2S(O)Et
CH2CH(OMe)2 CH(Et)CH2S(O)CF3
CH2CH(OMe)2 CH(Et)CH2S(O)CH2CF3
CH2CH(OMe)2 CH(Et)CH2S(O)2Me
CH2CH(OMe)2 CH(Et)CH2S(O)2Et
CH2CH(OMe)2 CH(Et)CH2S(O)2CF3
CH2CH(OMe)2 CH(Et)CH2S(O)2CH2CF3
CH2CH(OMe)2 C(Me)2CH2SMe
CH2CH(OMe)2 C(Me)2CH2SEt
CH2CH(OMe)2 C(Me)2CH2SCF3
CH2CH(OMe)2 C(Me)2CH2SCH2CF3
CH2CH(OMe)2 C(Me)2CH2S(O)Me
CH2CH(OMe)2 C(Me)2CH2S(O)Et
CH2CH(OMe)2 C(Me)2CH2S(O)CF3
CH2CH(OMe)2 C(Me)2CH2S(O)CH2CF3
CH2CH(OMe)2 C(Me)2CH2S(O)2Me
CH2CH(OMe)2 C(Me)2CH2S(O)2Et
CH2CH(OMe)2 C(Me)2CH2S(O)2CF3
CH2CH(OMe)2 C(Me)2CH2S(O)2CH2CF3
CH2CH(OMe)2 CH2CH(Me)SMe
CH2CH(OMe)2 CH2CH(Me)SEt
CH2CH(OMe)2 CH2CH(Me)SCF3
CH2CH(OMe)2 CH2CH(Me)SCH2CF3
CH2CH(OMe)2 CH2CH(Me)S(O)Me
CH2CH(OMe)2 CH2CH(Me)S(O)Et
CH2CH(OMe)2 CH2CH(Me)S(O)CF3
CH2CH(OMe)2 CH2CH(Me)S(O)CH2CF3
CH2CH(OMe)2 CH2CH(Me)S(O)2Me
CH2CH(OMe)2 CH2CH(Me)S(O)2Et
CH2CH(OMe)2 CH2CH(Me)S(O)2CF3
CH2CH(OMe)2 CH2CH(Me)S(O)2CH2CF3
CH2CH(OMe)2 CH2CH(Et)SMe
CH2CH(OMe)2 CH2CH(Et)SEt
CH2CH(OMe)2 CH2CH(Et)SCF3
CH2CH(OMe)2 CH2CH(Et)SCH2CF3
CH2CH(OMe)2 CH2CH(Et)S(O)Me
CH2CH(OMe)2 CH2CH(Et)S(O)Et
CH2CH(OMe)2 CH2CH(Et)S(O)CF3
CH2CH(OMe)2 CH2CH(Et)S(O)CH2CF3
CH2CH(OMe)2 CH2CH(Et)S(O)2Me
CH2CH(OMe)2 CH2CH(Et)S(O)2Et
CH2CH(OMe)2 CH2CH(Et)S(O)2CF3
CH2CH(OMe)2 CH2CH(Et)S(O)2CH2CF3
CH2CH(OMe)2 CH(Me)CH(Me)SMe
CH2CH(OMe)2 CH(Me)CH(Me)SEt
CH2CH(OMe)2 CH(Me)CH(Me)SCF3
CH2CH(OMe)2 CH(Me)CH(Me)SCH2CF3
CH2CH(OMe)2 CH(Me)CH(Me)S(O)Me
CH2CH(OMe)2 CH(Me)CH(Me)S(O)Et
CH2CH(OMe)2 CH(Me)CH(Me)S(O)CF3
CH2CH(OMe)2 CH(Me)CH(Me)S(O)CH2CF3
CH2CH(OMe)2 CH(Me)CH(Me)S(O)2Me
CH2CH(OMe)2 CH(Me)CH(Me)S(O)2Et
CH2CH(OMe)2 CH(Me)CH(Me)S(O)2CF3
CH2CH(OMe)2 CH(Me)CH(Me)S(O)2CH2CF3
CH(Me)OEt CH2SMe
CH(Me)OEt CH2SEt
CH(Me)OEt CH2SCF3
CH(Me)OEt CH2SCH2CF3
CH(Me)OEt CH2S(O)Me
CH(Me)OEt CH2S(O)Et
CH(Me)OEt CH2S(O)CF3
CH(Me)OEt CH2S(O)CH2CF3
CH(Me)OEt CH2S(O)2Me
CH(Me)OEt CH2S(O)2Et
CH(Me)OEt CH2S(O)2CF3
CH(Me)OEt CH2S(O)2CH2CF3
CH(Me)OEt CH(Me)SMe
CH(Me)OEt CH(Me)SEt
CH(Me)OEt CH(Me)SCF3
CH(Me)OEt CH(Me)SCH2CF3
CH(Me)OEt CH(Me)S(O)Me
CH(Me)OEt CH(Me)S(O)Et
CH(Me)OEt CH(Me)S(O)CF3
CH(Me)OEt CH(Me)S(O)CH2CF3
CH(Me)OEt CH(Me)S(O)2Me
CH(Me)OEt CH(Me)S(O)2Et
CH(Me)OEt CH(Me)S(O)2CF3
CH(Me)OEt CH(Me)S(O)2CH2CF3
CH(Me)OEt CH(Et)SMe
CH(Me)OEt CH(Et)SEt
CH(Me)OEt CH(Et)SCF3
CH(Me)OEt CH(Et)SCH2CF3
CH(Me)OEt CH(Et)S(O)Me
CH(Me)OEt CH(Et)S(O)Et
CH(Me)OEt CH(Et)S(O)CF3
CH(Me)OEt CH(Et)S(O)CH2CF3
CH(Me)OEt CH(Et)S(O)2Me
CH(Me)OEt CH(Et)S(O)2Et
CH(Me)OEt CH(Et)S(O)2CF3
CH(Me)OEt CH(Et)S(O)2CH2CF3
CH(Me)OEt CH(n-Pr)SMe
CH(Me)OEt CH(n-Pr)SEt
CH(Me)OEt CH(n-Pr)SCF3
CH(Me)OEt CH(n-Pr)SCH2CF3
CH(Me)OEt CH(n-Pr)S(O)Me
CH(Me)OEt CH(n-Pr)S(O)Et
CH(Me)OEt CH(n-Pr)S(O)CF3
CH(Me)OEt CH(n-Pr)S(O)CH2CF3
CH(Me)OEt CH(n-Pr)S(O)2Me
CH(Me)OEt CH(n-Pr)S(O)2Et
CH(Me)OEt CH(n-Pr)S(O)2CF3
CH(Me)OEt CH(n-Pr)S(O)2CH2CF3
CH(Me)OEt CH(i-Pr)SMe
CH(Me)OEt CH(i-Pr)SEt
CH(Me)OEt CH(i-Pr)SCF3
CH(Me)OEt CH(i-Pr)SCH2CF3
CH(Me)OEt CH(i-Pr)S(O)Me
CH(Me)OEt CH(i-Pr)S(O)Et
CH(Me)OEt CH(i-Pr)S(O)CF3
CH(Me)OEt CH(i-Pr)S(O)CH2CF3
CH(Me)OEt CH(i-Pr)S(O)2Me
CH(Me)OEt CH(i-Pr)S(O)2Et
CH(Me)OEt CH(i-Pr)S(O)2CF3
CH(Me)OEt CH(i-Pr)S(O)2CH2CF3
CH(Me)OEt CH(n-Bu)SMe
CH(Me)OEt CH(n-Bu)SEt
CH(Me)OEt CH(n-Bu)SCF3
CH(Me)OEt CH(n-Bu)SCH2CF3
CH(Me)OEt CH(n-Bu)S(O)Me
CH(Me)OEt CH(n-Bu)S(O)Et
CH(Me)OEt CH(n-Bu)S(O)CF3
CH(Me)OEt CH(n-Bu)S(O)CH2CF3
CH(Me)OEt CH(n-Bu)S(O)2Me
CH(Me)OEt CH(n-Bu)S(O)2Et
CH(Me)OEt CH(n-Bu)S(O)2CF3
CH(Me)OEt CH(n-Bu)S(O)2CH2CF3
CH(Me)OEt CH(i-Bu)SMe
CH(Me)OEt CH(i-Bu)SEt
CH(Me)OEt CH(i-Bu)SCF3
CH(Me)OEt CH(i-Bu)SCH2CF3
CH(Me)OEt CH(i-Bu)S(O)Me
CH(Me)OEt CH(i-Bu)S(O)Et
CH(Me)OEt CH(i-Bu)S(O)CF3
CH(Me)OEt CH(i-Bu)S(O)CH2CF3
CH(Me)OEt CH(i-Bu)S(O)2Me
CH(Me)OEt CH(i-Bu)S(O)2Et
CH(Me)OEt CH(i-Bu)S(O)2CF3
CH(Me)OEt CH(i-Bu)S(O)2CH2CF3
CH(Me)OEt CH(s-Bu)SMe
CH(Me)OEt CH(s-Bu)SEt
CH(Me)OEt CH(s-Bu)SCF3
CH(Me)OEt CH(s-Bu)SCH2CF3
CH(Me)OEt CH(s-Bu)S(O)Me
CH(Me)OEt CH(s-Bu)S(O)Et
CH(Me)OEt CH(s-Bu)S(O)CF3
CH(Me)OEt CH(s-Bu)S(O)CH2CF3
CH(Me)OEt CH(s-Bu)S(O)2Me
CH(Me)OEt CH(s-Bu)S(O)2Et
CH(Me)OEt CH(s-Bu)S(O)2CF3
CH(Me)OEt CH(s-Bu)S(O)2CH2CF3
CH(Me)OEt CH(t-Bu)SMe
CH(Me)OEt CH(t-Bu)SEt
CH(Me)OEt CH(t-Bu)SCF3
CH(Me)OEt CH(t-Bu)SCH2CF3
CH(Me)OEt CH(t-Bu)S(O)Me
CH(Me)OEt CH(t-Bu)S(O)Et
CH(Me)OEt CH(t-Bu)S(O)CF3
CH(Me)OEt CH(t-Bu)S(O)CH2CF3
CH(Me)OEt CH(t-Bu)S(O)2Me
CH(Me)OEt CH(t-Bu)S(O)2Et
CH(Me)OEt CH(t-Bu)S(O)2CF3
CH(Me)OEt CH(t-Bu)S(O)2CH2CF3
CH(Me)OEt CH(CF3)SMe
CH(Me)OEt CH(CF3)SEt
CH(Me)OEt CH(CF3)SCF3
CH(Me)OEt CH(CF3)SCH2CF3
CH(Me)OEt CH(CF3)S(O)Me
CH(Me)OEt CH(CF3)S(O)Et
CH(Me)OEt CH(CF3)S(O)CF3
CH(Me)OEt CH(CF3)S(O)CH2CF3
CH(Me)OEt CH(CF3)S(O)2Me
CH(Me)OEt CH(CF3)S(O)2Et
CH(Me)OEt CH(CF3)S(O)2CF3
CH(Me)OEt CH(CF3)S(O)2CH2CF3
CH(Me)OEt CH2CH2SMe
CH(Me)OEt CH2CH2SEt
CH(Me)OEt CH2CH2SCF3
CH(Me)OEt CH2CH2SCH2CF3
CH(Me)OEt CH2CH2S(O)Me
CH(Me)OEt CH2CH2S(O)Et
CH(Me)OEt CH2CH2S(O)CF3
CH(Me)OEt CH2CH2S(O)CH2CF3
CH(Me)OEt CH2CH2S(O)2Me
CH(Me)OEt CH2CH2S(O)2Et
CH(Me)OEt CH2CH2S(O)2CF3
CH(Me)OEt CH2CH2S(O)2CH2CF3
CH(Me)OEt CH(Me)CH2SMe
CH(Me)OEt CH(Me)CH2SEt
CH(Me)OEt CH(Me)CH2SCF3
CH(Me)OEt CH(Me)CH2SCH2CF3
CH(Me)OEt CH(Me)CH2S(O)Me
CH(Me)OEt CH(Me)CH2S(O)Et
CH(Me)OEt CH(Me)CH2S(O)CF3
CH(Me)OEt CH(Me)CH2S(O)CH2CF3
CH(Me)OEt CH(Me)CH2S(O)2Me
CH(Me)OEt CH(Me)CH2S(O)2Et
CH(Me)OEt CH(Me)CH2S(O)2CF3
CH(Me)OEt CH(Me)CH2S(O)2CH2CF3
CH(Me)OEt CH(Et)CH2SMe
CH(Me)OEt CH(Et)CH2SEt
CH(Me)OEt CH(Et)CH2SCF3
CH(Me)OEt CH(Et)CH2SCH2CF3
CH(Me)OEt CH(Et)CH2S(O)Me
CH(Me)OEt CH(Et)CH2S(O)Et
CH(Me)OEt CH(Et)CH2S(O)CF3
CH(Me)OEt CH(Et)CH2S(O)CH2CF3
CH(Me)OEt CH(Et)CH2S(O)2Me
CH(Me)OEt CH(Et)CH2S(O)2Et
CH(Me)OEt CH(Et)CH2S(O)2CF3
CH(Me)OEt CH(Et)CH2S(O)2CH2CF3
CH(Me)OEt C(Me)2CH2SMe
CH(Me)OEt C(Me)2CH2SEt
CH(Me)OEt C(Me)2CH2SCF3
CH(Me)OEt C(Me)2CH2SCH2CF3
CH(Me)OEt C(Me)2CH2S(O)Me
CH(Me)OEt C(Me)2CH2S(O)Et
CH(Me)OEt C(Me)2CH2S(O)CF3
CH(Me)OEt C(Me)2CH2S(O)CH2CF3
CH(Me)OEt C(Me)2CH2S(O)2Me
CH(Me)OEt C(Me)2CH2S(O)2Et
CH(Me)OEt C(Me)2CH2S(O)2CF3
CH(Me)OEt C(Me)2CH2S(O)2CH2CF3
CH(Me)OEt CH2CH(Me)SMe
CH(Me)OEt CH2CH(Me)SEt
CH(Me)OEt CH2CH(Me)SCF3
CH(Me)OEt CH2CH(Me)SCH2CF3
CH(Me)OEt CH2CH(Me)S(O)Me
CH(Me)OEt CH2CH(Me)S(O)Et
CH(Me)OEt CH2CH(Me)S(O)CF3
CH(Me)OEt CH2CH(Me)S(O)CH2CF3
CH(Me)OEt CH2CH(Me)S(O)2Me
CH(Me)OEt CH2CH(Me)S(O)2Et
CH(Me)OEt CH2CH(Me)S(O)2CF3
CH(Me)OEt CH2CH(Me)S(O)2CH2CF3
CH(Me)OEt CH2CH(Et)SMe
CH(Me)OEt CH2CH(Et)SEt
CH(Me)OEt CH2CH(Et)SCF3
CH(Me)OEt CH2CH(Et)SCH2CF3
CH(Me)OEt CH2CH(Et)S(O)Me
CH(Me)OEt CH2CH(Et)S(O)Et
CH(Me)OEt CH2CH(Et)S(O)CF3
CH(Me)OEt CH2CH(Et)S(O)CH2CF3
CH(Me)OEt CH2CH(Et)S(O)2Me
CH(Me)OEt CH2CH(Et)S(O)2Et
CH(Me)OEt CH2CH(Et)S(O)2CF3
CH(Me)OEt CH2CH(Et)S(O)2CH2CF3
CH(Me)OEt CH(Me)CH(Me)SMe
CH(Me)OEt CH(Me)CH(Me)SEt
CH(Me)OEt CH(Me)CH(Me)SCF3
CH(Me)OEt CH(Me)CH(Me)SCH2CF3
CH(Me)OEt CH(Me)CH(Me)S(O)Me
CH(Me)OEt CH(Me)CH(Me)S(O)Et
CH(Me)OEt CH(Me)CH(Me)S(O)CF3
CH(Me)OEt CH(Me)CH(Me)S(O)CH2CF3
CH(Me)OEt CH(Me)CH(Me)S(O)2Me
CH(Me)OEt CH(Me)CH(Me)S(O)2Et
CH(Me)OEt CH(Me)CH(Me)S(O)2CF3
CH(Me)OEt CH(Me)CH(Me)S(O)2CH2CF3
S(O)2Me CH2SMe
S(O)2Me CH2SEt
S(O)2Me CH2SCF3
S(O)2Me CH2SCH2CF3
S(O)2Me CH2S(O)Me
S(O)2Me CH2S(O)Et
S(O)2Me CH2S(O)CF3
S(O)2Me CH2S(O)CH2CF3
S(O)2Me CH2S(O)2Me
S(O)2Me CH2S(O)2Et
S(O)2Me CH2S(O)2CF3
S(O)2Me CH2S(O)2CH2CF3
S(O)2Me CH(Me)SMe
S(O)2Me CH(Me)SEt
S(O)2Me CH(Me)SCF3
S(O)2Me CH(Me)SCH2CF3
S(O)2Me CH(Me)S(O)Me
S(O)2Me CH(Me)S(O)Et
S(O)2Me CH(Me)S(O)CF3
S(O)2Me CH(Me)S(O)CH2CF3
S(O)2Me CH(Me)S(O)2Me
S(O)2Me CH(Me)S(O)2Et
S(O)2Me CH(Me)S(O)2CF3
S(O)2Me CH(Me)S(O)2CH2CF3
S(O)2Me CH(Et)SMe
S(O)2Me CH(Et)SEt
S(O)2Me CH(Et)SCF3
S(O)2Me CH(Et)SCH2CF3
S(O)2Me CH(Et)S(O)Me
S(O)2Me CH(Et)S(O)Et
S(O)2Me CH(Et)S(O)CF3
S(O)2Me CH(Et)S(O)CH2CF3
S(O)2Me CH(Et)S(O)2Me
S(O)2Me CH(Et)S(O)2Et
S(O)2Me CH(Et)S(O)2CF3
S(O)2Me CH(Et)S(O)2CH2CF3
S(O)2Me CH(n-Pr)SMe
S(O)2Me CH(n-Pr)SEt
S(O)2Me CH(n-Pr)SCF3
S(O)2Me CH(n-Pr)SCH2CF3
S(O)2Me CH(n-Pr)S(O)Me
S(O)2Me CH(n-Pr)S(O)Et
S(O)2Me CH(n-Pr)S(O)CF3
S(O)2Me CH(n-Pr)S(O)CH2CF3
S(O)2Me CH(n-Pr)S(O)2Me
S(O)2Me CH(n-Pr)S(O)2Et
S(O)2Me CH(n-Pr)S(O)2CF3
S(O)2Me CH(n-Pr)S(O)2CH2CF3
S(O)2Me CH(i-Pr)SMe
S(O)2Me CH(i-Pr)SEt
S(O)2Me CH(i-Pr)SCF3
S(O)2Me CH(i-Pr)SCH2CF3
S(O)2Me CH(i-Pr)S(O)Me
S(O)2Me CH(i-Pr)S(O)Et
S(O)2Me CH(i-Pr)S(O)CF3
S(O)2Me CH(i-Pr)S(O)CH2CF3
S(O)2Me CH(i-Pr)S(O)2Me
S(O)2Me CH(i-Pr)S(O)2Et
S(O)2Me CH(i-Pr)S(O)2CF3
S(O)2Me CH(i-Pr)S(O)2CH2CF3
S(O)2Me CH(n-Bu)SMe
S(O)2Me CH(n-Bu)SEt
S(O)2Me CH(n-Bu)SCF3
S(O)2Me CH(n-Bu)SCH2CF3
S(O)2Me CH(n-Bu)S(O)Me
S(O)2Me CH(n-Bu)S(O)Et
S(O)2Me CH(n-Bu)S(O)CF3
S(O)2Me CH(n-Bu)S(O)CH2CF3
S(O)2Me CH(n-Bu)S(O)2Me
S(O)2Me CH(n-Bu)S(O)2Et
S(O)2Me CH(n-Bu)S(O)2CF3
S(O)2Me CH(n-Bu)S(O)2CH2CF3
S(O)2Me CH(i-Bu)SMe
S(O)2Me CH(i-Bu)SEt
S(O)2Me CH(i-Bu)SCF3
S(O)2Me CH(i-Bu)SCH2CF3
S(O)2Me CH(i-Bu)S(O)Me
S(O)2Me CH(i-Bu)S(O)Et
S(O)2Me CH(i-Bu)S(O)CF3
S(O)2Me CH(i-Bu)S(O)CH2CF3
S(O)2Me CH(i-Bu)S(O)2Me
S(O)2Me CH(i-Bu)S(O)2Et
S(O)2Me CH(i-Bu)S(O)2CF3
S(O)2Me CH(i-Bu)S(O)2CH2CF3
S(O)2Me CH(s-Bu)SMe
S(O)2Me CH(s-Bu)SEt
S(O)2Me CH(s-Bu)SCF3
S(O)2Me CH(s-Bu)SCH2CF3
S(O)2Me CH(s-Bu)S(O)Me
S(O)2Me CH(s-Bu)S(O)Et
S(O)2Me CH(s-Bu)S(O)CF3
S(O)2Me CH(s-Bu)S(O)CH2CF3
S(O)2Me CH(s-Bu)S(O)2Me
S(O)2Me CH(s-Bu)S(O)2Et
S(O)2Me CH(s-Bu)S(O)2CF3
S(O)2Me CH(s-Bu)S(O)2CH2CF3
S(O)2Me CH(t-Bu)SMe
S(O)2Me CH(t-Bu)SEt
S(O)2Me CH(t-Bu)SCF3
S(O)2Me CH(t-Bu)SCH2CF3
S(O)2Me CH(t-Bu)S(O)Me
S(O)2Me CH(t-Bu)S(O)Et
S(O)2Me CH(t-Bu)S(O)CF3
S(O)2Me CH(t-Bu)S(O)CH2CF3
S(O)2Me CH(t-Bu)S(O)2Me
S(O)2Me CH(t-Bu)S(O)2Et
S(O)2Me CH(t-Bu)S(O)2CF3
S(O)2Me CH(t-Bu)S(O)2CH2CF3
S(O)2Me CH(CF3)SMe
S(O)2Me CH(CF3)SEt
S(O)2Me CH(CF3)SCF3
S(O)2Me CH(CF3)SCH2CF3
S(O)2Me CH(CF3)S(O)Me
S(O)2Me CH(CF3)S(O)Et
S(O)2Me CH(CF3)S(O)CF3
S(O)2Me CH(CF3)S(O)CH2CF3
S(O)2Me CH(CF3)S(O)2Me
S(O)2Me CH(CF3)S(O)2Et
S(O)2Me CH(CF3)S(O)2CF3
S(O)2Me CH(CF3)S(O)2CH2CF3
S(O)2Me CH2CH2SMe
S(O)2Me CH2CH2SEt
S(O)2Me CH2CH2SCF3
S(O)2Me CH2CH2SCH2CF3
S(O)2Me CH2CH2S(O)Me
S(O)2Me CH2CH2S(O)Et
S(O)2Me CH2CH2S(O)CF3
S(O)2Me CH2CH2S(O)CH2CF3
S(O)2Me CH2CH2S(O)2Me
S(O)2Me CH2CH2S(O)2Et
S(O)2Me CH2CH2S(O)2CF3
S(O)2Me CH2CH2S(O)2CH2CF3
S(O)2Me CH(Me)CH2SMe
S(O)2Me CH(Me)CH2SEt
S(O)2Me CH(Me)CH2SCF3
S(O)2Me CH(Me)CH2SCH2CF3
S(O)2Me CH(Me)CH2S(O)Me
S(O)2Me CH(Me)CH2S(O)Et
S(O)2Me CH(Me)CH2S(O)CF3
S(O)2Me CH(Me)CH2S(O)CH2CF3
S(O)2Me CH(Me)CH2S(O)2Me
S(O)2Me CH(Me)CH2S(O)2Et
S(O)2Me CH(Me)CH2S(O)2CF3
S(O)2Me CH(Me)CH2S(O)2CH2CF3
S(O)2Me CH(Et)CH2SMe
S(O)2Me CH(Et)CH2SEt
S(O)2Me CH(Et)CH2SCF3
S(O)2Me CH(Et)CH2SCH2CF3
S(O)2Me CH(Et)CH2S(O)Me
S(O)2Me CH(Et)CH2S(O)Et
S(O)2Me CH(Et)CH2S(O)CF3
S(O)2Me CH(Et)CH2S(O)CH2CF3
S(O)2Me CH(Et)CH2S(O)2Me
S(O)2Me CH(Et)CH2S(O)2Et
S(O)2Me CH(Et)CH2S(O)2CF3
S(O)2Me CH(Et)CH2S(O)2CH2CF3
S(O)2Me C(Me)2CH2SMe
S(O)2Me C(Me)2CH2SEt
S(O)2Me C(Me)2CH2SCF3
S(O)2Me C(Me)2CH2SCH2CF3
S(O)2Me C(Me)2CH2S(O)Me
S(O)2Me C(Me)2CH2S(O)Et
S(O)2Me C(Me)2CH2S(O)CF3
S(O)2Me C(Me)2CH2S(O)CH2CF3
S(O)2Me C(Me)2CH2S(O)2Me
S(O)2Me C(Me)2CH2S(O)2Et
S(O)2Me C(Me)2CH2S(O)2CF3
S(O)2Me C(Me)2CH2S(O)2CH2CF3
S(O)2Me CH2CH(Me)SMe
S(O)2Me CH2CH(Me)SEt
S(O)2Me CH2CH(Me)SCF3
S(O)2Me CH2CH(Me)SCH2CF3
S(O)2Me CH2CH(Me)S(O)Me
S(O)2Me CH2CH(Me)S(O)Et
S(O)2Me CH2CH(Me)S(O)CF3
S(O)2Me CH2CH(Me)S(O)CH2CF3
S(O)2Me CH2CH(Me)S(O)2Me
S(O)2Me CH2CH(Me)S(O)2Et
S(O)2Me CH2CH(Me)S(O)2CF3
S(O)2Me CH2CH(Me)S(O)2CH2CF3
S(O)2Me CH2CH(Et)SMe
S(O)2Me CH2CH(Et)SEt
S(O)2Me CH2CH(Et)SCF3
S(O)2Me CH2CH(Et)SCH2CF3
S(O)2Me CH2CH(Et)S(O)Me
S(O)2Me CH2CH(Et)S(O)Et
S(O)2Me CH2CH(Et)S(O)CF3
S(O)2Me CH2CH(Et)S(O)CH2CF3
S(O)2Me CH2CH(Et)S(O)2Me
S(O)2Me CH2CH(Et)S(O)2Et
S(O)2Me CH2CH(Et)S(O)2CF3
S(O)2Me CH2CH(Et)S(O)2CH2CF3
S(O)2Me CH(Me)CH(Me)SMe
S(O)2Me CH(Me)CH(Me)SEt
S(O)2Me CH(Me)CH(Me)SCF3
S(O)2Me CH(Me)CH(Me)SCH2CF3
S(O)2Me CH(Me)CH(Me)S(O)Me
S(O)2Me CH(Me)CH(Me)S(O)Et
S(O)2Me CH(Me)CH(Me)S(O)CF3
S(O)2Me CH(Me)CH(Me)S(O)CH2CF3
S(O)2Me CH(Me)CH(Me)S(O)2Me
S(O)2Me CH(Me)CH(Me)S(O)2Et
S(O)2Me CH(Me)CH(Me)S(O)2CF3
S(O)2Me CH(Me)CH(Me)S(O)2CH2CF3
D2-32a CH2SMe
D2-32a CH2SEt
D2-32a CH2SCF3
D2-32a CH2SCH2CF3
D2-32a CH2S(O)Me
D2-32a CH2S(O)Et
D2-32a CH2S(O)CF3
D2-32a CH2S(O)CH2CF3
D2-32a CH2S(O)2Me
D2-32a CH2S(O)2Et
D2-32a CH2S(O)2CF3
D2-32a CH2S(O)2CH2CF3
D2-32a CH(Me)SMe
D2-32a CH(Me)SEt
D2-32a CH(Me)SCF3
D2-32a CH(Me)SCH2CF3
D2-32a CH(Me)S(O)Me
D2-32a CH(Me)S(O)Et
D2-32a CH(Me)S(O)CF3
D2-32a CH(Me)S(O)CH2CF3
D2-32a CH(Me)S(O)2Me
D2-32a CH(Me)S(O)2Et
D2-32a CH(Me)S(O)2CF3
D2-32a CH(Me)S(O)2CH2CF3
D2-32a CH(Et)SMe
D2-32a CH(Et)SEt
D2-32a CH(Et)SCF3
D2-32a CH(Et)SCH2CF3
D2-32a CH(Et)S(O)Me
D2-32a CH(Et)S(O)Et
D2-32a CH(Et)S(O)CF3
D2-32a CH(Et)S(O)CH2CF3
D2-32a CH(Et)S(O)2Me
D2-32a CH(Et)S(O)2Et
D2-32a CH(Et)S(O)2CF3
D2-32a CH(Et)S(O)2CH2CF3
D2-32a CH(n-Pr)SMe
D2-32a CH(n-Pr)SEt
D2-32a CH(n-Pr)SCF3
D2-32a CH(n-Pr)SCH2CF3
D2-32a CH(n-Pr)S(O)Me
D2-32a CH(n-Pr)S(O)Et
D2-32a CH(n-Pr)S(O)CF3
D2-32a CH(n-Pr)S(O)CH2CF3
D2-32a CH(n-Pr)S(O)2Me
D2-32a CH(n-Pr)S(O)2Et
D2-32a CH(n-Pr)S(O)2CF3
D2-32a CH(n-Pr)S(O)2CH2CF3
D2-32a CH(i-Pr)SMe
D2-32a CH(i-Pr)SEt
D2-32a CH(i-Pr)SCF3
D2-32a CH(i-Pr)SCH2CF3
D2-32a CH(i-Pr)S(O)Me
D2-32a CH(i-Pr)S(O)Et
D2-32a CH(i-Pr)S(O)CF3
D2-32a CH(i-Pr)S(O)CH2CF3
D2-32a CH(i-Pr)S(O)2Me
D2-32a CH(i-Pr)S(O)2Et
D2-32a CH(i-Pr)S(O)2CF3
D2-32a CH(i-Pr)S(O)2CH2CF3
D2-32a CH(n-Bu)SMe
D2-32a CH(n-Bu)SEt
D2-32a CH(n-Bu)SCF3
D2-32a CH(n-Bu)SCH2CF3
D2-32a CH(n-Bu)S(O)Me
D2-32a CH(n-Bu)S(O)Et
D2-32a CH(n-Bu)S(O)CF3
D2-32a CH(n-Bu)S(O)CH2CF3
D2-32a CH(n-Bu)S(O)2Me
D2-32a CH(n-Bu)S(O)2Et
D2-32a CH(n-Bu)S(O)2CF3
D2-32a CH(n-Bu)S(O)2CH2CF3
D2-32a CH(i-Bu)SMe
D2-32a CH(i-Bu)SEt
D2-32a CH(i-Bu)SCF3
D2-32a CH(i-Bu)SCH2CF3
D2-32a CH(i-Bu)S(O)Me
D2-32a CH(i-Bu)S(O)Et
D2-32a CH(i-Bu)S(O)CF3
D2-32a CH(i-Bu)S(O)CH2CF3
D2-32a CH(i-Bu)S(O)2Me
D2-32a CH(i-Bu)S(O)2Et
D2-32a CH(i-Bu)S(O)2CF3
D2-32a CH(i-Bu)S(O)2CH2CF3
D2-32a CH(s-Bu)SMe
D2-32a CH(s-Bu)SEt
D2-32a CH(s-Bu)SCF3
D2-32a CH(s-Bu)SCH2CF3
D2-32a CH(s-Bu)S(O)Me
D2-32a CH(s-Bu)S(O)Et
D2-32a CH(s-Bu)S(O)CF3
D2-32a CH(s-Bu)S(O)CH2CF3
D2-32a CH(s-Bu)S(O)2Me
D2-32a CH(s-Bu)S(O)2Et
D2-32a CH(s-Bu)S(O)2CF3
D2-32a CH(s-Bu)S(O)2CH2CF3
D2-32a CH(t-Bu)SMe
D2-32a CH(t-Bu)SEt
D2-32a CH(t-Bu)SCF3
D2-32a CH(t-Bu)SCH2CF3
D2-32a CH(t-Bu)S(O)Me
D2-32a CH(t-Bu)S(O)Et
D2-32a CH(t-Bu)S(O)CF3
D2-32a CH(t-Bu)S(O)CH2CF3
D2-32a CH(t-Bu)S(O)2Me
D2-32a CH(t-Bu)S(O)2Et
D2-32a CH(t-Bu)S(O)2CF3
D2-32a CH(t-Bu)S(O)2CH2CF3
D2-32a CH(CF3)SMe
D2-32a CH(CF3)SEt
D2-32a CH(CF3)SCF3
D2-32a CH(CF3)SCH2CF3
D2-32a CH(CF3)S(O)Me
D2-32a CH(CF3)S(O)Et
D2-32a CH(CF3)S(O)CF3
D2-32a CH(CF3)S(O)CH2CF3
D2-32a CH(CF3)S(O)2Me
D2-32a CH(CF3)S(O)2Et
D2-32a CH(CF3)S(O)2CF3
D2-32a CH(CF3)S(O)2CH2CF3
D2-32a CH2CH2SMe
D2-32a CH2CH2SEt
D2-32a CH2CH2SCF3
D2-32a CH2CH2SCH2CF3
D2-32a CH2CH2S(O)Me
D2-32a CH2CH2S(O)Et
D2-32a CH2CH2S(O)CF3
D2-32a CH2CH2S(O)CH2CF3
D2-32a CH2CH2S(O)2Me
D2-32a CH2CH2S(O)2Et
D2-32a CH2CH2S(O)2CF3
D2-32a CH2CH2S(O)2CH2CF3
D2-32a CH(Me)CH2SMe
D2-32a CH(Me)CH2SEt
D2-32a CH(Me)CH2SCF3
D2-32a CH(Me)CH2SCH2CF3
D2-32a CH(Me)CH2S(O)Me
D2-32a CH(Me)CH2S(O)Et
D2-32a CH(Me)CH2S(O)CF3
D2-32a CH(Me)CH2S(O)CH2CF3
D2-32a CH(Me)CH2S(O)2Me
D2-32a CH(Me)CH2S(O)2Et
D2-32a CH(Me)CH2S(O)2CF3
D2-32a CH(Me)CH2S(O)2CH2CF3
D2-32a CH(Et)CH2SMe
D2-32a CH(Et)CH2SEt
D2-32a CH(Et)CH2SCF3
D2-32a CH(Et)CH2SCH2CF3
D2-32a CH(Et)CH2S(O)Me
D2-32a CH(Et)CH2S(O)Et
D2-32a CH(Et)CH2S(O)CF3
D2-32a CH(Et)CH2S(O)CH2CF3
D2-32a CH(Et)CH2S(O)2Me
D2-32a CH(Et)CH2S(O)2Et
D2-32a CH(Et)CH2S(O)2CF3
D2-32a CH(Et)CH2S(O)2CH2CF3
D2-32a C(Me)2CH2SMe
D2-32a C(Me)2CH2SEt
D2-32a C(Me)2CH2SCF3
D2-32a C(Me)2CH2SCH2CF3
D2-32a C(Me)2CH2S(O)Me
D2-32a C(Me)2CH2S(O)Et
D2-32a C(Me)2CH2S(O)CF3
D2-32a C(Me)2CH2S(O)CH2CF3
D2-32a C(Me)2CH2S(O)2Me
D2-32a C(Me)2CH2S(O)2Et
D2-32a C(Me)2CH2S(O)2CF3
D2-32a C(Me)2CH2S(O)2CH2CF3
D2-32a CH2CH(Me)SMe
D2-32a CH2CH(Me)SEt
D2-32a CH2CH(Me)SCF3
D2-32a CH2CH(Me)SCH2CF3
D2-32a CH2CH(Me)S(O)Me
D2-32a CH2CH(Me)S(O)Et
D2-32a CH2CH(Me)S(O)CF3
D2-32a CH2CH(Me)S(O)CH2CF3
D2-32a CH2CH(Me)S(O)2Me
D2-32a CH2CH(Me)S(O)2Et
D2-32a CH2CH(Me)S(O)2CF3
D2-32a CH2CH(Me)S(O)2CH2CF3
D2-32a CH2CH(Et)SMe
D2-32a CH2CH(Et)SEt
D2-32a CH2CH(Et)SCF3
D2-32a CH2CH(Et)SCH2CF3
D2-32a CH2CH(Et)S(O)Me
D2-32a CH2CH(Et)S(O)Et
D2-32a CH2CH(Et)S(O)CF3
D2-32a CH2CH(Et)S(O)CH2CF3
D2-32a CH2CH(Et)S(O)2Me
D2-32a CH2CH(Et)S(O)2Et
D2-32a CH2CH(Et)S(O)2CF3
D2-32a CH2CH(Et)S(O)2CH2CF3
D2-32a CH(Me)CH(Me)SMe
D2-32a CH(Me)CH(Me)SEt
D2-32a CH(Me)CH(Me)SCF3
D2-32a CH(Me)CH(Me)SCH2CF3
D2-32a CH(Me)CH(Me)S(O)Me
D2-32a CH(Me)CH(Me)S(O)Et
D2-32a CH(Me)CH(Me)S(O)CF3
D2-32a CH(Me)CH(Me)S(O)CH2CF3
D2-32a CH(Me)CH(Me)S(O)2Me
D2-32a CH(Me)CH(Me)S(O)2Et
D2-32a CH(Me)CH(Me)S(O)2CF3
D2-32a CH(Me)CH(Me)S(O)2CH2CF3
D2-33a CH2SMe
D2-33a CH2SEt
D2-33a CH2SCF3
D2-33a CH2SCH2CF3
D2-33a CH2S(O)Me
D2-33a CH2S(O)Et
D2-33a CH2S(O)CF3
D2-33a CH2S(O)CH2CF3
D2-33a CH2S(O)2Me
D2-33a CH2S(O)2Et
D2-33a CH2S(O)2CF3
D2-33a CH2S(O)2CH2CF3
D2-33a CH(Me)SMe
D2-33a CH(Me)SEt
D2-33a CH(Me)SCF3
D2-33a CH(Me)SCH2CF3
D2-33a CH(Me)S(O)Me
D2-33a CH(Me)S(O)Et
D2-33a CH(Me)S(O)CF3
D2-33a CH(Me)S(O)CH2CF3
D2-33a CH(Me)S(O)2Me
D2-33a CH(Me)S(O)2Et
D2-33a CH(Me)S(O)2CF3
D2-33a CH(Me)S(O)2CH2CF3
D2-33a CH(Et)SMe
D2-33a CH(Et)SEt
D2-33a CH(Et)SCF3
D2-33a CH(Et)SCH2CF3
D2-33a CH(Et)S(O)Me
D2-33a CH(Et)S(O)Et
D2-33a CH(Et)S(O)CF3
D2-33a CH(Et)S(O)CH2CF3
D2-33a CH(Et)S(O)2Me
D2-33a CH(Et)S(O)2Et
D2-33a CH(Et)S(O)2CF3
D2-33a CH(Et)S(O)2CH2CF3
D2-33a CH(n-Pr)SMe
D2-33a CH(n-Pr)SEt
D2-33a CH(n-Pr)SCF3
D2-33a CH(n-Pr)SCH2CF3
D2-33a CH(n-Pr)S(O)Me
D2-33a CH(n-Pr)S(O)Et
D2-33a CH(n-Pr)S(O)CF3
D2-33a CH(n-Pr)S(O)CH2CF3
D2-33a CH(n-Pr)S(O)2Me
D2-33a CH(n-Pr)S(O)2Et
D2-33a CH(n-Pr)S(O)2CF3
D2-33a CH(n-Pr)S(O)2CH2CF3
D2-33a CH(i-Pr)SMe
D2-33a CH(i-Pr)SEt
D2-33a CH(i-Pr)SCF3
D2-33a CH(i-Pr)SCH2CF3
D2-33a CH(i-Pr)S(O)Me
D2-33a CH(i-Pr)S(O)Et
D2-33a CH(i-Pr)S(O)CF3
D2-33a CH(i-Pr)S(O)CH2CF3
D2-33a CH(i-Pr)S(O)2Me
D2-33a CH(i-Pr)S(O)2Et
D2-33a CH(i-Pr)S(O)2CF3
D2-33a CH(i-Pr)S(O)2CH2CF3
D2-33a CH(n-Bu)SMe
D2-33a CH(n-Bu)SEt
D2-33a CH(n-Bu)SCF3
D2-33a CH(n-Bu)SCH2CF3
D2-33a CH(n-Bu)S(O)Me
D2-33a CH(n-Bu)S(O)Et
D2-33a CH(n-Bu)S(O)CF3
D2-33a CH(n-Bu)S(O)CH2CF3
D2-33a CH(n-Bu)S(O)2Me
D2-33a CH(n-Bu)S(O)2Et
D2-33a CH(n-Bu)S(O)2CF3
D2-33a CH(n-Bu)S(O)2CH2CF3
D2-33a CH(i-Bu)SMe
D2-33a CH(i-Bu)SEt
D2-33a CH(i-Bu)SCF3
D2-33a CH(i-Bu)SCH2CF3
D2-33a CH(i-Bu)S(O)Me
D2-33a CH(i-Bu)S(O)Et
D2-33a CH(i-Bu)S(O)CF3
D2-33a CH(i-Bu)S(O)CH2CF3
D2-33a CH(i-Bu)S(O)2Me
D2-33a CH(i-Bu)S(O)2Et
D2-33a CH(i-Bu)S(O)2CF3
D2-33a CH(i-Bu)S(O)2CH2CF3
D2-33a CH(s-Bu)SMe
D2-33a CH(s-Bu)SEt
D2-33a CH(s-Bu)SCF3
D2-33a CH(s-Bu)SCH2CF3
D2-33a CH(s-Bu)S(O)Me
D2-33a CH(s-Bu)S(O)Et
D2-33a CH(s-Bu)S(O)CF3
D2-33a CH(s-Bu)S(O)CH2CF3
D2-33a CH(s-Bu)S(O)2Me
D2-33a CH(s-Bu)S(O)2Et
D2-33a CH(s-Bu)S(O)2CF3
D2-33a CH(s-Bu)S(O)2CH2CF3
D2-33a CH(t-Bu)SMe
D2-33a CH(t-Bu)SEt
D2-33a CH(t-Bu)SCF3
D2-33a CH(t-Bu)SCH2CF3
D2-33a CH(t-Bu)S(O)Me
D2-33a CH(t-Bu)S(O)Et
D2-33a CH(t-Bu)S(O)CF3
D2-33a CH(t-Bu)S(O)CH2CF3
D2-33a CH(t-Bu)S(O)2Me
D2-33a CH(t-Bu)S(O)2Et
D2-33a CH(t-Bu)S(O)2CF3
D2-33a CH(t-Bu)S(O)2CH2CF3
D2-33a CH(CF3)SMe
D2-33a CH(CF3)SEt
D2-33a CH(CF3)SCF3
D2-33a CH(CF3)SCH2CF3
D2-33a CH(CF3)S(O)Me
D2-33a CH(CF3)S(O)Et
D2-33a CH(CF3)S(O)CF3
D2-33a CH(CF3)S(O)CH2CF3
D2-33a CH(CF3)S(O)2Me
D2-33a CH(CF3)S(O)2Et
D2-33a CH(CF3)S(O)2CF3
D2-33a CH(CF3)S(O)2CH2CF3
D2-33a CH2CH2SMe
D2-33a CH2CH2SEt
D2-33a CH2CH2SCF3
D2-33a CH2CH2SCH2CF3
D2-33a CH2CH2S(O)Me
D2-33a CH2CH2S(O)Et
D2-33a CH2CH2S(O)CF3
D2-33a CH2CH2S(O)CH2CF3
D2-33a CH2CH2S(O)2Me
D2-33a CH2CH2S(O)2Et
D2-33a CH2CH2S(O)2CF3
D2-33a CH2CH2S(O)2CH2CF3
D2-33a CH(Me)CH2SMe
D2-33a CH(Me)CH2SEt
D2-33a CH(Me)CH2SCF3
D2-33a CH(Me)CH2SCH2CF3
D2-33a CH(Me)CH2S(O)Me
D2-33a CH(Me)CH2S(O)Et
D2-33a CH(Me)CH2S(O)CF3
D2-33a CH(Me)CH2S(O)CH2CF3
D2-33a CH(Me)CH2S(O)2Me
D2-33a CH(Me)CH2S(O)2Et
D2-33a CH(Me)CH2S(O)2CF3
D2-33a CH(Me)CH2S(O)2CH2CF3
D2-33a CH(Et)CH2SMe
D2-33a CH(Et)CH2SEt
D2-33a CH(Et)CH2SCF3
D2-33a CH(Et)CH2SCH2CF3
D2-33a CH(Et)CH2S(O)Me
D2-33a CH(Et)CH2S(O)Et
D2-33a CH(Et)CH2S(O)CF3
D2-33a CH(Et)CH2S(O)CH2CF3
D2-33a CH(Et)CH2S(O)2Me
D2-33a CH(Et)CH2S(O)2Et
D2-33a CH(Et)CH2S(O)2CF3
D2-33a CH(Et)CH2S(O)2CH2CF3
D2-33a C(Me)2CH2SMe
D2-33a C(Me)2CH2SEt
D2-33a C(Me)2CH2SCF3
D2-33a C(Me)2CH2SCH2CF3
D2-33a C(Me)2CH2S(O)Me
D2-33a C(Me)2CH2S(O)Et
D2-33a C(Me)2CH2S(O)CF3
D2-33a C(Me)2CH2S(O)CH2CF3
D2-33a C(Me)2CH2S(O)2Me
D2-33a C(Me)2CH2S(O)2Et
D2-33a C(Me)2CH2S(O)2CF3
D2-33a C(Me)2CH2S(O)2CH2CF3
D2-33a CH2CH(Me)SMe
D2-33a CH2CH(Me)SEt
D2-33a CH2CH(Me)SCF3
D2-33a CH2CH(Me)SCH2CF3
D2-33a CH2CH(Me)S(O)Me
D2-33a CH2CH(Me)S(O)Et
D2-33a CH2CH(Me)S(O)CF3
D2-33a CH2CH(Me)S(O)CH2CF3
D2-33a CH2CH(Me)S(O)2Me
D2-33a CH2CH(Me)S(O)2Et
D2-33a CH2CH(Me)S(O)2CF3
D2-33a CH2CH(Me)S(O)2CH2CF3
D2-33a CH2CH(Et)SMe
D2-33a CH2CH(Et)SEt
D2-33a CH2CH(Et)SCF3
D2-33a CH2CH(Et)SCH2CF3
D2-33a CH2CH(Et)S(O)Me
D2-33a CH2CH(Et)S(O)Et
D2-33a CH2CH(Et)S(O)CF3
D2-33a CH2CH(Et)S(O)CH2CF3
D2-33a CH2CH(Et)S(O)2Me
D2-33a CH2CH(Et)S(O)2Et
D2-33a CH2CH(Et)S(O)2CF3
D2-33a CH2CH(Et)S(O)2CH2CF3
D2-33a CH(Me)CH(Me)SMe
D2-33a CH(Me)CH(Me)SEt
D2-33a CH(Me)CH(Me)SCF3
D2-33a CH(Me)CH(Me)SCH2CF3
D2-33a CH(Me)CH(Me)S(O)Me
D2-33a CH(Me)CH(Me)S(O)Et
D2-33a CH(Me)CH(Me)S(O)CF3
D2-33a CH(Me)CH(Me)S(O)CH2CF3
D2-33a CH(Me)CH(Me)S(O)2Me
D2-33a CH(Me)CH(Me)S(O)2Et
D2-33a CH(Me)CH(Me)S(O)2CF3
D2-33a CH(Me)CH(Me)S(O)2CH2CF3
D2-34a CH2SMe
D2-34a CH2SEt
D2-34a CH2SCF3
D2-34a CH2SCH2CF3
D2-34a CH2S(O)Me
D2-34a CH2S(O)Et
D2-34a CH2S(O)CF3
D2-34a CH2S(O)CH2CF3
D2-34a CH2S(O)2Me
D2-34a CH2S(O)2Et
D2-34a CH2S(O)2CF3
D2-34a CH2S(O)2CH2CF3
D2-34a CH(Me)SMe
D2-34a CH(Me)SEt
D2-34a CH(Me)SCF3
D2-34a CH(Me)SCH2CF3
D2-34a CH(Me)S(O)Me
D2-34a CH(Me)S(O)Et
D2-34a CH(Me)S(O)CF3
D2-34a CH(Me)S(O)CH2CF3
D2-34a CH(Me)S(O)2Me
D2-34a CH(Me)S(O)2Et
D2-34a CH(Me)S(O)2CF3
D2-34a CH(Me)S(O)2CH2CF3
D2-34a CH(Et)SMe
D2-34a CH(Et)SEt
D2-34a CH(Et)SCF3
D2-34a CH(Et)SCH2CF3
D2-34a CH(Et)S(O)Me
D2-34a CH(Et)S(O)Et
D2-34a CH(Et)S(O)CF3
D2-34a CH(Et)S(O)CH2CF3
D2-34a CH(Et)S(O)2Me
D2-34a CH(Et)S(O)2Et
D2-34a CH(Et)S(O)2CF3
D2-34a CH(Et)S(O)2CH2CF3
D2-34a CH(n-Pr)SMe
D2-34a CH(n-Pr)SEt
D2-34a CH(n-Pr)SCF3
D2-34a CH(n-Pr)SCH2CF3
D2-34a CH(n-Pr)S(O)Me
D2-34a CH(n-Pr)S(O)Et
D2-34a CH(n-Pr)S(O)CF3
D2-34a CH(n-Pr)S(O)CH2CF3
D2-34a CH(n-Pr)S(O)2Me
D2-34a CH(n-Pr)S(O)2Et
D2-34a CH(n-Pr)S(O)2CF3
D2-34a CH(n-Pr)S(O)2CH2CF3
D2-34a CH(i-Pr)SMe
D2-34a CH(i-Pr)SEt
D2-34a CH(i-Pr)SCF3
D2-34a CH(i-Pr)SCH2CF3
D2-34a CH(i-Pr)S(O)Me
D2-34a CH(i-Pr)S(O)Et
D2-34a CH(i-Pr)S(O)CF3
D2-34a CH(i-Pr)S(O)CH2CF3
D2-34a CH(i-Pr)S(O)2Me
D2-34a CH(i-Pr)S(O)2Et
D2-34a CH(i-Pr)S(O)2CF3
D2-34a CH(i-Pr)S(O)2CH2CF3
D2-34a CH(n-Bu)SMe
D2-34a CH(n-Bu)SEt
D2-34a CH(n-Bu)SCF3
D2-34a CH(n-Bu)SCH2CF3
D2-34a CH(n-Bu)S(O)Me
D2-34a CH(n-Bu)S(O)Et
D2-34a CH(n-Bu)S(O)CF3
D2-34a CH(n-Bu)S(O)CH2CF3
D2-34a CH(n-Bu)S(O)2Me
D2-34a CH(n-Bu)S(O)2Et
D2-34a CH(n-Bu)S(O)2CF3
D2-34a CH(n-Bu)S(O)2CH2CF3
D2-34a CH(i-Bu)SMe
D2-34a CH(i-Bu)SEt
D2-34a CH(i-Bu)SCF3
D2-34a CH(i-Bu)SCH2CF3
D2-34a CH(i-Bu)S(O)Me
D2-34a CH(i-Bu)S(O)Et
D2-34a CH(i-Bu)S(O)CF3
D2-34a CH(i-Bu)S(O)CH2CF3
D2-34a CH(i-Bu)S(O)2Me
D2-34a CH(i-Bu)S(O)2Et
D2-34a CH(i-Bu)S(O)2CF3
D2-34a CH(i-Bu)S(O)2CH2CF3
D2-34a CH(s-Bu)SMe
D2-34a CH(s-Bu)SEt
D2-34a CH(s-Bu)SCF3
D2-34a CH(s-Bu)SCH2CF3
D2-34a CH(s-Bu)S(O)Me
D2-34a CH(s-Bu)S(O)Et
D2-34a CH(s-Bu)S(O)CF3
D2-34a CH(s-Bu)S(O)CH2CF3
D2-34a CH(s-Bu)S(O)2Me
D2-34a CH(s-Bu)S(O)2Et
D2-34a CH(s-Bu)S(O)2CF3
D2-34a CH(s-Bu)S(O)2CH2CF3
D2-34a CH(t-Bu)SMe
D2-34a CH(t-Bu)SEt
D2-34a CH(t-Bu)SCF3
D2-34a CH(t-Bu)SCH2CF3
D2-34a CH(t-Bu)S(O)Me
D2-34a CH(t-Bu)S(O)Et
D2-34a CH(t-Bu)S(O)CF3
D2-34a CH(t-Bu)S(O)CH2CF3
D2-34a CH(t-Bu)S(O)2Me
D2-34a CH(t-Bu)S(O)2Et
D2-34a CH(t-Bu)S(O)2CF3
D2-34a CH(t-Bu)S(O)2CH2CF3
D2-34a CH(CF3)SMe
D2-34a CH(CF3)SEt
D2-34a CH(CF3)SCF3
D2-34a CH(CF3)SCH2CF3
D2-34a CH(CF3)S(O)Me
D2-34a CH(CF3)S(O)Et
D2-34a CH(CF3)S(O)CF3
D2-34a CH(CF3)S(O)CH2CF3
D2-34a CH(CF3)S(O)2Me
D2-34a CH(CF3)S(O)2Et
D2-34a CH(CF3)S(O)2CF3
D2-34a CH(CF3)S(O)2CH2CF3
D2-34a CH2CH2SMe
D2-34a CH2CH2SEt
D2-34a CH2CH2SCF3
D2-34a CH2CH2SCH2CF3
D2-34a CH2CH2S(O)Me
D2-34a CH2CH2S(O)Et
D2-34a CH2CH2S(O)CF3
D2-34a CH2CH2S(O)CH2CF3
D2-34a CH2CH2S(O)2Me
D2-34a CH2CH2S(O)2Et
D2-34a CH2CH2S(O)2CF3
D2-34a CH2CH2S(O)2CH2CF3
D2-34a CH(Me)CH2SMe
D2-34a CH(Me)CH2SEt
D2-34a CH(Me)CH2SCF3
D2-34a CH(Me)CH2SCH2CF3
D2-34a CH(Me)CH2S(O)Me
D2-34a CH(Me)CH2S(O)Et
D2-34a CH(Me)CH2S(O)CF3
D2-34a CH(Me)CH2S(O)CH2CF3
D2-34a CH(Me)CH2S(O)2Me
D2-34a CH(Me)CH2S(O)2Et
D2-34a CH(Me)CH2S(O)2CF3
D2-34a CH(Me)CH2S(O)2CH2CF3
D2-34a CH(Et)CH2SMe
D2-34a CH(Et)CH2SEt
D2-34a CH(Et)CH2SCF3
D2-34a CH(Et)CH2SCH2CF3
D2-34a CH(Et)CH2S(O)Me
D2-34a CH(Et)CH2S(O)Et
D2-34a CH(Et)CH2S(O)CF3
D2-34a CH(Et)CH2S(O)CH2CF3
D2-34a CH(Et)CH2S(O)2Me
D2-34a CH(Et)CH2S(O)2Et
D2-34a CH(Et)CH2S(O)2CF3
D2-34a CH(Et)CH2S(O)2CH2CF3
D2-34a C(Me)2CH2SMe
D2-34a C(Me)2CH2SEt
D2-34a C(Me)2CH2SCF3
D2-34a C(Me)2CH2SCH2CF3
D2-34a C(Me)2CH2S(O)Me
D2-34a C(Me)2CH2S(O)Et
D2-34a C(Me)2CH2S(O)CF3
D2-34a C(Me)2CH2S(O)CH2CF3
D2-34a C(Me)2CH2S(O)2Me
D2-34a C(Me)2CH2S(O)2Et
D2-34a C(Me)2CH2S(O)2CF3
D2-34a C(Me)2CH2S(O)2CH2CF3
D2-34a CH2CH(Me)SMe
D2-34a CH2CH(Me)SEt
D2-34a CH2CH(Me)SCF3
D2-34a CH2CH(Me)SCH2CF3
D2-34a CH2CH(Me)S(O)Me
D2-34a CH2CH(Me)S(O)Et
D2-34a CH2CH(Me)S(O)CF3
D2-34a CH2CH(Me)S(O)CH2CF3
D2-34a CH2CH(Me)S(O)2Me
D2-34a CH2CH(Me)S(O)2Et
D2-34a CH2CH(Me)S(O)2CF3
D2-34a CH2CH(Me)S(O)2CH2CF3
D2-34a CH2CH(Et)SMe
D2-34a CH2CH(Et)SEt
D2-34a CH2CH(Et)SCF3
D2-34a CH2CH(Et)SCH2CF3
D2-34a CH2CH(Et)S(O)Me
D2-34a CH2CH(Et)S(O)Et
D2-34a CH2CH(Et)S(O)CF3
D2-34a CH2CH(Et)S(O)CH2CF3
D2-34a CH2CH(Et)S(O)2Me
D2-34a CH2CH(Et)S(O)2Et
D2-34a CH2CH(Et)S(O)2CF3
D2-34a CH2CH(Et)S(O)2CH2CF3
D2-34a CH(Me)CH(Me)SMe
D2-34a CH(Me)CH(Me)SEt
D2-34a CH(Me)CH(Me)SCF3
D2-34a CH(Me)CH(Me)SCH2CF3
D2-34a CH(Me)CH(Me)S(O)Me
D2-34a CH(Me)CH(Me)S(O)Et
D2-34a CH(Me)CH(Me)S(O)CF3
D2-34a CH(Me)CH(Me)S(O)CH2CF3
D2-34a CH(Me)CH(Me)S(O)2Me
D2-34a CH(Me)CH(Me)S(O)2Et
D2-34a CH(Me)CH(Me)S(O)2CF3
D2-34a CH(Me)CH(Me)S(O)2CH2CF3
D2-36a CH2SMe
D2-36a CH2SEt
D2-36a CH2SCF3
D2-36a CH2SCH2CF3
D2-36a CH2S(O)Me
D2-36a CH2S(O)Et
D2-36a CH2S(O)CF3
D2-36a CH2S(O)CH2CF3
D2-36a CH2S(O)2Me
D2-36a CH2S(O)2Et
D2-36a CH2S(O)2CF3
D2-36a CH2S(O)2CH2CF3
D2-36a CH(Me)SMe
D2-36a CH(Me)SEt
D2-36a CH(Me)SCF3
D2-36a CH(Me)SCH2CF3
D2-36a CH(Me)S(O)Me
D2-36a CH(Me)S(O)Et
D2-36a CH(Me)S(O)CF3
D2-36a CH(Me)S(O)CH2CF3
D2-36a CH(Me)S(O)2Me
D2-36a CH(Me)S(O)2Et
D2-36a CH(Me)S(O)2CF3
D2-36a CH(Me)S(O)2CH2CF3
D2-36a CH(Et)SMe
D2-36a CH(Et)SEt
D2-36a CH(Et)SCF3
D2-36a CH(Et)SCH2CF3
D2-36a CH(Et)S(O)Me
D2-36a CH(Et)S(O)Et
D2-36a CH(Et)S(O)CF3
D2-36a CH(Et)S(O)CH2CF3
D2-36a CH(Et)S(O)2Me
D2-36a CH(Et)S(O)2Et
D2-36a CH(Et)S(O)2CF3
D2-36a CH(Et)S(O)2CH2CF3
D2-36a CH(n-Pr)SMe
D2-36a CH(n-Pr)SEt
D2-36a CH(n-Pr)SCF3
D2-36a CH(n-Pr)SCH2CF3
D2-36a CH(n-Pr)S(O)Me
D2-36a CH(n-Pr)S(O)Et
D2-36a CH(n-Pr)S(O)CF3
D2-36a CH(n-Pr)S(O)CH2CF3
D2-36a CH(n-Pr)S(O)2Me
D2-36a CH(n-Pr)S(O)2Et
D2-36a CH(n-Pr)S(O)2CF3
D2-36a CH(n-Pr)S(O)2CH2CF3
D2-36a CH(i-Pr)SMe
D2-36a CH(i-Pr)SEt
D2-36a CH(i-Pr)SCF3
D2-36a CH(i-Pr)SCH2CF3
D2-36a CH(i-Pr)S(O)Me
D2-36a CH(i-Pr)S(O)Et
D2-36a CH(i-Pr)S(O)CF3
D2-36a CH(i-Pr)S(O)CH2CF3
D2-36a CH(i-Pr)S(O)2Me
D2-36a CH(i-Pr)S(O)2Et
D2-36a CH(i-Pr)S(O)2CF3
D2-36a CH(i-Pr)S(O)2CH2CF3
D2-36a CH(n-Bu)SMe
D2-36a CH(n-Bu)SEt
D2-36a CH(n-Bu)SCF3
D2-36a CH(n-Bu)SCH2CF3
D2-36a CH(n-Bu)S(O)Me
D2-36a CH(n-Bu)S(O)Et
D2-36a CH(n-Bu)S(O)CF3
D2-36a CH(n-Bu)S(O)CH2CF3
D2-36a CH(n-Bu)S(O)2Me
D2-36a CH(n-Bu)S(O)2Et
D2-36a CH(n-Bu)S(O)2CF3
D2-36a CH(n-Bu)S(O)2CH2CF3
D2-36a CH(i-Bu)SMe
D2-36a CH(i-Bu)SEt
D2-36a CH(i-Bu)SCF3
D2-36a CH(i-Bu)SCH2CF3
D2-36a CH(i-Bu)S(O)Me
D2-36a CH(i-Bu)S(O)Et
D2-36a CH(i-Bu)S(O)CF3
D2-36a CH(i-Bu)S(O)CH2CF3
D2-36a CH(i-Bu)S(O)2Me
D2-36a CH(i-Bu)S(O)2Et
D2-36a CH(i-Bu)S(O)2CF3
D2-36a CH(i-Bu)S(O)2CH2CF3
D2-36a CH(s-Bu)SMe
D2-36a CH(s-Bu)SEt
D2-36a CH(s-Bu)SCF3
D2-36a CH(s-Bu)SCH2CF3
D2-36a CH(s-Bu)S(O)Me
D2-36a CH(s-Bu)S(O)Et
D2-36a CH(s-Bu)S(O)CF3
D2-36a CH(s-Bu)S(O)CH2CF3
D2-36a CH(s-Bu)S(O)2Me
D2-36a CH(s-Bu)S(O)2Et
D2-36a CH(s-Bu)S(O)2CF3
D2-36a CH(s-Bu)S(O)2CH2CF3
D2-36a CH(t-Bu)SMe
D2-36a CH(t-Bu)SEt
D2-36a CH(t-Bu)SCF3
D2-36a CH(t-Bu)SCH2CF3
D2-36a CH(t-Bu)S(O)Me
D2-36a CH(t-Bu)S(O)Et
D2-36a CH(t-Bu)S(O)CF3
D2-36a CH(t-Bu)S(O)CH2CF3
D2-36a CH(t-Bu)S(O)2Me
D2-36a CH(t-Bu)S(O)2Et
D2-36a CH(t-Bu)S(O)2CF3
D2-36a CH(t-Bu)S(O)2CH2CF3
D2-36a CH(CF3)SMe
D2-36a CH(CF3)SEt
D2-36a CH(CF3)SCF3
D2-36a CH(CF3)SCH2CF3
D2-36a CH(CF3)S(O)Me
D2-36a CH(CF3)S(O)Et
D2-36a CH(CF3)S(O)CF3
D2-36a CH(CF3)S(O)CH2CF3
D2-36a CH(CF3)S(O)2Me
D2-36a CH(CF3)S(O)2Et
D2-36a CH(CF3)S(O)2CF3
D2-36a CH(CF3)S(O)2CH2CF3
D2-36a CH2CH2SMe
D2-36a CH2CH2SEt
D2-36a CH2CH2SCF3
D2-36a CH2CH2SCH2CF3
D2-36a CH2CH2S(O)Me
D2-36a CH2CH2S(O)Et
D2-36a CH2CH2S(O)CF3
D2-36a CH2CH2S(O)CH2CF3
D2-36a CH2CH2S(O)2Me
D2-36a CH2CH2S(O)2Et
D2-36a CH2CH2S(O)2CF3
D2-36a CH2CH2S(O)2CH2CF3
D2-36a CH(Me)CH2SMe
D2-36a CH(Me)CH2SEt
D2-36a CH(Me)CH2SCF3
D2-36a CH(Me)CH2SCH2CF3
D2-36a CH(Me)CH2S(O)Me
D2-36a CH(Me)CH2S(O)Et
D2-36a CH(Me)CH2S(O)CF3
D2-36a CH(Me)CH2S(O)CH2CF3
D2-36a CH(Me)CH2S(O)2Me
D2-36a CH(Me)CH2S(O)2Et
D2-36a CH(Me)CH2S(O)2CF3
D2-36a CH(Me)CH2S(O)2CH2CF3
D2-36a CH(Et)CH2SMe
D2-36a CH(Et)CH2SEt
D2-36a CH(Et)CH2SCF3
D2-36a CH(Et)CH2SCH2CF3
D2-36a CH(Et)CH2S(O)Me
D2-36a CH(Et)CH2S(O)Et
D2-36a CH(Et)CH2S(O)CF3
D2-36a CH(Et)CH2S(O)CH2CF3
D2-36a CH(Et)CH2S(O)2Me
D2-36a CH(Et)CH2S(O)2Et
D2-36a CH(Et)CH2S(O)2CF3
D2-36a CH(Et)CH2S(O)2CH2CF3
D2-36a C(Me)2CH2SMe
D2-36a C(Me)2CH2SEt
D2-36a C(Me)2CH2SCF3
D2-36a C(Me)2CH2SCH2CF3
D2-36a C(Me)2CH2S(O)Me
D2-36a C(Me)2CH2S(O)Et
D2-36a C(Me)2CH2S(O)CF3
D2-36a C(Me)2CH2S(O)CH2CF3
D2-36a C(Me)2CH2S(O)2Me
D2-36a C(Me)2CH2S(O)2Et
D2-36a C(Me)2CH2S(O)2CF3
D2-36a C(Me)2CH2S(O)2CH2CF3
D2-36a CH2CH(Me)SMe
D2-36a CH2CH(Me)SEt
D2-36a CH2CH(Me)SCF3
D2-36a CH2CH(Me)SCH2CF3
D2-36a CH2CH(Me)S(O)Me
D2-36a CH2CH(Me)S(O)Et
D2-36a CH2CH(Me)S(O)CF3
D2-36a CH2CH(Me)S(O)CH2CF3
D2-36a CH2CH(Me)S(O)2Me
D2-36a CH2CH(Me)S(O)2Et
D2-36a CH2CH(Me)S(O)2CF3
D2-36a CH2CH(Me)S(O)2CH2CF3
D2-36a CH2CH(Et)SMe
D2-36a CH2CH(Et)SEt
D2-36a CH2CH(Et)SCF3
D2-36a CH2CH(Et)SCH2CF3
D2-36a CH2CH(Et)S(O)Me
D2-36a CH2CH(Et)S(O)Et
D2-36a CH2CH(Et)S(O)CF3
D2-36a CH2CH(Et)S(O)CH2CF3
D2-36a CH2CH(Et)S(O)2Me
D2-36a CH2CH(Et)S(O)2Et
D2-36a CH2CH(Et)S(O)2CF3
D2-36a CH2CH(Et)S(O)2CH2CF3
D2-36a CH(Me)CH(Me)SMe
D2-36a CH(Me)CH(Me)SEt
D2-36a CH(Me)CH(Me)SCF3
D2-36a CH(Me)CH(Me)SCH2CF3
D2-36a CH(Me)CH(Me)S(O)Me
D2-36a CH(Me)CH(Me)S(O)Et
D2-36a CH(Me)CH(Me)S(O)CF3
D2-36a CH(Me)CH(Me)S(O)CH2CF3
D2-36a CH(Me)CH(Me)S(O)2Me
D2-36a CH(Me)CH(Me)S(O)2Et
D2-36a CH(Me)CH(Me)S(O)2CF3
D2-36a CH(Me)CH(Me)S(O)2CH2CF3
D2-37a CH2SMe
D2-37a CH2SEt
D2-37a CH2SCF3
D2-37a CH2SCH2CF3
D2-37a CH2S(O)Me
D2-37a CH2S(O)Et
D2-37a CH2S(O)CF3
D2-37a CH2S(O)CH2CF3
D2-37a CH2S(O)2Me
D2-37a CH2S(O)2Et
D2-37a CH2S(O)2CF3
D2-37a CH2S(O)2CH2CF3
D2-37a CH(Me)SMe
D2-37a CH(Me)SEt
D2-37a CH(Me)SCF3
D2-37a CH(Me)SCH2CF3
D2-37a CH(Me)S(O)Me
D2-37a CH(Me)S(O)Et
D2-37a CH(Me)S(O)CF3
D2-37a CH(Me)S(O)CH2CF3
D2-37a CH(Me)S(O)2Me
D2-37a CH(Me)S(O)2Et
D2-37a CH(Me)S(O)2CF3
D2-37a CH(Me)S(O)2CH2CF3
D2-37a CH(Et)SMe
D2-37a CH(Et)SEt
D2-37a CH(Et)SCF3
D2-37a CH(Et)SCH2CF3
D2-37a CH(Et)S(O)Me
D2-37a CH(Et)S(O)Et
D2-37a CH(Et)S(O)CF3
D2-37a CH(Et)S(O)CH2CF3
D2-37a CH(Et)S(O)2Me
D2-37a CH(Et)S(O)2Et
D2-37a CH(Et)S(O)2CF3
D2-37a CH(Et)S(O)2CH2CF3
D2-37a CH(n-Pr)SMe
D2-37a CH(n-Pr)SEt
D2-37a CH(n-Pr)SCF3
D2-37a CH(n-Pr)SCH2CF3
D2-37a CH(n-Pr)S(O)Me
D2-37a CH(n-Pr)S(O)Et
D2-37a CH(n-Pr)S(O)CF3
D2-37a CH(n-Pr)S(O)CH2CF3
D2-37a CH(n-Pr)S(O)2Me
D2-37a CH(n-Pr)S(O)2Et
D2-37a CH(n-Pr)S(O)2CF3
D2-37a CH(n-Pr)S(O)2CH2CF3
D2-37a CH(i-Pr)SMe
D2-37a CH(i-Pr)SEt
D2-37a CH(i-Pr)SCF3
D2-37a CH(i-Pr)SCH2CF3
D2-37a CH(i-Pr)S(O)Me
D2-37a CH(i-Pr)S(O)Et
D2-37a CH(i-Pr)S(O)CF3
D2-37a CH(i-Pr)S(O)CH2CF3
D2-37a CH(i-Pr)S(O)2Me
D2-37a CH(i-Pr)S(O)2Et
D2-37a CH(i-Pr)S(O)2CF3
D2-37a CH(i-Pr)S(O)2CH2CF3
D2-37a CH(n-Bu)SMe
D2-37a CH(n-Bu)SEt
D2-37a CH(n-Bu)SCF3
D2-37a CH(n-Bu)SCH2CF3
D2-37a CH(n-Bu)S(O)Me
D2-37a CH(n-Bu)S(O)Et
D2-37a CH(n-Bu)S(O)CF3
D2-37a CH(n-Bu)S(O)CH2CF3
D2-37a CH(n-Bu)S(O)2Me
D2-37a CH(n-Bu)S(O)2Et
D2-37a CH(n-Bu)S(O)2CF3
D2-37a CH(n-Bu)S(O)2CH2CF3
D2-37a CH(i-Bu)SMe
D2-37a CH(i-Bu)SEt
D2-37a CH(i-Bu)SCF3
D2-37a CH(i-Bu)SCH2CF3
D2-37a CH(i-Bu)S(O)Me
D2-37a CH(i-Bu)S(O)Et
D2-37a CH(i-Bu)S(O)CF3
D2-37a CH(i-Bu)S(O)CH2CF3
D2-37a CH(i-Bu)S(O)2Me
D2-37a CH(i-Bu)S(O)2Et
D2-37a CH(i-Bu)S(O)2CF3
D2-37a CH(i-Bu)S(O)2CH2CF3
D2-37a CH(s-Bu)SMe
D2-37a CH(s-Bu)SEt
D2-37a CH(s-Bu)SCF3
D2-37a CH(s-Bu)SCH2CF3
D2-37a CH(s-Bu)S(O)Me
D2-37a CH(s-Bu)S(O)Et
D2-37a CH(s-Bu)S(O)CF3
D2-37a CH(s-Bu)S(O)CH2CF3
D2-37a CH(s-Bu)S(O)2Me
D2-37a CH(s-Bu)S(O)2Et
D2-37a CH(s-Bu)S(O)2CF3
D2-37a CH(s-Bu)S(O)2CH2CF3
D2-37a CH(t-Bu)SMe
D2-37a CH(t-Bu)SEt
D2-37a CH(t-Bu)SCF3
D2-37a CH(t-Bu)SCH2CF3
D2-37a CH(t-Bu)S(O)Me
D2-37a CH(t-Bu)S(O)Et
D2-37a CH(t-Bu)S(O)CF3
D2-37a CH(t-Bu)S(O)CH2CF3
D2-37a CH(t-Bu)S(O)2Me
D2-37a CH(t-Bu)S(O)2Et
D2-37a CH(t-Bu)S(O)2CF3
D2-37a CH(t-Bu)S(O)2CH2CF3
D2-37a CH(CF3)SMe
D2-37a CH(CF3)SEt
D2-37a CH(CF3)SCF3
D2-37a CH(CF3)SCH2CF3
D2-37a CH(CF3)S(O)Me
D2-37a CH(CF3)S(O)Et
D2-37a CH(CF3)S(O)CF3
D2-37a CH(CF3)S(O)CH2CF3
D2-37a CH(CF3)S(O)2Me
D2-37a CH(CF3)S(O)2Et
D2-37a CH(CF3)S(O)2CF3
D2-37a CH(CF3)S(O)2CH2CF3
D2-37a CH2CH2SMe
D2-37a CH2CH2SEt
D2-37a CH2CH2SCF3
D2-37a CH2CH2SCH2CF3
D2-37a CH2CH2S(O)Me
D2-37a CH2CH2S(O)Et
D2-37a CH2CH2S(O)CF3
D2-37a CH2CH2S(O)CH2CF3
D2-37a CH2CH2S(O)2Me
D2-37a CH2CH2S(O)2Et
D2-37a CH2CH2S(O)2CF3
D2-37a CH2CH2S(O)2CH2CF3
D2-37a CH(Me)CH2SMe
D2-37a CH(Me)CH2SEt
D2-37a CH(Me)CH2SCF3
D2-37a CH(Me)CH2SCH2CF3
D2-37a CH(Me)CH2S(O)Me
D2-37a CH(Me)CH2S(O)Et
D2-37a CH(Me)CH2S(O)CF3
D2-37a CH(Me)CH2S(O)CH2CF3
D2-37a CH(Me)CH2S(O)2Me
D2-37a CH(Me)CH2S(O)2Et
D2-37a CH(Me)CH2S(O)2CF3
D2-37a CH(Me)CH2S(O)2CH2CF3
D2-37a CH(Et)CH2SMe
D2-37a CH(Et)CH2SEt
D2-37a CH(Et)CH2SCF3
D2-37a CH(Et)CH2SCH2CF3
D2-37a CH(Et)CH2S(O)Me
D2-37a CH(Et)CH2S(O)Et
D2-37a CH(Et)CH2S(O)CF3
D2-37a CH(Et)CH2S(O)CH2CF3
D2-37a CH(Et)CH2S(O)2Me
D2-37a CH(Et)CH2S(O)2Et
D2-37a CH(Et)CH2S(O)2CF3
D2-37a CH(Et)CH2S(O)2CH2CF3
D2-37a C(Me)2CH2SMe
D2-37a C(Me)2CH2SEt
D2-37a C(Me)2CH2SCF3
D2-37a C(Me)2CH2SCH2CF3
D2-37a C(Me)2CH2S(O)Me
D2-37a C(Me)2CH2S(O)Et
D2-37a C(Me)2CH2S(O)CF3
D2-37a C(Me)2CH2S(O)CH2CF3
D2-37a C(Me)2CH2S(O)2Me
D2-37a C(Me)2CH2S(O)2Et
D2-37a C(Me)2CH2S(O)2CF3
D2-37a C(Me)2CH2S(O)2CH2CF3
D2-37a CH2CH(Me)SMe
D2-37a CH2CH(Me)SEt
D2-37a CH2CH(Me)SCF3
D2-37a CH2CH(Me)SCH2CF3
D2-37a CH2CH(Me)S(O)Me
D2-37a CH2CH(Me)S(O)Et
D2-37a CH2CH(Me)S(O)CF3
D2-37a CH2CH(Me)S(O)CH2CF3
D2-37a CH2CH(Me)S(O)2Me
D2-37a CH2CH(Me)S(O)2Et
D2-37a CH2CH(Me)S(O)2CF3
D2-37a CH2CH(Me)S(O)2CH2CF3
D2-37a CH2CH(Et)SMe
D2-37a CH2CH(Et)SEt
D2-37a CH2CH(Et)SCF3
D2-37a CH2CH(Et)SCH2CF3
D2-37a CH2CH(Et)S(O)Me
D2-37a CH2CH(Et)S(O)Et
D2-37a CH2CH(Et)S(O)CF3
D2-37a CH2CH(Et)S(O)CH2CF3
D2-37a CH2CH(Et)S(O)2Me
D2-37a CH2CH(Et)S(O)2Et
D2-37a CH2CH(Et)S(O)2CF3
D2-37a CH2CH(Et)S(O)2CH2CF3
D2-37a CH(Me)CH(Me)SMe
D2-37a CH(Me)CH(Me)SEt
D2-37a CH(Me)CH(Me)SCF3
D2-37a CH(Me)CH(Me)SCH2CF3
D2-37a CH(Me)CH(Me)S(O)Me
D2-37a CH(Me)CH(Me)S(O)Et
D2-37a CH(Me)CH(Me)S(O)CF3
D2-37a CH(Me)CH(Me)S(O)CH2CF3
D2-37a CH(Me)CH(Me)S(O)2Me
D2-37a CH(Me)CH(Me)S(O)2Et
D2-37a CH(Me)CH(Me)S(O)2CF3
D2-37a CH(Me)CH(Me)S(O)2CH2CF3
D2-38a CH2SMe
D2-38a CH2SEt
D2-38a CH2SCF3
D2-38a CH2SCH2CF3
D2-38a CH2S(O)Me
D2-38a CH2S(O)Et
D2-38a CH2S(O)CF3
D2-38a CH2S(O)CH2CF3
D2-38a CH2S(O)2Me
D2-38a CH2S(O)2Et
D2-38a CH2S(O)2CF3
D2-38a CH2S(O)2CH2CF3
D2-38a CH(Me)SMe
D2-38a CH(Me)SEt
D2-38a CH(Me)SCF3
D2-38a CH(Me)SCH2CF3
D2-38a CH(Me)S(O)Me
D2-38a CH(Me)S(O)Et
D2-38a CH(Me)S(O)CF3
D2-38a CH(Me)S(O)CH2CF3
D2-38a CH(Me)S(O)2Me
D2-38a CH(Me)S(O)2Et
D2-38a CH(Me)S(O)2CF3
D2-38a CH(Me)S(O)2CH2CF3
D2-38a CH(Et)SMe
D2-38a CH(Et)SEt
D2-38a CH(Et)SCF3
D2-38a CH(Et)SCH2CF3
D2-38a CH(Et)S(O)Me
D2-38a CH(Et)S(O)Et
D2-38a CH(Et)S(O)CF3
D2-38a CH(Et)S(O)CH2CF3
D2-38a CH(Et)S(O)2Me
D2-38a CH(Et)S(O)2Et
D2-38a CH(Et)S(O)2CF3
D2-38a CH(Et)S(O)2CH2CF3
D2-38a CH(n-Pr)SMe
D2-38a CH(n-Pr)SEt
D2-38a CH(n-Pr)SCF3
D2-38a CH(n-Pr)SCH2CF3
D2-38a CH(n-Pr)S(O)Me
D2-38a CH(n-Pr)S(O)Et
D2-38a CH(n-Pr)S(O)CF3
D2-38a CH(n-Pr)S(O)CH2CF3
D2-38a CH(n-Pr)S(O)2Me
D2-38a CH(n-Pr)S(O)2Et
D2-38a CH(n-Pr)S(O)2CF3
D2-38a CH(n-Pr)S(O)2CH2CF3
D2-38a CH(i-Pr)SMe
D2-38a CH(i-Pr)SEt
D2-38a CH(i-Pr)SCF3
D2-38a CH(i-Pr)SCH2CF3
D2-38a CH(i-Pr)S(O)Me
D2-38a CH(i-Pr)S(O)Et
D2-38a CH(i-Pr)S(O)CF3
D2-38a CH(i-Pr)S(O)CH2CF3
D2-38a CH(i-Pr)S(O)2Me
D2-38a CH(i-Pr)S(O)2Et
D2-38a CH(i-Pr)S(O)2CF3
D2-38a CH(i-Pr)S(O)2CH2CF3
D2-38a CH(n-Bu)SMe
D2-38a CH(n-Bu)SEt
D2-38a CH(n-Bu)SCF3
D2-38a CH(n-Bu)SCH2CF3
D2-38a CH(n-Bu)S(O)Me
D2-38a CH(n-Bu)S(O)Et
D2-38a CH(n-Bu)S(O)CF3
D2-38a CH(n-Bu)S(O)CH2CF3
D2-38a CH(n-Bu)S(O)2Me
D2-38a CH(n-Bu)S(O)2Et
D2-38a CH(n-Bu)S(O)2CF3
D2-38a CH(n-Bu)S(O)2CH2CF3
D2-38a CH(i-Bu)SMe
D2-38a CH(i-Bu)SEt
D2-38a CH(i-Bu)SCF3
D2-38a CH(i-Bu)SCH2CF3
D2-38a CH(i-Bu)S(O)Me
D2-38a CH(i-Bu)S(O)Et
D2-38a CH(i-Bu)S(O)CF3
D2-38a CH(i-Bu)S(O)CH2CF3
D2-38a CH(i-Bu)S(O)2Me
D2-38a CH(i-Bu)S(O)2Et
D2-38a CH(i-Bu)S(O)2CF3
D2-38a CH(i-Bu)S(O)2CH2CF3
D2-38a CH(s-Bu)SMe
D2-38a CH(s-Bu)SEt
D2-38a CH(s-Bu)SCF3
D2-38a CH(s-Bu)SCH2CF3
D2-38a CH(s-Bu)S(O)Me
D2-38a CH(s-Bu)S(O)Et
D2-38a CH(s-Bu)S(O)CF3
D2-38a CH(s-Bu)S(O)CH2CF3
D2-38a CH(s-Bu)S(O)2Me
D2-38a CH(s-Bu)S(O)2Et
D2-38a CH(s-Bu)S(O)2CF3
D2-38a CH(s-Bu)S(O)2CH2CF3
D2-38a CH(t-Bu)SMe
D2-38a CH(t-Bu)SEt
D2-38a CH(t-Bu)SCF3
D2-38a CH(t-Bu)SCH2CF3
D2-38a CH(t-Bu)S(O)Me
D2-38a CH(t-Bu)S(O)Et
D2-38a CH(t-Bu)S(O)CF3
D2-38a CH(t-Bu)S(O)CH2CF3
D2-38a CH(t-Bu)S(O)2Me
D2-38a CH(t-Bu)S(O)2Et
D2-38a CH(t-Bu)S(O)2CF3
D2-38a CH(t-Bu)S(O)2CH2CF3
D2-38a CH(CF3)SMe
D2-38a CH(CF3)SEt
D2-38a CH(CF3)SCF3
D2-38a CH(CF3)SCH2CF3
D2-38a CH(CF3)S(O)Me
D2-38a CH(CF3)S(O)Et
D2-38a CH(CF3)S(O)CF3
D2-38a CH(CF3)S(O)CH2CF3
D2-38a CH(CF3)S(O)2Me
D2-38a CH(CF3)S(O)2Et
D2-38a CH(CF3)S(O)2CF3
D2-38a CH(CF3)S(O)2CH2CF3
D2-38a CH2CH2SMe
D2-38a CH2CH2SEt
D2-38a CH2CH2SCF3
D2-38a CH2CH2SCH2CF3
D2-38a CH2CH2S(O)Me
D2-38a CH2CH2S(O)Et
D2-38a CH2CH2S(O)CF3
D2-38a CH2CH2S(O)CH2CF3
D2-38a CH2CH2S(O)2Me
D2-38a CH2CH2S(O)2Et
D2-38a CH2CH2S(O)2CF3
D2-38a CH2CH2S(O)2CH2CF3
D2-38a CH(Me)CH2SMe
D2-38a CH(Me)CH2SEt
D2-38a CH(Me)CH2SCF3
D2-38a CH(Me)CH2SCH2CF3
D2-38a CH(Me)CH2S(O)Me
D2-38a CH(Me)CH2S(O)Et
D2-38a CH(Me)CH2S(O)CF3
D2-38a CH(Me)CH2S(O)CH2CF3
D2-38a CH(Me)CH2S(O)2Me
D2-38a CH(Me)CH2S(O)2Et
D2-38a CH(Me)CH2S(O)2CF3
D2-38a CH(Me)CH2S(O)2CH2CF3
D2-38a CH(Et)CH2SMe
D2-38a CH(Et)CH2SEt
D2-38a CH(Et)CH2SCF3
D2-38a CH(Et)CH2SCH2CF3
D2-38a CH(Et)CH2S(O)Me
D2-38a CH(Et)CH2S(O)Et
D2-38a CH(Et)CH2S(O)CF3
D2-38a CH(Et)CH2S(O)CH2CF3
D2-38a CH(Et)CH2S(O)2Me
D2-38a CH(Et)CH2S(O)2Et
D2-38a CH(Et)CH2S(O)2CF3
D2-38a CH(Et)CH2S(O)2CH2CF3
D2-38a C(Me)2CH2SMe
D2-38a C(Me)2CH2SEt
D2-38a C(Me)2CH2SCF3
D2-38a C(Me)2CH2SCH2CF3
D2-38a C(Me)2CH2S(O)Me
D2-38a C(Me)2CH2S(O)Et
D2-38a C(Me)2CH2S(O)CF3
D2-38a C(Me)2CH2S(O)CH2CF3
D2-38a C(Me)2CH2S(O)2Me
D2-38a C(Me)2CH2S(O)2Et
D2-38a C(Me)2CH2S(O)2CF3
D2-38a C(Me)2CH2S(O)2CH2CF3
D2-38a CH2CH(Me)SMe
D2-38a CH2CH(Me)SEt
D2-38a CH2CH(Me)SCF3
D2-38a CH2CH(Me)SCH2CF3
D2-38a CH2CH(Me)S(O)Me
D2-38a CH2CH(Me)S(O)Et
D2-38a CH2CH(Me)S(O)CF3
D2-38a CH2CH(Me)S(O)CH2CF3
D2-38a CH2CH(Me)S(O)2Me
D2-38a CH2CH(Me)S(O)2Et
D2-38a CH2CH(Me)S(O)2CF3
D2-38a CH2CH(Me)S(O)2CH2CF3
D2-38a CH2CH(Et)SMe
D2-38a CH2CH(Et)SEt
D2-38a CH2CH(Et)SCF3
D2-38a CH2CH(Et)SCH2CF3
D2-38a CH2CH(Et)S(O)Me
D2-38a CH2CH(Et)S(O)Et
D2-38a CH2CH(Et)S(O)CF3
D2-38a CH2CH(Et)S(O)CH2CF3
D2-38a CH2CH(Et)S(O)2Me
D2-38a CH2CH(Et)S(O)2Et
D2-38a CH2CH(Et)S(O)2CF3
D2-38a CH2CH(Et)S(O)2CH2CF3
D2-38a CH(Me)CH(Me)SMe
D2-38a CH(Me)CH(Me)SEt
D2-38a CH(Me)CH(Me)SCF3
D2-38a CH(Me)CH(Me)SCH2CF3
D2-38a CH(Me)CH(Me)S(O)Me
D2-38a CH(Me)CH(Me)S(O)Et
D2-38a CH(Me)CH(Me)S(O)CF3
D2-38a CH(Me)CH(Me)S(O)CH2CF3
D2-38a CH(Me)CH(Me)S(O)2Me
D2-38a CH(Me)CH(Me)S(O)2Et
D2-38a CH(Me)CH(Me)S(O)2CF3
D2-38a CH(Me)CH(Me)S(O)2CH2CF3
D2-92a CH2SMe
D2-92a CH2SEt
D2-92a CH2SCF3
D2-92a CH2SCH2CF3
D2-92a CH2S(O)Me
D2-92a CH2S(O)Et
D2-92a CH2S(O)CF3
D2-92a CH2S(O)CH2CF3
D2-92a CH2S(O)2Me
D2-92a CH2S(O)2Et
D2-92a CH2S(O)2CF3
D2-92a CH2S(O)2CH2CF3
D2-92a CH(Me)SMe
D2-92a CH(Me)SEt
D2-92a CH(Me)SCF3
D2-92a CH(Me)SCH2CF3
D2-92a CH(Me)S(O)Me
D2-92a CH(Me)S(O)Et
D2-92a CH(Me)S(O)CF3
D2-92a CH(Me)S(O)CH2CF3
D2-92a CH(Me)S(O)2Me
D2-92a CH(Me)S(O)2Et
D2-92a CH(Me)S(O)2CF3
D2-92a CH(Me)S(O)2CH2CF3
D2-92a CH(Et)SMe
D2-92a CH(Et)SEt
D2-92a CH(Et)SCF3
D2-92a CH(Et)SCH2CF3
D2-92a CH(Et)S(O)Me
D2-92a CH(Et)S(O)Et
D2-92a CH(Et)S(O)CF3
D2-92a CH(Et)S(O)CH2CF3
D2-92a CH(Et)S(O)2Me
D2-92a CH(Et)S(O)2Et
D2-92a CH(Et)S(O)2CF3
D2-92a CH(Et)S(O)2CH2CF3
D2-92a CH(n-Pr)SMe
D2-92a CH(n-Pr)SEt
D2-92a CH(n-Pr)SCF3
D2-92a CH(n-Pr)SCH2CF3
D2-92a CH(n-Pr)S(O)Me
D2-92a CH(n-Pr)S(O)Et
D2-92a CH(n-Pr)S(O)CF3
D2-92a CH(n-Pr)S(O)CH2CF3
D2-92a CH(n-Pr)S(O)2Me
D2-92a CH(n-Pr)S(O)2Et
D2-92a CH(n-Pr)S(O)2CF3
D2-92a CH(n-Pr)S(O)2CH2CF3
D2-92a CH(i-Pr)SMe
D2-92a CH(i-Pr)SEt
D2-92a CH(i-Pr)SCF3
D2-92a CH(i-Pr)SCH2CF3
D2-92a CH(i-Pr)S(O)Me
D2-92a CH(i-Pr)S(O)Et
D2-92a CH(i-Pr)S(O)CF3
D2-92a CH(i-Pr)S(O)CH2CF3
D2-92a CH(i-Pr)S(O)2Me
D2-92a CH(i-Pr)S(O)2Et
D2-92a CH(i-Pr)S(O)2CF3
D2-92a CH(i-Pr)S(O)2CH2CF3
D2-92a CH(n-Bu)SMe
D2-92a CH(n-Bu)SEt
D2-92a CH(n-Bu)SCF3
D2-92a CH(n-Bu)SCH2CF3
D2-92a CH(n-Bu)S(O)Me
D2-92a CH(n-Bu)S(O)Et
D2-92a CH(n-Bu)S(O)CF3
D2-92a CH(n-Bu)S(O)CH2CF3
D2-92a CH(n-Bu)S(O)2Me
D2-92a CH(n-Bu)S(O)2Et
D2-92a CH(n-Bu)S(O)2CF3
D2-92a CH(n-Bu)S(O)2CH2CF3
D2-92a CH(i-Bu)SMe
D2-92a CH(i-Bu)SEt
D2-92a CH(i-Bu)SCF3
D2-92a CH(i-Bu)SCH2CF3
D2-92a CH(i-Bu)S(O)Me
D2-92a CH(i-Bu)S(O)Et
D2-92a CH(i-Bu)S(O)CF3
D2-92a CH(i-Bu)S(O)CH2CF3
D2-92a CH(i-Bu)S(O)2Me
D2-92a CH(i-Bu)S(O)2Et
D2-92a CH(i-Bu)S(O)2CF3
D2-92a CH(i-Bu)S(O)2CH2CF3
D2-92a CH(s-Bu)SMe
D2-92a CH(s-Bu)SEt
D2-92a CH(s-Bu)SCF3
D2-92a CH(s-Bu)SCH2CF3
D2-92a CH(s-Bu)S(O)Me
D2-92a CH(s-Bu)S(O)Et
D2-92a CH(s-Bu)S(O)CF3
D2-92a CH(s-Bu)S(O)CH2CF3
D2-92a CH(s-Bu)S(O)2Me
D2-92a CH(s-Bu)S(O)2Et
D2-92a CH(s-Bu)S(O)2CF3
D2-92a CH(s-Bu)S(O)2CH2CF3
D2-92a CH(t-Bu)SMe
D2-92a CH(t-Bu)SEt
D2-92a CH(t-Bu)SCF3
D2-92a CH(t-Bu)SCH2CF3
D2-92a CH(t-Bu)S(O)Me
D2-92a CH(t-Bu)S(O)Et
D2-92a CH(t-Bu)S(O)CF3
D2-92a CH(t-Bu)S(O)CH2CF3
D2-92a CH(t-Bu)S(O)2Me
D2-92a CH(t-Bu)S(O)2Et
D2-92a CH(t-Bu)S(O)2CF3
D2-92a CH(t-Bu)S(O)2CH2CF3
D2-92a CH(CF3)SMe
D2-92a CH(CF3)SEt
D2-92a CH(CF3)SCF3
D2-92a CH(CF3)SCH2CF3
D2-92a CH(CF3)S(O)Me
D2-92a CH(CF3)S(O)Et
D2-92a CH(CF3)S(O)CF3
D2-92a CH(CF3)S(O)CH2CF3
D2-92a CH(CF3)S(O)2Me
D2-92a CH(CF3)S(O)2Et
D2-92a CH(CF3)S(O)2CF3
D2-92a CH(CF3)S(O)2CH2CF3
D2-92a CH2CH2SMe
D2-92a CH2CH2SEt
D2-92a CH2CH2SCF3
D2-92a CH2CH2SCH2CF3
D2-92a CH2CH2S(O)Me
D2-92a CH2CH2S(O)Et
D2-92a CH2CH2S(O)CF3
D2-92a CH2CH2S(O)CH2CF3
D2-92a CH2CH2S(O)2Me
D2-92a CH2CH2S(O)2Et
D2-92a CH2CH2S(O)2CF3
D2-92a CH2CH2S(O)2CH2CF3
D2-92a CH(Me)CH2SMe
D2-92a CH(Me)CH2SEt
D2-92a CH(Me)CH2SCF3
D2-92a CH(Me)CH2SCH2CF3
D2-92a CH(Me)CH2S(O)Me
D2-92a CH(Me)CH2S(O)Et
D2-92a CH(Me)CH2S(O)CF3
D2-92a CH(Me)CH2S(O)CH2CF3
D2-92a CH(Me)CH2S(O)2Me
D2-92a CH(Me)CH2S(O)2Et
D2-92a CH(Me)CH2S(O)2CF3
D2-92a CH(Me)CH2S(O)2CH2CF3
D2-92a CH(Et)CH2SMe
D2-92a CH(Et)CH2SEt
D2-92a CH(Et)CH2SCF3
D2-92a CH(Et)CH2SCH2CF3
D2-92a CH(Et)CH2S(O)Me
D2-92a CH(Et)CH2S(O)Et
D2-92a CH(Et)CH2S(O)CF3
D2-92a CH(Et)CH2S(O)CH2CF3
D2-92a CH(Et)CH2S(O)2Me
D2-92a CH(Et)CH2S(O)2Et
D2-92a CH(Et)CH2S(O)2CF3
D2-92a CH(Et)CH2S(O)2CH2CF3
D2-92a C(Me)2CH2SMe
D2-92a C(Me)2CH2SEt
D2-92a C(Me)2CH2SCF3
D2-92a C(Me)2CH2SCH2CF3
D2-92a C(Me)2CH2S(O)Me
D2-92a C(Me)2CH2S(O)Et
D2-92a C(Me)2CH2S(O)CF3
D2-92a C(Me)2CH2S(O)CH2CF3
D2-92a C(Me)2CH2S(O)2Me
D2-92a C(Me)2CH2S(O)2Et
D2-92a C(Me)2CH2S(O)2CF3
D2-92a C(Me)2CH2S(O)2CH2CF3
D2-92a CH2CH(Me)SMe
D2-92a CH2CH(Me)SEt
D2-92a CH2CH(Me)SCF3
D2-92a CH2CH(Me)SCH2CF3
D2-92a CH2CH(Me)S(O)Me
D2-92a CH2CH(Me)S(O)Et
D2-92a CH2CH(Me)S(O)CF3
D2-92a CH2CH(Me)S(O)CH2CF3
D2-92a CH2CH(Me)S(O)2Me
D2-92a CH2CH(Me)S(O)2Et
D2-92a CH2CH(Me)S(O)2CF3
D2-92a CH2CH(Me)S(O)2CH2CF3
D2-92a CH2CH(Et)SMe
D2-92a CH2CH(Et)SEt
D2-92a CH2CH(Et)SCF3
D2-92a CH2CH(Et)SCH2CF3
D2-92a CH2CH(Et)S(O)Me
D2-92a CH2CH(Et)S(O)Et
D2-92a CH2CH(Et)S(O)CF3
D2-92a CH2CH(Et)S(O)CH2CF3
D2-92a CH2CH(Et)S(O)2Me
D2-92a CH2CH(Et)S(O)2Et
D2-92a CH2CH(Et)S(O)2CF3
D2-92a CH2CH(Et)S(O)2CH2CF3
D2-92a CH(Me)CH(Me)SMe
D2-92a CH(Me)CH(Me)SEt
D2-92a CH(Me)CH(Me)SCF3
D2-92a CH(Me)CH(Me)SCH2CF3
D2-92a CH(Me)CH(Me)S(O)Me
D2-92a CH(Me)CH(Me)S(O)Et
D2-92a CH(Me)CH(Me)S(O)CF3
D2-92a CH(Me)CH(Me)S(O)CH2CF3
D2-92a CH(Me)CH(Me)S(O)2Me
D2-92a CH(Me)CH(Me)S(O)2Et
D2-92a CH(Me)CH(Me)S(O)2CF3
D2-92a CH(Me)CH(Me)S(O)2CH2CF3
CH(Me)SMe CH2SMe
CH(Me)SMe CH2SEt
CH(Me)SMe CH2SCF3
CH(Me)SMe CH2SCH2CF3
CH(Me)SMe CH2S(O)Me
CH(Me)SMe CH2S(O)Et
CH(Me)SMe CH2S(O)CF3
CH(Me)SMe CH2S(O)CH2CF3
CH(Me)SMe CH2S(O)2Me
CH(Me)SMe CH2S(O)2Et
CH(Me)SMe CH2S(O)2CF3
CH(Me)SMe CH2S(O)2CH2CF3
CH(Me)SMe CH(Me)SMe
CH(Me)SMe CH(Me)SEt
CH(Me)SMe CH(Me)SCF3
CH(Me)SMe CH(Me)SCH2CF3
CH(Me)SMe CH(Me)S(O)Me
CH(Me)SMe CH(Me)S(O)Et
CH(Me)SMe CH(Me)S(O)CF3
CH(Me)SMe CH(Me)S(O)CH2CF3
CH(Me)SMe CH(Me)S(O)2Me
CH(Me)SMe CH(Me)S(O)2Et
CH(Me)SMe CH(Me)S(O)2CF3
CH(Me)SMe CH(Me)S(O)2CH2CF3
CH(Me)SMe CH(Et)SMe
CH(Me)SMe CH(Et)SEt
CH(Me)SMe CH(Et)SCF3
CH(Me)SMe CH(Et)SCH2CF3
CH(Me)SMe CH(Et)S(O)Me
CH(Me)SMe CH(Et)S(O)Et
CH(Me)SMe CH(Et)S(O)CF3
CH(Me)SMe CH(Et)S(O)CH2CF3
CH(Me)SMe CH(Et)S(O)2Me
CH(Me)SMe CH(Et)S(O)2Et
CH(Me)SMe CH(Et)S(O)2CF3
CH(Me)SMe CH(Et)S(O)2CH2CF3
CH(Me)SMe CH(n-Pr)SMe
CH(Me)SMe CH(n-Pr)SEt
CH(Me)SMe CH(n-Pr)SCF3
CH(Me)SMe CH(n-Pr)SCH2CF3
CH(Me)SMe CH(n-Pr)S(O)Me
CH(Me)SMe CH(n-Pr)S(O)Et
CH(Me)SMe CH(n-Pr)S(O)CF3
CH(Me)SMe CH(n-Pr)S(O)CH2CF3
CH(Me)SMe CH(n-Pr)S(O)2Me
CH(Me)SMe CH(n-Pr)S(O)2Et
CH(Me)SMe CH(n-Pr)S(O)2CF3
CH(Me)SMe CH(n-Pr)S(O)2CH2CF3
CH(Me)SMe CH(i-Pr)SMe
CH(Me)SMe CH(i-Pr)SEt
CH(Me)SMe CH(i-Pr)SCF3
CH(Me)SMe CH(i-Pr)SCH2CF3
CH(Me)SMe CH(i-Pr)S(O)Me
CH(Me)SMe CH(i-Pr)S(O)Et
CH(Me)SMe CH(i-Pr)S(O)CF3
CH(Me)SMe CH(i-Pr)S(O)CH2CF3
CH(Me)SMe CH(i-Pr)S(O)2Me
CH(Me)SMe CH(i-Pr)S(O)2Et
CH(Me)SMe CH(i-Pr)S(O)2CF3
CH(Me)SMe CH(i-Pr)S(O)2CH2CF3
CH(Me)SMe CH(n-Bu)SMe
CH(Me)SMe CH(n-Bu)SEt
CH(Me)SMe CH(n-Bu)SCF3
CH(Me)SMe CH(n-Bu)SCH2CF3
CH(Me)SMe CH(n-Bu)S(O)Me
CH(Me)SMe CH(n-Bu)S(O)Et
CH(Me)SMe CH(n-Bu)S(O)CF3
CH(Me)SMe CH(n-Bu)S(O)CH2CF3
CH(Me)SMe CH(n-Bu)S(O)2Me
CH(Me)SMe CH(n-Bu)S(O)2Et
CH(Me)SMe CH(n-Bu)S(O)2CF3
CH(Me)SMe CH(n-Bu)S(O)2CH2CF3
CH(Me)SMe CH(i-Bu)SMe
CH(Me)SMe CH(i-Bu)SEt
CH(Me)SMe CH(i-Bu)SCF3
CH(Me)SMe CH(i-Bu)SCH2CF3
CH(Me)SMe CH(i-Bu)S(O)Me
CH(Me)SMe CH(i-Bu)S(O)Et
CH(Me)SMe CH(i-Bu)S(O)CF3
CH(Me)SMe CH(i-Bu)S(O)CH2CF3
CH(Me)SMe CH(i-Bu)S(O)2Me
CH(Me)SMe CH(i-Bu)S(O)2Et
CH(Me)SMe CH(i-Bu)S(O)2CF3
CH(Me)SMe CH(i-Bu)S(O)2CH2CF3
CH(Me)SMe CH(s-Bu)SMe
CH(Me)SMe CH(s-Bu)SEt
CH(Me)SMe CH(s-Bu)SCF3
CH(Me)SMe CH(s-Bu)SCH2CF3
CH(Me)SMe CH(s-Bu)S(O)Me
CH(Me)SMe CH(s-Bu)S(O)Et
CH(Me)SMe CH(s-Bu)S(O)CF3
CH(Me)SMe CH(s-Bu)S(O)CH2CF3
CH(Me)SMe CH(s-Bu)S(O)2Me
CH(Me)SMe CH(s-Bu)S(O)2Et
CH(Me)SMe CH(s-Bu)S(O)2CF3
CH(Me)SMe CH(s-Bu)S(O)2CH2CF3
CH(Me)SMe CH(t-Bu)SMe
CH(Me)SMe CH(t-Bu)SEt
CH(Me)SMe CH(t-Bu)SCF3
CH(Me)SMe CH(t-Bu)SCH2CF3
CH(Me)SMe CH(t-Bu)S(O)Me
CH(Me)SMe CH(t-Bu)S(O)Et
CH(Me)SMe CH(t-Bu)S(O)CF3
CH(Me)SMe CH(t-Bu)S(O)CH2CF3
CH(Me)SMe CH(t-Bu)S(O)2Me
CH(Me)SMe CH(t-Bu)S(O)2Et
CH(Me)SMe CH(t-Bu)S(O)2CF3
CH(Me)SMe CH(t-Bu)S(O)2CH2CF3
CH(Me)SMe CH(CF3)SMe
CH(Me)SMe CH(CF3)SEt
CH(Me)SMe CH(CF3)SCF3
CH(Me)SMe CH(CF3)SCH2CF3
CH(Me)SMe CH(CF3)S(O)Me
CH(Me)SMe CH(CF3)S(O)Et
CH(Me)SMe CH(CF3)S(O)CF3
CH(Me)SMe CH(CF3)S(O)CH2CF3
CH(Me)SMe CH(CF3)S(O)2Me
CH(Me)SMe CH(CF3)S(O)2Et
CH(Me)SMe CH(CF3)S(O)2CF3
CH(Me)SMe CH(CF3)S(O)2CH2CF3
CH(Me)SMe CH2CH2SMe
CH(Me)SMe CH2CH2SEt
CH(Me)SMe CH2CH2SCF3
CH(Me)SMe CH2CH2SCH2CF3
CH(Me)SMe CH2CH2S(O)Me
CH(Me)SMe CH2CH2S(O)Et
CH(Me)SMe CH2CH2S(O)CF3
CH(Me)SMe CH2CH2S(O)CH2CF3
CH(Me)SMe CH2CH2S(O)2Me
CH(Me)SMe CH2CH2S(O)2Et
CH(Me)SMe CH2CH2S(O)2CF3
CH(Me)SMe CH2CH2S(O)2CH2CF3
CH(Me)SMe CH(Me)CH2SMe
CH(Me)SMe CH(Me)CH2SEt
CH(Me)SMe CH(Me)CH2SCF3
CH(Me)SMe CH(Me)CH2SCH2CF3
CH(Me)SMe CH(Me)CH2S(O)Me
CH(Me)SMe CH(Me)CH2S(O)Et
CH(Me)SMe CH(Me)CH2S(O)CF3
CH(Me)SMe CH(Me)CH2S(O)CH2CF3
CH(Me)SMe CH(Me)CH2S(O)2Me
CH(Me)SMe CH(Me)CH2S(O)2Et
CH(Me)SMe CH(Me)CH2S(O)2CF3
CH(Me)SMe CH(Me)CH2S(O)2CH2CF3
CH(Me)SMe CH(Et)CH2SMe
CH(Me)SMe CH(Et)CH2SEt
CH(Me)SMe CH(Et)CH2SCF3
CH(Me)SMe CH(Et)CH2SCH2CF3
CH(Me)SMe CH(Et)CH2S(O)Me
CH(Me)SMe CH(Et)CH2S(O)Et
CH(Me)SMe CH(Et)CH2S(O)CF3
CH(Me)SMe CH(Et)CH2S(O)CH2CF3
CH(Me)SMe CH(Et)CH2S(O)2Me
CH(Me)SMe CH(Et)CH2S(O)2Et
CH(Me)SMe CH(Et)CH2S(O)2CF3
CH(Me)SMe CH(Et)CH2S(O)2CH2CF3
CH(Me)SMe C(Me)2CH2SMe
CH(Me)SMe C(Me)2CH2SEt
CH(Me)SMe C(Me)2CH2SCF3
CH(Me)SMe C(Me)2CH2SCH2CF3
CH(Me)SMe C(Me)2CH2S(O)Me
CH(Me)SMe C(Me)2CH2S(O)Et
CH(Me)SMe C(Me)2CH2S(O)CF3
CH(Me)SMe C(Me)2CH2S(O)CH2CF3
CH(Me)SMe C(Me)2CH2S(O)2Me
CH(Me)SMe C(Me)2CH2S(O)2Et
CH(Me)SMe C(Me)2CH2S(O)2CF3
CH(Me)SMe C(Me)2CH2S(O)2CH2CF3
CH(Me)SMe CH2CH(Me)SMe
CH(Me)SMe CH2CH(Me)SEt
CH(Me)SMe CH2CH(Me)SCF3
CH(Me)SMe CH2CH(Me)SCH2CF3
CH(Me)SMe CH2CH(Me)S(O)Me
CH(Me)SMe CH2CH(Me)S(O)Et
CH(Me)SMe CH2CH(Me)S(O)CF3
CH(Me)SMe CH2CH(Me)S(O)CH2CF3
CH(Me)SMe CH2CH(Me)S(O)2Me
CH(Me)SMe CH2CH(Me)S(O)2Et
CH(Me)SMe CH2CH(Me)S(O)2CF3
CH(Me)SMe CH2CH(Me)S(O)2CH2CF3
CH(Me)SMe CH2CH(Et)SMe
CH(Me)SMe CH2CH(Et)SEt
CH(Me)SMe CH2CH(Et)SCF3
CH(Me)SMe CH2CH(Et)SCH2CF3
CH(Me)SMe CH2CH(Et)S(O)Me
CH(Me)SMe CH2CH(Et)S(O)Et
CH(Me)SMe CH2CH(Et)S(O)CF3
CH(Me)SMe CH2CH(Et)S(O)CH2CF3
CH(Me)SMe CH2CH(Et)S(O)2Me
CH(Me)SMe CH2CH(Et)S(O)2Et
CH(Me)SMe CH2CH(Et)S(O)2CF3
CH(Me)SMe CH2CH(Et)S(O)2CH2CF3
CH(Me)SMe CH(Me)CH(Me)SMe
CH(Me)SMe CH(Me)CH(Me)SEt
CH(Me)SMe CH(Me)CH(Me)SCF3
CH(Me)SMe CH(Me)CH(Me)SCH2CF3
CH(Me)SMe CH(Me)CH(Me)S(O)Me
CH(Me)SMe CH(Me)CH(Me)S(O)Et
CH(Me)SMe CH(Me)CH(Me)S(O)CF3
CH(Me)SMe CH(Me)CH(Me)S(O)CH2CF3
CH(Me)SMe CH(Me)CH(Me)S(O)2Me
CH(Me)SMe CH(Me)CH(Me)S(O)2Et
CH(Me)SMe CH(Me)CH(Me)S(O)2CF3
CH(Me)SMe CH(Me)CH(Me)S(O)2CH2CF3
C(O)Me CH2SMe
C(O)Me CH2SEt
C(O)Me CH2SCF3
C(O)Me CH2SCH2CF3
C(O)Me CH2S(O)Me
C(O)Me CH2S(O)Et
C(O)Me CH2S(O)CF3
C(O)Me CH2S(O)CH2CF3
C(O)Me CH2S(O)2Me
C(O)Me CH2S(O)2Et
C(O)Me CH2S(O)2CF3
C(O)Me CH2S(O)2CH2CF3
C(O)Me CH(Me)SMe
C(O)Me CH(Me)SEt
C(O)Me CH(Me)SCF3
C(O)Me CH(Me)SCH2CF3
C(O)Me CH(Me)S(O)Me
C(O)Me CH(Me)S(O)Et
C(O)Me CH(Me)S(O)CF3
C(O)Me CH(Me)S(O)CH2CF3
C(O)Me CH(Me)S(O)2Me
C(O)Me CH(Me)S(O)2Et
C(O)Me CH(Me)S(O)2CF3
C(O)Me CH(Me)S(O)2CH2CF3
C(O)Me CH(Et)SMe
C(O)Me CH(Et)SEt
C(O)Me CH(Et)SCF3
C(O)Me CH(Et)SCH2CF3
C(O)Me CH(Et)S(O)Me
C(O)Me CH(Et)S(O)Et
C(O)Me CH(Et)S(O)CF3
C(O)Me CH(Et)S(O)CH2CF3
C(O)Me CH(Et)S(O)2Me
C(O)Me CH(Et)S(O)2Et
C(O)Me CH(Et)S(O)2CF3
C(O)Me CH(Et)S(O)2CH2CF3
C(O)Me CH(n-Pr)SMe
C(O)Me CH(n-Pr)SEt
C(O)Me CH(n-Pr)SCF3
C(O)Me CH(n-Pr)SCH2CF3
C(O)Me CH(n-Pr)S(O)Me
C(O)Me CH(n-Pr)S(O)Et
C(O)Me CH(n-Pr)S(O)CF3
C(O)Me CH(n-Pr)S(O)CH2CF3
C(O)Me CH(n-Pr)S(O)2Me
C(O)Me CH(n-Pr)S(O)2Et
C(O)Me CH(n-Pr)S(O)2CF3
C(O)Me CH(n-Pr)S(O)2CH2CF3
C(O)Me CH(i-Pr)SMe
C(O)Me CH(i-Pr)SEt
C(O)Me CH(i-Pr)SCF3
C(O)Me CH(i-Pr)SCH2CF3
C(O)Me CH(i-Pr)S(O)Me
C(O)Me CH(i-Pr)S(O)Et
C(O)Me CH(i-Pr)S(O)CF3
C(O)Me CH(i-Pr)S(O)CH2CF3
C(O)Me CH(i-Pr)S(O)2Me
C(O)Me CH(i-Pr)S(O)2Et
C(O)Me CH(i-Pr)S(O)2CF3
C(O)Me CH(i-Pr)S(O)2CH2CF3
C(O)Me CH(n-Bu)SMe
C(O)Me CH(n-Bu)SEt
C(O)Me CH(n-Bu)SCF3
C(O)Me CH(n-Bu)SCH2CF3
C(O)Me CH(n-Bu)S(O)Me
C(O)Me CH(n-Bu)S(O)Et
C(O)Me CH(n-Bu)S(O)CF3
C(O)Me CH(n-Bu)S(O)CH2CF3
C(O)Me CH(n-Bu)S(O)2Me
C(O)Me CH(n-Bu)S(O)2Et
C(O)Me CH(n-Bu)S(O)2CF3
C(O)Me CH(n-Bu)S(O)2CH2CF3
C(O)Me CH(i-Bu)SMe
C(O)Me CH(i-Bu)SEt
C(O)Me CH(i-Bu)SCF3
C(O)Me CH(i-Bu)SCH2CF3
C(O)Me CH(i-Bu)S(O)Me
C(O)Me CH(i-Bu)S(O)Et
C(O)Me CH(i-Bu)S(O)CF3
C(O)Me CH(i-Bu)S(O)CH2CF3
C(O)Me CH(i-Bu)S(O)2Me
C(O)Me CH(i-Bu)S(O)2Et
C(O)Me CH(i-Bu)S(O)2CF3
C(O)Me CH(i-Bu)S(O)2CH2CF3
C(O)Me CH(s-Bu)SMe
C(O)Me CH(s-Bu)SEt
C(O)Me CH(s-Bu)SCF3
C(O)Me CH(s-Bu)SCH2CF3
C(O)Me CH(s-Bu)S(O)Me
C(O)Me CH(s-Bu)S(O)Et
C(O)Me CH(s-Bu)S(O)CF3
C(O)Me CH(s-Bu)S(O)CH2CF3
C(O)Me CH(s-Bu)S(O)2Me
C(O)Me CH(s-Bu)S(O)2Et
C(O)Me CH(s-Bu)S(O)2CF3
C(O)Me CH(s-Bu)S(O)2CH2CF3
C(O)Me CH(t-Bu)SMe
C(O)Me CH(t-Bu)SEt
C(O)Me CH(t-Bu)SCF3
C(O)Me CH(t-Bu)SCH2CF3
C(O)Me CH(t-Bu)S(O)Me
C(O)Me CH(t-Bu)S(O)Et
C(O)Me CH(t-Bu)S(O)CF3
C(O)Me CH(t-Bu)S(O)CH2CF3
C(O)Me CH(t-Bu)S(O)2Me
C(O)Me CH(t-Bu)S(O)2Et
C(O)Me CH(t-Bu)S(O)2CF3
C(O)Me CH(t-Bu)S(O)2CH2CF3
C(O)Me CH(CF3)SMe
C(O)Me CH(CF3)SEt
C(O)Me CH(CF3)SCF3
C(O)Me CH(CF3)SCH2CF3
C(O)Me CH(CF3)S(O)Me
C(O)Me CH(CF3)S(O)Et
C(O)Me CH(CF3)S(O)CF3
C(O)Me CH(CF3)S(O)CH2CF3
C(O)Me CH(CF3)S(O)2Me
C(O)Me CH(CF3)S(O)2Et
C(O)Me CH(CF3)S(O)2CF3
C(O)Me CH(CF3)S(O)2CH2CF3
C(O)Me CH2CH2SMe
C(O)Me CH2CH2SEt
C(O)Me CH2CH2SCF3
C(O)Me CH2CH2SCH2CF3
C(O)Me CH2CH2S(O)Me
C(O)Me CH2CH2S(O)Et
C(O)Me CH2CH2S(O)CF3
C(O)Me CH2CH2S(O)CH2CF3
C(O)Me CH2CH2S(O)2Me
C(O)Me CH2CH2S(O)2Et
C(O)Me CH2CH2S(O)2CF3
C(O)Me CH2CH2S(O)2CH2CF3
C(O)Me CH(Me)CH2SMe
C(O)Me CH(Me)CH2SEt
C(O)Me CH(Me)CH2SCF3
C(O)Me CH(Me)CH2SCH2CF3
C(O)Me CH(Me)CH2S(O)Me
C(O)Me CH(Me)CH2S(O)Et
C(O)Me CH(Me)CH2S(O)CF3
C(O)Me CH(Me)CH2S(O)CH2CF3
C(O)Me CH(Me)CH2S(O)2Me
C(O)Me CH(Me)CH2S(O)2Et
C(O)Me CH(Me)CH2S(O)2CF3
C(O)Me CH(Me)CH2S(O)2CH2CF3
C(O)Me CH(Et)CH2SMe
C(O)Me CH(Et)CH2SEt
C(O)Me CH(Et)CH2SCF3
C(O)Me CH(Et)CH2SCH2CF3
C(O)Me CH(Et)CH2S(O)Me
C(O)Me CH(Et)CH2S(O)Et
C(O)Me CH(Et)CH2S(O)CF3
C(O)Me CH(Et)CH2S(O)CH2CF3
C(O)Me CH(Et)CH2S(O)2Me
C(O)Me CH(Et)CH2S(O)2Et
C(O)Me CH(Et)CH2S(O)2CF3
C(O)Me CH(Et)CH2S(O)2CH2CF3
C(O)Me C(Me)2CH2SMe
C(O)Me C(Me)2CH2SEt
C(O)Me C(Me)2CH2SCF3
C(O)Me C(Me)2CH2SCH2CF3
C(O)Me C(Me)2CH2S(O)Me
C(O)Me C(Me)2CH2S(O)Et
C(O)Me C(Me)2CH2S(O)CF3
C(O)Me C(Me)2CH2S(O)CH2CF3
C(O)Me C(Me)2CH2S(O)2Me
C(O)Me C(Me)2CH2S(O)2Et
C(O)Me C(Me)2CH2S(O)2CF3
C(O)Me C(Me)2CH2S(O)2CH2CF3
C(O)Me CH2CH(Me)SMe
C(O)Me CH2CH(Me)SEt
C(O)Me CH2CH(Me)SCF3
C(O)Me CH2CH(Me)SCH2CF3
C(O)Me CH2CH(Me)S(O)Me
C(O)Me CH2CH(Me)S(O)Et
C(O)Me CH2CH(Me)S(O)CF3
C(O)Me CH2CH(Me)S(O)CH2CF3
C(O)Me CH2CH(Me)S(O)2Me
C(O)Me CH2CH(Me)S(O)2Et
C(O)Me CH2CH(Me)S(O)2CF3
C(O)Me CH2CH(Me)S(O)2CH2CF3
C(O)Me CH2CH(Et)SMe
C(O)Me CH2CH(Et)SEt
C(O)Me CH2CH(Et)SCF3
C(O)Me CH2CH(Et)SCH2CF3
C(O)Me CH2CH(Et)S(O)Me
C(O)Me CH2CH(Et)S(O)Et
C(O)Me CH2CH(Et)S(O)CF3
C(O)Me CH2CH(Et)S(O)CH2CF3
C(O)Me CH2CH(Et)S(O)2Me
C(O)Me CH2CH(Et)S(O)2Et
C(O)Me CH2CH(Et)S(O)2CF3
C(O)Me CH2CH(Et)S(O)2CH2CF3
C(O)Me CH(Me)CH(Me)SMe
C(O)Me CH(Me)CH(Me)SEt
C(O)Me CH(Me)CH(Me)SCF3
C(O)Me CH(Me)CH(Me)SCH2CF3
C(O)Me CH(Me)CH(Me)S(O)Me
C(O)Me CH(Me)CH(Me)S(O)Et
C(O)Me CH(Me)CH(Me)S(O)CF3
C(O)Me CH(Me)CH(Me)S(O)CH2CF3
C(O)Me CH(Me)CH(Me)S(O)2Me
C(O)Me CH(Me)CH(Me)S(O)2Et
C(O)Me CH(Me)CH(Me)S(O)2CF3
C(O)Me CH(Me)CH(Me)S(O)2CH2CF3
C(O)OMe CH2SMe
C(O)OMe CH2SEt
C(O)OMe CH2SCF3
C(O)OMe CH2SCH2CF3
C(O)OMe CH2S(O)Me
C(O)OMe CH2S(O)Et
C(O)OMe CH2S(O)CF3
C(O)OMe CH2S(O)CH2CF3
C(O)OMe CH2S(O)2Me
C(O)OMe CH2S(O)2Et
C(O)OMe CH2S(O)2CF3
C(O)OMe CH2S(O)2CH2CF3
C(O)OMe CH(Me)SMe
C(O)OMe CH(Me)SEt
C(O)OMe CH(Me)SCF3
C(O)OMe CH(Me)SCH2CF3
C(O)OMe CH(Me)S(O)Me
C(O)OMe CH(Me)S(O)Et
C(O)OMe CH(Me)S(O)CF3
C(O)OMe CH(Me)S(O)CH2CF3
C(O)OMe CH(Me)S(O)2Me
C(O)OMe CH(Me)S(O)2Et
C(O)OMe CH(Me)S(O)2CF3
C(O)OMe CH(Me)S(O)2CH2CF3
C(O)OMe CH(Et)SMe
C(O)OMe CH(Et)SEt
C(O)OMe CH(Et)SCF3
C(O)OMe CH(Et)SCH2CF3
C(O)OMe CH(Et)S(O)Me
C(O)OMe CH(Et)S(O)Et
C(O)OMe CH(Et)S(O)CF3
C(O)OMe CH(Et)S(O)CH2CF3
C(O)OMe CH(Et)S(O)2Me
C(O)OMe CH(Et)S(O)2Et
C(O)OMe CH(Et)S(O)2CF3
C(O)OMe CH(Et)S(O)2CH2CF3
C(O)OMe CH(n-Pr)SMe
C(O)OMe CH(n-Pr)SEt
C(O)OMe CH(n-Pr)SCF3
C(O)OMe CH(n-Pr)SCH2CF3
C(O)OMe CH(n-Pr)S(O)Me
C(O)OMe CH(n-Pr)S(O)Et
C(O)OMe CH(n-Pr)S(O)CF3
C(O)OMe CH(n-Pr)S(O)CH2CF3
C(O)OMe CH(n-Pr)S(O)2Me
C(O)OMe CH(n-Pr)S(O)2Et
C(O)OMe CH(n-Pr)S(O)2CF3
C(O)OMe CH(n-Pr)S(O)2CH2CF3
C(O)OMe CH(i-Pr)SMe
C(O)OMe CH(i-Pr)SEt
C(O)OMe CH(i-Pr)SCF3
C(O)OMe CH(i-Pr)SCH2CF3
C(O)OMe CH(i-Pr)S(O)Me
C(O)OMe CH(i-Pr)S(O)Et
C(O)OMe CH(i-Pr)S(O)CF3
C(O)OMe CH(i-Pr)S(O)CH2CF3
C(O)OMe CH(i-Pr)S(O)2Me
C(O)OMe CH(i-Pr)S(O)2Et
C(O)OMe CH(i-Pr)S(O)2CF3
C(O)OMe CH(i-Pr)S(O)2CH2CF3
C(O)OMe CH(n-Bu)SMe
C(O)OMe CH(n-Bu)SEt
C(O)OMe CH(n-Bu)SCF3
C(O)OMe CH(n-Bu)SCH2CF3
C(O)OMe CH(n-Bu)S(O)Me
C(O)OMe CH(n-Bu)S(O)Et
C(O)OMe CH(n-Bu)S(O)CF3
C(O)OMe CH(n-Bu)S(O)CH2CF3
C(O)OMe CH(n-Bu)S(O)2Me
C(O)OMe CH(n-Bu)S(O)2Et
C(O)OMe CH(n-Bu)S(O)2CF3
C(O)OMe CH(n-Bu)S(O)2CH2CF3
C(O)OMe CH(i-Bu)SMe
C(O)OMe CH(i-Bu)SEt
C(O)OMe CH(i-Bu)SCF3
C(O)OMe CH(i-Bu)SCH2CF3
C(O)OMe CH(i-Bu)S(O)Me
C(O)OMe CH(i-Bu)S(O)Et
C(O)OMe CH(i-Bu)S(O)CF3
C(O)OMe CH(i-Bu)S(O)CH2CF3
C(O)OMe CH(i-Bu)S(O)2Me
C(O)OMe CH(i-Bu)S(O)2Et
C(O)OMe CH(i-Bu)S(O)2CF3
C(O)OMe CH(i-Bu)S(O)2CH2CF3
C(O)OMe CH(s-Bu)SMe
C(O)OMe CH(s-Bu)SEt
C(O)OMe CH(s-Bu)SCF3
C(O)OMe CH(s-Bu)SCH2CF3
C(O)OMe CH(s-Bu)S(O)Me
C(O)OMe CH(s-Bu)S(O)Et
C(O)OMe CH(s-Bu)S(O)CF3
C(O)OMe CH(s-Bu)S(O)CH2CF3
C(O)OMe CH(s-Bu)S(O)2Me
C(O)OMe CH(s-Bu)S(O)2Et
C(O)OMe CH(s-Bu)S(O)2CF3
C(O)OMe CH(s-Bu)S(O)2CH2CF3
C(O)OMe CH(t-Bu)SMe
C(O)OMe CH(t-Bu)SEt
C(O)OMe CH(t-Bu)SCF3
C(O)OMe CH(t-Bu)SCH2CF3
C(O)OMe CH(t-Bu)S(O)Me
C(O)OMe CH(t-Bu)S(O)Et
C(O)OMe CH(t-Bu)S(O)CF3
C(O)OMe CH(t-Bu)S(O)CH2CF3
C(O)OMe CH(t-Bu)S(O)2Me
C(O)OMe CH(t-Bu)S(O)2Et
C(O)OMe CH(t-Bu)S(O)2CF3
C(O)OMe CH(t-Bu)S(O)2CH2CF3
C(O)OMe CH(CF3)SMe
C(O)OMe CH(CF3)SEt
C(O)OMe CH(CF3)SCF3
C(O)OMe CH(CF3)SCH2CF3
C(O)OMe CH(CF3)S(O)Me
C(O)OMe CH(CF3)S(O)Et
C(O)OMe CH(CF3)S(O)CF3
C(O)OMe CH(CF3)S(O)CH2CF3
C(O)OMe CH(CF3)S(O)2Me
C(O)OMe CH(CF3)S(O)2Et
C(O)OMe CH(CF3)S(O)2CF3
C(O)OMe CH(CF3)S(O)2CH2CF3
C(O)OMe CH2CH2SMe
C(O)OMe CH2CH2SEt
C(O)OMe CH2CH2SCF3
C(O)OMe CH2CH2SCH2CF3
C(O)OMe CH2CH2S(O)Me
C(O)OMe CH2CH2S(O)Et
C(O)OMe CH2CH2S(O)CF3
C(O)OMe CH2CH2S(O)CH2CF3
C(O)OMe CH2CH2S(O)2Me
C(O)OMe CH2CH2S(O)2Et
C(O)OMe CH2CH2S(O)2CF3
C(O)OMe CH2CH2S(O)2CH2CF3
C(O)OMe CH(Me)CH2SMe
C(O)OMe CH(Me)CH2SEt
C(O)OMe CH(Me)CH2SCF3
C(O)OMe CH(Me)CH2SCH2CF3
C(O)OMe CH(Me)CH2S(O)Me
C(O)OMe CH(Me)CH2S(O)Et
C(O)OMe CH(Me)CH2S(O)CF3
C(O)OMe CH(Me)CH2S(O)CH2CF3
C(O)OMe CH(Me)CH2S(O)2Me
C(O)OMe CH(Me)CH2S(O)2Et
C(O)OMe CH(Me)CH2S(O)2CF3
C(O)OMe CH(Me)CH2S(O)2CH2CF3
C(O)OMe CH(Et)CH2SMe
C(O)OMe CH(Et)CH2SEt
C(O)OMe CH(Et)CH2SCF3
C(O)OMe CH(Et)CH2SCH2CF3
C(O)OMe CH(Et)CH2S(O)Me
C(O)OMe CH(Et)CH2S(O)Et
C(O)OMe CH(Et)CH2S(O)CF3
C(O)OMe CH(Et)CH2S(O)CH2CF3
C(O)OMe CH(Et)CH2S(O)2Me
C(O)OMe CH(Et)CH2S(O)2Et
C(O)OMe CH(Et)CH2S(O)2CF3
C(O)OMe CH(Et)CH2S(O)2CH2CF3
C(O)OMe C(Me)2CH2SMe
C(O)OMe C(Me)2CH2SEt
C(O)OMe C(Me)2CH2SCF3
C(O)OMe C(Me)2CH2SCH2CF3
C(O)OMe C(Me)2CH2S(O)Me
C(O)OMe C(Me)2CH2S(O)Et
C(O)OMe C(Me)2CH2S(O)CF3
C(O)OMe C(Me)2CH2S(O)CH2CF3
C(O)OMe C(Me)2CH2S(O)2Me
C(O)OMe C(Me)2CH2S(O)2Et
C(O)OMe C(Me)2CH2S(O)2CF3
C(O)OMe C(Me)2CH2S(O)2CH2CF3
C(O)OMe CH2CH(Me)SMe
C(O)OMe CH2CH(Me)SEt
C(O)OMe CH2CH(Me)SCF3
C(O)OMe CH2CH(Me)SCH2CF3
C(O)OMe CH2CH(Me)S(O)Me
C(O)OMe CH2CH(Me)S(O)Et
C(O)OMe CH2CH(Me)S(O)CF3
C(O)OMe CH2CH(Me)S(O)CH2CF3
C(O)OMe CH2CH(Me)S(O)2Me
C(O)OMe CH2CH(Me)S(O)2Et
C(O)OMe CH2CH(Me)S(O)2CF3
C(O)OMe CH2CH(Me)S(O)2CH2CF3
C(O)OMe CH2CH(Et)SMe
C(O)OMe CH2CH(Et)SEt
C(O)OMe CH2CH(Et)SCF3
C(O)OMe CH2CH(Et)SCH2CF3
C(O)OMe CH2CH(Et)S(O)Me
C(O)OMe CH2CH(Et)S(O)Et
C(O)OMe CH2CH(Et)S(O)CF3
C(O)OMe CH2CH(Et)S(O)CH2CF3
C(O)OMe CH2CH(Et)S(O)2Me
C(O)OMe CH2CH(Et)S(O)2Et
C(O)OMe CH2CH(Et)S(O)2CF3
C(O)OMe CH2CH(Et)S(O)2CH2CF3
C(O)OMe CH(Me)CH(Me)SMe
C(O)OMe CH(Me)CH(Me)SEt
C(O)OMe CH(Me)CH(Me)SCF3
C(O)OMe CH(Me)CH(Me)SCH2CF3
C(O)OMe CH(Me)CH(Me)S(O)Me
C(O)OMe CH(Me)CH(Me)S(O)Et
C(O)OMe CH(Me)CH(Me)S(O)CF3
C(O)OMe CH(Me)CH(Me)S(O)CH2CF3
C(O)OMe CH(Me)CH(Me)S(O)2Me
C(O)OMe CH(Me)CH(Me)S(O)2Et
C(O)OMe CH(Me)CH(Me)S(O)2CF3
C(O)OMe CH(Me)CH(Me)S(O)2CH2CF3
CH2OMe CH2SMe
CH2OMe CH2SEt
CH2OMe CH2SCF3
CH2OMe CH2SCH2CF3
CH2OMe CH2S(O)Me
CH2OMe CH2S(O)Et
CH2OMe CH2S(O)CF3
CH2OMe CH2S(O)CH2CF3
CH2OMe CH2S(O)2Me
CH2OMe CH2S(O)2Et
CH2OMe CH2S(O)2CF3
CH2OMe CH2S(O)2CH2CF3
CH2OMe CH(Me)SMe
CH2OMe CH(Me)SEt
CH2OMe CH(Me)SCF3
CH2OMe CH(Me)SCH2CF3
CH2OMe CH(Me)S(O)Me
CH2OMe CH(Me)S(O)Et
CH2OMe CH(Me)S(O)CF3
CH2OMe CH(Me)S(O)CH2CF3
CH2OMe CH(Me)S(O)2Me
CH2OMe CH(Me)S(O)2Et
CH2OMe CH(Me)S(O)2CF3
CH2OMe CH(Me)S(O)2CH2CF3
CH2OMe CH(Et)SMe
CH2OMe CH(Et)SEt
CH2OMe CH(Et)SCF3
CH2OMe CH(Et)SCH2CF3
CH2OMe CH(Et)S(O)Me
CH2OMe CH(Et)S(O)Et
CH2OMe CH(Et)S(O)CF3
CH2OMe CH(Et)S(O)CH2CF3
CH2OMe CH(Et)S(O)2Me
CH2OMe CH(Et)S(O)2Et
CH2OMe CH(Et)S(O)2CF3
CH2OMe CH(Et)S(O)2CH2CF3
CH2OMe CH(n-Pr)SMe
CH2OMe CH(n-Pr)SEt
CH2OMe CH(n-Pr)SCF3
CH2OMe CH(n-Pr)SCH2CF3
CH2OMe CH(n-Pr)S(O)Me
CH2OMe CH(n-Pr)S(O)Et
CH2OMe CH(n-Pr)S(O)CF3
CH2OMe CH(n-Pr)S(O)CH2CF3
CH2OMe CH(n-Pr)S(O)2Me
CH2OMe CH(n-Pr)S(O)2Et
CH2OMe CH(n-Pr)S(O)2CF3
CH2OMe CH(n-Pr)S(O)2CH2CF3
CH2OMe CH(i-Pr)SMe
CH2OMe CH(i-Pr)SEt
CH2OMe CH(i-Pr)SCF3
CH2OMe CH(i-Pr)SCH2CF3
CH2OMe CH(i-Pr)S(O)Me
CH2OMe CH(i-Pr)S(O)Et
CH2OMe CH(i-Pr)S(O)CF3
CH2OMe CH(i-Pr)S(O)CH2CF3
CH2OMe CH(i-Pr)S(O)2Me
CH2OMe CH(i-Pr)S(O)2Et
CH2OMe CH(i-Pr)S(O)2CF3
CH2OMe CH(i-Pr)S(O)2CH2CF3
CH2OMe CH(n-Bu)SMe
CH2OMe CH(n-Bu)SEt
CH2OMe CH(n-Bu)SCF3
CH2OMe CH(n-Bu)SCH2CF3
CH2OMe CH(n-Bu)S(O)Me
CH2OMe CH(n-Bu)S(O)Et
CH2OMe CH(n-Bu)S(O)CF3
CH2OMe CH(n-Bu)S(O)CH2CF3
CH2OMe CH(n-Bu)S(O)2Me
CH2OMe CH(n-Bu)S(O)2Et
CH2OMe CH(n-Bu)S(O)2CF3
CH2OMe CH(n-Bu)S(O)2CH2CF3
CH2OMe CH(i-Bu)SMe
CH2OMe CH(i-Bu)SEt
CH2OMe CH(i-Bu)SCF3
CH2OMe CH(i-Bu)SCH2CF3
CH2OMe CH(i-Bu)S(O)Me
CH2OMe CH(i-Bu)S(O)Et
CH2OMe CH(i-Bu)S(O)CF3
CH2OMe CH(i-Bu)S(O)CH2CF3
CH2OMe CH(i-Bu)S(O)2Me
CH2OMe CH(i-Bu)S(O)2Et
CH2OMe CH(i-Bu)S(O)2CF3
CH2OMe CH(i-Bu)S(O)2CH2CF3
CH2OMe CH(s-Bu)SMe
CH2OMe CH(s-Bu)SEt
CH2OMe CH(s-Bu)SCF3
CH2OMe CH(s-Bu)SCH2CF3
CH2OMe CH(s-Bu)S(O)Me
CH2OMe CH(s-Bu)S(O)Et
CH2OMe CH(s-Bu)S(O)CF3
CH2OMe CH(s-Bu)S(O)CH2CF3
CH2OMe CH(s-Bu)S(O)2Me
CH2OMe CH(s-Bu)S(O)2Et
CH2OMe CH(s-Bu)S(O)2CF3
CH2OMe CH(s-Bu)S(O)2CH2CF3
CH2OMe CH(t-Bu)SMe
CH2OMe CH(t-Bu)SEt
CH2OMe CH(t-Bu)SCF3
CH2OMe CH(t-Bu)SCH2CF3
CH2OMe CH(t-Bu)S(O)Me
CH2OMe CH(t-Bu)S(O)Et
CH2OMe CH(t-Bu)S(O)CF3
CH2OMe CH(t-Bu)S(O)CH2CF3
CH2OMe CH(t-Bu)S(O)2Me
CH2OMe CH(t-Bu)S(O)2Et
CH2OMe CH(t-Bu)S(O)2CF3
CH2OMe CH(t-Bu)S(O)2CH2CF3
CH2OMe CH(CF3)SMe
CH2OMe CH(CF3)SEt
CH2OMe CH(CF3)SCF3
CH2OMe CH(CF3)SCH2CF3
CH2OMe CH(CF3)S(O)Me
CH2OMe CH(CF3)S(O)Et
CH2OMe CH(CF3)S(O)CF3
CH2OMe CH(CF3)S(O)CH2CF3
CH2OMe CH(CF3)S(O)2Me
CH2OMe CH(CF3)S(O)2Et
CH2OMe CH(CF3)S(O)2CF3
CH2OMe CH(CF3)S(O)2CH2CF3
CH2OMe CH2CH2SMe
CH2OMe CH2CH2SEt
CH2OMe CH2CH2SCF3
CH2OMe CH2CH2SCH2CF3
CH2OMe CH2CH2S(O)Me
CH2OMe CH2CH2S(O)Et
CH2OMe CH2CH2S(O)CF3
CH2OMe CH2CH2S(O)CH2CF3
CH2OMe CH2CH2S(O)2Me
CH2OMe CH2CH2S(O)2Et
CH2OMe CH2CH2S(O)2CF3
CH2OMe CH2CH2S(O)2CH2CF3
CH2OMe CH(Me)CH2SMe
CH2OMe CH(Me)CH2SEt
CH2OMe CH(Me)CH2SCF3
CH2OMe CH(Me)CH2SCH2CF3
CH2OMe CH(Me)CH2S(O)Me
CH2OMe CH(Me)CH2S(O)Et
CH2OMe CH(Me)CH2S(O)CF3
CH2OMe CH(Me)CH2S(O)CH2CF3
CH2OMe CH(Me)CH2S(O)2Me
CH2OMe CH(Me)CH2S(O)2Et
CH2OMe CH(Me)CH2S(O)2CF3
CH2OMe CH(Me)CH2S(O)2CH2CF3
CH2OMe CH(Et)CH2SMe
CH2OMe CH(Et)CH2SEt
CH2OMe CH(Et)CH2SCF3
CH2OMe CH(Et)CH2SCH2CF3
CH2OMe CH(Et)CH2S(O)Me
CH2OMe CH(Et)CH2S(O)Et
CH2OMe CH(Et)CH2S(O)CF3
CH2OMe CH(Et)CH2S(O)CH2CF3
CH2OMe CH(Et)CH2S(O)2Me
CH2OMe CH(Et)CH2S(O)2Et
CH2OMe CH(Et)CH2S(O)2CF3
CH2OMe CH(Et)CH2S(O)2CH2CF3
CH2OMe C(Me)2CH2SMe
CH2OMe C(Me)2CH2SEt
CH2OMe C(Me)2CH2SCF3
CH2OMe C(Me)2CH2SCH2CF3
CH2OMe C(Me)2CH2S(O)Me
CH2OMe C(Me)2CH2S(O)Et
CH2OMe C(Me)2CH2S(O)CF3
CH2OMe C(Me)2CH2S(O)CH2CF3
CH2OMe C(Me)2CH2S(O)2Me
CH2OMe C(Me)2CH2S(O)2Et
CH2OMe C(Me)2CH2S(O)2CF3
CH2OMe C(Me)2CH2S(O)2CH2CF3
CH2OMe CH2CH(Me)SMe
CH2OMe CH2CH(Me)SEt
CH2OMe CH2CH(Me)SCF3
CH2OMe CH2CH(Me)SCH2CF3
CH2OMe CH2CH(Me)S(O)Me
CH2OMe CH2CH(Me)S(O)Et
CH2OMe CH2CH(Me)S(O)CF3
CH2OMe CH2CH(Me)S(O)CH2CF3
CH2OMe CH2CH(Me)S(O)2Me
CH2OMe CH2CH(Me)S(O)2Et
CH2OMe CH2CH(Me)S(O)2CF3
CH2OMe CH2CH(Me)S(O)2CH2CF3
CH2OMe CH2CH(Et)SMe
CH2OMe CH2CH(Et)SEt
CH2OMe CH2CH(Et)SCF3
CH2OMe CH2CH(Et)SCH2CF3
CH2OMe CH2CH(Et)S(O)Me
CH2OMe CH2CH(Et)S(O)Et
CH2OMe CH2CH(Et)S(O)CF3
CH2OMe CH2CH(Et)S(O)CH2CF3
CH2OMe CH2CH(Et)S(O)2Me
CH2OMe CH2CH(Et)S(O)2Et
CH2OMe CH2CH(Et)S(O)2CF3
CH2OMe CH2CH(Et)S(O)2CH2CF3
CH2OMe CH(Me)CH(Me)SMe
CH2OMe CH(Me)CH(Me)SEt
CH2OMe CH(Me)CH(Me)SCF3
CH2OMe CH(Me)CH(Me)SCH2CF3
CH2OMe CH(Me)CH(Me)S(O)Me
CH2OMe CH(Me)CH(Me)S(O)Et
CH2OMe CH(Me)CH(Me)S(O)CF3
CH2OMe CH(Me)CH(Me)S(O)CH2CF3
CH2OMe CH(Me)CH(Me)S(O)2Me
CH2OMe CH(Me)CH(Me)S(O)2Et
CH2OMe CH(Me)CH(Me)S(O)2CF3
CH2OMe CH(Me)CH(Me)S(O)2CH2CF3
CH2SMe CH2SMe
CH2SEt CH2SMe
CH2S(O)Me CH2SMe
CH2S(O)Et CH2SMe
CH2S(O)2Me CH2SMe
CH2S(O)2Et CH2SMe
CH(Me)SMe CH2SMe
CH(Me)SEt CH2SMe
CH(Me)S(O)Me CH2SMe
CH(Me)S(O)Et CH2SMe
CH(Me)S(O)2Me CH2SMe
CH(Me)S(O)2Et CH2SMe
CH(Et)SMe CH2SMe
CH(Et)SEt CH2SMe
CH(Et)S(O)Me CH2SMe
CH(Et)S(O)Et CH2SMe
CH(Et)S(O)2Me CH2SMe
CH(Et)S(O)2Et CH2SMe
CH(n-Pr)SMe CH2SMe
CH(n-Pr)SEt CH2SMe
CH(n-Pr)S(O)Me CH2SMe
CH(n-Pr)S(O)Et CH2SMe
CH(n-Pr)S(O)2Me CH2SMe
CH(n-Pr)S(O)2Et CH2SMe
CH(i-Pr)SMe CH2SMe
CH(i-Pr)SEt CH2SMe
CH(i-Pr)S(O)Me CH2SMe
CH(i-Pr)S(O)Et CH2SMe
CH(i-Pr)S(O)2Me CH2SMe
CH(i-Pr)S(O)2Et CH2SMe
CH(n-Bu)SMe CH2SMe
CH(n-Bu)SEt CH2SMe
CH(n-Bu)S(O)Me CH2SMe
CH(n-Bu)S(O)Et CH2SMe
CH(n-Bu)S(O)2Me CH2SMe
CH(n-Bu)S(O)2Et CH2SMe
CH(i-Bu)SMe CH2SMe
CH(i-Bu)SEt CH2SMe
CH(i-Bu)S(O)Me CH2SMe
CH(i-Bu)S(O)Et CH2SMe
CH(i-Bu)S(O)2Me CH2SMe
CH(i-Bu)S(O)2Et CH2SMe
CH(s-Bu)SMe CH2SMe
CH(s-Bu)SEt CH2SMe
CH(s-Bu)S(O)Me CH2SMe
CH(s-Bu)S(O)Et CH2SMe
CH(s-Bu)S(O)2Me CH2SMe
CH(s-Bu)S(O)2Et CH2SMe
CH(t-Bu)SMe CH2SMe
CH(t-Bu)SEt CH2SMe
CH(t-Bu)S(O)Me CH2SMe
CH(t-Bu)S(O)Et CH2SMe
CH(t-Bu)S(O)2Me CH2SMe
CH(t-Bu)S(O)2Et CH2SMe
CH2CH2SMe CH2SMe
CH2CH2SEt CH2SMe
CH2CH2S(O)2Me CH2SMe
CH2CH2S(O)2Et CH2SMe
CH(Me)CH2SMe CH2SMe
CH(Me)CH2SEt CH2SMe
CH(Me)CH2S(O)Me CH2SMe
CH(Me)CH2S(O)Et CH2SMe
CH(Me)CH2S(O)2Me CH2SMe
CH(Me)CH2S(O)2Et CH2SMe
CH(Et)CH2SMe CH2SMe
CH(Et)CH2SEt CH2SMe
CH(Et)CH2S(O)Me CH2SMe
CH(Et)CH2S(O)Et CH2SMe
CH(Et)CH2S(O)2Me CH2SMe
CH(Et)CH2S(O)2Et CH2SMe
C(Me)2CH2SMe CH2SMe
C(Me)2CH2SEt CH2SMe
C(Me)2CH2S(O)Me CH2SMe
C(Me)2CH2S(O)Et CH2SMe
C(Me)2CH2S(O)2Me CH2SMe
C(Me)2CH2S(O)2Et CH2SMe
CH2CH(Me)SMe CH2SMe
CH2CH(Me)SEt CH2SMe
CH2CH(Me)S(O)Me CH2SMe
CH2CH(Me)S(O)Et CH2SMe
CH2CH(Me)S(O)2Me CH2SMe
CH2CH(Me)S(O)2Et CH2SMe
CH2CH(Et)SMe CH2SMe
CH2CH(Et)SEt CH2SMe
CH2CH(Et)S(O)Me CH2SMe
CH2CH(Et)S(O)Et CH2SMe
CH2CH(Et)S(O)2Me CH2SMe
CH2CH(Et)S(O)2Et CH2SMe
CH(Me)CH(Me)SMe CH2SMe
CH(Me)CH(Me)SEt CH2SMe
CH(Me)CH(Me)S(O)Me CH2SMe
CH(Me)CH(Me)S(O)Et CH2SMe
CH(Me)CH(Me)S(O)2Me CH2SMe
CH(Me)CH(Me)S(O)2Et CH2SMe
CH2SMe CH2S(O)Me
CH2SEt CH2S(O)Me
CH2S(O)Me CH2S(O)Me
CH2S(O)Et CH2S(O)Me
CH2S(O)2Me CH2S(O)Me
CH2S(O)2Et CH2S(O)Me
CH(Me)SMe CH2S(O)Me
CH(Me)SEt CH2S(O)Me
CH(Me)S(O)Me CH2S(O)Me
CH(Me)S(O)Et CH2S(O)Me
CH(Me)S(O)2Me CH2S(O)Me
CH(Me)S(O)2Et CH2S(O)Me
CH(Et)SMe CH2S(O)Me
CH(Et)SEt CH2S(O)Me
CH(Et)S(O)Me CH2S(O)Me
CH(Et)S(O)Et CH2S(O)Me
CH(Et)S(O)2Me CH2S(O)Me
CH(Et)S(O)2Et CH2S(O)Me
CH(n-Pr)SMe CH2S(O)Me
CH(n-Pr)SEt CH2S(O)Me
CH(n-Pr)S(O)Me CH2S(O)Me
CH(n-Pr)S(O)Et CH2S(O)Me
CH(n-Pr)S(O)2Me CH2S(O)Me
CH(n-Pr)S(O)2Et CH2S(O)Me
CH(i-Pr)SMe CH2S(O)Me
CH(i-Pr)SEt CH2S(O)Me
CH(i-Pr)S(O)Me CH2S(O)Me
CH(i-Pr)S(O)Et CH2S(O)Me
CH(i-Pr)S(O)2Me CH2S(O)Me
CH(i-Pr)S(O)2Et CH2S(O)Me
CH(n-Bu)SMe CH2S(O)Me
CH(n-Bu)SEt CH2S(O)Me
CH(n-Bu)S(O)Me CH2S(O)Me
CH(n-Bu)S(O)Et CH2S(O)Me
CH(n-Bu)S(O)2Me CH2S(O)Me
CH(n-Bu)S(O)2Et CH2S(O)Me
CH(i-Bu)SMe CH2S(O)Me
CH(i-Bu)SEt CH2S(O)Me
CH(i-Bu)S(O)Me CH2S(O)Me
CH(i-Bu)S(O)Et CH2S(O)Me
CH(i-Bu)S(O)2Me CH2S(O)Me
CH(i-Bu)S(O)2Et CH2S(O)Me
CH(s-Bu)SMe CH2S(O)Me
CH(s-Bu)SEt CH2S(O)Me
CH(s-Bu)S(O)Me CH2S(O)Me
CH(s-Bu)S(O)Et CH2S(O)Me
CH(s-Bu)S(O)2Me CH2S(O)Me
CH(s-Bu)S(O)2Et CH2S(O)Me
CH(t-Bu)SMe CH2S(O)Me
CH(t-Bu)SEt CH2S(O)Me
CH(t-Bu)S(O)Me CH2S(O)Me
CH(t-Bu)S(O)Et CH2S(O)Me
CH(t-Bu)S(O)2Me CH2S(O)Me
CH(t-Bu)S(O)2Et CH2S(O)Me
CH2CH2SMe CH2S(O)Me
CH2CH2SEt CH2S(O)Me
CH2CH2S(O)2Me CH2S(O)Me
CH2CH2S(O)2Et CH2S(O)Me
CH(Me)CH2SMe CH2S(O)Me
CH(Me)CH2SEt CH2S(O)Me
CH(Me)CH2S(O)Me CH2S(O)Me
CH(Me)CH2S(O)Et CH2S(O)Me
CH(Me)CH2S(O)2Me CH2S(O)Me
CH(Me)CH2S(O)2Et CH2S(O)Me
CH(Et)CH2SMe CH2S(O)Me
CH(Et)CH2SEt CH2S(O)Me
CH(Et)CH2S(O)Me CH2S(O)Me
CH(Et)CH2S(O)Et CH2S(O)Me
CH(Et)CH2S(O)2Me CH2S(O)Me
CH(Et)CH2S(O)2Et CH2S(O)Me
C(Me)2CH2SMe CH2S(O)Me
C(Me)2CH2SEt CH2S(O)Me
C(Me)2CH2S(O)Me CH2S(O)Me
C(Me)2CH2S(O)Et CH2S(O)Me
C(Me)2CH2S(O)2Me CH2S(O)Me
C(Me)2CH2S(O)2Et CH2S(O)Me
CH2CH(Me)SMe CH2S(O)Me
CH2CH(Me)SEt CH2S(O)Me
CH2CH(Me)S(O)Me CH2S(O)Me
CH2CH(Me)S(O)Et CH2S(O)Me
CH2CH(Me)S(O)2Me CH2S(O)Me
CH2CH(Me)S(O)2Et CH2S(O)Me
CH2CH(Et)SMe CH2S(O)Me
CH2CH(Et)SEt CH2S(O)Me
CH2CH(Et)S(O)Me CH2S(O)Me
CH2CH(Et)S(O)Et CH2S(O)Me
CH2CH(Et)S(O)2Me CH2S(O)Me
CH2CH(Et)S(O)2Et CH2S(O)Me
CH(Me)CH(Me)SMe CH2S(O)Me
CH(Me)CH(Me)SEt CH2S(O)Me
CH(Me)CH(Me)S(O)Me CH2S(O)Me
CH(Me)CH(Me)S(O)Et CH2S(O)Me
CH(Me)CH(Me)S(O)2Me CH2S(O)Me
CH(Me)CH(Me)S(O)2Et CH2S(O)Me
CH2SMe CH2S(O)2Me
CH2SEt CH2S(O)2Me
CH2S(O)Me CH2S(O)2Me
CH2S(O)Et CH2S(O)2Me
CH2S(O)2Me CH2S(O)2Me
CH2S(O)2Et CH2S(O)2Me
CH(Me)SMe CH2S(O)2Me
CH(Me)SEt CH2S(O)2Me
CH(Me)S(O)Me CH2S(O)2Me
CH(Me)S(O)Et CH2S(O)2Me
CH(Me)S(O)2Me CH2S(O)2Me
CH(Me)S(O)2Et CH2S(O)2Me
CH(Et)SMe CH2S(O)2Me
CH(Et)SEt CH2S(O)2Me
CH(Et)S(O)Me CH2S(O)2Me
CH(Et)S(O)Et CH2S(O)2Me
CH(Et)S(O)2Me CH2S(O)2Me
CH(Et)S(O)2Et CH2S(O)2Me
CH(n-Pr)SMe CH2S(O)2Me
CH(n-Pr)SEt CH2S(O)2Me
CH(n-Pr)S(O)Me CH2S(O)2Me
CH(n-Pr)S(O)Et CH2S(O)2Me
CH(n-Pr)S(O)2Me CH2S(O)2Me
CH(n-Pr)S(O)2Et CH2S(O)2Me
CH(i-Pr)SMe CH2S(O)2Me
CH(i-Pr)SEt CH2S(O)2Me
CH(i-Pr)S(O)Me CH2S(O)2Me
CH(i-Pr)S(O)Et CH2S(O)2Me
CH(i-Pr)S(O)2Me CH2S(O)2Me
CH(i-Pr)S(O)2Et CH2S(O)2Me
CH(n-Bu)SMe CH2S(O)2Me
CH(n-Bu)SEt CH2S(O)2Me
CH(n-Bu)S(O)Me CH2S(O)2Me
CH(n-Bu)S(O)Et CH2S(O)2Me
CH(n-Bu)S(O)2Me CH2S(O)2Me
CH(n-Bu)S(O)2Et CH2S(O)2Me
CH(i-Bu)SMe CH2S(O)2Me
CH(i-Bu)SEt CH2S(O)2Me
CH(i-Bu)S(O)Me CH2S(O)2Me
CH(i-Bu)S(O)Et CH2S(O)2Me
CH(i-Bu)S(O)2Me CH2S(O)2Me
CH(i-Bu)S(O)2Et CH2S(O)2Me
CH(s-Bu)SMe CH2S(O)2Me
CH(s-Bu)SEt CH2S(O)2Me
CH(s-Bu)S(O)Me CH2S(O)2Me
CH(s-Bu)S(O)Et CH2S(O)2Me
CH(s-Bu)S(O)2Me CH2S(O)2Me
CH(s-Bu)S(O)2Et CH2S(O)2Me
CH(t-Bu)SMe CH2S(O)2Me
CH(t-Bu)SEt CH2S(O)2Me
CH(t-Bu)S(O)Me CH2S(O)2Me
CH(t-Bu)S(O)Et CH2S(O)2Me
CH(t-Bu)S(O)2Me CH2S(O)2Me
CH(t-Bu)S(O)2Et CH2S(O)2Me
CH2CH2SMe CH2S(O)2Me
CH2CH2SEt CH2S(O)2Me
CH2CH2S(O)2Me CH2S(O)2Me
CH2CH2S(O)2Et CH2S(O)2Me
CH(Me)CH2SMe CH2S(O)2Me
CH(Me)CH2SEt CH2S(O)2Me
CH(Me)CH2S(O)Me CH2S(O)2Me
CH(Me)CH2S(O)Et CH2S(O)2Me
CH(Me)CH2S(O)2Me CH2S(O)2Me
CH(Me)CH2S(O)2Et CH2S(O)2Me
CH(Et)CH2SMe CH2S(O)2Me
CH(Et)CH2SEt CH2S(O)2Me
CH(Et)CH2S(O)Me CH2S(O)2Me
CH(Et)CH2S(O)Et CH2S(O)2Me
CH(Et)CH2S(O)2Me CH2S(O)2Me
CH(Et)CH2S(O)2Et CH2S(O)2Me
C(Me)2CH2SMe CH2S(O)2Me
C(Me)2CH2SEt CH2S(O)2Me
C(Me)2CH2S(O)Me CH2S(O)2Me
C(Me)2CH2S(O)Et CH2S(O)2Me
C(Me)2CH2S(O)2Me CH2S(O)2Me
C(Me)2CH2S(O)2Et CH2S(O)2Me
CH2CH(Me)SMe CH2S(O)2Me
CH2CH(Me)SEt CH2S(O)2Me
CH2CH(Me)S(O)Me CH2S(O)2Me
CH2CH(Me)S(O)Et CH2S(O)2Me
CH2CH(Me)S(O)2Me CH2S(O)2Me
CH2CH(Me)S(O)2Et CH2S(O)2Me
CH2CH(Et)SMe CH2S(O)2Me
CH2CH(Et)SEt CH2S(O)2Me
CH2CH(Et)S(O)Me CH2S(O)2Me
CH2CH(Et)S(O)Et CH2S(O)2Me
CH2CH(Et)S(O)2Me CH2S(O)2Me
CH2CH(Et)S(O)2Et CH2S(O)2Me
CH(Me)CH(Me)SMe CH2S(O)2Me
CH(Me)CH(Me)SEt CH2S(O)2Me
CH(Me)CH(Me)S(O)Me CH2S(O)2Me
CH(Me)CH(Me)S(O)Et CH2S(O)2Me
CH(Me)CH(Me)S(O)2Me CH2S(O)2Me
CH(Me)CH(Me)S(O)2Et CH2S(O)2Me
CH2SMe SMe
CH2SEt SMe
CH2S(O)Me SMe
CH2S(O)Et SMe
CH2S(O)2Me SMe
CH2S(O)2Et SMe
CH(Me)SMe SMe
CH(Me)SEt SMe
CH(Me)S(O)Me SMe
CH(Me)S(O)Et SMe
CH(Me)S(O)2Me SMe
CH(Me)S(O)2Et SMe
CH(Et)SMe SMe
CH(Et)SEt SMe
CH(Et)S(O)Me SMe
CH(Et)S(O)Et SMe
CH(Et)S(O)2Me SMe
CH(Et)S(O)2Et SMe
CH(n-Pr)SMe SMe
CH(n-Pr)SEt SMe
CH(n-Pr)S(O)Me SMe
CH(n-Pr)S(O)Et SMe
CH(n-Pr)S(O)2Me SMe
CH(n-Pr)S(O)2Et SMe
CH(i-Pr)SMe SMe
CH(i-Pr)SEt SMe
CH(i-Pr)S(O)Me SMe
CH(i-Pr)S(O)Et SMe
CH(i-Pr)S(O)2Me SMe
CH(i-Pr)S(O)2Et SMe
CH(n-Bu)SMe SMe
CH(n-Bu)SEt SMe
CH(n-Bu)S(O)Me SMe
CH(n-Bu)S(O)Et SMe
CH(n-Bu)S(O)2Me SMe
CH(n-Bu)S(O)2Et SMe
CH(i-Bu)SMe SMe
CH(i-Bu)SEt SMe
CH(i-Bu)S(O)Me SMe
CH(i-Bu)S(O)Et SMe
CH(i-Bu)S(O)2Me SMe
CH(i-Bu)S(O)2Et SMe
CH(s-Bu)SMe SMe
CH(s-Bu)SEt SMe
CH(s-Bu)S(O)Me SMe
CH(s-Bu)S(O)Et SMe
CH(s-Bu)S(O)2Me SMe
CH(s-Bu)S(O)2Et SMe
CH(t-Bu)SMe SMe
CH(t-Bu)SEt SMe
CH(t-Bu)S(O)Me SMe
CH(t-Bu)S(O)Et SMe
CH(t-Bu)S(O)2Me SMe
CH(t-Bu)S(O)2Et SMe
CH2CH2SMe SMe
CH2CH2SEt SMe
CH2CH2S(O)2Me SMe
CH2CH2S(O)2Et SMe
CH(Me)CH2SMe SMe
CH(Me)CH2SEt SMe
CH(Me)CH2S(O)Me SMe
CH(Me)CH2S(O)Et SMe
CH(Me)CH2S(O)2Me SMe
CH(Me)CH2S(O)2Et SMe
CH(Et)CH2SMe SMe
CH(Et)CH2SEt SMe
CH(Et)CH2S(O)Me SMe
CH(Et)CH2S(O)Et SMe
CH(Et)CH2S(O)2Me SMe
CH(Et)CH2S(O)2Et SMe
C(Me)2CH2SMe SMe
C(Me)2CH2SEt SMe
C(Me)2CH2S(O)Me SMe
C(Me)2CH2S(O)Et SMe
C(Me)2CH2S(O)2Me SMe
C(Me)2CH2S(O)2Et SMe
CH2CH(Me)SMe SMe
CH2CH(Me)SEt SMe
CH2CH(Me)S(O)Me SMe
CH2CH(Me)S(O)Et SMe
CH2CH(Me)S(O)2Me SMe
CH2CH(Me)S(O)2Et SMe
CH2CH(Et)SMe SMe
CH2CH(Et)SEt SMe
CH2CH(Et)S(O)Me SMe
CH2CH(Et)S(O)Et SMe
CH2CH(Et)S(O)2Me SMe
CH2CH(Et)S(O)2Et SMe
CH(Me)CH(Me)SMe SMe
CH(Me)CH(Me)SEt SMe
CH(Me)CH(Me)S(O)Me SMe
CH(Me)CH(Me)S(O)Et SMe
CH(Me)CH(Me)S(O)2Me SMe
CH(Me)CH(Me)S(O)2Et SMe
CH2SMe S(O)Me
CH2SEt S(O)Me
CH2S(O)Me S(O)Me
CH2S(O)Et S(O)Me
CH2S(O)2Me S(O)Me
CH2S(O)2Et S(O)Me
CH(Me)SMe S(O)Me
CH(Me)SEt S(O)Me
CH(Me)S(O)Me S(O)Me
CH(Me)S(O)Et S(O)Me
CH(Me)S(O)2Me S(O)Me
CH(Me)S(O)2Et S(O)Me
CH(Et)SMe S(O)Me
CH(Et)SEt S(O)Me
CH(Et)S(O)Me S(O)Me
CH(Et)S(O)Et S(O)Me
CH(Et)S(O)2Me S(O)Me
CH(Et)S(O)2Et S(O)Me
CH(n-Pr)SMe S(O)Me
CH(n-Pr)SEt S(O)Me
CH(n-Pr)S(O)Me S(O)Me
CH(n-Pr)S(O)Et S(O)Me
CH(n-Pr)S(O)2Me S(O)Me
CH(n-Pr)S(O)2Et S(O)Me
CH(i-Pr)SMe S(O)Me
CH(i-Pr)SEt S(O)Me
CH(i-Pr)S(O)Me S(O)Me
CH(i-Pr)S(O)Et S(O)Me
CH(i-Pr)S(O)2Me S(O)Me
CH(i-Pr)S(O)2Et S(O)Me
CH(n-Bu)SMe S(O)Me
CH(n-Bu)SEt S(O)Me
CH(n-Bu)S(O)Me S(O)Me
CH(n-Bu)S(O)Et S(O)Me
CH(n-Bu)S(O)2Me S(O)Me
CH(n-Bu)S(O)2Et S(O)Me
CH(i-Bu)SMe S(O)Me
CH(i-Bu)SEt S(O)Me
CH(i-Bu)S(O)Me S(O)Me
CH(i-Bu)S(O)Et S(O)Me
CH(i-Bu)S(O)2Me S(O)Me
CH(i-Bu)S(O)2Et S(O)Me
CH(s-Bu)SMe S(O)Me
CH(s-Bu)SEt S(O)Me
CH(s-Bu)S(O)Me S(O)Me
CH(s-Bu)S(O)Et S(O)Me
CH(s-Bu)S(O)2Me S(O)Me
CH(s-Bu)S(O)2Et S(O)Me
CH(t-Bu)SMe S(O)Me
CH(t-Bu)SEt S(O)Me
CH(t-Bu)S(O)Me S(O)Me
CH(t-Bu)S(O)Et S(O)Me
CH(t-Bu)S(O)2Me S(O)Me
CH(t-Bu)S(O)2Et S(O)Me
CH2CH2SMe S(O)Me
CH2CH2SEt S(O)Me
CH2CH2S(O)2Me S(O)Me
CH2CH2S(O)2Et S(O)Me
CH(Me)CH2SMe S(O)Me
CH(Me)CH2SEt S(O)Me
CH(Me)CH2S(O)Me S(O)Me
CH(Me)CH2S(O)Et S(O)Me
CH(Me)CH2S(O)2Me S(O)Me
CH(Me)CH2S(O)2Et S(O)Me
CH(Et)CH2SMe S(O)Me
CH(Et)CH2SEt S(O)Me
CH(Et)CH2S(O)Me S(O)Me
CH(Et)CH2S(O)Et S(O)Me
CH(Et)CH2S(O)2Me S(O)Me
CH(Et)CH2S(O)2Et S(O)Me
C(Me)2CH2SMe S(O)Me
C(Me)2CH2SEt S(O)Me
C(Me)2CH2S(O)Me S(O)Me
C(Me)2CH2S(O)Et S(O)Me
C(Me)2CH2S(O)2Me S(O)Me
C(Me)2CH2S(O)2Et S(O)Me
CH2CH(Me)SMe S(O)Me
CH2CH(Me)SEt S(O)Me
CH2CH(Me)S(O)Me S(O)Me
CH2CH(Me)S(O)Et S(O)Me
CH2CH(Me)S(O)2Me S(O)Me
CH2CH(Me)S(O)2Et S(O)Me
CH2CH(Et)SMe S(O)Me
CH2CH(Et)SEt S(O)Me
CH2CH(Et)S(O)Me S(O)Me
CH2CH(Et)S(O)Et S(O)Me
CH2CH(Et)S(O)2Me S(O)Me
CH2CH(Et)S(O)2Et S(O)Me
CH(Me)CH(Me)SMe S(O)Me
CH(Me)CH(Me)SEt S(O)Me
CH(Me)CH(Me)S(O)Me S(O)Me
CH(Me)CH(Me)S(O)Et S(O)Me
CH(Me)CH(Me)S(O)2Me S(O)Me
CH(Me)CH(Me)S(O)2Et S(O)Me
CH2SMe S(O)2Me
CH2SEt S(O)2Me
CH2S(O)Me S(O)2Me
CH2S(O)Et S(O)2Me
CH2S(O)2Me S(O)2Me
CH2S(O)2Et S(O)2Me
CH(Me)SMe S(O)2Me
CH(Me)SEt S(O)2Me
CH(Me)S(O)Me S(O)2Me
CH(Me)S(O)Et S(O)2Me
CH(Me)S(O)2Me S(O)2Me
CH(Me)S(O)2Et S(O)2Me
CH(Et)SMe S(O)2Me
CH(Et)SEt S(O)2Me
CH(Et)S(O)Me S(O)2Me
CH(Et)S(O)Et S(O)2Me
CH(Et)S(O)2Me S(O)2Me
CH(Et)S(O)2Et S(O)2Me
CH(n-Pr)SMe S(O)2Me
CH(n-Pr)SEt S(O)2Me
CH(n-Pr)S(O)Me S(O)2Me
CH(n-Pr)S(O)Et S(O)2Me
CH(n-Pr)S(O)2Me S(O)2Me
CH(n-Pr)S(O)2Et S(O)2Me
CH(i-Pr)SMe S(O)2Me
CH(i-Pr)SEt S(O)2Me
CH(i-Pr)S(O)Me S(O)2Me
CH(i-Pr)S(O)Et S(O)2Me
CH(i-Pr)S(O)2Me S(O)2Me
CH(i-Pr)S(O)2Et S(O)2Me
CH(n-Bu)SMe S(O)2Me
CH(n-Bu)SEt S(O)2Me
CH(n-Bu)S(O)Me S(O)2Me
CH(n-Bu)S(O)Et S(O)2Me
CH(n-Bu)S(O)2Me S(O)2Me
CH(n-Bu)S(O)2Et S(O)2Me
CH(i-Bu)SMe S(O)2Me
CH(i-Bu)SEt S(O)2Me
CH(i-Bu)S(O)Me S(O)2Me
CH(i-Bu)S(O)Et S(O)2Me
CH(i-Bu)S(O)2Me S(O)2Me
CH(i-Bu)S(O)2Et S(O)2Me
CH(s-Bu)SMe S(O)2Me
CH(s-Bu)SEt S(O)2Me
CH(s-Bu)S(O)Me S(O)2Me
CH(s-Bu)S(O)Et S(O)2Me
CH(s-Bu)S(O)2Me S(O)2Me
CH(s-Bu)S(O)2Et S(O)2Me
CH(t-Bu)SMe S(O)2Me
CH(t-Bu)SEt S(O)2Me
CH(t-Bu)S(O)Me S(O)2Me
CH(t-Bu)S(O)Et S(O)2Me
CH(t-Bu)S(O)2Me S(O)2Me
CH(t-Bu)S(O)2Et S(O)2Me
CH2CH2SMe S(O)2Me
CH2CH2SEt S(O)2Me
CH2CH2S(O)2Me S(O)2Me
CH2CH2S(O)2Et S(O)2Me
CH(Me)CH2SMe S(O)2Me
CH(Me)CH2SEt S(O)2Me
CH(Me)CH2S(O)Me S(O)2Me
CH(Me)CH2S(O)Et S(O)2Me
CH(Me)CH2S(O)2Me S(O)2Me
CH(Me)CH2S(O)2Et S(O)2Me
CH(Et)CH2SMe S(O)2Me
CH(Et)CH2SEt S(O)2Me
CH(Et)CH2S(O)Me S(O)2Me
CH(Et)CH2S(O)Et S(O)2Me
CH(Et)CH2S(O)2Me S(O)2Me
CH(Et)CH2S(O)2Et S(O)2Me
C(Me)2CH2SMe S(O)2Me
C(Me)2CH2SEt S(O)2Me
C(Me)2CH2S(O)Me S(O)2Me
C(Me)2CH2S(O)Et S(O)2Me
C(Me)2CH2S(O)2Me S(O)2Me
C(Me)2CH2S(O)2Et S(O)2Me
CH2CH(Me)SMe S(O)2Me
CH2CH(Me)SEt S(O)2Me
CH2CH(Me)S(O)Me S(O)2Me
CH2CH(Me)S(O)Et S(O)2Me
CH2CH(Me)S(O)2Me S(O)2Me
CH2CH(Me)S(O)2Et S(O)2Me
CH2CH(Et)SMe S(O)2Me
CH2CH(Et)SEt S(O)2Me
CH2CH(Et)S(O)Me S(O)2Me
CH2CH(Et)S(O)Et S(O)2Me
CH2CH(Et)S(O)2Me S(O)2Me
CH2CH(Et)S(O)2Et S(O)2Me
CH(Me)CH(Me)SMe S(O)2Me
CH(Me)CH(Me)SEt S(O)2Me
CH(Me)CH(Me)S(O)Me S(O)2Me
CH(Me)CH(Me)S(O)Et S(O)2Me
CH(Me)CH(Me)S(O)2Me S(O)2Me
CH(Me)CH(Me)S(O)2Et S(O)2Me
CH2SMe H
CH2SEt H
CH2S(O)Me H
CH2S(O)Et H
CH2S(O)2Me H
CH2S(O)2Et H
CH(Me)SMe H
CH(Me)SEt H
CH(Me)S(O)Me H
CH(Me)S(O)Et H
CH(Me)S(O)2Me H
CH(Me)S(O)2Et H
CH(Et)SMe H
CH(Et)SEt H
CH(Et)S(O)Me H
CH(Et)S(O)Et H
CH(Et)S(O)2Me H
CH(Et)S(O)2Et H
CH(n-Pr)SMe H
CH(n-Pr)SEt H
CH(n-Pr)S(O)Me H
CH(n-Pr)S(O)Et H
CH(n-Pr)S(O)2Me H
CH(n-Pr)S(O)2Et H
CH(i-Pr)SMe H
CH(i-Pr)SEt H
CH(i-Pr)S(O)Me H
CH(i-Pr)S(O)Et H
CH(i-Pr)S(O)2Me H
CH(i-Pr)S(O)2Et H
CH(n-Bu)SMe H
CH(n-Bu)SEt H
CH(n-Bu)S(O)Me H
CH(n-Bu)S(O)Et H
CH(n-Bu)S(O)2Me H
CH(n-Bu)S(O)2Et H
CH(i-Bu)SMe H
CH(i-Bu)SEt H
CH(i-Bu)S(O)Me H
CH(i-Bu)S(O)Et H
CH(i-Bu)S(O)2Me H
CH(i-Bu)S(O)2Et H
CH(s-Bu)SMe H
CH(s-Bu)SEt H
CH(s-Bu)S(O)Me H
CH(s-Bu)S(O)Et H
CH(s-Bu)S(O)2Me H
CH(s-Bu)S(O)2Et H
CH(t-Bu)SMe H
CH(t-Bu)SEt H
CH(t-Bu)S(O)Me H
CH(t-Bu)S(O)Et H
CH(t-Bu)S(O)2Me H
CH(t-Bu)S(O)2Et H
CH2CH2SMe H
CH2CH2SEt H
CH2CH2S(O)2Me H
CH2CH2S(O)2Et H
CH(Me)CH2SMe H
CH(Me)CH2SEt H
CH(Me)CH2S(O)Me H
CH(Me)CH2S(O)Et H
CH(Me)CH2S(O)2Me H
CH(Me)CH2S(O)2Et H
CH(Et)CH2SMe H
CH(Et)CH2SEt H
CH(Et)CH2S(O)Me H
CH(Et)CH2S(O)Et H
CH(Et)CH2S(O)2Me H
CH(Et)CH2S(O)2Et H
C(Me)2CH2SMe H
C(Me)2CH2SEt H
C(Me)2CH2S(O)Me H
C(Me)2CH2S(O)Et H
C(Me)2CH2S(O)2Me H
C(Me)2CH2S(O)2Et H
CH2CH(Me)SMe H
CH2CH(Me)SEt H
CH2CH(Me)S(O)Me H
CH2CH(Me)S(O)Et H
CH2CH(Me)S(O)2Me H
CH2CH(Me)S(O)2Et H
CH2CH(Et)SMe H
CH2CH(Et)SEt H
CH2CH(Et)S(O)Me H
CH2CH(Et)S(O)Et H
CH2CH(Et)S(O)2Me H
CH2CH(Et)S(O)2Et H
CH(Me)CH(Me)SMe H
CH(Me)CH(Me)SEt H
CH(Me)CH(Me)S(O)Me H
CH(Me)CH(Me)S(O)Et H
CH(Me)CH(Me)S(O)2Me H
CH(Me)CH(Me)S(O)2Et H
CH2SMe Me
CH2SEt Me
CH2S(O)Me Me
CH2S(O)Et Me
CH2S(O)2Me Me
CH2S(O)2Et Me
CH(Me)SMe Me
CH(Me)SEt Me
CH(Me)S(O)Me Me
CH(Me)S(O)Et Me
CH(Me)S(O)2Me Me
CH(Me)S(O)2Et Me
CH(Et)SMe Me
CH(Et)SEt Me
CH(Et)S(O)Me Me
CH(Et)S(O)Et Me
CH(Et)S(O)2Me Me
CH(Et)S(O)2Et Me
CH(n-Pr)SMe Me
CH(n-Pr)SEt Me
CH(n-Pr)S(O)Me Me
CH(n-Pr)S(O)Et Me
CH(n-Pr)S(O)2Me Me
CH(n-Pr)S(O)2Et Me
CH(i-Pr)SMe Me
CH(i-Pr)SEt Me
CH(i-Pr)S(O)Me Me
CH(i-Pr)S(O)Et Me
CH(i-Pr)S(O)2Me Me
CH(i-Pr)S(O)2Et Me
CH(n-Bu)SMe Me
CH(n-Bu)SEt Me
CH(n-Bu)S(O)Me Me
CH(n-Bu)S(O)Et Me
CH(n-Bu)S(O)2Me Me
CH(n-Bu)S(O)2Et Me
CH(i-Bu)SMe Me
CH(i-Bu)SEt Me
CH(i-Bu)S(O)Me Me
CH(i-Bu)S(O)Et Me
CH(i-Bu)S(O)2Me Me
CH(i-Bu)S(O)2Et Me
CH(s-Bu)SMe Me
CH(s-Bu)SEt Me
CH(s-Bu)S(O)Me Me
CH(s-Bu)S(O)Et Me
CH(s-Bu)S(O)2Me Me
CH(s-Bu)S(O)2Et Me
CH(t-Bu)SMe Me
CH(t-Bu)SEt Me
CH(t-Bu)S(O)Me Me
CH(t-Bu)S(O)Et Me
CH(t-Bu)S(O)2Me Me
CH(t-Bu)S(O)2Et Me
CH2CH2SMe Me
CH2CH2SEt Me
CH2CH2S(O)2Me Me
CH2CH2S(O)2Et Me
CH(Me)CH2SMe Me
CH(Me)CH2SEt Me
CH(Me)CH2S(O)Me Me
CH(Me)CH2S(O)Et Me
CH(Me)CH2S(O)2Me Me
CH(Me)CH2S(O)2Et Me
CH(Et)CH2SMe Me
CH(Et)CH2SEt Me
CH(Et)CH2S(O)Me Me
CH(Et)CH2S(O)Et Me
CH(Et)CH2S(O)2Me Me
CH(Et)CH2S(O)2Et Me
C(Me)2CH2SMe Me
C(Me)2CH2SEt Me
C(Me)2CH2S(O)Me Me
C(Me)2CH2S(O)Et Me
C(Me)2CH2S(O)2Me Me
C(Me)2CH2S(O)2Et Me
CH2CH(Me)SMe Me
CH2CH(Me)SEt Me
CH2CH(Me)S(O)Me Me
CH2CH(Me)S(O)Et Me
CH2CH(Me)S(O)2Me Me
CH2CH(Me)S(O)2Et Me
CH2CH(Et)SMe Me
CH2CH(Et)SEt Me
CH2CH(Et)S(O)Me Me
CH2CH(Et)S(O)Et Me
CH2CH(Et)S(O)2Me Me
CH2CH(Et)S(O)2Et Me
CH(Me)CH(Me)SMe Me
CH(Me)CH(Me)SEt Me
CH(Me)CH(Me)S(O)Me Me
CH(Me)CH(Me)S(O)Et Me
CH(Me)CH(Me)S(O)2Me Me
CH(Me)CH(Me)S(O)2Et Me
CH2SMe CF3
CH2SEt CF3
CH2S(O)Me CF3
CH2S(O)Et CF3
CH2S(O)2Me CF3
CH2S(O)2Et CF3
CH(Me)SMe CF3
CH(Me)SEt CF3
CH(Me)S(O)Me CF3
CH(Me)S(O)Et CF3
CH(Me)S(O)2Me CF3
CH(Me)S(O)2Et CF3
CH(Et)SMe CF3
CH(Et)SEt CF3
CH(Et)S(O)Me CF3
CH(Et)S(O)Et CF3
CH(Et)S(O)2Me CF3
CH(Et)S(O)2Et CF3
CH(n-Pr)SMe CF3
CH(n-Pr)SEt CF3
CH(n-Pr)S(O)Me CF3
CH(n-Pr)S(O)Et CF3
CH(n-Pr)S(O)2Me CF3
CH(n-Pr)S(O)2Et CF3
CH(i-Pr)SMe CF3
CH(i-Pr)SEt CF3
CH(i-Pr)S(O)Me CF3
CH(i-Pr)S(O)Et CF3
CH(i-Pr)S(O)2Me CF3
CH(i-Pr)S(O)2Et CF3
CH(n-Bu)SMe CF3
CH(n-Bu)SEt CF3
CH(n-Bu)S(O)Me CF3
CH(n-Bu)S(O)Et CF3
CH(n-Bu)S(O)2Me CF3
CH(n-Bu)S(O)2Et CF3
CH(i-Bu)SMe CF3
CH(i-Bu)SEt CF3
CH(i-Bu)S(O)Me CF3
CH(i-Bu)S(O)Et CF3
CH(i-Bu)S(O)2Me CF3
CH(i-Bu)S(O)2Et CF3
CH(s-Bu)SMe CF3
CH(s-Bu)SEt CF3
CH(s-Bu)S(O)Me CF3
CH(s-Bu)S(O)Et CF3
CH(s-Bu)S(O)2Me CF3
CH(s-Bu)S(O)2Et CF3
CH(t-Bu)SMe CF3
CH(t-Bu)SEt CF3
CH(t-Bu)S(O)Me CF3
CH(t-Bu)S(O)Et CF3
CH(t-Bu)S(O)2Me CF3
CH(t-Bu)S(O)2Et CF3
CH2CH2SMe CF3
CH2CH2SEt CF3
CH2CH2S(O)2Me CF3
CH2CH2S(O)2Et CF3
CH(Me)CH2SMe CF3
CH(Me)CH2SEt CF3
CH(Me)CH2S(O)Me CF3
CH(Me)CH2S(O)Et CF3
CH(Me)CH2S(O)2Me CF3
CH(Me)CH2S(O)2Et CF3
CH(Et)CH2SMe CF3
CH(Et)CH2SEt CF3
CH(Et)CH2S(O)Me CF3
CH(Et)CH2S(O)Et CF3
CH(Et)CH2S(O)2Me CF3
CH(Et)CH2S(O)2Et CF3
C(Me)2CH2SMe CF3
C(Me)2CH2SEt CF3
C(Me)2CH2S(O)Me CF3
C(Me)2CH2S(O)Et CF3
C(Me)2CH2S(O)2Me CF3
C(Me)2CH2S(O)2Et CF3
CH2CH(Me)SMe CF3
CH2CH(Me)SEt CF3
CH2CH(Me)S(O)Me CF3
CH2CH(Me)S(O)Et CF3
CH2CH(Me)S(O)2Me CF3
CH2CH(Me)S(O)2Et CF3
CH2CH(Et)SMe CF3
CH2CH(Et)SEt CF3
CH2CH(Et)S(O)Me CF3
CH2CH(Et)S(O)Et CF3
CH2CH(Et)S(O)2Me CF3
CH2CH(Et)S(O)2Et CF3
CH(Me)CH(Me)SMe CF3
CH(Me)CH(Me)SEt CF3
CH(Me)CH(Me)S(O)Me CF3
CH(Me)CH(Me)S(O)Et CF3
CH(Me)CH(Me)S(O)2Me CF3
CH(Me)CH(Me)S(O)2Et CF3
CH2SMe CN
CH2SEt CN
CH2S(O)Me CN
CH2S(O)Et CN
CH2S(O)2Me CN
CH2S(O)2Et CN
CH(Me)SMe CN
CH(Me)SEt CN
CH(Me)S(O)Me CN
CH(Me)S(O)Et CN
CH(Me)S(O)2Me CN
CH(Me)S(O)2Et CN
CH(Et)SMe CN
CH(Et)SEt CN
CH(Et)S(O)Me CN
CH(Et)S(O)Et CN
CH(Et)S(O)2Me CN
CH(Et)S(O)2Et CN
CH(n-Pr)SMe CN
CH(n-Pr)SEt CN
CH(n-Pr)S(O)Me CN
CH(n-Pr)S(O)Et CN
CH(n-Pr)S(O)2Me CN
CH(n-Pr)S(O)2Et CN
CH(i-Pr)SMe CN
CH(i-Pr)SEt CN
CH(i-Pr)S(O)Me CN
CH(i-Pr)S(O)Et CN
CH(i-Pr)S(O)2Me CN
CH(i-Pr)S(O)2Et CN
CH(n-Bu)SMe CN
CH(n-Bu)SEt CN
CH(n-Bu)S(O)Me CN
CH(n-Bu)S(O)Et CN
CH(n-Bu)S(O)2Me CN
CH(n-Bu)S(O)2Et CN
CH(i-Bu)SMe CN
CH(i-Bu)SEt CN
CH(i-Bu)S(O)Me CN
CH(i-Bu)S(O)Et CN
CH(i-Bu)S(O)2Me CN
CH(i-Bu)S(O)2Et CN
CH(s-Bu)SMe CN
CH(s-Bu)SEt CN
CH(s-Bu)S(O)Me CN
CH(s-Bu)S(O)Et CN
CH(s-Bu)S(O)2Me CN
CH(s-Bu)S(O)2Et CN
CH(t-Bu)SMe CN
CH(t-Bu)SEt CN
CH(t-Bu)S(O)Me CN
CH(t-Bu)S(O)Et CN
CH(t-Bu)S(O)2Me CN
CH(t-Bu)S(O)2Et CN
CH2CH2SMe CN
CH2CH2SEt CN
CH2CH2S(O)2Me CN
CH2CH2S(O)2Et CN
CH(Me)CH2SMe CN
CH(Me)CH2SEt CN
CH(Me)CH2S(O)Me CN
CH(Me)CH2S(O)Et CN
CH(Me)CH2S(O)2Me CN
CH(Me)CH2S(O)2Et CN
CH(Et)CH2SMe CN
CH(Et)CH2SEt CN
CH(Et)CH2S(O)Me CN
CH(Et)CH2S(O)Et CN
CH(Et)CH2S(O)2Me CN
CH(Et)CH2S(O)2Et CN
C(Me)2CH2SMe CN
C(Me)2CH2SEt CN
C(Me)2CH2S(O)Me CN
C(Me)2CH2S(O)Et CN
C(Me)2CH2S(O)2Me CN
C(Me)2CH2S(O)2Et CN
CH2CH(Me)SMe CN
CH2CH(Me)SEt CN
CH2CH(Me)S(O)Me CN
CH2CH(Me)S(O)Et CN
CH2CH(Me)S(O)2Me CN
CH2CH(Me)S(O)2Et CN
CH2CH(Et)SMe CN
CH2CH(Et)SEt CN
CH2CH(Et)S(O)Me CN
CH2CH(Et)S(O)Et CN
CH2CH(Et)S(O)2Me CN
CH2CH(Et)S(O)2Et CN
CH(Me)CH(Me)SMe CN
CH(Me)CH(Me)SEt CN
CH(Me)CH(Me)S(O)Me CN
CH(Me)CH(Me)S(O)Et CN
CH(Me)CH(Me)S(O)2Me CN
CH(Me)CH(Me)S(O)2Et CN
CH2SMe Cl
CH2SEt Cl
CH2S(O)Me Cl
CH2S(O)Et Cl
CH2S(O)2Me Cl
CH2S(O)2Et Cl
CH(Me)SMe Cl
CH(Me)SEt Cl
CH(Me)S(O)Me Cl
CH(Me)S(O)Et Cl
CH(Me)S(O)2Me Cl
CH(Me)S(O)2Et Cl
CH(Et)SMe Cl
CH(Et)SEt Cl
CH(Et)S(O)Me Cl
CH(Et)S(O)Et Cl
CH(Et)S(O)2Me Cl
CH(Et)S(O)2Et Cl
CH(n-Pr)SMe Cl
CH(n-Pr)SEt Cl
CH(n-Pr)S(O)Me Cl
CH(n-Pr)S(O)Et Cl
CH(n-Pr)S(O)2Me Cl
CH(n-Pr)S(O)2Et Cl
CH(i-Pr)SMe Cl
CH(i-Pr)SEt Cl
CH(i-Pr)S(O)Me Cl
CH(i-Pr)S(O)Et Cl
CH(i-Pr)S(O)2Me Cl
CH(i-Pr)S(O)2Et Cl
CH(n-Bu)SMe Cl
CH(n-Bu)SEt Cl
CH(n-Bu)S(O)Me Cl
CH(n-Bu)S(O)Et Cl
CH(n-Bu)S(O)2Me Cl
CH(n-Bu)S(O)2Et Cl
CH(i-Bu)SMe Cl
CH(i-Bu)SEt Cl
CH(i-Bu)S(O)Me Cl
CH(i-Bu)S(O)Et Cl
CH(i-Bu)S(O)2Me Cl
CH(i-Bu)S(O)2Et Cl
CH(s-Bu)SMe Cl
CH(s-Bu)SEt Cl
CH(s-Bu)S(O)Me Cl
CH(s-Bu)S(O)Et Cl
CH(s-Bu)S(O)2Me Cl
CH(s-Bu)S(O)2Et Cl
CH(t-Bu)SMe Cl
CH(t-Bu)SEt Cl
CH(t-Bu)S(O)Me Cl
CH(t-Bu)S(O)Et Cl
CH(t-Bu)S(O)2Me Cl
CH(t-Bu)S(O)2Et Cl
CH2CH2SMe Cl
CH2CH2SEt Cl
CH2CH2S(O)2Me Cl
CH2CH2S(O)2Et Cl
CH(Me)CH2SMe Cl
CH(Me)CH2SEt Cl
CH(Me)CH2S(O)Me Cl
CH(Me)CH2S(O)Et Cl
CH(Me)CH2S(O)2Me Cl
CH(Me)CH2S(O)2Et Cl
CH(Et)CH2SMe Cl
CH(Et)CH2SEt Cl
CH(Et)CH2S(O)Me Cl
CH(Et)CH2S(O)Et Cl
CH(Et)CH2S(O)2Me Cl
CH(Et)CH2S(O)2Et Cl
C(Me)2CH2SMe Cl
C(Me)2CH2SEt Cl
C(Me)2CH2S(O)Me Cl
C(Me)2CH2S(O)Et Cl
C(Me)2CH2S(O)2Me Cl
C(Me)2CH2S(O)2Et Cl
CH2CH(Me)SMe Cl
CH2CH(Me)SEt Cl
CH2CH(Me)S(O)Me Cl
CH2CH(Me)S(O)Et Cl
CH2CH(Me)S(O)2Me Cl
CH2CH(Me)S(O)2Et Cl
CH2CH(Et)SMe Cl
CH2CH(Et)SEt Cl
CH2CH(Et)S(O)Me Cl
CH2CH(Et)S(O)Et Cl
CH2CH(Et)S(O)2Me Cl
CH2CH(Et)S(O)2Et Cl
CH(Me)CH(Me)SMe Cl
CH(Me)CH(Me)SEt Cl
CH(Me)CH(Me)S(O)Me Cl
CH(Me)CH(Me)S(O)Et Cl
CH(Me)CH(Me)S(O)2Me Cl
CH(Me)CH(Me)S(O)2Et Cl
CH2SMe C(O)OMe
CH2SEt C(O)OMe
CH2S(O)Me C(O)OMe
CH2S(O)Et C(O)OMe
CH2S(O)2Me C(O)OMe
CH2S(O)2Et C(O)OMe
CH(Me)SMe C(O)OMe
CH(Me)SEt C(O)OMe
CH(Me)S(O)Me C(O)OMe
CH(Me)S(O)Et C(O)OMe
CH(Me)S(O)2Me C(O)OMe
CH(Me)S(O)2Et C(O)OMe
CH(Et)SMe C(O)OMe
CH(Et)SEt C(O)OMe
CH(Et)S(O)Me C(O)OMe
CH(Et)S(O)Et C(O)OMe
CH(Et)S(O)2Me C(O)OMe
CH(Et)S(O)2Et C(O)OMe
CH(n-Pr)SMe C(O)OMe
CH(n-Pr)SEt C(O)OMe
CH(n-Pr)S(O)Me C(O)OMe
CH(n-Pr)S(O)Et C(O)OMe
CH(n-Pr)S(O)2Me C(O)OMe
CH(n-Pr)S(O)2Et C(O)OMe
CH(i-Pr)SMe C(O)OMe
CH(i-Pr)SEt C(O)OMe
CH(i-Pr)S(O)Me C(O)OMe
CH(i-Pr)S(O)Et C(O)OMe
CH(i-Pr)S(O)2Me C(O)OMe
CH(i-Pr)S(O)2Et C(O)OMe
CH(n-Bu)SMe C(O)OMe
CH(n-Bu)SEt C(O)OMe
CH(n-Bu)S(O)Me C(O)OMe
CH(n-Bu)S(O)Et C(O)OMe
CH(n-Bu)S(O)2Me C(O)OMe
CH(n-Bu)S(O)2Et C(O)OMe
CH(i-Bu)SMe C(O)OMe
CH(i-Bu)SEt C(O)OMe
CH(i-Bu)S(O)Me C(O)OMe
CH(i-Bu)S(O)Et C(O)OMe
CH(i-Bu)S(O)2Me C(O)OMe
CH(i-Bu)S(O)2Et C(O)OMe
CH(s-Bu)SMe C(O)OMe
CH(s-Bu)SEt C(O)OMe
CH(s-Bu)S(O)Me C(O)OMe
CH(s-Bu)S(O)Et C(O)OMe
CH(s-Bu)S(O)2Me C(O)OMe
CH(s-Bu)S(O)2Et C(O)OMe
CH(t-Bu)SMe C(O)OMe
CH(t-Bu)SEt C(O)OMe
CH(t-Bu)S(O)Me C(O)OMe
CH(t-Bu)S(O)Et C(O)OMe
CH(t-Bu)S(O)2Me C(O)OMe
CH(t-Bu)S(O)2Et C(O)OMe
CH2CH2SMe C(O)OMe
CH2CH2SEt C(O)OMe
CH2CH2S(O)2Me C(O)OMe
CH2CH2S(O)2Et C(O)OMe
CH(Me)CH2SMe C(O)OMe
CH(Me)CH2SEt C(O)OMe
CH(Me)CH2S(O)Me C(O)OMe
CH(Me)CH2S(O)Et C(O)OMe
CH(Me)CH2S(O)2Me C(O)OMe
CH(Me)CH2S(O)2Et C(O)OMe
CH(Et)CH2SMe C(O)OMe
CH(Et)CH2SEt C(O)OMe
CH(Et)CH2S(O)Me C(O)OMe
CH(Et)CH2S(O)Et C(O)OMe
CH(Et)CH2S(O)2Me C(O)OMe
CH(Et)CH2S(O)2Et C(O)OMe
C(Me)2CH2SMe C(O)OMe
C(Me)2CH2SEt C(O)OMe
C(Me)2CH2S(O)Me C(O)OMe
C(Me)2CH2S(O)Et C(O)OMe
C(Me)2CH2S(O)2Me C(O)OMe
C(Me)2CH2S(O)2Et C(O)OMe
CH2CH(Me)SMe C(O)OMe
CH2CH(Me)SEt C(O)OMe
CH2CH(Me)S(O)Me C(O)OMe
CH2CH(Me)S(O)Et C(O)OMe
CH2CH(Me)S(O)2Me C(O)OMe
CH2CH(Me)S(O)2Et C(O)OMe
CH2CH(Et)SMe C(O)OMe
CH2CH(Et)SEt C(O)OMe
CH2CH(Et)S(O)Me C(O)OMe
CH2CH(Et)S(O)Et C(O)OMe
CH2CH(Et)S(O)2Me C(O)OMe
CH2CH(Et)S(O)2Et C(O)OMe
CH(Me)CH(Me)SMe C(O)OMe
CH(Me)CH(Me)SEt C(O)OMe
CH(Me)CH(Me)S(O)Me C(O)OMe
CH(Me)CH(Me)S(O)Et C(O)OMe
CH(Me)CH(Me)S(O)2Me C(O)OMe
CH(Me)CH(Me)S(O)2Et C(O)OMe
CH2OMe CH2SMe
CH2OMe CH2SEt
CH2OMe CH2SCF3
CH2OMe CH2SCH2CF3
CH2OMe CH2S(O)Me
CH2OMe CH2S(O)Et
CH2OMe CH2S(O)CF3
CH2OMe CH2S(O)CH2CF3
CH2OMe CH2S(O)2Me
CH2OMe CH2S(O)2Et
CH2OMe CH2S(O)2CF3
CH2OMe CH2S(O)2CH2CF3
CH2OMe CH(Me)SMe
CH2OMe CH(Me)SEt
CH2OMe CH(Me)SCF3
CH2OMe CH(Me)SCH2CF3
CH2OMe CH(Me)S(O)Me
CH2OMe CH(Me)S(O)Et
CH2OMe CH(Me)S(O)CF3
CH2OMe CH(Me)S(O)CH2CF3
CH2OMe CH(Me)S(O)2Me
CH2OMe CH(Me)S(O)2Et
CH2OMe CH(Me)S(O)2CF3
CH2OMe CH(Me)S(O)2CH2CF3
CH2OMe CH(Et)SMe
CH2OMe CH(Et)SEt
CH2OMe CH(Et)SCF3
CH2OMe CH(Et)SCH2CF3
CH2OMe CH(Et)S(O)Me
CH2OMe CH(Et)S(O)Et
CH2OMe CH(Et)S(O)CF3
CH2OMe CH(Et)S(O)CH2CF3
CH2OMe CH(Et)S(O)2Me
CH2OMe CH(Et)S(O)2Et
CH2OMe CH(Et)S(O)2CF3
CH2OMe CH(Et)S(O)2CH2CF3
CH2OMe CH(n-Pr)SMe
CH2OMe CH(n-Pr)SEt
CH2OMe CH(n-Pr)SCF3
CH2OMe CH(n-Pr)SCH2CF3
CH2OMe CH(n-Pr)S(O)Me
CH2OMe CH(n-Pr)S(O)Et
CH2OMe CH(n-Pr)S(O)CF3
CH2OMe CH(n-Pr)S(O)CH2CF3
CH2OMe CH(n-Pr)S(O)2Me
CH2OMe CH(n-Pr)S(O)2Et
CH2OMe CH(n-Pr)S(O)2CF3
CH2OMe CH(n-Pr)S(O)2CH2CF3
CH2OMe CH(i-Pr)SMe
CH2OMe CH(i-Pr)SEt
CH2OMe CH(i-Pr)SCF3
CH2OMe CH(i-Pr)SCH2CF3
CH2OMe CH(i-Pr)S(O)Me
CH2OMe CH(i-Pr)S(O)Et
CH2OMe CH(i-Pr)S(O)CF3
CH2OMe CH(i-Pr)S(O)CH2CF3
CH2OMe CH(i-Pr)S(O)2Me
CH2OMe CH(i-Pr)S(O)2Et
CH2OMe CH(i-Pr)S(O)2CF3
CH2OMe CH(i-Pr)S(O)2CH2CF3
CH2OMe CH(n-Bu)SMe
CH2OMe CH(n-Bu)SEt
CH2OMe CH(n-Bu)SCF3
CH2OMe CH(n-Bu)SCH2CF3
CH2OMe CH(n-Bu)S(O)Me
CH2OMe CH(n-Bu)S(O)Et
CH2OMe CH(n-Bu)S(O)CF3
CH2OMe CH(n-Bu)S(O)CH2CF3
CH2OMe CH(n-Bu)S(O)2Me
CH2OMe CH(n-Bu)S(O)2Et
CH2OMe CH(n-Bu)S(O)2CF3
CH2OMe CH(n-Bu)S(O)2CH2CF3
CH2OMe CH(i-Bu)SMe
CH2OMe CH(i-Bu)SEt
CH2OMe CH(i-Bu)SCF3
CH2OMe CH(i-Bu)SCH2CF3
CH2OMe CH(i-Bu)S(O)Me
CH2OMe CH(i-Bu)S(O)Et
CH2OMe CH(i-Bu)S(O)CF3
CH2OMe CH(i-Bu)S(O)CH2CF3
CH2OMe CH(i-Bu)S(O)2Me
CH2OMe CH(i-Bu)S(O)2Et
CH2OMe CH(i-Bu)S(O)2CF3
CH2OMe CH(i-Bu)S(O)2CH2CF3
CH2OMe CH(s-Bu)SMe
CH2OMe CH(s-Bu)SEt
CH2OMe CH(s-Bu)SCF3
CH2OMe CH(s-Bu)SCH2CF3
CH2OMe CH(s-Bu)S(O)Me
CH2OMe CH(s-Bu)S(O)Et
CH2OMe CH(s-Bu)S(O)CF3
CH2OMe CH(s-Bu)S(O)CH2CF3
CH2OMe CH(s-Bu)S(O)2Me
CH2OMe CH(s-Bu)S(O)2Et
CH2OMe CH(s-Bu)S(O)2CF3
CH2OMe CH(s-Bu)S(O)2CH2CF3
CH2OMe CH(t-Bu)SMe
CH2OMe CH(t-Bu)SEt
CH2OMe CH(t-Bu)SCF3
CH2OMe CH(t-Bu)SCH2CF3
CH2OMe CH(t-Bu)S(O)Me
CH2OMe CH(t-Bu)S(O)Et
CH2OMe CH(t-Bu)S(O)CF3
CH2OMe CH(t-Bu)S(O)CH2CF3
CH2OMe CH(t-Bu)S(O)2Me
CH2OMe CH(t-Bu)S(O)2Et
CH2OMe CH(t-Bu)S(O)2CF3
CH2OMe CH(t-Bu)S(O)2CH2CF3
CH2OMe CH(CF3)SMe
CH2OMe CH(CF3)SEt
CH2OMe CH(CF3)SCF3
CH2OMe CH(CF3)SCH2CF3
CH2OMe CH(CF3)S(O)Me
CH2OMe CH(CF3)S(O)Et
CH2OMe CH(CF3)S(O)CF3
CH2OMe CH(CF3)S(O)CH2CF3
CH2OMe CH(CF3)S(O)2Me
CH2OMe CH(CF3)S(O)2Et
CH2OMe CH(CF3)S(O)2CF3
CH2OMe CH(CF3)S(O)2CH2CF3
CH2OMe CH2CH2SMe
CH2OMe CH2CH2SEt
CH2OMe CH2CH2SCF3
CH2OMe CH2CH2SCH2CF3
CH2OMe CH2CH2S(O)Me
CH2OMe CH2CH2S(O)Et
CH2OMe CH2CH2S(O)CF3
CH2OMe CH2CH2S(O)CH2CF3
CH2OMe CH2CH2S(O)2Me
CH2OMe CH2CH2S(O)2Et
CH2OMe CH2CH2S(O)2CF3
CH2OMe CH2CH2S(O)2CH2CF3
CH2OMe CH(Me)CH2SMe
CH2OMe CH(Me)CH2SEt
CH2OMe CH(Me)CH2SCF3
CH2OMe CH(Me)CH2SCH2CF3
CH2OMe CH(Me)CH2S(O)Me
CH2OMe CH(Me)CH2S(O)Et
CH2OMe CH(Me)CH2S(O)CF3
CH2OMe CH(Me)CH2S(O)CH2CF3
CH2OMe CH(Me)CH2S(O)2Me
CH2OMe CH(Me)CH2S(O)2Et
CH2OMe CH(Me)CH2S(O)2CF3
CH2OMe CH(Me)CH2S(O)2CH2CF3
CH2OMe CH(Et)CH2SMe
CH2OMe CH(Et)CH2SEt
CH2OMe CH(Et)CH2SCF3
CH2OMe CH(Et)CH2SCH2CF3
CH2OMe CH(Et)CH2S(O)Me
CH2OMe CH(Et)CH2S(O)Et
CH2OMe CH(Et)CH2S(O)CF3
CH2OMe CH(Et)CH2S(O)CH2CF3
CH2OMe CH(Et)CH2S(O)2Me
CH2OMe CH(Et)CH2S(O)2Et
CH2OMe CH(Et)CH2S(O)2CF3
CH2OMe CH(Et)CH2S(O)2CH2CF3
CH2OMe C(Me)2CH2SMe
CH2OMe C(Me)2CH2SEt
CH2OMe C(Me)2CH2SCF3
CH2OMe C(Me)2CH2SCH2CF3
CH2OMe C(Me)2CH2S(O)Me
CH2OMe C(Me)2CH2S(O)Et
CH2OMe C(Me)2CH2S(O)CF3
CH2OMe C(Me)2CH2S(O)CH2CF3
CH2OMe C(Me)2CH2S(O)2Me
CH2OMe C(Me)2CH2S(O)2Et
CH2OMe C(Me)2CH2S(O)2CF3
CH2OMe C(Me)2CH2S(O)2CH2CF3
CH2OMe CH2CH(Me)SMe
CH2OMe CH2CH(Me)SEt
CH2OMe CH2CH(Me)SCF3
CH2OMe CH2CH(Me)SCH2CF3
CH2OMe CH2CH(Me)S(O)Me
CH2OMe CH2CH(Me)S(O)Et
CH2OMe CH2CH(Me)S(O)CF3
CH2OMe CH2CH(Me)S(O)CH2CF3
CH2OMe CH2CH(Me)S(O)2Me
CH2OMe CH2CH(Me)S(O)2Et
CH2OMe CH2CH(Me)S(O)2CF3
CH2OMe CH2CH(Me)S(O)2CH2CF3
CH2OMe CH2CH(Et)SMe
CH2OMe CH2CH(Et)SEt
CH2OMe CH2CH(Et)SCF3
CH2OMe CH2CH(Et)SCH2CF3
CH2OMe CH2CH(Et)S(O)Me
CH2OMe CH2CH(Et)S(O)Et
CH2OMe CH2CH(Et)S(O)CF3
CH2OMe CH2CH(Et)S(O)CH2CF3
CH2OMe CH2CH(Et)S(O)2Me
CH2OMe CH2CH(Et)S(O)2Et
CH2OMe CH2CH(Et)S(O)2CF3
CH2OMe CH2CH(Et)S(O)2CH2CF3
CH2OMe CH(Me)CH(Me)SMe
CH2OMe CH(Me)CH(Me)SEt
CH2OMe CH(Me)CH(Me)SCF3
CH2OMe CH(Me)CH(Me)SCH2CF3
CH2OMe CH(Me)CH(Me)S(O)Me
CH2OMe CH(Me)CH(Me)S(O)Et
CH2OMe CH(Me)CH(Me)S(O)CF3
CH2OMe CH(Me)CH(Me)S(O)CH2CF3
CH2OMe CH(Me)CH(Me)S(O)2Me
CH2OMe CH(Me)CH(Me)S(O)2Et
CH2OMe CH(Me)CH(Me)S(O)2CF3
CH2OMe CH(Me)CH(Me)S(O)2CH2CF3
CH2C(=NOMe)Me CH2SMe
CH2C(=NOMe)Me CH2SEt
CH2C(=NOMe)Me CH2SCF3
CH2C(=NOMe)Me CH2SCH2CF3
CH2C(=NOMe)Me CH2S(O)Me
CH2C(=NOMe)Me CH2S(O)Et
CH2C(=NOMe)Me CH2S(O)CF3
CH2C(=NOMe)Me CH2S(O)CH2CF3
CH2C(=NOMe)Me CH2S(O)2Me
CH2C(=NOMe)Me CH2S(O)2Et
CH2C(=NOMe)Me CH2S(O)2CF3
CH2C(=NOMe)Me CH2S(O)2CH2CF3
CH2C(=NOMe)Me CH(Me)SMe
CH2C(=NOMe)Me CH(Me)SEt
CH2C(=NOMe)Me CH(Me)SCF3
CH2C(=NOMe)Me CH(Me)SCH2CF3
CH2C(=NOMe)Me CH(Me)S(O)Me
CH2C(=NOMe)Me CH(Me)S(O)Et
CH2C(=NOMe)Me CH(Me)S(O)CF3
CH2C(=NOMe)Me CH(Me)S(O)CH2CF3
CH2C(=NOMe)Me CH(Me)S(O)2Me
CH2C(=NOMe)Me CH(Me)S(O)2Et
CH2C(=NOMe)Me CH(Me)S(O)2CF3
CH2C(=NOMe)Me CH(Me)S(O)2CH2CF3
CH2C(=NOMe)Me CH(Et)SMe
CH2C(=NOMe)Me CH(Et)SEt
CH2C(=NOMe)Me CH(Et)SCF3
CH2C(=NOMe)Me CH(Et)SCH2CF3
CH2C(=NOMe)Me CH(Et)S(O)Me
CH2C(=NOMe)Me CH(Et)S(O)Et
CH2C(=NOMe)Me CH(Et)S(O)CF3
CH2C(=NOMe)Me CH(Et)S(O)CH2CF3
CH2C(=NOMe)Me CH(Et)S(O)2Me
CH2C(=NOMe)Me CH(Et)S(O)2Et
CH2C(=NOMe)Me CH(Et)S(O)2CF3
CH2C(=NOMe)Me CH(Et)S(O)2CH2CF3
CH2C(=NOMe)Me CH(n-Pr)SMe
CH2C(=NOMe)Me CH(n-Pr)SEt
CH2C(=NOMe)Me CH(n-Pr)SCF3
CH2C(=NOMe)Me CH(n-Pr)SCH2CF3
CH2C(=NOMe)Me CH(n-Pr)S(O)Me
CH2C(=NOMe)Me CH(n-Pr)S(O)Et
CH2C(=NOMe)Me CH(n-Pr)S(O)CF3
CH2C(=NOMe)Me CH(n-Pr)S(O)CH2CF3
CH2C(=NOMe)Me CH(n-Pr)S(O)2Me
CH2C(=NOMe)Me CH(n-Pr)S(O)2Et
CH2C(=NOMe)Me CH(n-Pr)S(O)2CF3
CH2C(=NOMe)Me CH(n-Pr)S(O)2CH2CF3
CH2C(=NOMe)Me CH(i-Pr)SMe
CH2C(=NOMe)Me CH(i-Pr)SEt
CH2C(=NOMe)Me CH(i-Pr)SCF3
CH2C(=NOMe)Me CH(i-Pr)SCH2CF3
CH2C(=NOMe)Me CH(i-Pr)S(O)Me
CH2C(=NOMe)Me CH(i-Pr)S(O)Et
CH2C(=NOMe)Me CH(i-Pr)S(O)CF3
CH2C(=NOMe)Me CH(i-Pr)S(O)CH2CF3
CH2C(=NOMe)Me CH(i-Pr)S(O)2Me
CH2C(=NOMe)Me CH(i-Pr)S(O)2Et
CH2C(=NOMe)Me CH(i-Pr)S(O)2CF3
CH2C(=NOMe)Me CH(i-Pr)S(O)2CH2CF3
CH2C(=NOMe)Me CH(n-Bu)SMe
CH2C(=NOMe)Me CH(n-Bu)SEt
CH2C(=NOMe)Me CH(n-Bu)SCF3
CH2C(=NOMe)Me CH(n-Bu)SCH2CF3
CH2C(=NOMe)Me CH(n-Bu)S(O)Me
CH2C(=NOMe)Me CH(n-Bu)S(O)Et
CH2C(=NOMe)Me CH(n-Bu)S(O)CF3
CH2C(=NOMe)Me CH(n-Bu)S(O)CH2CF3
CH2C(=NOMe)Me CH(n-Bu)S(O)2Me
CH2C(=NOMe)Me CH(n-Bu)S(O)2Et
CH2C(=NOMe)Me CH(n-Bu)S(O)2CF3
CH2C(=NOMe)Me CH(n-Bu)S(O)2CH2CF3
CH2C(=NOMe)Me CH(i-Bu)SMe
CH2C(=NOMe)Me CH(i-Bu)SEt
CH2C(=NOMe)Me CH(i-Bu)SCF3
CH2C(=NOMe)Me CH(i-Bu)SCH2CF3
CH2C(=NOMe)Me CH(i-Bu)S(O)Me
CH2C(=NOMe)Me CH(i-Bu)S(O)Et
CH2C(=NOMe)Me CH(i-Bu)S(O)CF3
CH2C(=NOMe)Me CH(i-Bu)S(O)CH2CF3
CH2C(=NOMe)Me CH(i-Bu)S(O)2Me
CH2C(=NOMe)Me CH(i-Bu)S(O)2Et
CH2C(=NOMe)Me CH(i-Bu)S(O)2CF3
CH2C(=NOMe)Me CH(i-Bu)S(O)2CH2CF3
CH2C(=NOMe)Me CH(s-Bu)SMe
CH2C(=NOMe)Me CH(s-Bu)SEt
CH2C(=NOMe)Me CH(s-Bu)SCF3
CH2C(=NOMe)Me CH(s-Bu)SCH2CF3
CH2C(=NOMe)Me CH(s-Bu)S(O)Me
CH2C(=NOMe)Me CH(s-Bu)S(O)Et
CH2C(=NOMe)Me CH(s-Bu)S(O)CF3
CH2C(=NOMe)Me CH(s-Bu)S(O)CH2CF3
CH2C(=NOMe)Me CH(s-Bu)S(O)2Me
CH2C(=NOMe)Me CH(s-Bu)S(O)2Et
CH2C(=NOMe)Me CH(s-Bu)S(O)2CF3
CH2C(=NOMe)Me CH(s-Bu)S(O)2CH2CF3
CH2C(=NOMe)Me CH(t-Bu)SMe
CH2C(=NOMe)Me CH(t-Bu)SEt
CH2C(=NOMe)Me CH(t-Bu)SCF3
CH2C(=NOMe)Me CH(t-Bu)SCH2CF3
CH2C(=NOMe)Me CH(t-Bu)S(O)Me
CH2C(=NOMe)Me CH(t-Bu)S(O)Et
CH2C(=NOMe)Me CH(t-Bu)S(O)CF3
CH2C(=NOMe)Me CH(t-Bu)S(O)CH2CF3
CH2C(=NOMe)Me CH(t-Bu)S(O)2Me
CH2C(=NOMe)Me CH(t-Bu)S(O)2Et
CH2C(=NOMe)Me CH(t-Bu)S(O)2CF3
CH2C(=NOMe)Me CH(t-Bu)S(O)2CH2CF3
CH2C(=NOMe)Me CH(CF3)SMe
CH2C(=NOMe)Me CH(CF3)SEt
CH2C(=NOMe)Me CH(CF3)SCF3
CH2C(=NOMe)Me CH(CF3)SCH2CF3
CH2C(=NOMe)Me CH(CF3)S(O)Me
CH2C(=NOMe)Me CH(CF3)S(O)Et
CH2C(=NOMe)Me CH(CF3)S(O)CF3
CH2C(=NOMe)Me CH(CF3)S(O)CH2CF3
CH2C(=NOMe)Me CH(CF3)S(O)2Me
CH2C(=NOMe)Me CH(CF3)S(O)2Et
CH2C(=NOMe)Me CH(CF3)S(O)2CF3
CH2C(=NOMe)Me CH(CF3)S(O)2CH2CF3
CH2C(=NOMe)Me CH2CH2SMe
CH2C(=NOMe)Me CH2CH2SEt
CH2C(=NOMe)Me CH2CH2SCF3
CH2C(=NOMe)Me CH2CH2SCH2CF3
CH2C(=NOMe)Me CH2CH2S(O)Me
CH2C(=NOMe)Me CH2CH2S(O)Et
CH2C(=NOMe)Me CH2CH2S(O)CF3
CH2C(=NOMe)Me CH2CH2S(O)CH2CF3
CH2C(=NOMe)Me CH2CH2S(O)2Me
CH2C(=NOMe)Me CH2CH2S(O)2Et
CH2C(=NOMe)Me CH2CH2S(O)2CF3
CH2C(=NOMe)Me CH2CH2S(O)2CH2CF3
CH2C(=NOMe)Me CH(Me)CH2SMe
CH2C(=NOMe)Me CH(Me)CH2SEt
CH2C(=NOMe)Me CH(Me)CH2SCF3
CH2C(=NOMe)Me CH(Me)CH2SCH2CF3
CH2C(=NOMe)Me CH(Me)CH2S(O)Me
CH2C(=NOMe)Me CH(Me)CH2S(O)Et
CH2C(=NOMe)Me CH(Me)CH2S(O)CF3
CH2C(=NOMe)Me CH(Me)CH2S(O)CH2CF3
CH2C(=NOMe)Me CH(Me)CH2S(O)2Me
CH2C(=NOMe)Me CH(Me)CH2S(O)2Et
CH2C(=NOMe)Me CH(Me)CH2S(O)2CF3
CH2C(=NOMe)Me CH(Me)CH2S(O)2CH2CF3
CH2C(=NOMe)Me CH(Et)CH2SMe
CH2C(=NOMe)Me CH(Et)CH2SEt
CH2C(=NOMe)Me CH(Et)CH2SCF3
CH2C(=NOMe)Me CH(Et)CH2SCH2CF3
CH2C(=NOMe)Me CH(Et)CH2S(O)Me
CH2C(=NOMe)Me CH(Et)CH2S(O)Et
CH2C(=NOMe)Me CH(Et)CH2S(O)CF3
CH2C(=NOMe)Me CH(Et)CH2S(O)CH2CF3
CH2C(=NOMe)Me CH(Et)CH2S(O)2Me
CH2C(=NOMe)Me CH(Et)CH2S(O)2Et
CH2C(=NOMe)Me CH(Et)CH2S(O)2CF3
CH2C(=NOMe)Me CH(Et)CH2S(O)2CH2CF3
CH2C(=NOMe)Me C(Me)2CH2SMe
CH2C(=NOMe)Me C(Me)2CH2SEt
CH2C(=NOMe)Me C(Me)2CH2SCF3
CH2C(=NOMe)Me C(Me)2CH2SCH2CF3
CH2C(=NOMe)Me C(Me)2CH2S(O)Me
CH2C(=NOMe)Me C(Me)2CH2S(O)Et
CH2C(=NOMe)Me C(Me)2CH2S(O)CF3
CH2C(=NOMe)Me C(Me)2CH2S(O)CH2CF3
CH2C(=NOMe)Me C(Me)2CH2S(O)2Me
CH2C(=NOMe)Me C(Me)2CH2S(O)2Et
CH2C(=NOMe)Me C(Me)2CH2S(O)2CF3
CH2C(=NOMe)Me C(Me)2CH2S(O)2CH2CF3
CH2C(=NOMe)Me CH2CH(Me)SMe
CH2C(=NOMe)Me CH2CH(Me)SEt
CH2C(=NOMe)Me CH2CH(Me)SCF3
CH2C(=NOMe)Me CH2CH(Me)SCH2CF3
CH2C(=NOMe)Me CH2CH(Me)S(O)Me
CH2C(=NOMe)Me CH2CH(Me)S(O)Et
CH2C(=NOMe)Me CH2CH(Me)S(O)CF3
CH2C(=NOMe)Me CH2CH(Me)S(O)CH2CF3
CH2C(=NOMe)Me CH2CH(Me)S(O)2Me
CH2C(=NOMe)Me CH2CH(Me)S(O)2Et
CH2C(=NOMe)Me CH2CH(Me)S(O)2CF3
CH2C(=NOMe)Me CH2CH(Me)S(O)2CH2CF3
CH2C(=NOMe)Me CH2CH(Et)SMe
CH2C(=NOMe)Me CH2CH(Et)SEt
CH2C(=NOMe)Me CH2CH(Et)SCF3
CH2C(=NOMe)Me CH2CH(Et)SCH2CF3
CH2C(=NOMe)Me CH2CH(Et)S(O)Me
CH2C(=NOMe)Me CH2CH(Et)S(O)Et
CH2C(=NOMe)Me CH2CH(Et)S(O)CF3
CH2C(=NOMe)Me CH2CH(Et)S(O)CH2CF3
CH2C(=NOMe)Me CH2CH(Et)S(O)2Me
CH2C(=NOMe)Me CH2CH(Et)S(O)2Et
CH2C(=NOMe)Me CH2CH(Et)S(O)2CF3
CH2C(=NOMe)Me CH2CH(Et)S(O)2CH2CF3
CH2C(=NOMe)Me CH(Me)CH(Me)SMe
CH2C(=NOMe)Me CH(Me)CH(Me)SEt
CH2C(=NOMe)Me CH(Me)CH(Me)SCF3
CH2C(=NOMe)Me CH(Me)CH(Me)SCH2CF3
CH2C(=NOMe)Me CH(Me)CH(Me)S(O)Me
CH2C(=NOMe)Me CH(Me)CH(Me)S(O)Et
CH2C(=NOMe)Me CH(Me)CH(Me)S(O)CF3
CH2C(=NOMe)Me CH(Me)CH(Me)S(O)CH2CF3
CH2C(=NOMe)Me CH(Me)CH(Me)S(O)2Me
CH2C(=NOMe)Me CH(Me)CH(Me)S(O)2Et
CH2C(=NOMe)Me CH(Me)CH(Me)S(O)2CF3
CH2C(=NOMe)Me CH(Me)CH(Me)S(O)2CH2CF3
――――――――――――――――――
本発明化合物は、農園芸作物及び樹木などを加害する所謂農業害虫、家畜・家禽類に寄生する所謂家畜害虫、家屋等の人間の生活環境で様々な悪影響を与える所謂衛生害虫、倉庫に貯蔵された穀物等を加害する所謂貯穀害虫等としての昆虫類、及び同様の場面で発生、加害するダニ類、甲殻類、軟体動物、線虫類の何れの有害生物も低濃度で有効に防除できる。
――――――――――――――――――
X1-2 X1-1
――――――――――――――――――
H CH2SMe
H CH2SEt
H CH2SCFThree
H CH2SCH2CFThree
H CH2S (O) Me
H CH2S (O) Et
H CH2S (O) CFThree
H CH2S (O) CH2CFThree
H CH2S (O)2Me
H CH2S (O)2Et
H CH2S (O)2CFThree
H CH2S (O)2CH2CFThree
H CH (Me) SMe
H CH (Me) SEt
H CH (Me) SCFThree
H CH (Me) SCH2CFThree
H CH (Me) S (O) Me
H CH (Me) S (O) Et
H CH (Me) S (O) CFThree
H CH (Me) S (O) CH2CFThree
H CH (Me) S (O)2Me
H CH (Me) S (O)2Et
H CH (Me) S (O)2CFThree
H CH (Me) S (O)2CH2CFThree
H CH (Et) SMe
H CH (Et) SEt
H CH (Et) SCFThree
H CH (Et) SCH2CFThree
H CH (Et) S (O) Me
H CH (Et) S (O) Et
H CH (Et) S (O) CFThree
H CH (Et) S (O) CH2CFThree
H CH (Et) S (O)2Me
H CH (Et) S (O)2Et
H CH (Et) S (O)2CFThree
H CH (Et) S (O)2CH2CFThree
H CH (n-Pr) SMe
H CH (n-Pr) SEt
H CH (n-Pr) SCFThree
H CH (n-Pr) SCH2CFThree
H CH (n-Pr) S (O) Me
H CH (n-Pr) S (O) Et
H CH (n-Pr) S (O) CFThree
H CH (n-Pr) S (O) CH2CFThree
H CH (n-Pr) S (O)2Me
H CH (n-Pr) S (O)2Et
H CH (n-Pr) S (O)2CFThree
H CH (n-Pr) S (O)2CH2CFThree
H CH (i-Pr) SMe
H CH (i-Pr) SEt
H CH (i-Pr) SCFThree
H CH (i-Pr) SCH2CFThree
H CH (i-Pr) S (O) Me
H CH (i-Pr) S (O) Et
H CH (i-Pr) S (O) CFThree
H CH (i-Pr) S (O) CH2CFThree
H CH (i-Pr) S (O)2Me
H CH (i-Pr) S (O)2Et
H CH (i-Pr) S (O)2CFThree
H CH (i-Pr) S (O)2CH2CFThree
H CH (n-Bu) SMe
H CH (n-Bu) SEt
H CH (n-Bu) SCFThree
H CH (n-Bu) SCH2CFThree
H CH (n-Bu) S (O) Me
H CH (n-Bu) S (O) Et
H CH (n-Bu) S (O) CFThree
H CH (n-Bu) S (O) CH2CFThree
H CH (n-Bu) S (O)2Me
H CH (n-Bu) S (O)2Et
H CH (n-Bu) S (O)2CFThree
H CH (n-Bu) S (O)2CH2CFThree
H CH (i-Bu) SMe
H CH (i-Bu) SEt
H CH (i-Bu) SCFThree
H CH (i-Bu) SCH2CFThree
H CH (i-Bu) S (O) Me
H CH (i-Bu) S (O) Et
H CH (i-Bu) S (O) CFThree
H CH (i-Bu) S (O) CH2CFThree
H CH (i-Bu) S (O)2Me
H CH (i-Bu) S (O)2Et
H CH (i-Bu) S (O)2CFThree
H CH (i-Bu) S (O)2CH2CFThree
H CH (s-Bu) SMe
H CH (s-Bu) SEt
H CH (s-Bu) SCFThree
H CH (s-Bu) SCH2CFThree
H CH (s-Bu) S (O) Me
H CH (s-Bu) S (O) Et
H CH (s-Bu) S (O) CFThree
H CH (s-Bu) S (O) CH2CFThree
H CH (s-Bu) S (O)2Me
H CH (s-Bu) S (O)2Et
H CH (s-Bu) S (O)2CFThree
H CH (s-Bu) S (O)2CH2CFThree
H CH (t-Bu) SMe
H CH (t-Bu) SEt
H CH (t-Bu) SCFThree
H CH (t-Bu) SCH2CFThree
H CH (t-Bu) S (O) Me
H CH (t-Bu) S (O) Et
H CH (t-Bu) S (O) CFThree
H CH (t-Bu) S (O) CH2CFThree
H CH (t-Bu) S (O)2Me
H CH (t-Bu) S (O)2Et
H CH (t-Bu) S (O)2CFThree
H CH (t-Bu) S (O)2CH2CFThree
H CH (CFThreeSMe
H CH (CFThree) SEt
H CH (CFThree) SCFThree
H CH (CFThree) SCH2CFThree
H CH (CFThree) S (O) Me
H CH (CFThree) S (O) Et
H CH (CFThree) S (O) CFThree
H CH (CFThree) S (O) CH2CFThree
H CH (CFThree) S (O)2Me
H CH (CFThree) S (O)2Et
H CH (CFThree) S (O)2CFThree
H CH (CFThree) S (O)2CH2CFThree
H CH2CH2SMe
H CH2CH2SEt
H CH2CH2SCFThree
H CH2CH2SCH2CFThree
H CH2CH2S (O) Me
H CH2CH2S (O) Et
H CH2CH2S (O) CFThree
H CH2CH2S (O) CH2CFThree
H CH2CH2S (O)2Me
H CH2CH2S (O)2Et
H CH2CH2S (O)2CFThree
H CH2CH2S (O)2CH2CFThree
H CH (Me) CH2SMe
H CH (Me) CH2SEt
H CH (Me) CH2SCFThree
H CH (Me) CH2SCH2CFThree
H CH (Me) CH2S (O) Me
H CH (Me) CH2S (O) Et
H CH (Me) CH2S (O) CFThree
H CH (Me) CH2S (O) CH2CFThree
H CH (Me) CH2S (O)2Me
H CH (Me) CH2S (O)2Et
H CH (Me) CH2S (O)2CFThree
H CH (Me) CH2S (O)2CH2CFThree
H CH (Et) CH2SMe
H CH (Et) CH2SEt
H CH (Et) CH2SCFThree
H CH (Et) CH2SCH2CFThree
H CH (Et) CH2S (O) Me
H CH (Et) CH2S (O) Et
H CH (Et) CH2S (O) CFThree
H CH (Et) CH2S (O) CH2CFThree
H CH (Et) CH2S (O)2Me
H CH (Et) CH2S (O)2Et
H CH (Et) CH2S (O)2CFThree
H CH (Et) CH2S (O)2CH2CFThree
H C (Me)2CH2SMe
H C (Me)2CH2SEt
H C (Me)2CH2SCFThree
H C (Me)2CH2SCH2CFThree
H C (Me)2CH2S (O) Me
H C (Me)2CH2S (O) Et
H C (Me)2CH2S (O) CFThree
H C (Me)2CH2S (O) CH2CFThree
H C (Me)2CH2S (O)2Me
H C (Me)2CH2S (O)2Et
H C (Me)2CH2S (O)2CFThree
H C (Me)2CH2S (O)2CH2CFThree
H CH2CH (Me) SMe
H CH2CH (Me) SEt
H CH2CH (Me) SCFThree
H CH2CH (Me) SCH2CFThree
H CH2CH (Me) S (O) Me
H CH2CH (Me) S (O) Et
H CH2CH (Me) S (O) CFThree
H CH2CH (Me) S (O) CH2CFThree
H CH2CH (Me) S (O)2Me
H CH2CH (Me) S (O)2Et
H CH2CH (Me) S (O)2CFThree
H CH2CH (Me) S (O)2CH2CFThree
H CH2CH (Et) SMe
H CH2CH (Et) SEt
H CH2CH (Et) SCFThree
H CH2CH (Et) SCH2CFThree
H CH2CH (Et) S (O) Me
H CH2CH (Et) S (O) Et
H CH2CH (Et) S (O) CFThree
H CH2CH (Et) S (O) CH2CFThree
H CH2CH (Et) S (O)2Me
H CH2CH (Et) S (O)2Et
H CH2CH (Et) S (O)2CFThree
H CH2CH (Et) S (O)2CH2CFThree
H CH (Me) CH (Me) SMe
H CH (Me) CH (Me) SEt
H CH (Me) CH (Me) SCFThree
H CH (Me) CH (Me) SCH2CFThree
H CH (Me) CH (Me) S (O) Me
H CH (Me) CH (Me) S (O) Et
H CH (Me) CH (Me) S (O) CFThree
H CH (Me) CH (Me) S (O) CH2CFThree
H CH (Me) CH (Me) S (O)2Me
H CH (Me) CH (Me) S (O)2Et
H CH (Me) CH (Me) S (O)2CFThree
H CH (Me) CH (Me) S (O)2CH2CFThree
Me CH2SMe
Me CH2SEt
Me CH2SCFThree
Me CH2SCH2CFThree
Me CH2S (O) Me
Me CH2S (O) Et
Me CH2S (O) CFThree
Me CH2S (O) CH2CFThree
Me CH2S (O)2Me
Me CH2S (O)2Et
Me CH2S (O)2CFThree
Me CH2S (O)2CH2CFThree
Me CH (Me) SMe
Me CH (Me) SEt
Me CH (Me) SCFThree
Me CH (Me) SCH2CFThree
Me CH (Me) S (O) Me
Me CH (Me) S (O) Et
Me CH (Me) S (O) CFThree
Me CH (Me) S (O) CH2CFThree
Me CH (Me) S (O)2Me
Me CH (Me) S (O)2Et
Me CH (Me) S (O)2CFThree
Me CH (Me) S (O)2CH2CFThree
Me CH (Et) SMe
Me CH (Et) SEt
Me CH (Et) SCFThree
Me CH (Et) SCH2CFThree
Me CH (Et) S (O) Me
Me CH (Et) S (O) Et
Me CH (Et) S (O) CFThree
Me CH (Et) S (O) CH2CFThree
Me CH (Et) S (O)2Me
Me CH (Et) S (O)2Et
Me CH (Et) S (O)2CFThree
Me CH (Et) S (O)2CH2CFThree
Me CH (n-Pr) SMe
Me CH (n-Pr) SEt
Me CH (n-Pr) SCFThree
Me CH (n-Pr) SCH2CFThree
Me CH (n-Pr) S (O) Me
Me CH (n-Pr) S (O) Et
Me CH (n-Pr) S (O) CFThree
Me CH (n-Pr) S (O) CH2CFThree
Me CH (n-Pr) S (O)2Me
Me CH (n-Pr) S (O)2Et
Me CH (n-Pr) S (O)2CFThree
Me CH (n-Pr) S (O)2CH2CFThree
Me CH (i-Pr) SMe
Me CH (i-Pr) SEt
Me CH (i-Pr) SCFThree
Me CH (i-Pr) SCH2CFThree
Me CH (i-Pr) S (O) Me
Me CH (i-Pr) S (O) Et
Me CH (i-Pr) S (O) CFThree
Me CH (i-Pr) S (O) CH2CFThree
Me CH (i-Pr) S (O)2Me
Me CH (i-Pr) S (O)2Et
Me CH (i-Pr) S (O)2CFThree
Me CH (i-Pr) S (O)2CH2CFThree
Me CH (n-Bu) SMe
Me CH (n-Bu) SEt
Me CH (n-Bu) SCFThree
Me CH (n-Bu) SCH2CFThree
Me CH (n-Bu) S (O) Me
Me CH (n-Bu) S (O) Et
Me CH (n-Bu) S (O) CFThree
Me CH (n-Bu) S (O) CH2CFThree
Me CH (n-Bu) S (O)2Me
Me CH (n-Bu) S (O)2Et
Me CH (n-Bu) S (O)2CFThree
Me CH (n-Bu) S (O)2CH2CFThree
Me CH (i-Bu) SMe
Me CH (i-Bu) SEt
Me CH (i-Bu) SCFThree
Me CH (i-Bu) SCH2CFThree
Me CH (i-Bu) S (O) Me
Me CH (i-Bu) S (O) Et
Me CH (i-Bu) S (O) CFThree
Me CH (i-Bu) S (O) CH2CFThree
Me CH (i-Bu) S (O)2Me
Me CH (i-Bu) S (O)2Et
Me CH (i-Bu) S (O)2CFThree
Me CH (i-Bu) S (O)2CH2CFThree
Me CH (s-Bu) SMe
Me CH (s-Bu) SEt
Me CH (s-Bu) SCFThree
Me CH (s-Bu) SCH2CFThree
Me CH (s-Bu) S (O) Me
Me CH (s-Bu) S (O) Et
Me CH (s-Bu) S (O) CFThree
Me CH (s-Bu) S (O) CH2CFThree
Me CH (s-Bu) S (O)2Me
Me CH (s-Bu) S (O)2Et
Me CH (s-Bu) S (O)2CFThree
Me CH (s-Bu) S (O)2CH2CFThree
Me CH (t-Bu) SMe
Me CH (t-Bu) SEt
Me CH (t-Bu) SCFThree
Me CH (t-Bu) SCH2CFThree
Me CH (t-Bu) S (O) Me
Me CH (t-Bu) S (O) Et
Me CH (t-Bu) S (O) CFThree
Me CH (t-Bu) S (O) CH2CFThree
Me CH (t-Bu) S (O)2Me
Me CH (t-Bu) S (O)2Et
Me CH (t-Bu) S (O)2CFThree
Me CH (t-Bu) S (O)2CH2CFThree
Me CH (CFThreeSMe
Me CH (CFThree) SEt
Me CH (CFThree) SCFThree
Me CH (CFThree) SCH2CFThree
Me CH (CFThree) S (O) Me
Me CH (CFThree) S (O) Et
Me CH (CFThree) S (O) CFThree
Me CH (CFThree) S (O) CH2CFThree
Me CH (CFThree) S (O)2Me
Me CH (CFThree) S (O)2Et
Me CH (CFThree) S (O)2CFThree
Me CH (CFThree) S (O)2CH2CFThree
Me CH2CH2SMe
Me CH2CH2SEt
Me CH2CH2SCFThree
Me CH2CH2SCH2CFThree
Me CH2CH2S (O) Me
Me CH2CH2S (O) Et
Me CH2CH2S (O) CFThree
Me CH2CH2S (O) CH2CFThree
Me CH2CH2S (O)2Me
Me CH2CH2S (O)2Et
Me CH2CH2S (O)2CFThree
Me CH2CH2S (O)2CH2CFThree
Me CH (Me) CH2SMe
Me CH (Me) CH2SEt
Me CH (Me) CH2SCFThree
Me CH (Me) CH2SCH2CFThree
Me CH (Me) CH2S (O) Me
Me CH (Me) CH2S (O) Et
Me CH (Me) CH2S (O) CFThree
Me CH (Me) CH2S (O) CH2CFThree
Me CH (Me) CH2S (O)2Me
Me CH (Me) CH2S (O)2Et
Me CH (Me) CH2S (O)2CFThree
Me CH (Me) CH2S (O)2CH2CFThree
Me CH (Et) CH2SMe
Me CH (Et) CH2SEt
Me CH (Et) CH2SCFThree
Me CH (Et) CH2SCH2CFThree
Me CH (Et) CH2S (O) Me
Me CH (Et) CH2S (O) Et
Me CH (Et) CH2S (O) CFThree
Me CH (Et) CH2S (O) CH2CFThree
Me CH (Et) CH2S (O)2Me
Me CH (Et) CH2S (O)2Et
Me CH (Et) CH2S (O)2CFThree
Me CH (Et) CH2S (O)2CH2CFThree
Me C (Me)2CH2SMe
Me C (Me)2CH2SEt
Me C (Me)2CH2SCFThree
Me C (Me)2CH2SCH2CFThree
Me C (Me)2CH2S (O) Me
Me C (Me)2CH2S (O) Et
Me C (Me)2CH2S (O) CFThree
Me C (Me)2CH2S (O) CH2CFThree
Me C (Me)2CH2S (O)2Me
Me C (Me)2CH2S (O)2Et
Me C (Me)2CH2S (O)2CFThree
Me C (Me)2CH2S (O)2CH2CFThree
Me CH2CH (Me) SMe
Me CH2CH (Me) SEt
Me CH2CH (Me) SCFThree
Me CH2CH (Me) SCH2CFThree
Me CH2CH (Me) S (O) Me
Me CH2CH (Me) S (O) Et
Me CH2CH (Me) S (O) CFThree
Me CH2CH (Me) S (O) CH2CFThree
Me CH2CH (Me) S (O)2Me
Me CH2CH (Me) S (O)2Et
Me CH2CH (Me) S (O)2CFThree
Me CH2CH (Me) S (O)2CH2CFThree
Me CH2CH (Et) SMe
Me CH2CH (Et) SEt
Me CH2CH (Et) SCFThree
Me CH2CH (Et) SCH2CFThree
Me CH2CH (Et) S (O) Me
Me CH2CH (Et) S (O) Et
Me CH2CH (Et) S (O) CFThree
Me CH2CH (Et) S (O) CH2CFThree
Me CH2CH (Et) S (O)2Me
Me CH2CH (Et) S (O)2Et
Me CH2CH (Et) S (O)2CFThree
Me CH2CH (Et) S (O)2CH2CFThree
Me CH (Me) CH (Me) SMe
Me CH (Me) CH (Me) SEt
Me CH (Me) CH (Me) SCFThree
Me CH (Me) CH (Me) SCH2CFThree
Me CH (Me) CH (Me) S (O) Me
Me CH (Me) CH (Me) S (O) Et
Me CH (Me) CH (Me) S (O) CFThree
Me CH (Me) CH (Me) S (O) CH2CFThree
Me CH (Me) CH (Me) S (O)2Me
Me CH (Me) CH (Me) S (O)2Et
Me CH (Me) CH (Me) S (O)2CFThree
Me CH (Me) CH (Me) S (O)2CH2CFThree
CH2CFThree CH2SMe
CH2CFThree CH2SEt
CH2CFThree CH2SCFThree
CH2CFThree CH2SCH2CFThree
CH2CFThree CH2S (O) Me
CH2CFThree CH2S (O) Et
CH2CFThree CH2S (O) CFThree
CH2CFThree CH2S (O) CH2CFThree
CH2CFThree CH2S (O)2Me
CH2CFThree CH2S (O)2Et
CH2CFThree CH2S (O)2CFThree
CH2CFThree CH2S (O)2CH2CFThree
CH2CFThree CH (Me) SMe
CH2CFThree CH (Me) SEt
CH2CFThree CH (Me) SCFThree
CH2CFThree CH (Me) SCH2CFThree
CH2CFThree CH (Me) S (O) Me
CH2CFThree CH (Me) S (O) Et
CH2CFThree CH (Me) S (O) CFThree
CH2CFThree CH (Me) S (O) CH2CFThree
CH2CFThree CH (Me) S (O)2Me
CH2CFThree CH (Me) S (O)2Et
CH2CFThree CH (Me) S (O)2CFThree
CH2CFThree CH (Me) S (O)2CH2CFThree
CH2CFThree CH (Et) SMe
CH2CFThree CH (Et) SEt
CH2CFThree CH (Et) SCFThree
CH2CFThree CH (Et) SCH2CFThree
CH2CFThree CH (Et) S (O) Me
CH2CFThree CH (Et) S (O) Et
CH2CFThree CH (Et) S (O) CFThree
CH2CFThree CH (Et) S (O) CH2CFThree
CH2CFThree CH (Et) S (O)2Me
CH2CFThree CH (Et) S (O)2Et
CH2CFThree CH (Et) S (O)2CFThree
CH2CFThree CH (Et) S (O)2CH2CFThree
CH2CFThree CH (n-Pr) SMe
CH2CFThree CH (n-Pr) SEt
CH2CFThree CH (n-Pr) SCFThree
CH2CFThree CH (n-Pr) SCH2CFThree
CH2CFThree CH (n-Pr) S (O) Me
CH2CFThree CH (n-Pr) S (O) Et
CH2CFThree CH (n-Pr) S (O) CFThree
CH2CFThree CH (n-Pr) S (O) CH2CFThree
CH2CFThree CH (n-Pr) S (O)2Me
CH2CFThree CH (n-Pr) S (O)2Et
CH2CFThree CH (n-Pr) S (O)2CFThree
CH2CFThree CH (n-Pr) S (O)2CH2CFThree
CH2CFThree CH (i-Pr) SMe
CH2CFThree CH (i-Pr) SEt
CH2CFThree CH (i-Pr) SCFThree
CH2CFThree CH (i-Pr) SCH2CFThree
CH2CFThree CH (i-Pr) S (O) Me
CH2CFThree CH (i-Pr) S (O) Et
CH2CFThree CH (i-Pr) S (O) CFThree
CH2CFThree CH (i-Pr) S (O) CH2CFThree
CH2CFThree CH (i-Pr) S (O)2Me
CH2CFThree CH (i-Pr) S (O)2Et
CH2CFThree CH (i-Pr) S (O)2CFThree
CH2CFThree CH (i-Pr) S (O)2CH2CFThree
CH2CFThree CH (n-Bu) SMe
CH2CFThree CH (n-Bu) SEt
CH2CFThree CH (n-Bu) SCFThree
CH2CFThree CH (n-Bu) SCH2CFThree
CH2CFThree CH (n-Bu) S (O) Me
CH2CFThree CH (n-Bu) S (O) Et
CH2CFThree CH (n-Bu) S (O) CFThree
CH2CFThree CH (n-Bu) S (O) CH2CFThree
CH2CFThree CH (n-Bu) S (O)2Me
CH2CFThree CH (n-Bu) S (O)2Et
CH2CFThree CH (n-Bu) S (O)2CFThree
CH2CFThree CH (n-Bu) S (O)2CH2CFThree
CH2CFThree CH (i-Bu) SMe
CH2CFThree CH (i-Bu) SEt
CH2CFThree CH (i-Bu) SCFThree
CH2CFThree CH (i-Bu) SCH2CFThree
CH2CFThree CH (i-Bu) S (O) Me
CH2CFThree CH (i-Bu) S (O) Et
CH2CFThree CH (i-Bu) S (O) CFThree
CH2CFThree CH (i-Bu) S (O) CH2CFThree
CH2CFThree CH (i-Bu) S (O)2Me
CH2CFThree CH (i-Bu) S (O)2Et
CH2CFThree CH (i-Bu) S (O)2CFThree
CH2CFThree CH (i-Bu) S (O)2CH2CFThree
CH2CFThree CH (s-Bu) SMe
CH2CFThree CH (s-Bu) SEt
CH2CFThree CH (s-Bu) SCFThree
CH2CFThree CH (s-Bu) SCH2CFThree
CH2CFThree CH (s-Bu) S (O) Me
CH2CFThree CH (s-Bu) S (O) Et
CH2CFThree CH (s-Bu) S (O) CFThree
CH2CFThree CH (s-Bu) S (O) CH2CFThree
CH2CFThree CH (s-Bu) S (O)2Me
CH2CFThree CH (s-Bu) S (O)2Et
CH2CFThree CH (s-Bu) S (O)2CFThree
CH2CFThree CH (s-Bu) S (O)2CH2CFThree
CH2CFThree CH (t-Bu) SMe
CH2CFThree CH (t-Bu) SEt
CH2CFThree CH (t-Bu) SCFThree
CH2CFThree CH (t-Bu) SCH2CFThree
CH2CFThree CH (t-Bu) S (O) Me
CH2CFThree CH (t-Bu) S (O) Et
CH2CFThree CH (t-Bu) S (O) CFThree
CH2CFThree CH (t-Bu) S (O) CH2CFThree
CH2CFThree CH (t-Bu) S (O)2Me
CH2CFThree CH (t-Bu) S (O)2Et
CH2CFThree CH (t-Bu) S (O)2CFThree
CH2CFThree CH (t-Bu) S (O)2CH2CFThree
CH2CFThree CH (CFThreeSMe
CH2CFThree CH (CFThree) SEt
CH2CFThree CH (CFThree) SCFThree
CH2CFThree CH (CFThree) SCH2CFThree
CH2CFThree CH (CFThree) S (O) Me
CH2CFThree CH (CFThree) S (O) Et
CH2CFThree CH (CFThree) S (O) CFThree
CH2CFThree CH (CFThree) S (O) CH2CFThree
CH2CFThree CH (CFThree) S (O)2Me
CH2CFThree CH (CFThree) S (O)2Et
CH2CFThree CH (CFThree) S (O)2CFThree
CH2CFThree CH (CFThree) S (O)2CH2CFThree
CH2CFThree CH2CH2SMe
CH2CFThree CH2CH2SEt
CH2CFThree CH2CH2SCFThree
CH2CFThree CH2CH2SCH2CFThree
CH2CFThree CH2CH2S (O) Me
CH2CFThree CH2CH2S (O) Et
CH2CFThree CH2CH2S (O) CFThree
CH2CFThree CH2CH2S (O) CH2CFThree
CH2CFThree CH2CH2S (O)2Me
CH2CFThree CH2CH2S (O)2Et
CH2CFThree CH2CH2S (O)2CFThree
CH2CFThree CH2CH2S (O)2CH2CFThree
CH2CFThree CH (Me) CH2SMe
CH2CFThree CH (Me) CH2SEt
CH2CFThree CH (Me) CH2SCFThree
CH2CFThree CH (Me) CH2SCH2CFThree
CH2CFThree CH (Me) CH2S (O) Me
CH2CFThree CH (Me) CH2S (O) Et
CH2CFThree CH (Me) CH2S (O) CFThree
CH2CFThree CH (Me) CH2S (O) CH2CFThree
CH2CFThree CH (Me) CH2S (O)2Me
CH2CFThree CH (Me) CH2S (O)2Et
CH2CFThree CH (Me) CH2S (O)2CFThree
CH2CFThree CH (Me) CH2S (O)2CH2CFThree
CH2CFThree CH (Et) CH2SMe
CH2CFThree CH (Et) CH2SEt
CH2CFThree CH (Et) CH2SCFThree
CH2CFThree CH (Et) CH2SCH2CFThree
CH2CFThree CH (Et) CH2S (O) Me
CH2CFThree CH (Et) CH2S (O) Et
CH2CFThree CH (Et) CH2S (O) CFThree
CH2CFThree CH (Et) CH2S (O) CH2CFThree
CH2CFThree CH (Et) CH2S (O)2Me
CH2CFThree CH (Et) CH2S (O)2Et
CH2CFThree CH (Et) CH2S (O)2CFThree
CH2CFThree CH (Et) CH2S (O)2CH2CFThree
CH2CFThree C (Me)2CH2SMe
CH2CFThree C (Me)2CH2SEt
CH2CFThree C (Me)2CH2SCFThree
CH2CFThree C (Me)2CH2SCH2CFThree
CH2CFThree C (Me)2CH2S (O) Me
CH2CFThree C (Me)2CH2S (O) Et
CH2CFThree C (Me)2CH2S (O) CFThree
CH2CFThree C (Me)2CH2S (O) CH2CFThree
CH2CFThree C (Me)2CH2S (O)2Me
CH2CFThree C (Me)2CH2S (O)2Et
CH2CFThree C (Me)2CH2S (O)2CFThree
CH2CFThree C (Me)2CH2S (O)2CH2CFThree
CH2CFThree CH2CH (Me) SMe
CH2CFThree CH2CH (Me) SEt
CH2CFThree CH2CH (Me) SCFThree
CH2CFThree CH2CH (Me) SCH2CFThree
CH2CFThree CH2CH (Me) S (O) Me
CH2CFThree CH2CH (Me) S (O) Et
CH2CFThree CH2CH (Me) S (O) CFThree
CH2CFThree CH2CH (Me) S (O) CH2CFThree
CH2CFThree CH2CH (Me) S (O)2Me
CH2CFThree CH2CH (Me) S (O)2Et
CH2CFThree CH2CH (Me) S (O)2CFThree
CH2CFThree CH2CH (Me) S (O)2CH2CFThree
CH2CFThree CH2CH (Et) SMe
CH2CFThree CH2CH (Et) SEt
CH2CFThree CH2CH (Et) SCFThree
CH2CFThree CH2CH (Et) SCH2CFThree
CH2CFThree CH2CH (Et) S (O) Me
CH2CFThree CH2CH (Et) S (O) Et
CH2CFThree CH2CH (Et) S (O) CFThree
CH2CFThree CH2CH (Et) S (O) CH2CFThree
CH2CFThree CH2CH (Et) S (O)2Me
CH2CFThree CH2CH (Et) S (O)2Et
CH2CFThree CH2CH (Et) S (O)2CFThree
CH2CFThree CH2CH (Et) S (O)2CH2CFThree
CH2CFThree CH (Me) CH (Me) SMe
CH2CFThree CH (Me) CH (Me) SEt
CH2CFThree CH (Me) CH (Me) SCFThree
CH2CFThree CH (Me) CH (Me) SCH2CFThree
CH2CFThree CH (Me) CH (Me) S (O) Me
CH2CFThree CH (Me) CH (Me) S (O) Et
CH2CFThree CH (Me) CH (Me) S (O) CFThree
CH2CFThree CH (Me) CH (Me) S (O) CH2CFThree
CH2CFThree CH (Me) CH (Me) S (O)2Me
CH2CFThree CH (Me) CH (Me) S (O)2Et
CH2CFThree CH (Me) CH (Me) S (O)2CFThree
CH2CFThree CH (Me) CH (Me) S (O)2CH2CFThree
CH2CN CH2SMe
CH2CN CH2SEt
CH2CN CH2SCFThree
CH2CN CH2SCH2CFThree
CH2CN CH2S (O) Me
CH2CN CH2S (O) Et
CH2CN CH2S (O) CFThree
CH2CN CH2S (O) CH2CFThree
CH2CN CH2S (O)2Me
CH2CN CH2S (O)2Et
CH2CN CH2S (O)2CFThree
CH2CN CH2S (O)2CH2CFThree
CH2CN CH (Me) SMe
CH2CN CH (Me) SEt
CH2CN CH (Me) SCFThree
CH2CN CH (Me) SCH2CFThree
CH2CN CH (Me) S (O) Me
CH2CN CH (Me) S (O) Et
CH2CN CH (Me) S (O) CFThree
CH2CN CH (Me) S (O) CH2CFThree
CH2CN CH (Me) S (O)2Me
CH2CN CH (Me) S (O)2Et
CH2CN CH (Me) S (O)2CFThree
CH2CN CH (Me) S (O)2CH2CFThree
CH2CN CH (Et) SMe
CH2CN CH (Et) SEt
CH2CN CH (Et) SCFThree
CH2CN CH (Et) SCH2CFThree
CH2CN CH (Et) S (O) Me
CH2CN CH (Et) S (O) Et
CH2CN CH (Et) S (O) CFThree
CH2CN CH (Et) S (O) CH2CFThree
CH2CN CH (Et) S (O)2Me
CH2CN CH (Et) S (O)2Et
CH2CN CH (Et) S (O)2CFThree
CH2CN CH (Et) S (O)2CH2CFThree
CH2CN CH (n-Pr) SMe
CH2CN CH (n-Pr) SEt
CH2CN CH (n-Pr) SCFThree
CH2CN CH (n-Pr) SCH2CFThree
CH2CN CH (n-Pr) S (O) Me
CH2CN CH (n-Pr) S (O) Et
CH2CN CH (n-Pr) S (O) CFThree
CH2CN CH (n-Pr) S (O) CH2CFThree
CH2CN CH (n-Pr) S (O)2Me
CH2CN CH (n-Pr) S (O)2Et
CH2CN CH (n-Pr) S (O)2CFThree
CH2CN CH (n-Pr) S (O)2CH2CFThree
CH2CN CH (i-Pr) SMe
CH2CN CH (i-Pr) SEt
CH2CN CH (i-Pr) SCFThree
CH2CN CH (i-Pr) SCH2CFThree
CH2CN CH (i-Pr) S (O) Me
CH2CN CH (i-Pr) S (O) Et
CH2CN CH (i-Pr) S (O) CFThree
CH2CN CH (i-Pr) S (O) CH2CFThree
CH2CN CH (i-Pr) S (O)2Me
CH2CN CH (i-Pr) S (O)2Et
CH2CN CH (i-Pr) S (O)2CFThree
CH2CN CH (i-Pr) S (O)2CH2CFThree
CH2CN CH (n-Bu) SMe
CH2CN CH (n-Bu) SEt
CH2CN CH (n-Bu) SCFThree
CH2CN CH (n-Bu) SCH2CFThree
CH2CN CH (n-Bu) S (O) Me
CH2CN CH (n-Bu) S (O) Et
CH2CN CH (n-Bu) S (O) CFThree
CH2CN CH (n-Bu) S (O) CH2CFThree
CH2CN CH (n-Bu) S (O)2Me
CH2CN CH (n-Bu) S (O)2Et
CH2CN CH (n-Bu) S (O)2CFThree
CH2CN CH (n-Bu) S (O)2CH2CFThree
CH2CN CH (i-Bu) SMe
CH2CN CH (i-Bu) SEt
CH2CN CH (i-Bu) SCFThree
CH2CN CH (i-Bu) SCH2CFThree
CH2CN CH (i-Bu) S (O) Me
CH2CN CH (i-Bu) S (O) Et
CH2CN CH (i-Bu) S (O) CFThree
CH2CN CH (i-Bu) S (O) CH2CFThree
CH2CN CH (i-Bu) S (O)2Me
CH2CN CH (i-Bu) S (O)2Et
CH2CN CH (i-Bu) S (O)2CFThree
CH2CN CH (i-Bu) S (O)2CH2CFThree
CH2CN CH (s-Bu) SMe
CH2CN CH (s-Bu) SEt
CH2CN CH (s-Bu) SCFThree
CH2CN CH (s-Bu) SCH2CFThree
CH2CN CH (s-Bu) S (O) Me
CH2CN CH (s-Bu) S (O) Et
CH2CN CH (s-Bu) S (O) CFThree
CH2CN CH (s-Bu) S (O) CH2CFThree
CH2CN CH (s-Bu) S (O)2Me
CH2CN CH (s-Bu) S (O)2Et
CH2CN CH (s-Bu) S (O)2CFThree
CH2CN CH (s-Bu) S (O)2CH2CFThree
CH2CN CH (t-Bu) SMe
CH2CN CH (t-Bu) SEt
CH2CN CH (t-Bu) SCFThree
CH2CN CH (t-Bu) SCH2CFThree
CH2CN CH (t-Bu) S (O) Me
CH2CN CH (t-Bu) S (O) Et
CH2CN CH (t-Bu) S (O) CFThree
CH2CN CH (t-Bu) S (O) CH2CFThree
CH2CN CH (t-Bu) S (O)2Me
CH2CN CH (t-Bu) S (O)2Et
CH2CN CH (t-Bu) S (O)2CFThree
CH2CN CH (t-Bu) S (O)2CH2CFThree
CH2CN CH (CFThreeSMe
CH2CN CH (CFThree) SEt
CH2CN CH (CFThree) SCFThree
CH2CN CH (CFThree) SCH2CFThree
CH2CN CH (CFThree) S (O) Me
CH2CN CH (CFThree) S (O) Et
CH2CN CH (CFThree) S (O) CFThree
CH2CN CH (CFThree) S (O) CH2CFThree
CH2CN CH (CFThree) S (O)2Me
CH2CN CH (CFThree) S (O)2Et
CH2CN CH (CFThree) S (O)2CFThree
CH2CN CH (CFThree) S (O)2CH2CFThree
CH2CN CH2CH2SMe
CH2CN CH2CH2SEt
CH2CN CH2CH2SCFThree
CH2CN CH2CH2SCH2CFThree
CH2CN CH2CH2S (O) Me
CH2CN CH2CH2S (O) Et
CH2CN CH2CH2S (O) CFThree
CH2CN CH2CH2S (O) CH2CFThree
CH2CN CH2CH2S (O)2Me
CH2CN CH2CH2S (O)2Et
CH2CN CH2CH2S (O)2CFThree
CH2CN CH2CH2S (O)2CH2CFThree
CH2CN CH (Me) CH2SMe
CH2CN CH (Me) CH2SEt
CH2CN CH (Me) CH2SCFThree
CH2CN CH (Me) CH2SCH2CFThree
CH2CN CH (Me) CH2S (O) Me
CH2CN CH (Me) CH2S (O) Et
CH2CN CH (Me) CH2S (O) CFThree
CH2CN CH (Me) CH2S (O) CH2CFThree
CH2CN CH (Me) CH2S (O)2Me
CH2CN CH (Me) CH2S (O)2Et
CH2CN CH (Me) CH2S (O)2CFThree
CH2CN CH (Me) CH2S (O)2CH2CFThree
CH2CN CH (Et) CH2SMe
CH2CN CH (Et) CH2SEt
CH2CN CH (Et) CH2SCFThree
CH2CN CH (Et) CH2SCH2CFThree
CH2CN CH (Et) CH2S (O) Me
CH2CN CH (Et) CH2S (O) Et
CH2CN CH (Et) CH2S (O) CFThree
CH2CN CH (Et) CH2S (O) CH2CFThree
CH2CN CH (Et) CH2S (O)2Me
CH2CN CH (Et) CH2S (O)2Et
CH2CN CH (Et) CH2S (O)2CFThree
CH2CN CH (Et) CH2S (O)2CH2CFThree
CH2CN C (Me)2CH2SMe
CH2CN C (Me)2CH2SEt
CH2CN C (Me)2CH2SCFThree
CH2CN C (Me)2CH2SCH2CFThree
CH2CN C (Me)2CH2S (O) Me
CH2CN C (Me)2CH2S (O) Et
CH2CN C (Me)2CH2S (O) CFThree
CH2CN C (Me)2CH2S (O) CH2CFThree
CH2CN C (Me)2CH2S (O)2Me
CH2CN C (Me)2CH2S (O)2Et
CH2CN C (Me)2CH2S (O)2CFThree
CH2CN C (Me)2CH2S (O)2CH2CFThree
CH2CN CH2CH (Me) SMe
CH2CN CH2CH (Me) SEt
CH2CN CH2CH (Me) SCFThree
CH2CN CH2CH (Me) SCH2CFThree
CH2CN CH2CH (Me) S (O) Me
CH2CN CH2CH (Me) S (O) Et
CH2CN CH2CH (Me) S (O) CFThree
CH2CN CH2CH (Me) S (O) CH2CFThree
CH2CN CH2CH (Me) S (O)2Me
CH2CN CH2CH (Me) S (O)2Et
CH2CN CH2CH (Me) S (O)2CFThree
CH2CN CH2CH (Me) S (O)2CH2CFThree
CH2CN CH2CH (Et) SMe
CH2CN CH2CH (Et) SEt
CH2CN CH2CH (Et) SCFThree
CH2CN CH2CH (Et) SCH2CFThree
CH2CN CH2CH (Et) S (O) Me
CH2CN CH2CH (Et) S (O) Et
CH2CN CH2CH (Et) S (O) CFThree
CH2CN CH2CH (Et) S (O) CH2CFThree
CH2CN CH2CH (Et) S (O)2Me
CH2CN CH2CH (Et) S (O)2Et
CH2CN CH2CH (Et) S (O)2CFThree
CH2CN CH2CH (Et) S (O)2CH2CFThree
CH2CN CH (Me) CH (Me) SMe
CH2CN CH (Me) CH (Me) SEt
CH2CN CH (Me) CH (Me) SCFThree
CH2CN CH (Me) CH (Me) SCH2CFThree
CH2CN CH (Me) CH (Me) S (O) Me
CH2CN CH (Me) CH (Me) S (O) Et
CH2CN CH (Me) CH (Me) S (O) CFThree
CH2CN CH (Me) CH (Me) S (O) CH2CFThree
CH2CN CH (Me) CH (Me) S (O)2Me
CH2CN CH (Me) CH (Me) S (O)2Et
CH2CN CH (Me) CH (Me) S (O)2CFThree
CH2CN CH (Me) CH (Me) S (O)2CH2CFThree
CH2CH = CH2 CH2SMe
CH2CH = CH2 CH2SEt
CH2CH = CH2 CH2SCFThree
CH2CH = CH2 CH2SCH2CFThree
CH2CH = CH2 CH2S (O) Me
CH2CH = CH2 CH2S (O) Et
CH2CH = CH2 CH2S (O) CFThree
CH2CH = CH2 CH2S (O) CH2CFThree
CH2CH = CH2 CH2S (O)2Me
CH2CH = CH2 CH2S (O)2Et
CH2CH = CH2 CH2S (O)2CFThree
CH2CH = CH2 CH2S (O)2CH2CFThree
CH2CH = CH2 CH (Me) SMe
CH2CH = CH2 CH (Me) SEt
CH2CH = CH2 CH (Me) SCFThree
CH2CH = CH2 CH (Me) SCH2CFThree
CH2CH = CH2 CH (Me) S (O) Me
CH2CH = CH2 CH (Me) S (O) Et
CH2CH = CH2 CH (Me) S (O) CFThree
CH2CH = CH2 CH (Me) S (O) CH2CFThree
CH2CH = CH2 CH (Me) S (O)2Me
CH2CH = CH2 CH (Me) S (O)2Et
CH2CH = CH2 CH (Me) S (O)2CFThree
CH2CH = CH2 CH (Me) S (O)2CH2CFThree
CH2CH = CH2 CH (Et) SMe
CH2CH = CH2 CH (Et) SEt
CH2CH = CH2 CH (Et) SCFThree
CH2CH = CH2 CH (Et) SCH2CFThree
CH2CH = CH2 CH (Et) S (O) Me
CH2CH = CH2 CH (Et) S (O) Et
CH2CH = CH2 CH (Et) S (O) CFThree
CH2CH = CH2 CH (Et) S (O) CH2CFThree
CH2CH = CH2 CH (Et) S (O)2Me
CH2CH = CH2 CH (Et) S (O)2Et
CH2CH = CH2 CH (Et) S (O)2CFThree
CH2CH = CH2 CH (Et) S (O)2CH2CFThree
CH2CH = CH2 CH (n-Pr) SMe
CH2CH = CH2 CH (n-Pr) SEt
CH2CH = CH2 CH (n-Pr) SCFThree
CH2CH = CH2 CH (n-Pr) SCH2CFThree
CH2CH = CH2 CH (n-Pr) S (O) Me
CH2CH = CH2 CH (n-Pr) S (O) Et
CH2CH = CH2 CH (n-Pr) S (O) CFThree
CH2CH = CH2 CH (n-Pr) S (O) CH2CFThree
CH2CH = CH2 CH (n-Pr) S (O)2Me
CH2CH = CH2 CH (n-Pr) S (O)2Et
CH2CH = CH2 CH (n-Pr) S (O)2CFThree
CH2CH = CH2 CH (n-Pr) S (O)2CH2CFThree
CH2CH = CH2 CH (i-Pr) SMe
CH2CH = CH2 CH (i-Pr) SEt
CH2CH = CH2 CH (i-Pr) SCFThree
CH2CH = CH2 CH (i-Pr) SCH2CFThree
CH2CH = CH2 CH (i-Pr) S (O) Me
CH2CH = CH2 CH (i-Pr) S (O) Et
CH2CH = CH2 CH (i-Pr) S (O) CFThree
CH2CH = CH2 CH (i-Pr) S (O) CH2CFThree
CH2CH = CH2 CH (i-Pr) S (O)2Me
CH2CH = CH2 CH (i-Pr) S (O)2Et
CH2CH = CH2 CH (i-Pr) S (O)2CFThree
CH2CH = CH2 CH (i-Pr) S (O)2CH2CFThree
CH2CH = CH2 CH (n-Bu) SMe
CH2CH = CH2 CH (n-Bu) SEt
CH2CH = CH2 CH (n-Bu) SCFThree
CH2CH = CH2 CH (n-Bu) SCH2CFThree
CH2CH = CH2 CH (n-Bu) S (O) Me
CH2CH = CH2 CH (n-Bu) S (O) Et
CH2CH = CH2 CH (n-Bu) S (O) CFThree
CH2CH = CH2 CH (n-Bu) S (O) CH2CFThree
CH2CH = CH2 CH (n-Bu) S (O)2Me
CH2CH = CH2 CH (n-Bu) S (O)2Et
CH2CH = CH2 CH (n-Bu) S (O)2CFThree
CH2CH = CH2 CH (n-Bu) S (O)2CH2CFThree
CH2CH = CH2 CH (i-Bu) SMe
CH2CH = CH2 CH (i-Bu) SEt
CH2CH = CH2 CH (i-Bu) SCFThree
CH2CH = CH2 CH (i-Bu) SCH2CFThree
CH2CH = CH2 CH (i-Bu) S (O) Me
CH2CH = CH2 CH (i-Bu) S (O) Et
CH2CH = CH2 CH (i-Bu) S (O) CFThree
CH2CH = CH2 CH (i-Bu) S (O) CH2CFThree
CH2CH = CH2 CH (i-Bu) S (O)2Me
CH2CH = CH2 CH (i-Bu) S (O)2Et
CH2CH = CH2 CH (i-Bu) S (O)2CFThree
CH2CH = CH2 CH (i-Bu) S (O)2CH2CFThree
CH2CH = CH2 CH (s-Bu) SMe
CH2CH = CH2 CH (s-Bu) SEt
CH2CH = CH2 CH (s-Bu) SCFThree
CH2CH = CH2 CH (s-Bu) SCH2CFThree
CH2CH = CH2 CH (s-Bu) S (O) Me
CH2CH = CH2 CH (s-Bu) S (O) Et
CH2CH = CH2 CH (s-Bu) S (O) CFThree
CH2CH = CH2 CH (s-Bu) S (O) CH2CFThree
CH2CH = CH2 CH (s-Bu) S (O)2Me
CH2CH = CH2 CH (s-Bu) S (O)2Et
CH2CH = CH2 CH (s-Bu) S (O)2CFThree
CH2CH = CH2 CH (s-Bu) S (O)2CH2CFThree
CH2CH = CH2 CH (t-Bu) SMe
CH2CH = CH2 CH (t-Bu) SEt
CH2CH = CH2 CH (t-Bu) SCFThree
CH2CH = CH2 CH (t-Bu) SCH2CFThree
CH2CH = CH2 CH (t-Bu) S (O) Me
CH2CH = CH2 CH (t-Bu) S (O) Et
CH2CH = CH2 CH (t-Bu) S (O) CFThree
CH2CH = CH2 CH (t-Bu) S (O) CH2CFThree
CH2CH = CH2 CH (t-Bu) S (O)2Me
CH2CH = CH2 CH (t-Bu) S (O)2Et
CH2CH = CH2 CH (t-Bu) S (O)2CFThree
CH2CH = CH2 CH (t-Bu) S (O)2CH2CFThree
CH2CH = CH2 CH (CFThreeSMe
CH2CH = CH2 CH (CFThree) SEt
CH2CH = CH2 CH (CFThree) SCFThree
CH2CH = CH2 CH (CFThree) SCH2CFThree
CH2CH = CH2 CH (CFThree) S (O) Me
CH2CH = CH2 CH (CFThree) S (O) Et
CH2CH = CH2 CH (CFThree) S (O) CFThree
CH2CH = CH2 CH (CFThree) S (O) CH2CFThree
CH2CH = CH2 CH (CFThree) S (O)2Me
CH2CH = CH2 CH (CFThree) S (O)2Et
CH2CH = CH2 CH (CFThree) S (O)2CFThree
CH2CH = CH2 CH (CFThree) S (O)2CH2CFThree
CH2CH = CH2 CH2CH2SMe
CH2CH = CH2 CH2CH2SEt
CH2CH = CH2 CH2CH2SCFThree
CH2CH = CH2 CH2CH2SCH2CFThree
CH2CH = CH2 CH2CH2S (O) Me
CH2CH = CH2 CH2CH2S (O) Et
CH2CH = CH2 CH2CH2S (O) CFThree
CH2CH = CH2 CH2CH2S (O) CH2CFThree
CH2CH = CH2 CH2CH2S (O)2Me
CH2CH = CH2 CH2CH2S (O)2Et
CH2CH = CH2 CH2CH2S (O)2CFThree
CH2CH = CH2 CH2CH2S (O)2CH2CFThree
CH2CH = CH2 CH (Me) CH2SMe
CH2CH = CH2 CH (Me) CH2SEt
CH2CH = CH2 CH (Me) CH2SCFThree
CH2CH = CH2 CH (Me) CH2SCH2CFThree
CH2CH = CH2 CH (Me) CH2S (O) Me
CH2CH = CH2 CH (Me) CH2S (O) Et
CH2CH = CH2 CH (Me) CH2S (O) CFThree
CH2CH = CH2 CH (Me) CH2S (O) CH2CFThree
CH2CH = CH2 CH (Me) CH2S (O)2Me
CH2CH = CH2 CH (Me) CH2S (O)2Et
CH2CH = CH2 CH (Me) CH2S (O)2CFThree
CH2CH = CH2 CH (Me) CH2S (O)2CH2CFThree
CH2CH = CH2 CH (Et) CH2SMe
CH2CH = CH2 CH (Et) CH2SEt
CH2CH = CH2 CH (Et) CH2SCFThree
CH2CH = CH2 CH (Et) CH2SCH2CFThree
CH2CH = CH2 CH (Et) CH2S (O) Me
CH2CH = CH2 CH (Et) CH2S (O) Et
CH2CH = CH2 CH (Et) CH2S (O) CFThree
CH2CH = CH2 CH (Et) CH2S (O) CH2CFThree
CH2CH = CH2 CH (Et) CH2S (O)2Me
CH2CH = CH2 CH (Et) CH2S (O)2Et
CH2CH = CH2 CH (Et) CH2S (O)2CFThree
CH2CH = CH2 CH (Et) CH2S (O)2CH2CFThree
CH2CH = CH2 C (Me)2CH2SMe
CH2CH = CH2 C (Me)2CH2SEt
CH2CH = CH2 C (Me)2CH2SCFThree
CH2CH = CH2 C (Me)2CH2SCH2CFThree
CH2CH = CH2 C (Me)2CH2S (O) Me
CH2CH = CH2 C (Me)2CH2S (O) Et
CH2CH = CH2 C (Me)2CH2S (O) CFThree
CH2CH = CH2 C (Me)2CH2S (O) CH2CFThree
CH2CH = CH2 C (Me)2CH2S (O)2Me
CH2CH = CH2 C (Me)2CH2S (O)2Et
CH2CH = CH2 C (Me)2CH2S (O)2CFThree
CH2CH = CH2 C (Me)2CH2S (O)2CH2CFThree
CH2CH = CH2 CH2CH (Me) SMe
CH2CH = CH2 CH2CH (Me) SEt
CH2CH = CH2 CH2CH (Me) SCFThree
CH2CH = CH2 CH2CH (Me) SCH2CFThree
CH2CH = CH2 CH2CH (Me) S (O) Me
CH2CH = CH2 CH2CH (Me) S (O) Et
CH2CH = CH2 CH2CH (Me) S (O) CFThree
CH2CH = CH2 CH2CH (Me) S (O) CH2CFThree
CH2CH = CH2 CH2CH (Me) S (O)2Me
CH2CH = CH2 CH2CH (Me) S (O)2Et
CH2CH = CH2 CH2CH (Me) S (O)2CFThree
CH2CH = CH2 CH2CH (Me) S (O)2CH2CFThree
CH2CH = CH2 CH2CH (Et) SMe
CH2CH = CH2 CH2CH (Et) SEt
CH2CH = CH2 CH2CH (Et) SCFThree
CH2CH = CH2 CH2CH (Et) SCH2CFThree
CH2CH = CH2 CH2CH (Et) S (O) Me
CH2CH = CH2 CH2CH (Et) S (O) Et
CH2CH = CH2 CH2CH (Et) S (O) CFThree
CH2CH = CH2 CH2CH (Et) S (O) CH2CFThree
CH2CH = CH2 CH2CH (Et) S (O)2Me
CH2CH = CH2 CH2CH (Et) S (O)2Et
CH2CH = CH2 CH2CH (Et) S (O)2CFThree
CH2CH = CH2 CH2CH (Et) S (O)2CH2CFThree
CH2CH = CH2 CH (Me) CH (Me) SMe
CH2CH = CH2 CH (Me) CH (Me) SEt
CH2CH = CH2 CH (Me) CH (Me) SCFThree
CH2CH = CH2 CH (Me) CH (Me) SCH2CFThree
CH2CH = CH2 CH (Me) CH (Me) S (O) Me
CH2CH = CH2 CH (Me) CH (Me) S (O) Et
CH2CH = CH2 CH (Me) CH (Me) S (O) CFThree
CH2CH = CH2 CH (Me) CH (Me) S (O) CH2CFThree
CH2CH = CH2 CH (Me) CH (Me) S (O)2Me
CH2CH = CH2 CH (Me) CH (Me) S (O)2Et
CH2CH = CH2 CH (Me) CH (Me) S (O)2CFThree
CH2CH = CH2 CH (Me) CH (Me) S (O)2CH2CFThree
CH2CH (OMe)2 CH2SMe
CH2CH (OMe)2 CH2SEt
CH2CH (OMe)2 CH2SCFThree
CH2CH (OMe)2 CH2SCH2CFThree
CH2CH (OMe)2 CH2S (O) Me
CH2CH (OMe)2 CH2S (O) Et
CH2CH (OMe)2 CH2S (O) CFThree
CH2CH (OMe)2 CH2S (O) CH2CFThree
CH2CH (OMe)2 CH2S (O)2Me
CH2CH (OMe)2 CH2S (O)2Et
CH2CH (OMe)2 CH2S (O)2CFThree
CH2CH (OMe)2 CH2S (O)2CH2CFThree
CH2CH (OMe)2 CH (Me) SMe
CH2CH (OMe)2 CH (Me) SEt
CH2CH (OMe)2 CH (Me) SCFThree
CH2CH (OMe)2 CH (Me) SCH2CFThree
CH2CH (OMe)2 CH (Me) S (O) Me
CH2CH (OMe)2 CH (Me) S (O) Et
CH2CH (OMe)2 CH (Me) S (O) CFThree
CH2CH (OMe)2 CH (Me) S (O) CH2CFThree
CH2CH (OMe)2 CH (Me) S (O)2Me
CH2CH (OMe)2 CH (Me) S (O)2Et
CH2CH (OMe)2 CH (Me) S (O)2CFThree
CH2CH (OMe)2 CH (Me) S (O)2CH2CFThree
CH2CH (OMe)2 CH (Et) SMe
CH2CH (OMe)2 CH (Et) SEt
CH2CH (OMe)2 CH (Et) SCFThree
CH2CH (OMe)2 CH (Et) SCH2CFThree
CH2CH (OMe)2 CH (Et) S (O) Me
CH2CH (OMe)2 CH (Et) S (O) Et
CH2CH (OMe)2 CH (Et) S (O) CFThree
CH2CH (OMe)2 CH (Et) S (O) CH2CFThree
CH2CH (OMe)2 CH (Et) S (O)2Me
CH2CH (OMe)2 CH (Et) S (O)2Et
CH2CH (OMe)2 CH (Et) S (O)2CFThree
CH2CH (OMe)2 CH (Et) S (O)2CH2CFThree
CH2CH (OMe)2 CH (n-Pr) SMe
CH2CH (OMe)2 CH (n-Pr) SEt
CH2CH (OMe)2 CH (n-Pr) SCFThree
CH2CH (OMe)2 CH (n-Pr) SCH2CFThree
CH2CH (OMe)2 CH (n-Pr) S (O) Me
CH2CH (OMe)2 CH (n-Pr) S (O) Et
CH2CH (OMe)2 CH (n-Pr) S (O) CFThree
CH2CH (OMe)2 CH (n-Pr) S (O) CH2CFThree
CH2CH (OMe)2 CH (n-Pr) S (O)2Me
CH2CH (OMe)2 CH (n-Pr) S (O)2Et
CH2CH (OMe)2 CH (n-Pr) S (O)2CFThree
CH2CH (OMe)2 CH (n-Pr) S (O)2CH2CFThree
CH2CH (OMe)2 CH (i-Pr) SMe
CH2CH (OMe)2 CH (i-Pr) SEt
CH2CH (OMe)2 CH (i-Pr) SCFThree
CH2CH (OMe)2 CH (i-Pr) SCH2CFThree
CH2CH (OMe)2 CH (i-Pr) S (O) Me
CH2CH (OMe)2 CH (i-Pr) S (O) Et
CH2CH (OMe)2 CH (i-Pr) S (O) CFThree
CH2CH (OMe)2 CH (i-Pr) S (O) CH2CFThree
CH2CH (OMe)2 CH (i-Pr) S (O)2Me
CH2CH (OMe)2 CH (i-Pr) S (O)2Et
CH2CH (OMe)2 CH (i-Pr) S (O)2CFThree
CH2CH (OMe)2 CH (i-Pr) S (O)2CH2CFThree
CH2CH (OMe)2 CH (n-Bu) SMe
CH2CH (OMe)2 CH (n-Bu) SEt
CH2CH (OMe)2 CH (n-Bu) SCFThree
CH2CH (OMe)2 CH (n-Bu) SCH2CFThree
CH2CH (OMe)2 CH (n-Bu) S (O) Me
CH2CH (OMe)2 CH (n-Bu) S (O) Et
CH2CH (OMe)2 CH (n-Bu) S (O) CFThree
CH2CH (OMe)2 CH (n-Bu) S (O) CH2CFThree
CH2CH (OMe)2 CH (n-Bu) S (O)2Me
CH2CH (OMe)2 CH (n-Bu) S (O)2Et
CH2CH (OMe)2 CH (n-Bu) S (O)2CFThree
CH2CH (OMe)2 CH (n-Bu) S (O)2CH2CFThree
CH2CH (OMe)2 CH (i-Bu) SMe
CH2CH (OMe)2 CH (i-Bu) SEt
CH2CH (OMe)2 CH (i-Bu) SCFThree
CH2CH (OMe)2 CH (i-Bu) SCH2CFThree
CH2CH (OMe)2 CH (i-Bu) S (O) Me
CH2CH (OMe)2 CH (i-Bu) S (O) Et
CH2CH (OMe)2 CH (i-Bu) S (O) CFThree
CH2CH (OMe)2 CH (i-Bu) S (O) CH2CFThree
CH2CH (OMe)2 CH (i-Bu) S (O)2Me
CH2CH (OMe)2 CH (i-Bu) S (O)2Et
CH2CH (OMe)2 CH (i-Bu) S (O)2CFThree
CH2CH (OMe)2 CH (i-Bu) S (O)2CH2CFThree
CH2CH (OMe)2 CH (s-Bu) SMe
CH2CH (OMe)2 CH (s-Bu) SEt
CH2CH (OMe)2 CH (s-Bu) SCFThree
CH2CH (OMe)2 CH (s-Bu) SCH2CFThree
CH2CH (OMe)2 CH (s-Bu) S (O) Me
CH2CH (OMe)2 CH (s-Bu) S (O) Et
CH2CH (OMe)2 CH (s-Bu) S (O) CFThree
CH2CH (OMe)2 CH (s-Bu) S (O) CH2CFThree
CH2CH (OMe)2 CH (s-Bu) S (O)2Me
CH2CH (OMe)2 CH (s-Bu) S (O)2Et
CH2CH (OMe)2 CH (s-Bu) S (O)2CFThree
CH2CH (OMe)2 CH (s-Bu) S (O)2CH2CFThree
CH2CH (OMe)2 CH (t-Bu) SMe
CH2CH (OMe)2 CH (t-Bu) SEt
CH2CH (OMe)2 CH (t-Bu) SCFThree
CH2CH (OMe)2 CH (t-Bu) SCH2CFThree
CH2CH (OMe)2 CH (t-Bu) S (O) Me
CH2CH (OMe)2 CH (t-Bu) S (O) Et
CH2CH (OMe)2 CH (t-Bu) S (O) CFThree
CH2CH (OMe)2 CH (t-Bu) S (O) CH2CFThree
CH2CH (OMe)2 CH (t-Bu) S (O)2Me
CH2CH (OMe)2 CH (t-Bu) S (O)2Et
CH2CH (OMe)2 CH (t-Bu) S (O)2CFThree
CH2CH (OMe)2 CH (t-Bu) S (O)2CH2CFThree
CH2CH (OMe)2 CH (CFThreeSMe
CH2CH (OMe)2 CH (CFThree) SEt
CH2CH (OMe)2 CH (CFThree) SCFThree
CH2CH (OMe)2 CH (CFThree) SCH2CFThree
CH2CH (OMe)2 CH (CFThree) S (O) Me
CH2CH (OMe)2 CH (CFThree) S (O) Et
CH2CH (OMe)2 CH (CFThree) S (O) CFThree
CH2CH (OMe)2 CH (CFThree) S (O) CH2CFThree
CH2CH (OMe)2 CH (CFThree) S (O)2Me
CH2CH (OMe)2 CH (CFThree) S (O)2Et
CH2CH (OMe)2 CH (CFThree) S (O)2CFThree
CH2CH (OMe)2 CH (CFThree) S (O)2CH2CFThree
CH2CH (OMe)2 CH2CH2SMe
CH2CH (OMe)2 CH2CH2SEt
CH2CH (OMe)2 CH2CH2SCFThree
CH2CH (OMe)2 CH2CH2SCH2CFThree
CH2CH (OMe)2 CH2CH2S (O) Me
CH2CH (OMe)2 CH2CH2S (O) Et
CH2CH (OMe)2 CH2CH2S (O) CFThree
CH2CH (OMe)2 CH2CH2S (O) CH2CFThree
CH2CH (OMe)2 CH2CH2S (O)2Me
CH2CH (OMe)2 CH2CH2S (O)2Et
CH2CH (OMe)2 CH2CH2S (O)2CFThree
CH2CH (OMe)2 CH2CH2S (O)2CH2CFThree
CH2CH (OMe)2 CH (Me) CH2SMe
CH2CH (OMe)2 CH (Me) CH2SEt
CH2CH (OMe)2 CH (Me) CH2SCFThree
CH2CH (OMe)2 CH (Me) CH2SCH2CFThree
CH2CH (OMe)2 CH (Me) CH2S (O) Me
CH2CH (OMe)2 CH (Me) CH2S (O) Et
CH2CH (OMe)2 CH (Me) CH2S (O) CFThree
CH2CH (OMe)2 CH (Me) CH2S (O) CH2CFThree
CH2CH (OMe)2 CH (Me) CH2S (O)2Me
CH2CH (OMe)2 CH (Me) CH2S (O)2Et
CH2CH (OMe)2 CH (Me) CH2S (O)2CFThree
CH2CH (OMe)2 CH (Me) CH2S (O)2CH2CFThree
CH2CH (OMe)2 CH (Et) CH2SMe
CH2CH (OMe)2 CH (Et) CH2SEt
CH2CH (OMe)2 CH (Et) CH2SCFThree
CH2CH (OMe)2 CH (Et) CH2SCH2CFThree
CH2CH (OMe)2 CH (Et) CH2S (O) Me
CH2CH (OMe)2 CH (Et) CH2S (O) Et
CH2CH (OMe)2 CH (Et) CH2S (O) CFThree
CH2CH (OMe)2 CH (Et) CH2S (O) CH2CFThree
CH2CH (OMe)2 CH (Et) CH2S (O)2Me
CH2CH (OMe)2 CH (Et) CH2S (O)2Et
CH2CH (OMe)2 CH (Et) CH2S (O)2CFThree
CH2CH (OMe)2 CH (Et) CH2S (O)2CH2CFThree
CH2CH (OMe)2 C (Me)2CH2SMe
CH2CH (OMe)2 C (Me)2CH2SEt
CH2CH (OMe)2 C (Me)2CH2SCFThree
CH2CH (OMe)2 C (Me)2CH2SCH2CFThree
CH2CH (OMe)2 C (Me)2CH2S (O) Me
CH2CH (OMe)2 C (Me)2CH2S (O) Et
CH2CH (OMe)2 C (Me)2CH2S (O) CFThree
CH2CH (OMe)2 C (Me)2CH2S (O) CH2CFThree
CH2CH (OMe)2 C (Me)2CH2S (O)2Me
CH2CH (OMe)2 C (Me)2CH2S (O)2Et
CH2CH (OMe)2 C (Me)2CH2S (O)2CFThree
CH2CH (OMe)2 C (Me)2CH2S (O)2CH2CFThree
CH2CH (OMe)2 CH2CH (Me) SMe
CH2CH (OMe)2 CH2CH (Me) SEt
CH2CH (OMe)2 CH2CH (Me) SCFThree
CH2CH (OMe)2 CH2CH (Me) SCH2CFThree
CH2CH (OMe)2 CH2CH (Me) S (O) Me
CH2CH (OMe)2 CH2CH (Me) S (O) Et
CH2CH (OMe)2 CH2CH (Me) S (O) CFThree
CH2CH (OMe)2 CH2CH (Me) S (O) CH2CFThree
CH2CH (OMe)2 CH2CH (Me) S (O)2Me
CH2CH (OMe)2 CH2CH (Me) S (O)2Et
CH2CH (OMe)2 CH2CH (Me) S (O)2CFThree
CH2CH (OMe)2 CH2CH (Me) S (O)2CH2CFThree
CH2CH (OMe)2 CH2CH (Et) SMe
CH2CH (OMe)2 CH2CH (Et) SEt
CH2CH (OMe)2 CH2CH (Et) SCFThree
CH2CH (OMe)2 CH2CH (Et) SCH2CFThree
CH2CH (OMe)2 CH2CH (Et) S (O) Me
CH2CH (OMe)2 CH2CH (Et) S (O) Et
CH2CH (OMe)2 CH2CH (Et) S (O) CFThree
CH2CH (OMe)2 CH2CH (Et) S (O) CH2CFThree
CH2CH (OMe)2 CH2CH (Et) S (O)2Me
CH2CH (OMe)2 CH2CH (Et) S (O)2Et
CH2CH (OMe)2 CH2CH (Et) S (O)2CFThree
CH2CH (OMe)2 CH2CH (Et) S (O)2CH2CFThree
CH2CH (OMe)2 CH (Me) CH (Me) SMe
CH2CH (OMe)2 CH (Me) CH (Me) SEt
CH2CH (OMe)2 CH (Me) CH (Me) SCFThree
CH2CH (OMe)2 CH (Me) CH (Me) SCH2CFThree
CH2CH (OMe)2 CH (Me) CH (Me) S (O) Me
CH2CH (OMe)2 CH (Me) CH (Me) S (O) Et
CH2CH (OMe)2 CH (Me) CH (Me) S (O) CFThree
CH2CH (OMe)2 CH (Me) CH (Me) S (O) CH2CFThree
CH2CH (OMe)2 CH (Me) CH (Me) S (O)2Me
CH2CH (OMe)2 CH (Me) CH (Me) S (O)2Et
CH2CH (OMe)2 CH (Me) CH (Me) S (O)2CFThree
CH2CH (OMe)2 CH (Me) CH (Me) S (O)2CH2CFThree
CH (Me) OEt CH2SMe
CH (Me) OEt CH2SEt
CH (Me) OEt CH2SCFThree
CH (Me) OEt CH2SCH2CFThree
CH (Me) OEt CH2S (O) Me
CH (Me) OEt CH2S (O) Et
CH (Me) OEt CH2S (O) CFThree
CH (Me) OEt CH2S (O) CH2CFThree
CH (Me) OEt CH2S (O)2Me
CH (Me) OEt CH2S (O)2Et
CH (Me) OEt CH2S (O)2CFThree
CH (Me) OEt CH2S (O)2CH2CFThree
CH (Me) OEt CH (Me) SMe
CH (Me) OEt CH (Me) SEt
CH (Me) OEt CH (Me) SCFThree
CH (Me) OEt CH (Me) SCH2CFThree
CH (Me) OEt CH (Me) S (O) Me
CH (Me) OEt CH (Me) S (O) Et
CH (Me) OEt CH (Me) S (O) CFThree
CH (Me) OEt CH (Me) S (O) CH2CFThree
CH (Me) OEt CH (Me) S (O)2Me
CH (Me) OEt CH (Me) S (O)2Et
CH (Me) OEt CH (Me) S (O)2CFThree
CH (Me) OEt CH (Me) S (O)2CH2CFThree
CH (Me) OEt CH (Et) SMe
CH (Me) OEt CH (Et) SEt
CH (Me) OEt CH (Et) SCFThree
CH (Me) OEt CH (Et) SCH2CFThree
CH (Me) OEt CH (Et) S (O) Me
CH (Me) OEt CH (Et) S (O) Et
CH (Me) OEt CH (Et) S (O) CFThree
CH (Me) OEt CH (Et) S (O) CH2CFThree
CH (Me) OEt CH (Et) S (O)2Me
CH (Me) OEt CH (Et) S (O)2Et
CH (Me) OEt CH (Et) S (O)2CFThree
CH (Me) OEt CH (Et) S (O)2CH2CFThree
CH (Me) OEt CH (n-Pr) SMe
CH (Me) OEt CH (n-Pr) SEt
CH (Me) OEt CH (n-Pr) SCFThree
CH (Me) OEt CH (n-Pr) SCH2CFThree
CH (Me) OEt CH (n-Pr) S (O) Me
CH (Me) OEt CH (n-Pr) S (O) Et
CH (Me) OEt CH (n-Pr) S (O) CFThree
CH (Me) OEt CH (n-Pr) S (O) CH2CFThree
CH (Me) OEt CH (n-Pr) S (O)2Me
CH (Me) OEt CH (n-Pr) S (O)2Et
CH (Me) OEt CH (n-Pr) S (O)2CFThree
CH (Me) OEt CH (n-Pr) S (O)2CH2CFThree
CH (Me) OEt CH (i-Pr) SMe
CH (Me) OEt CH (i-Pr) SEt
CH (Me) OEt CH (i-Pr) SCFThree
CH (Me) OEt CH (i-Pr) SCH2CFThree
CH (Me) OEt CH (i-Pr) S (O) Me
CH (Me) OEt CH (i-Pr) S (O) Et
CH (Me) OEt CH (i-Pr) S (O) CFThree
CH (Me) OEt CH (i-Pr) S (O) CH2CFThree
CH (Me) OEt CH (i-Pr) S (O)2Me
CH (Me) OEt CH (i-Pr) S (O)2Et
CH (Me) OEt CH (i-Pr) S (O)2CFThree
CH (Me) OEt CH (i-Pr) S (O)2CH2CFThree
CH (Me) OEt CH (n-Bu) SMe
CH (Me) OEt CH (n-Bu) SEt
CH (Me) OEt CH (n-Bu) SCFThree
CH (Me) OEt CH (n-Bu) SCH2CFThree
CH (Me) OEt CH (n-Bu) S (O) Me
CH (Me) OEt CH (n-Bu) S (O) Et
CH (Me) OEt CH (n-Bu) S (O) CFThree
CH (Me) OEt CH (n-Bu) S (O) CH2CFThree
CH (Me) OEt CH (n-Bu) S (O)2Me
CH (Me) OEt CH (n-Bu) S (O)2Et
CH (Me) OEt CH (n-Bu) S (O)2CFThree
CH (Me) OEt CH (n-Bu) S (O)2CH2CFThree
CH (Me) OEt CH (i-Bu) SMe
CH (Me) OEt CH (i-Bu) SEt
CH (Me) OEt CH (i-Bu) SCFThree
CH (Me) OEt CH (i-Bu) SCH2CFThree
CH (Me) OEt CH (i-Bu) S (O) Me
CH (Me) OEt CH (i-Bu) S (O) Et
CH (Me) OEt CH (i-Bu) S (O) CFThree
CH (Me) OEt CH (i-Bu) S (O) CH2CFThree
CH (Me) OEt CH (i-Bu) S (O)2Me
CH (Me) OEt CH (i-Bu) S (O)2Et
CH (Me) OEt CH (i-Bu) S (O)2CFThree
CH (Me) OEt CH (i-Bu) S (O)2CH2CFThree
CH (Me) OEt CH (s-Bu) SMe
CH (Me) OEt CH (s-Bu) SEt
CH (Me) OEt CH (s-Bu) SCFThree
CH (Me) OEt CH (s-Bu) SCH2CFThree
CH (Me) OEt CH (s-Bu) S (O) Me
CH (Me) OEt CH (s-Bu) S (O) Et
CH (Me) OEt CH (s-Bu) S (O) CFThree
CH (Me) OEt CH (s-Bu) S (O) CH2CFThree
CH (Me) OEt CH (s-Bu) S (O)2Me
CH (Me) OEt CH (s-Bu) S (O)2Et
CH (Me) OEt CH (s-Bu) S (O)2CFThree
CH (Me) OEt CH (s-Bu) S (O)2CH2CFThree
CH (Me) OEt CH (t-Bu) SMe
CH (Me) OEt CH (t-Bu) SEt
CH (Me) OEt CH (t-Bu) SCFThree
CH (Me) OEt CH (t-Bu) SCH2CFThree
CH (Me) OEt CH (t-Bu) S (O) Me
CH (Me) OEt CH (t-Bu) S (O) Et
CH (Me) OEt CH (t-Bu) S (O) CFThree
CH (Me) OEt CH (t-Bu) S (O) CH2CFThree
CH (Me) OEt CH (t-Bu) S (O)2Me
CH (Me) OEt CH (t-Bu) S (O)2Et
CH (Me) OEt CH (t-Bu) S (O)2CFThree
CH (Me) OEt CH (t-Bu) S (O)2CH2CFThree
CH (Me) OEt CH (CFThreeSMe
CH (Me) OEt CH (CFThree) SEt
CH (Me) OEt CH (CFThree) SCFThree
CH (Me) OEt CH (CFThree) SCH2CFThree
CH (Me) OEt CH (CFThree) S (O) Me
CH (Me) OEt CH (CFThree) S (O) Et
CH (Me) OEt CH (CFThree) S (O) CFThree
CH (Me) OEt CH (CFThree) S (O) CH2CFThree
CH (Me) OEt CH (CFThree) S (O)2Me
CH (Me) OEt CH (CFThree) S (O)2Et
CH (Me) OEt CH (CFThree) S (O)2CFThree
CH (Me) OEt CH (CFThree) S (O)2CH2CFThree
CH (Me) OEt CH2CH2SMe
CH (Me) OEt CH2CH2SEt
CH (Me) OEt CH2CH2SCFThree
CH (Me) OEt CH2CH2SCH2CFThree
CH (Me) OEt CH2CH2S (O) Me
CH (Me) OEt CH2CH2S (O) Et
CH (Me) OEt CH2CH2S (O) CFThree
CH (Me) OEt CH2CH2S (O) CH2CFThree
CH (Me) OEt CH2CH2S (O)2Me
CH (Me) OEt CH2CH2S (O)2Et
CH (Me) OEt CH2CH2S (O)2CFThree
CH (Me) OEt CH2CH2S (O)2CH2CFThree
CH (Me) OEt CH (Me) CH2SMe
CH (Me) OEt CH (Me) CH2SEt
CH (Me) OEt CH (Me) CH2SCFThree
CH (Me) OEt CH (Me) CH2SCH2CFThree
CH (Me) OEt CH (Me) CH2S (O) Me
CH (Me) OEt CH (Me) CH2S (O) Et
CH (Me) OEt CH (Me) CH2S (O) CFThree
CH (Me) OEt CH (Me) CH2S (O) CH2CFThree
CH (Me) OEt CH (Me) CH2S (O)2Me
CH (Me) OEt CH (Me) CH2S (O)2Et
CH (Me) OEt CH (Me) CH2S (O)2CFThree
CH (Me) OEt CH (Me) CH2S (O)2CH2CFThree
CH (Me) OEt CH (Et) CH2SMe
CH (Me) OEt CH (Et) CH2SEt
CH (Me) OEt CH (Et) CH2SCFThree
CH (Me) OEt CH (Et) CH2SCH2CFThree
CH (Me) OEt CH (Et) CH2S (O) Me
CH (Me) OEt CH (Et) CH2S (O) Et
CH (Me) OEt CH (Et) CH2S (O) CFThree
CH (Me) OEt CH (Et) CH2S (O) CH2CFThree
CH (Me) OEt CH (Et) CH2S (O)2Me
CH (Me) OEt CH (Et) CH2S (O)2Et
CH (Me) OEt CH (Et) CH2S (O)2CFThree
CH (Me) OEt CH (Et) CH2S (O)2CH2CFThree
CH (Me) OEt C (Me)2CH2SMe
CH (Me) OEt C (Me)2CH2SEt
CH (Me) OEt C (Me)2CH2SCFThree
CH (Me) OEt C (Me)2CH2SCH2CFThree
CH (Me) OEt C (Me)2CH2S (O) Me
CH (Me) OEt C (Me)2CH2S (O) Et
CH (Me) OEt C (Me)2CH2S (O) CFThree
CH (Me) OEt C (Me)2CH2S (O) CH2CFThree
CH (Me) OEt C (Me)2CH2S (O)2Me
CH (Me) OEt C (Me)2CH2S (O)2Et
CH (Me) OEt C (Me)2CH2S (O)2CFThree
CH (Me) OEt C (Me)2CH2S (O)2CH2CFThree
CH (Me) OEt CH2CH (Me) SMe
CH (Me) OEt CH2CH (Me) SEt
CH (Me) OEt CH2CH (Me) SCFThree
CH (Me) OEt CH2CH (Me) SCH2CFThree
CH (Me) OEt CH2CH (Me) S (O) Me
CH (Me) OEt CH2CH (Me) S (O) Et
CH (Me) OEt CH2CH (Me) S (O) CFThree
CH (Me) OEt CH2CH (Me) S (O) CH2CFThree
CH (Me) OEt CH2CH (Me) S (O)2Me
CH (Me) OEt CH2CH (Me) S (O)2Et
CH (Me) OEt CH2CH (Me) S (O)2CFThree
CH (Me) OEt CH2CH (Me) S (O)2CH2CFThree
CH (Me) OEt CH2CH (Et) SMe
CH (Me) OEt CH2CH (Et) SEt
CH (Me) OEt CH2CH (Et) SCFThree
CH (Me) OEt CH2CH (Et) SCH2CFThree
CH (Me) OEt CH2CH (Et) S (O) Me
CH (Me) OEt CH2CH (Et) S (O) Et
CH (Me) OEt CH2CH (Et) S (O) CFThree
CH (Me) OEt CH2CH (Et) S (O) CH2CFThree
CH (Me) OEt CH2CH (Et) S (O)2Me
CH (Me) OEt CH2CH (Et) S (O)2Et
CH (Me) OEt CH2CH (Et) S (O)2CFThree
CH (Me) OEt CH2CH (Et) S (O)2CH2CFThree
CH (Me) OEt CH (Me) CH (Me) SMe
CH (Me) OEt CH (Me) CH (Me) SEt
CH (Me) OEt CH (Me) CH (Me) SCFThree
CH (Me) OEt CH (Me) CH (Me) SCH2CFThree
CH (Me) OEt CH (Me) CH (Me) S (O) Me
CH (Me) OEt CH (Me) CH (Me) S (O) Et
CH (Me) OEt CH (Me) CH (Me) S (O) CFThree
CH (Me) OEt CH (Me) CH (Me) S (O) CH2CFThree
CH (Me) OEt CH (Me) CH (Me) S (O)2Me
CH (Me) OEt CH (Me) CH (Me) S (O)2Et
CH (Me) OEt CH (Me) CH (Me) S (O)2CFThree
CH (Me) OEt CH (Me) CH (Me) S (O)2CH2CFThree
S (O)2Me CH2SMe
S (O)2Me CH2SEt
S (O)2Me CH2SCFThree
S (O)2Me CH2SCH2CFThree
S (O)2Me CH2S (O) Me
S (O)2Me CH2S (O) Et
S (O)2Me CH2S (O) CFThree
S (O)2Me CH2S (O) CH2CFThree
S (O)2Me CH2S (O)2Me
S (O)2Me CH2S (O)2Et
S (O)2Me CH2S (O)2CFThree
S (O)2Me CH2S (O)2CH2CFThree
S (O)2Me CH (Me) SMe
S (O)2Me CH (Me) SEt
S (O)2Me CH (Me) SCFThree
S (O)2Me CH (Me) SCH2CFThree
S (O)2Me CH (Me) S (O) Me
S (O)2Me CH (Me) S (O) Et
S (O)2Me CH (Me) S (O) CFThree
S (O)2Me CH (Me) S (O) CH2CFThree
S (O)2Me CH (Me) S (O)2Me
S (O)2Me CH (Me) S (O)2Et
S (O)2Me CH (Me) S (O)2CFThree
S (O)2Me CH (Me) S (O)2CH2CFThree
S (O)2Me CH (Et) SMe
S (O)2Me CH (Et) SEt
S (O)2Me CH (Et) SCFThree
S (O)2Me CH (Et) SCH2CFThree
S (O)2Me CH (Et) S (O) Me
S (O)2Me CH (Et) S (O) Et
S (O)2Me CH (Et) S (O) CFThree
S (O)2Me CH (Et) S (O) CH2CFThree
S (O)2Me CH (Et) S (O)2Me
S (O)2Me CH (Et) S (O)2Et
S (O)2Me CH (Et) S (O)2CFThree
S (O)2Me CH (Et) S (O)2CH2CFThree
S (O)2Me CH (n-Pr) SMe
S (O)2Me CH (n-Pr) SEt
S (O)2Me CH (n-Pr) SCFThree
S (O)2Me CH (n-Pr) SCH2CFThree
S (O)2Me CH (n-Pr) S (O) Me
S (O)2Me CH (n-Pr) S (O) Et
S (O)2Me CH (n-Pr) S (O) CFThree
S (O)2Me CH (n-Pr) S (O) CH2CFThree
S (O)2Me CH (n-Pr) S (O)2Me
S (O)2Me CH (n-Pr) S (O)2Et
S (O)2Me CH (n-Pr) S (O)2CFThree
S (O)2Me CH (n-Pr) S (O)2CH2CFThree
S (O)2Me CH (i-Pr) SMe
S (O)2Me CH (i-Pr) SEt
S (O)2Me CH (i-Pr) SCFThree
S (O)2Me CH (i-Pr) SCH2CFThree
S (O)2Me CH (i-Pr) S (O) Me
S (O)2Me CH (i-Pr) S (O) Et
S (O)2Me CH (i-Pr) S (O) CFThree
S (O)2Me CH (i-Pr) S (O) CH2CFThree
S (O)2Me CH (i-Pr) S (O)2Me
S (O)2Me CH (i-Pr) S (O)2Et
S (O)2Me CH (i-Pr) S (O)2CFThree
S (O)2Me CH (i-Pr) S (O)2CH2CFThree
S (O)2Me CH (n-Bu) SMe
S (O)2Me CH (n-Bu) SEt
S (O)2Me CH (n-Bu) SCFThree
S (O)2Me CH (n-Bu) SCH2CFThree
S (O)2Me CH (n-Bu) S (O) Me
S (O)2Me CH (n-Bu) S (O) Et
S (O)2Me CH (n-Bu) S (O) CFThree
S (O)2Me CH (n-Bu) S (O) CH2CFThree
S (O)2Me CH (n-Bu) S (O)2Me
S (O)2Me CH (n-Bu) S (O)2Et
S (O)2Me CH (n-Bu) S (O)2CFThree
S (O)2Me CH (n-Bu) S (O)2CH2CFThree
S (O)2Me CH (i-Bu) SMe
S (O)2Me CH (i-Bu) SEt
S (O)2Me CH (i-Bu) SCFThree
S (O)2Me CH (i-Bu) SCH2CFThree
S (O)2Me CH (i-Bu) S (O) Me
S (O)2Me CH (i-Bu) S (O) Et
S (O)2Me CH (i-Bu) S (O) CFThree
S (O)2Me CH (i-Bu) S (O) CH2CFThree
S (O)2Me CH (i-Bu) S (O)2Me
S (O)2Me CH (i-Bu) S (O)2Et
S (O)2Me CH (i-Bu) S (O)2CFThree
S (O)2Me CH (i-Bu) S (O)2CH2CFThree
S (O)2Me CH (s-Bu) SMe
S (O)2Me CH (s-Bu) SEt
S (O)2Me CH (s-Bu) SCFThree
S (O)2Me CH (s-Bu) SCH2CFThree
S (O)2Me CH (s-Bu) S (O) Me
S (O)2Me CH (s-Bu) S (O) Et
S (O)2Me CH (s-Bu) S (O) CFThree
S (O)2Me CH (s-Bu) S (O) CH2CFThree
S (O)2Me CH (s-Bu) S (O)2Me
S (O)2Me CH (s-Bu) S (O)2Et
S (O)2Me CH (s-Bu) S (O)2CFThree
S (O)2Me CH (s-Bu) S (O)2CH2CFThree
S (O)2Me CH (t-Bu) SMe
S (O)2Me CH (t-Bu) SEt
S (O)2Me CH (t-Bu) SCFThree
S (O)2Me CH (t-Bu) SCH2CFThree
S (O)2Me CH (t-Bu) S (O) Me
S (O)2Me CH (t-Bu) S (O) Et
S (O)2Me CH (t-Bu) S (O) CFThree
S (O)2Me CH (t-Bu) S (O) CH2CFThree
S (O)2Me CH (t-Bu) S (O)2Me
S (O)2Me CH (t-Bu) S (O)2Et
S (O)2Me CH (t-Bu) S (O)2CFThree
S (O)2Me CH (t-Bu) S (O)2CH2CFThree
S (O)2Me CH (CFThreeSMe
S (O)2Me CH (CFThree) SEt
S (O)2Me CH (CFThree) SCFThree
S (O)2Me CH (CFThree) SCH2CFThree
S (O)2Me CH (CFThree) S (O) Me
S (O)2Me CH (CFThree) S (O) Et
S (O)2Me CH (CFThree) S (O) CFThree
S (O)2Me CH (CFThree) S (O) CH2CFThree
S (O)2Me CH (CFThree) S (O)2Me
S (O)2Me CH (CFThree) S (O)2Et
S (O)2Me CH (CFThree) S (O)2CFThree
S (O)2Me CH (CFThree) S (O)2CH2CFThree
S (O)2Me CH2CH2SMe
S (O)2Me CH2CH2SEt
S (O)2Me CH2CH2SCFThree
S (O)2Me CH2CH2SCH2CFThree
S (O)2Me CH2CH2S (O) Me
S (O)2Me CH2CH2S (O) Et
S (O)2Me CH2CH2S (O) CFThree
S (O)2Me CH2CH2S (O) CH2CFThree
S (O)2Me CH2CH2S (O)2Me
S (O)2Me CH2CH2S (O)2Et
S (O)2Me CH2CH2S (O)2CFThree
S (O)2Me CH2CH2S (O)2CH2CFThree
S (O)2Me CH (Me) CH2SMe
S (O)2Me CH (Me) CH2SEt
S (O)2Me CH (Me) CH2SCFThree
S (O)2Me CH (Me) CH2SCH2CFThree
S (O)2Me CH (Me) CH2S (O) Me
S (O)2Me CH (Me) CH2S (O) Et
S (O)2Me CH (Me) CH2S (O) CFThree
S (O)2Me CH (Me) CH2S (O) CH2CFThree
S (O)2Me CH (Me) CH2S (O)2Me
S (O)2Me CH (Me) CH2S (O)2Et
S (O)2Me CH (Me) CH2S (O)2CFThree
S (O)2Me CH (Me) CH2S (O)2CH2CFThree
S (O)2Me CH (Et) CH2SMe
S (O)2Me CH (Et) CH2SEt
S (O)2Me CH (Et) CH2SCFThree
S (O)2Me CH (Et) CH2SCH2CFThree
S (O)2Me CH (Et) CH2S (O) Me
S (O)2Me CH (Et) CH2S (O) Et
S (O)2Me CH (Et) CH2S (O) CFThree
S (O)2Me CH (Et) CH2S (O) CH2CFThree
S (O)2Me CH (Et) CH2S (O)2Me
S (O)2Me CH (Et) CH2S (O)2Et
S (O)2Me CH (Et) CH2S (O)2CFThree
S (O)2Me CH (Et) CH2S (O)2CH2CFThree
S (O)2Me C (Me)2CH2SMe
S (O)2Me C (Me)2CH2SEt
S (O)2Me C (Me)2CH2SCFThree
S (O)2Me C (Me)2CH2SCH2CFThree
S (O)2Me C (Me)2CH2S (O) Me
S (O)2Me C (Me)2CH2S (O) Et
S (O)2Me C (Me)2CH2S (O) CFThree
S (O)2Me C (Me)2CH2S (O) CH2CFThree
S (O)2Me C (Me)2CH2S (O)2Me
S (O)2Me C (Me)2CH2S (O)2Et
S (O)2Me C (Me)2CH2S (O)2CFThree
S (O)2Me C (Me)2CH2S (O)2CH2CFThree
S (O)2Me CH2CH (Me) SMe
S (O)2Me CH2CH (Me) SEt
S (O)2Me CH2CH (Me) SCFThree
S (O)2Me CH2CH (Me) SCH2CFThree
S (O)2Me CH2CH (Me) S (O) Me
S (O)2Me CH2CH (Me) S (O) Et
S (O)2Me CH2CH (Me) S (O) CFThree
S (O)2Me CH2CH (Me) S (O) CH2CFThree
S (O)2Me CH2CH (Me) S (O)2Me
S (O)2Me CH2CH (Me) S (O)2Et
S (O)2Me CH2CH (Me) S (O)2CFThree
S (O)2Me CH2CH (Me) S (O)2CH2CFThree
S (O)2Me CH2CH (Et) SMe
S (O)2Me CH2CH (Et) SEt
S (O)2Me CH2CH (Et) SCFThree
S (O)2Me CH2CH (Et) SCH2CFThree
S (O)2Me CH2CH (Et) S (O) Me
S (O)2Me CH2CH (Et) S (O) Et
S (O)2Me CH2CH (Et) S (O) CFThree
S (O)2Me CH2CH (Et) S (O) CH2CFThree
S (O)2Me CH2CH (Et) S (O)2Me
S (O)2Me CH2CH (Et) S (O)2Et
S (O)2Me CH2CH (Et) S (O)2CFThree
S (O)2Me CH2CH (Et) S (O)2CH2CFThree
S (O)2Me CH (Me) CH (Me) SMe
S (O)2Me CH (Me) CH (Me) SEt
S (O)2Me CH (Me) CH (Me) SCFThree
S (O)2Me CH (Me) CH (Me) SCH2CFThree
S (O)2Me CH (Me) CH (Me) S (O) Me
S (O)2Me CH (Me) CH (Me) S (O) Et
S (O)2Me CH (Me) CH (Me) S (O) CFThree
S (O)2Me CH (Me) CH (Me) S (O) CH2CFThree
S (O)2Me CH (Me) CH (Me) S (O)2Me
S (O)2Me CH (Me) CH (Me) S (O)2Et
S (O)2Me CH (Me) CH (Me) S (O)2CFThree
S (O)2Me CH (Me) CH (Me) S (O)2CH2CFThree
D2-32a CH2SMe
D2-32a CH2SEt
D2-32a CH2SCFThree
D2-32a CH2SCH2CFThree
D2-32a CH2S (O) Me
D2-32a CH2S (O) Et
D2-32a CH2S (O) CFThree
D2-32a CH2S (O) CH2CFThree
D2-32a CH2S (O)2Me
D2-32a CH2S (O)2Et
D2-32a CH2S (O)2CFThree
D2-32a CH2S (O)2CH2CFThree
D2-32a CH (Me) SMe
D2-32a CH (Me) SEt
D2-32a CH (Me) SCFThree
D2-32a CH (Me) SCH2CFThree
D2-32a CH (Me) S (O) Me
D2-32a CH (Me) S (O) Et
D2-32a CH (Me) S (O) CFThree
D2-32a CH (Me) S (O) CH2CFThree
D2-32a CH (Me) S (O)2Me
D2-32a CH (Me) S (O)2Et
D2-32a CH (Me) S (O)2CFThree
D2-32a CH (Me) S (O)2CH2CFThree
D2-32a CH (Et) SMe
D2-32a CH (Et) SEt
D2-32a CH (Et) SCFThree
D2-32a CH (Et) SCH2CFThree
D2-32a CH (Et) S (O) Me
D2-32a CH (Et) S (O) Et
D2-32a CH (Et) S (O) CFThree
D2-32a CH (Et) S (O) CH2CFThree
D2-32a CH (Et) S (O)2Me
D2-32a CH (Et) S (O)2Et
D2-32a CH (Et) S (O)2CFThree
D2-32a CH (Et) S (O)2CH2CFThree
D2-32a CH (n-Pr) SMe
D2-32a CH (n-Pr) SEt
D2-32a CH (n-Pr) SCFThree
D2-32a CH (n-Pr) SCH2CFThree
D2-32a CH (n-Pr) S (O) Me
D2-32a CH (n-Pr) S (O) Et
D2-32a CH (n-Pr) S (O) CFThree
D2-32a CH (n-Pr) S (O) CH2CFThree
D2-32a CH (n-Pr) S (O)2Me
D2-32a CH (n-Pr) S (O)2Et
D2-32a CH (n-Pr) S (O)2CFThree
D2-32a CH (n-Pr) S (O)2CH2CFThree
D2-32a CH (i-Pr) SMe
D2-32a CH (i-Pr) SEt
D2-32a CH (i-Pr) SCFThree
D2-32a CH (i-Pr) SCH2CFThree
D2-32a CH (i-Pr) S (O) Me
D2-32a CH (i-Pr) S (O) Et
D2-32a CH (i-Pr) S (O) CFThree
D2-32a CH (i-Pr) S (O) CH2CFThree
D2-32a CH (i-Pr) S (O)2Me
D2-32a CH (i-Pr) S (O)2Et
D2-32a CH (i-Pr) S (O)2CFThree
D2-32a CH (i-Pr) S (O)2CH2CFThree
D2-32a CH (n-Bu) SMe
D2-32a CH (n-Bu) SEt
D2-32a CH (n-Bu) SCFThree
D2-32a CH (n-Bu) SCH2CFThree
D2-32a CH (n-Bu) S (O) Me
D2-32a CH (n-Bu) S (O) Et
D2-32a CH (n-Bu) S (O) CFThree
D2-32a CH (n-Bu) S (O) CH2CFThree
D2-32a CH (n-Bu) S (O)2Me
D2-32a CH (n-Bu) S (O)2Et
D2-32a CH (n-Bu) S (O)2CFThree
D2-32a CH (n-Bu) S (O)2CH2CFThree
D2-32a CH (i-Bu) SMe
D2-32a CH (i-Bu) SEt
D2-32a CH (i-Bu) SCFThree
D2-32a CH (i-Bu) SCH2CFThree
D2-32a CH (i-Bu) S (O) Me
D2-32a CH (i-Bu) S (O) Et
D2-32a CH (i-Bu) S (O) CFThree
D2-32a CH (i-Bu) S (O) CH2CFThree
D2-32a CH (i-Bu) S (O)2Me
D2-32a CH (i-Bu) S (O)2Et
D2-32a CH (i-Bu) S (O)2CFThree
D2-32a CH (i-Bu) S (O)2CH2CFThree
D2-32a CH (s-Bu) SMe
D2-32a CH (s-Bu) SEt
D2-32a CH (s-Bu) SCFThree
D2-32a CH (s-Bu) SCH2CFThree
D2-32a CH (s-Bu) S (O) Me
D2-32a CH (s-Bu) S (O) Et
D2-32a CH (s-Bu) S (O) CFThree
D2-32a CH (s-Bu) S (O) CH2CFThree
D2-32a CH (s-Bu) S (O)2Me
D2-32a CH (s-Bu) S (O)2Et
D2-32a CH (s-Bu) S (O)2CFThree
D2-32a CH (s-Bu) S (O)2CH2CFThree
D2-32a CH (t-Bu) SMe
D2-32a CH (t-Bu) SEt
D2-32a CH (t-Bu) SCFThree
D2-32a CH (t-Bu) SCH2CFThree
D2-32a CH (t-Bu) S (O) Me
D2-32a CH (t-Bu) S (O) Et
D2-32a CH (t-Bu) S (O) CFThree
D2-32a CH (t-Bu) S (O) CH2CFThree
D2-32a CH (t-Bu) S (O)2Me
D2-32a CH (t-Bu) S (O)2Et
D2-32a CH (t-Bu) S (O)2CFThree
D2-32a CH (t-Bu) S (O)2CH2CFThree
D2-32a CH (CFThreeSMe
D2-32a CH (CFThree) SEt
D2-32a CH (CFThree) SCFThree
D2-32a CH (CFThree) SCH2CFThree
D2-32a CH (CFThree) S (O) Me
D2-32a CH (CFThree) S (O) Et
D2-32a CH (CFThree) S (O) CFThree
D2-32a CH (CFThree) S (O) CH2CFThree
D2-32a CH (CFThree) S (O)2Me
D2-32a CH (CFThree) S (O)2Et
D2-32a CH (CFThree) S (O)2CFThree
D2-32a CH (CFThree) S (O)2CH2CFThree
D2-32a CH2CH2SMe
D2-32a CH2CH2SEt
D2-32a CH2CH2SCFThree
D2-32a CH2CH2SCH2CFThree
D2-32a CH2CH2S (O) Me
D2-32a CH2CH2S (O) Et
D2-32a CH2CH2S (O) CFThree
D2-32a CH2CH2S (O) CH2CFThree
D2-32a CH2CH2S (O)2Me
D2-32a CH2CH2S (O)2Et
D2-32a CH2CH2S (O)2CFThree
D2-32a CH2CH2S (O)2CH2CFThree
D2-32a CH (Me) CH2SMe
D2-32a CH (Me) CH2SEt
D2-32a CH (Me) CH2SCFThree
D2-32a CH (Me) CH2SCH2CFThree
D2-32a CH (Me) CH2S (O) Me
D2-32a CH (Me) CH2S (O) Et
D2-32a CH (Me) CH2S (O) CFThree
D2-32a CH (Me) CH2S (O) CH2CFThree
D2-32a CH (Me) CH2S (O)2Me
D2-32a CH (Me) CH2S (O)2Et
D2-32a CH (Me) CH2S (O)2CFThree
D2-32a CH (Me) CH2S (O)2CH2CFThree
D2-32a CH (Et) CH2SMe
D2-32a CH (Et) CH2SEt
D2-32a CH (Et) CH2SCFThree
D2-32a CH (Et) CH2SCH2CFThree
D2-32a CH (Et) CH2S (O) Me
D2-32a CH (Et) CH2S (O) Et
D2-32a CH (Et) CH2S (O) CFThree
D2-32a CH (Et) CH2S (O) CH2CFThree
D2-32a CH (Et) CH2S (O)2Me
D2-32a CH (Et) CH2S (O)2Et
D2-32a CH (Et) CH2S (O)2CFThree
D2-32a CH (Et) CH2S (O)2CH2CFThree
D2-32a C (Me)2CH2SMe
D2-32a C (Me)2CH2SEt
D2-32a C (Me)2CH2SCFThree
D2-32a C (Me)2CH2SCH2CFThree
D2-32a C (Me)2CH2S (O) Me
D2-32a C (Me)2CH2S (O) Et
D2-32a C (Me)2CH2S (O) CFThree
D2-32a C (Me)2CH2S (O) CH2CFThree
D2-32a C (Me)2CH2S (O)2Me
D2-32a C (Me)2CH2S (O)2Et
D2-32a C (Me)2CH2S (O)2CFThree
D2-32a C (Me)2CH2S (O)2CH2CFThree
D2-32a CH2CH (Me) SMe
D2-32a CH2CH (Me) SEt
D2-32a CH2CH (Me) SCFThree
D2-32a CH2CH (Me) SCH2CFThree
D2-32a CH2CH (Me) S (O) Me
D2-32a CH2CH (Me) S (O) Et
D2-32a CH2CH (Me) S (O) CFThree
D2-32a CH2CH (Me) S (O) CH2CFThree
D2-32a CH2CH (Me) S (O)2Me
D2-32a CH2CH (Me) S (O)2Et
D2-32a CH2CH (Me) S (O)2CFThree
D2-32a CH2CH (Me) S (O)2CH2CFThree
D2-32a CH2CH (Et) SMe
D2-32a CH2CH (Et) SEt
D2-32a CH2CH (Et) SCFThree
D2-32a CH2CH (Et) SCH2CFThree
D2-32a CH2CH (Et) S (O) Me
D2-32a CH2CH (Et) S (O) Et
D2-32a CH2CH (Et) S (O) CFThree
D2-32a CH2CH (Et) S (O) CH2CFThree
D2-32a CH2CH (Et) S (O)2Me
D2-32a CH2CH (Et) S (O)2Et
D2-32a CH2CH (Et) S (O)2CFThree
D2-32a CH2CH (Et) S (O)2CH2CFThree
D2-32a CH (Me) CH (Me) SMe
D2-32a CH (Me) CH (Me) SEt
D2-32a CH (Me) CH (Me) SCFThree
D2-32a CH (Me) CH (Me) SCH2CFThree
D2-32a CH (Me) CH (Me) S (O) Me
D2-32a CH (Me) CH (Me) S (O) Et
D2-32a CH (Me) CH (Me) S (O) CFThree
D2-32a CH (Me) CH (Me) S (O) CH2CFThree
D2-32a CH (Me) CH (Me) S (O)2Me
D2-32a CH (Me) CH (Me) S (O)2Et
D2-32a CH (Me) CH (Me) S (O)2CFThree
D2-32a CH (Me) CH (Me) S (O)2CH2CFThree
D2-33a CH2SMe
D2-33a CH2SEt
D2-33a CH2SCFThree
D2-33a CH2SCH2CFThree
D2-33a CH2S (O) Me
D2-33a CH2S (O) Et
D2-33a CH2S (O) CFThree
D2-33a CH2S (O) CH2CFThree
D2-33a CH2S (O)2Me
D2-33a CH2S (O)2Et
D2-33a CH2S (O)2CFThree
D2-33a CH2S (O)2CH2CFThree
D2-33a CH (Me) SMe
D2-33a CH (Me) SEt
D2-33a CH (Me) SCFThree
D2-33a CH (Me) SCH2CFThree
D2-33a CH (Me) S (O) Me
D2-33a CH (Me) S (O) Et
D2-33a CH (Me) S (O) CFThree
D2-33a CH (Me) S (O) CH2CFThree
D2-33a CH (Me) S (O)2Me
D2-33a CH (Me) S (O)2Et
D2-33a CH (Me) S (O)2CFThree
D2-33a CH (Me) S (O)2CH2CFThree
D2-33a CH (Et) SMe
D2-33a CH (Et) SEt
D2-33a CH (Et) SCFThree
D2-33a CH (Et) SCH2CFThree
D2-33a CH (Et) S (O) Me
D2-33a CH (Et) S (O) Et
D2-33a CH (Et) S (O) CFThree
D2-33a CH (Et) S (O) CH2CFThree
D2-33a CH (Et) S (O)2Me
D2-33a CH (Et) S (O)2Et
D2-33a CH (Et) S (O)2CFThree
D2-33a CH (Et) S (O)2CH2CFThree
D2-33a CH (n-Pr) SMe
D2-33a CH (n-Pr) SEt
D2-33a CH (n-Pr) SCFThree
D2-33a CH (n-Pr) SCH2CFThree
D2-33a CH (n-Pr) S (O) Me
D2-33a CH (n-Pr) S (O) Et
D2-33a CH (n-Pr) S (O) CFThree
D2-33a CH (n-Pr) S (O) CH2CFThree
D2-33a CH (n-Pr) S (O)2Me
D2-33a CH (n-Pr) S (O)2Et
D2-33a CH (n-Pr) S (O)2CFThree
D2-33a CH (n-Pr) S (O)2CH2CFThree
D2-33a CH (i-Pr) SMe
D2-33a CH (i-Pr) SEt
D2-33a CH (i-Pr) SCFThree
D2-33a CH (i-Pr) SCH2CFThree
D2-33a CH (i-Pr) S (O) Me
D2-33a CH (i-Pr) S (O) Et
D2-33a CH (i-Pr) S (O) CFThree
D2-33a CH (i-Pr) S (O) CH2CFThree
D2-33a CH (i-Pr) S (O)2Me
D2-33a CH (i-Pr) S (O)2Et
D2-33a CH (i-Pr) S (O)2CFThree
D2-33a CH (i-Pr) S (O)2CH2CFThree
D2-33a CH (n-Bu) SMe
D2-33a CH (n-Bu) SEt
D2-33a CH (n-Bu) SCFThree
D2-33a CH (n-Bu) SCH2CFThree
D2-33a CH (n-Bu) S (O) Me
D2-33a CH (n-Bu) S (O) Et
D2-33a CH (n-Bu) S (O) CFThree
D2-33a CH (n-Bu) S (O) CH2CFThree
D2-33a CH (n-Bu) S (O)2Me
D2-33a CH (n-Bu) S (O)2Et
D2-33a CH (n-Bu) S (O)2CFThree
D2-33a CH (n-Bu) S (O)2CH2CFThree
D2-33a CH (i-Bu) SMe
D2-33a CH (i-Bu) SEt
D2-33a CH (i-Bu) SCFThree
D2-33a CH (i-Bu) SCH2CFThree
D2-33a CH (i-Bu) S (O) Me
D2-33a CH (i-Bu) S (O) Et
D2-33a CH (i-Bu) S (O) CFThree
D2-33a CH (i-Bu) S (O) CH2CFThree
D2-33a CH (i-Bu) S (O)2Me
D2-33a CH (i-Bu) S (O)2Et
D2-33a CH (i-Bu) S (O)2CFThree
D2-33a CH (i-Bu) S (O)2CH2CFThree
D2-33a CH (s-Bu) SMe
D2-33a CH (s-Bu) SEt
D2-33a CH (s-Bu) SCFThree
D2-33a CH (s-Bu) SCH2CFThree
D2-33a CH (s-Bu) S (O) Me
D2-33a CH (s-Bu) S (O) Et
D2-33a CH (s-Bu) S (O) CFThree
D2-33a CH (s-Bu) S (O) CH2CFThree
D2-33a CH (s-Bu) S (O)2Me
D2-33a CH (s-Bu) S (O)2Et
D2-33a CH (s-Bu) S (O)2CFThree
D2-33a CH (s-Bu) S (O)2CH2CFThree
D2-33a CH (t-Bu) SMe
D2-33a CH (t-Bu) SEt
D2-33a CH (t-Bu) SCFThree
D2-33a CH (t-Bu) SCH2CFThree
D2-33a CH (t-Bu) S (O) Me
D2-33a CH (t-Bu) S (O) Et
D2-33a CH (t-Bu) S (O) CFThree
D2-33a CH (t-Bu) S (O) CH2CFThree
D2-33a CH (t-Bu) S (O)2Me
D2-33a CH (t-Bu) S (O)2Et
D2-33a CH (t-Bu) S (O)2CFThree
D2-33a CH (t-Bu) S (O)2CH2CFThree
D2-33a CH (CFThreeSMe
D2-33a CH (CFThree) SEt
D2-33a CH (CFThree) SCFThree
D2-33a CH (CFThree) SCH2CFThree
D2-33a CH (CFThree) S (O) Me
D2-33a CH (CFThree) S (O) Et
D2-33a CH (CFThree) S (O) CFThree
D2-33a CH (CFThree) S (O) CH2CFThree
D2-33a CH (CFThree) S (O)2Me
D2-33a CH (CFThree) S (O)2Et
D2-33a CH (CFThree) S (O)2CFThree
D2-33a CH (CFThree) S (O)2CH2CFThree
D2-33a CH2CH2SMe
D2-33a CH2CH2SEt
D2-33a CH2CH2SCFThree
D2-33a CH2CH2SCH2CFThree
D2-33a CH2CH2S (O) Me
D2-33a CH2CH2S (O) Et
D2-33a CH2CH2S (O) CFThree
D2-33a CH2CH2S (O) CH2CFThree
D2-33a CH2CH2S (O)2Me
D2-33a CH2CH2S (O)2Et
D2-33a CH2CH2S (O)2CFThree
D2-33a CH2CH2S (O)2CH2CFThree
D2-33a CH (Me) CH2SMe
D2-33a CH (Me) CH2SEt
D2-33a CH (Me) CH2SCFThree
D2-33a CH (Me) CH2SCH2CFThree
D2-33a CH (Me) CH2S (O) Me
D2-33a CH (Me) CH2S (O) Et
D2-33a CH (Me) CH2S (O) CFThree
D2-33a CH (Me) CH2S (O) CH2CFThree
D2-33a CH (Me) CH2S (O)2Me
D2-33a CH (Me) CH2S (O)2Et
D2-33a CH (Me) CH2S (O)2CFThree
D2-33a CH (Me) CH2S (O)2CH2CFThree
D2-33a CH (Et) CH2SMe
D2-33a CH (Et) CH2SEt
D2-33a CH (Et) CH2SCFThree
D2-33a CH (Et) CH2SCH2CFThree
D2-33a CH (Et) CH2S (O) Me
D2-33a CH (Et) CH2S (O) Et
D2-33a CH (Et) CH2S (O) CFThree
D2-33a CH (Et) CH2S (O) CH2CFThree
D2-33a CH (Et) CH2S (O)2Me
D2-33a CH (Et) CH2S (O)2Et
D2-33a CH (Et) CH2S (O)2CFThree
D2-33a CH (Et) CH2S (O)2CH2CFThree
D2-33a C (Me)2CH2SMe
D2-33a C (Me)2CH2SEt
D2-33a C (Me)2CH2SCFThree
D2-33a C (Me)2CH2SCH2CFThree
D2-33a C (Me)2CH2S (O) Me
D2-33a C (Me)2CH2S (O) Et
D2-33a C (Me)2CH2S (O) CFThree
D2-33a C (Me)2CH2S (O) CH2CFThree
D2-33a C (Me)2CH2S (O)2Me
D2-33a C (Me)2CH2S (O)2Et
D2-33a C (Me)2CH2S (O)2CFThree
D2-33a C (Me)2CH2S (O)2CH2CFThree
D2-33a CH2CH (Me) SMe
D2-33a CH2CH (Me) SEt
D2-33a CH2CH (Me) SCFThree
D2-33a CH2CH (Me) SCH2CFThree
D2-33a CH2CH (Me) S (O) Me
D2-33a CH2CH (Me) S (O) Et
D2-33a CH2CH (Me) S (O) CFThree
D2-33a CH2CH (Me) S (O) CH2CFThree
D2-33a CH2CH (Me) S (O)2Me
D2-33a CH2CH (Me) S (O)2Et
D2-33a CH2CH (Me) S (O)2CFThree
D2-33a CH2CH (Me) S (O)2CH2CFThree
D2-33a CH2CH (Et) SMe
D2-33a CH2CH (Et) SEt
D2-33a CH2CH (Et) SCFThree
D2-33a CH2CH (Et) SCH2CFThree
D2-33a CH2CH (Et) S (O) Me
D2-33a CH2CH (Et) S (O) Et
D2-33a CH2CH (Et) S (O) CFThree
D2-33a CH2CH (Et) S (O) CH2CFThree
D2-33a CH2CH (Et) S (O)2Me
D2-33a CH2CH (Et) S (O)2Et
D2-33a CH2CH (Et) S (O)2CFThree
D2-33a CH2CH (Et) S (O)2CH2CFThree
D2-33a CH (Me) CH (Me) SMe
D2-33a CH (Me) CH (Me) SEt
D2-33a CH (Me) CH (Me) SCFThree
D2-33a CH (Me) CH (Me) SCH2CFThree
D2-33a CH (Me) CH (Me) S (O) Me
D2-33a CH (Me) CH (Me) S (O) Et
D2-33a CH (Me) CH (Me) S (O) CFThree
D2-33a CH (Me) CH (Me) S (O) CH2CFThree
D2-33a CH (Me) CH (Me) S (O)2Me
D2-33a CH (Me) CH (Me) S (O)2Et
D2-33a CH (Me) CH (Me) S (O)2CFThree
D2-33a CH (Me) CH (Me) S (O)2CH2CFThree
D2-34a CH2SMe
D2-34a CH2SEt
D2-34a CH2SCFThree
D2-34a CH2SCH2CFThree
D2-34a CH2S (O) Me
D2-34a CH2S (O) Et
D2-34a CH2S (O) CFThree
D2-34a CH2S (O) CH2CFThree
D2-34a CH2S (O)2Me
D2-34a CH2S (O)2Et
D2-34a CH2S (O)2CFThree
D2-34a CH2S (O)2CH2CFThree
D2-34a CH (Me) SMe
D2-34a CH (Me) SEt
D2-34a CH (Me) SCFThree
D2-34a CH (Me) SCH2CFThree
D2-34a CH (Me) S (O) Me
D2-34a CH (Me) S (O) Et
D2-34a CH (Me) S (O) CFThree
D2-34a CH (Me) S (O) CH2CFThree
D2-34a CH (Me) S (O)2Me
D2-34a CH (Me) S (O)2Et
D2-34a CH (Me) S (O)2CFThree
D2-34a CH (Me) S (O)2CH2CFThree
D2-34a CH (Et) SMe
D2-34a CH (Et) SEt
D2-34a CH (Et) SCFThree
D2-34a CH (Et) SCH2CFThree
D2-34a CH (Et) S (O) Me
D2-34a CH (Et) S (O) Et
D2-34a CH (Et) S (O) CFThree
D2-34a CH (Et) S (O) CH2CFThree
D2-34a CH (Et) S (O)2Me
D2-34a CH (Et) S (O)2Et
D2-34a CH (Et) S (O)2CFThree
D2-34a CH (Et) S (O)2CH2CFThree
D2-34a CH (n-Pr) SMe
D2-34a CH (n-Pr) SEt
D2-34a CH (n-Pr) SCFThree
D2-34a CH (n-Pr) SCH2CFThree
D2-34a CH (n-Pr) S (O) Me
D2-34a CH (n-Pr) S (O) Et
D2-34a CH (n-Pr) S (O) CFThree
D2-34a CH (n-Pr) S (O) CH2CFThree
D2-34a CH (n-Pr) S (O)2Me
D2-34a CH (n-Pr) S (O)2Et
D2-34a CH (n-Pr) S (O)2CFThree
D2-34a CH (n-Pr) S (O)2CH2CFThree
D2-34a CH (i-Pr) SMe
D2-34a CH (i-Pr) SEt
D2-34a CH (i-Pr) SCFThree
D2-34a CH (i-Pr) SCH2CFThree
D2-34a CH (i-Pr) S (O) Me
D2-34a CH (i-Pr) S (O) Et
D2-34a CH (i-Pr) S (O) CFThree
D2-34a CH (i-Pr) S (O) CH2CFThree
D2-34a CH (i-Pr) S (O)2Me
D2-34a CH (i-Pr) S (O)2Et
D2-34a CH (i-Pr) S (O)2CFThree
D2-34a CH (i-Pr) S (O)2CH2CFThree
D2-34a CH (n-Bu) SMe
D2-34a CH (n-Bu) SEt
D2-34a CH (n-Bu) SCFThree
D2-34a CH (n-Bu) SCH2CFThree
D2-34a CH (n-Bu) S (O) Me
D2-34a CH (n-Bu) S (O) Et
D2-34a CH (n-Bu) S (O) CFThree
D2-34a CH (n-Bu) S (O) CH2CFThree
D2-34a CH (n-Bu) S (O)2Me
D2-34a CH (n-Bu) S (O)2Et
D2-34a CH (n-Bu) S (O)2CFThree
D2-34a CH (n-Bu) S (O)2CH2CFThree
D2-34a CH (i-Bu) SMe
D2-34a CH (i-Bu) SEt
D2-34a CH (i-Bu) SCFThree
D2-34a CH (i-Bu) SCH2CFThree
D2-34a CH (i-Bu) S (O) Me
D2-34a CH (i-Bu) S (O) Et
D2-34a CH (i-Bu) S (O) CFThree
D2-34a CH (i-Bu) S (O) CH2CFThree
D2-34a CH (i-Bu) S (O)2Me
D2-34a CH (i-Bu) S (O)2Et
D2-34a CH (i-Bu) S (O)2CFThree
D2-34a CH (i-Bu) S (O)2CH2CFThree
D2-34a CH (s-Bu) SMe
D2-34a CH (s-Bu) SEt
D2-34a CH (s-Bu) SCFThree
D2-34a CH (s-Bu) SCH2CFThree
D2-34a CH (s-Bu) S (O) Me
D2-34a CH (s-Bu) S (O) Et
D2-34a CH (s-Bu) S (O) CFThree
D2-34a CH (s-Bu) S (O) CH2CFThree
D2-34a CH (s-Bu) S (O)2Me
D2-34a CH (s-Bu) S (O)2Et
D2-34a CH (s-Bu) S (O)2CFThree
D2-34a CH (s-Bu) S (O)2CH2CFThree
D2-34a CH (t-Bu) SMe
D2-34a CH (t-Bu) SEt
D2-34a CH (t-Bu) SCFThree
D2-34a CH (t-Bu) SCH2CFThree
D2-34a CH (t-Bu) S (O) Me
D2-34a CH (t-Bu) S (O) Et
D2-34a CH (t-Bu) S (O) CFThree
D2-34a CH (t-Bu) S (O) CH2CFThree
D2-34a CH (t-Bu) S (O)2Me
D2-34a CH (t-Bu) S (O)2Et
D2-34a CH (t-Bu) S (O)2CFThree
D2-34a CH (t-Bu) S (O)2CH2CFThree
D2-34a CH (CFThreeSMe
D2-34a CH (CFThree) SEt
D2-34a CH (CFThree) SCFThree
D2-34a CH (CFThree) SCH2CFThree
D2-34a CH (CFThree) S (O) Me
D2-34a CH (CFThree) S (O) Et
D2-34a CH (CFThree) S (O) CFThree
D2-34a CH (CFThree) S (O) CH2CFThree
D2-34a CH (CFThree) S (O)2Me
D2-34a CH (CFThree) S (O)2Et
D2-34a CH (CFThree) S (O)2CFThree
D2-34a CH (CFThree) S (O)2CH2CFThree
D2-34a CH2CH2SMe
D2-34a CH2CH2SEt
D2-34a CH2CH2SCFThree
D2-34a CH2CH2SCH2CFThree
D2-34a CH2CH2S (O) Me
D2-34a CH2CH2S (O) Et
D2-34a CH2CH2S (O) CFThree
D2-34a CH2CH2S (O) CH2CFThree
D2-34a CH2CH2S (O)2Me
D2-34a CH2CH2S (O)2Et
D2-34a CH2CH2S (O)2CFThree
D2-34a CH2CH2S (O)2CH2CFThree
D2-34a CH (Me) CH2SMe
D2-34a CH (Me) CH2SEt
D2-34a CH (Me) CH2SCFThree
D2-34a CH (Me) CH2SCH2CFThree
D2-34a CH (Me) CH2S (O) Me
D2-34a CH (Me) CH2S (O) Et
D2-34a CH (Me) CH2S (O) CFThree
D2-34a CH (Me) CH2S (O) CH2CFThree
D2-34a CH (Me) CH2S (O)2Me
D2-34a CH (Me) CH2S (O)2Et
D2-34a CH (Me) CH2S (O)2CFThree
D2-34a CH (Me) CH2S (O)2CH2CFThree
D2-34a CH (Et) CH2SMe
D2-34a CH (Et) CH2SEt
D2-34a CH (Et) CH2SCFThree
D2-34a CH (Et) CH2SCH2CFThree
D2-34a CH (Et) CH2S (O) Me
D2-34a CH (Et) CH2S (O) Et
D2-34a CH (Et) CH2S (O) CFThree
D2-34a CH (Et) CH2S (O) CH2CFThree
D2-34a CH (Et) CH2S (O)2Me
D2-34a CH (Et) CH2S (O)2Et
D2-34a CH (Et) CH2S (O)2CFThree
D2-34a CH (Et) CH2S (O)2CH2CFThree
D2-34a C (Me)2CH2SMe
D2-34a C (Me)2CH2SEt
D2-34a C (Me)2CH2SCFThree
D2-34a C (Me)2CH2SCH2CFThree
D2-34a C (Me)2CH2S (O) Me
D2-34a C (Me)2CH2S (O) Et
D2-34a C (Me)2CH2S (O) CFThree
D2-34a C (Me)2CH2S (O) CH2CFThree
D2-34a C (Me)2CH2S (O)2Me
D2-34a C (Me)2CH2S (O)2Et
D2-34a C (Me)2CH2S (O)2CFThree
D2-34a C (Me)2CH2S (O)2CH2CFThree
D2-34a CH2CH (Me) SMe
D2-34a CH2CH (Me) SEt
D2-34a CH2CH (Me) SCFThree
D2-34a CH2CH (Me) SCH2CFThree
D2-34a CH2CH (Me) S (O) Me
D2-34a CH2CH (Me) S (O) Et
D2-34a CH2CH (Me) S (O) CFThree
D2-34a CH2CH (Me) S (O) CH2CFThree
D2-34a CH2CH (Me) S (O)2Me
D2-34a CH2CH (Me) S (O)2Et
D2-34a CH2CH (Me) S (O)2CFThree
D2-34a CH2CH (Me) S (O)2CH2CFThree
D2-34a CH2CH (Et) SMe
D2-34a CH2CH (Et) SEt
D2-34a CH2CH (Et) SCFThree
D2-34a CH2CH (Et) SCH2CFThree
D2-34a CH2CH (Et) S (O) Me
D2-34a CH2CH (Et) S (O) Et
D2-34a CH2CH (Et) S (O) CFThree
D2-34a CH2CH (Et) S (O) CH2CFThree
D2-34a CH2CH (Et) S (O)2Me
D2-34a CH2CH (Et) S (O)2Et
D2-34a CH2CH (Et) S (O)2CFThree
D2-34a CH2CH (Et) S (O)2CH2CFThree
D2-34a CH (Me) CH (Me) SMe
D2-34a CH (Me) CH (Me) SEt
D2-34a CH (Me) CH (Me) SCFThree
D2-34a CH (Me) CH (Me) SCH2CFThree
D2-34a CH (Me) CH (Me) S (O) Me
D2-34a CH (Me) CH (Me) S (O) Et
D2-34a CH (Me) CH (Me) S (O) CFThree
D2-34a CH (Me) CH (Me) S (O) CH2CFThree
D2-34a CH (Me) CH (Me) S (O)2Me
D2-34a CH (Me) CH (Me) S (O)2Et
D2-34a CH (Me) CH (Me) S (O)2CFThree
D2-34a CH (Me) CH (Me) S (O)2CH2CFThree
D2-36a CH2SMe
D2-36a CH2SEt
D2-36a CH2SCFThree
D2-36a CH2SCH2CFThree
D2-36a CH2S (O) Me
D2-36a CH2S (O) Et
D2-36a CH2S (O) CFThree
D2-36a CH2S (O) CH2CFThree
D2-36a CH2S (O)2Me
D2-36a CH2S (O)2Et
D2-36a CH2S (O)2CFThree
D2-36a CH2S (O)2CH2CFThree
D2-36a CH (Me) SMe
D2-36a CH (Me) SEt
D2-36a CH (Me) SCFThree
D2-36a CH (Me) SCH2CFThree
D2-36a CH (Me) S (O) Me
D2-36a CH (Me) S (O) Et
D2-36a CH (Me) S (O) CFThree
D2-36a CH (Me) S (O) CH2CFThree
D2-36a CH (Me) S (O)2Me
D2-36a CH (Me) S (O)2Et
D2-36a CH (Me) S (O)2CFThree
D2-36a CH (Me) S (O)2CH2CFThree
D2-36a CH (Et) SMe
D2-36a CH (Et) SEt
D2-36a CH (Et) SCFThree
D2-36a CH (Et) SCH2CFThree
D2-36a CH (Et) S (O) Me
D2-36a CH (Et) S (O) Et
D2-36a CH (Et) S (O) CFThree
D2-36a CH (Et) S (O) CH2CFThree
D2-36a CH (Et) S (O)2Me
D2-36a CH (Et) S (O)2Et
D2-36a CH (Et) S (O)2CFThree
D2-36a CH (Et) S (O)2CH2CFThree
D2-36a CH (n-Pr) SMe
D2-36a CH (n-Pr) SEt
D2-36a CH (n-Pr) SCFThree
D2-36a CH (n-Pr) SCH2CFThree
D2-36a CH (n-Pr) S (O) Me
D2-36a CH (n-Pr) S (O) Et
D2-36a CH (n-Pr) S (O) CFThree
D2-36a CH (n-Pr) S (O) CH2CFThree
D2-36a CH (n-Pr) S (O)2Me
D2-36a CH (n-Pr) S (O)2Et
D2-36a CH (n-Pr) S (O)2CFThree
D2-36a CH (n-Pr) S (O)2CH2CFThree
D2-36a CH (i-Pr) SMe
D2-36a CH (i-Pr) SEt
D2-36a CH (i-Pr) SCFThree
D2-36a CH (i-Pr) SCH2CFThree
D2-36a CH (i-Pr) S (O) Me
D2-36a CH (i-Pr) S (O) Et
D2-36a CH (i-Pr) S (O) CFThree
D2-36a CH (i-Pr) S (O) CH2CFThree
D2-36a CH (i-Pr) S (O)2Me
D2-36a CH (i-Pr) S (O)2Et
D2-36a CH (i-Pr) S (O)2CFThree
D2-36a CH (i-Pr) S (O)2CH2CFThree
D2-36a CH (n-Bu) SMe
D2-36a CH (n-Bu) SEt
D2-36a CH (n-Bu) SCFThree
D2-36a CH (n-Bu) SCH2CFThree
D2-36a CH (n-Bu) S (O) Me
D2-36a CH (n-Bu) S (O) Et
D2-36a CH (n-Bu) S (O) CFThree
D2-36a CH (n-Bu) S (O) CH2CFThree
D2-36a CH (n-Bu) S (O)2Me
D2-36a CH (n-Bu) S (O)2Et
D2-36a CH (n-Bu) S (O)2CFThree
D2-36a CH (n-Bu) S (O)2CH2CFThree
D2-36a CH (i-Bu) SMe
D2-36a CH (i-Bu) SEt
D2-36a CH (i-Bu) SCFThree
D2-36a CH (i-Bu) SCH2CFThree
D2-36a CH (i-Bu) S (O) Me
D2-36a CH (i-Bu) S (O) Et
D2-36a CH (i-Bu) S (O) CFThree
D2-36a CH (i-Bu) S (O) CH2CFThree
D2-36a CH (i-Bu) S (O)2Me
D2-36a CH (i-Bu) S (O)2Et
D2-36a CH (i-Bu) S (O)2CFThree
D2-36a CH (i-Bu) S (O)2CH2CFThree
D2-36a CH (s-Bu) SMe
D2-36a CH (s-Bu) SEt
D2-36a CH (s-Bu) SCFThree
D2-36a CH (s-Bu) SCH2CFThree
D2-36a CH (s-Bu) S (O) Me
D2-36a CH (s-Bu) S (O) Et
D2-36a CH (s-Bu) S (O) CFThree
D2-36a CH (s-Bu) S (O) CH2CFThree
D2-36a CH (s-Bu) S (O)2Me
D2-36a CH (s-Bu) S (O)2Et
D2-36a CH (s-Bu) S (O)2CFThree
D2-36a CH (s-Bu) S (O)2CH2CFThree
D2-36a CH (t-Bu) SMe
D2-36a CH (t-Bu) SEt
D2-36a CH (t-Bu) SCFThree
D2-36a CH (t-Bu) SCH2CFThree
D2-36a CH (t-Bu) S (O) Me
D2-36a CH (t-Bu) S (O) Et
D2-36a CH (t-Bu) S (O) CFThree
D2-36a CH (t-Bu) S (O) CH2CFThree
D2-36a CH (t-Bu) S (O)2Me
D2-36a CH (t-Bu) S (O)2Et
D2-36a CH (t-Bu) S (O)2CFThree
D2-36a CH (t-Bu) S (O)2CH2CFThree
D2-36a CH (CFThreeSMe
D2-36a CH (CFThree) SEt
D2-36a CH (CFThree) SCFThree
D2-36a CH (CFThree) SCH2CFThree
D2-36a CH (CFThree) S (O) Me
D2-36a CH (CFThree) S (O) Et
D2-36a CH (CFThree) S (O) CFThree
D2-36a CH (CFThree) S (O) CH2CFThree
D2-36a CH (CFThree) S (O)2Me
D2-36a CH (CFThree) S (O)2Et
D2-36a CH (CFThree) S (O)2CFThree
D2-36a CH (CFThree) S (O)2CH2CFThree
D2-36a CH2CH2SMe
D2-36a CH2CH2SEt
D2-36a CH2CH2SCFThree
D2-36a CH2CH2SCH2CFThree
D2-36a CH2CH2S (O) Me
D2-36a CH2CH2S (O) Et
D2-36a CH2CH2S (O) CFThree
D2-36a CH2CH2S (O) CH2CFThree
D2-36a CH2CH2S (O)2Me
D2-36a CH2CH2S (O)2Et
D2-36a CH2CH2S (O)2CFThree
D2-36a CH2CH2S (O)2CH2CFThree
D2-36a CH (Me) CH2SMe
D2-36a CH (Me) CH2SEt
D2-36a CH (Me) CH2SCFThree
D2-36a CH (Me) CH2SCH2CFThree
D2-36a CH (Me) CH2S (O) Me
D2-36a CH (Me) CH2S (O) Et
D2-36a CH (Me) CH2S (O) CFThree
D2-36a CH (Me) CH2S (O) CH2CFThree
D2-36a CH (Me) CH2S (O)2Me
D2-36a CH (Me) CH2S (O)2Et
D2-36a CH (Me) CH2S (O)2CFThree
D2-36a CH (Me) CH2S (O)2CH2CFThree
D2-36a CH (Et) CH2SMe
D2-36a CH (Et) CH2SEt
D2-36a CH (Et) CH2SCFThree
D2-36a CH (Et) CH2SCH2CFThree
D2-36a CH (Et) CH2S (O) Me
D2-36a CH (Et) CH2S (O) Et
D2-36a CH (Et) CH2S (O) CFThree
D2-36a CH (Et) CH2S (O) CH2CFThree
D2-36a CH (Et) CH2S (O)2Me
D2-36a CH (Et) CH2S (O)2Et
D2-36a CH (Et) CH2S (O)2CFThree
D2-36a CH (Et) CH2S (O)2CH2CFThree
D2-36a C (Me)2CH2SMe
D2-36a C (Me)2CH2SEt
D2-36a C (Me)2CH2SCFThree
D2-36a C (Me)2CH2SCH2CFThree
D2-36a C (Me)2CH2S (O) Me
D2-36a C (Me)2CH2S (O) Et
D2-36a C (Me)2CH2S (O) CFThree
D2-36a C (Me)2CH2S (O) CH2CFThree
D2-36a C (Me)2CH2S (O)2Me
D2-36a C (Me)2CH2S (O)2Et
D2-36a C (Me)2CH2S (O)2CFThree
D2-36a C (Me)2CH2S (O)2CH2CFThree
D2-36a CH2CH (Me) SMe
D2-36a CH2CH (Me) SEt
D2-36a CH2CH (Me) SCFThree
D2-36a CH2CH (Me) SCH2CFThree
D2-36a CH2CH (Me) S (O) Me
D2-36a CH2CH (Me) S (O) Et
D2-36a CH2CH (Me) S (O) CFThree
D2-36a CH2CH (Me) S (O) CH2CFThree
D2-36a CH2CH (Me) S (O)2Me
D2-36a CH2CH (Me) S (O)2Et
D2-36a CH2CH (Me) S (O)2CFThree
D2-36a CH2CH (Me) S (O)2CH2CFThree
D2-36a CH2CH (Et) SMe
D2-36a CH2CH (Et) SEt
D2-36a CH2CH (Et) SCFThree
D2-36a CH2CH (Et) SCH2CFThree
D2-36a CH2CH (Et) S (O) Me
D2-36a CH2CH (Et) S (O) Et
D2-36a CH2CH (Et) S (O) CFThree
D2-36a CH2CH (Et) S (O) CH2CFThree
D2-36a CH2CH (Et) S (O)2Me
D2-36a CH2CH (Et) S (O)2Et
D2-36a CH2CH (Et) S (O)2CFThree
D2-36a CH2CH (Et) S (O)2CH2CFThree
D2-36a CH (Me) CH (Me) SMe
D2-36a CH (Me) CH (Me) SEt
D2-36a CH (Me) CH (Me) SCFThree
D2-36a CH (Me) CH (Me) SCH2CFThree
D2-36a CH (Me) CH (Me) S (O) Me
D2-36a CH (Me) CH (Me) S (O) Et
D2-36a CH (Me) CH (Me) S (O) CFThree
D2-36a CH (Me) CH (Me) S (O) CH2CFThree
D2-36a CH (Me) CH (Me) S (O)2Me
D2-36a CH (Me) CH (Me) S (O)2Et
D2-36a CH (Me) CH (Me) S (O)2CFThree
D2-36a CH (Me) CH (Me) S (O)2CH2CFThree
D2-37a CH2SMe
D2-37a CH2SEt
D2-37a CH2SCFThree
D2-37a CH2SCH2CFThree
D2-37a CH2S (O) Me
D2-37a CH2S (O) Et
D2-37a CH2S (O) CFThree
D2-37a CH2S (O) CH2CFThree
D2-37a CH2S (O)2Me
D2-37a CH2S (O)2Et
D2-37a CH2S (O)2CFThree
D2-37a CH2S (O)2CH2CFThree
D2-37a CH (Me) SMe
D2-37a CH (Me) SEt
D2-37a CH (Me) SCFThree
D2-37a CH (Me) SCH2CFThree
D2-37a CH (Me) S (O) Me
D2-37a CH (Me) S (O) Et
D2-37a CH (Me) S (O) CFThree
D2-37a CH (Me) S (O) CH2CFThree
D2-37a CH (Me) S (O)2Me
D2-37a CH (Me) S (O)2Et
D2-37a CH (Me) S (O)2CFThree
D2-37a CH (Me) S (O)2CH2CFThree
D2-37a CH (Et) SMe
D2-37a CH (Et) SEt
D2-37a CH (Et) SCFThree
D2-37a CH (Et) SCH2CFThree
D2-37a CH (Et) S (O) Me
D2-37a CH (Et) S (O) Et
D2-37a CH (Et) S (O) CFThree
D2-37a CH (Et) S (O) CH2CFThree
D2-37a CH (Et) S (O)2Me
D2-37a CH (Et) S (O)2Et
D2-37a CH (Et) S (O)2CFThree
D2-37a CH (Et) S (O)2CH2CFThree
D2-37a CH (n-Pr) SMe
D2-37a CH (n-Pr) SEt
D2-37a CH (n-Pr) SCFThree
D2-37a CH (n-Pr) SCH2CFThree
D2-37a CH (n-Pr) S (O) Me
D2-37a CH (n-Pr) S (O) Et
D2-37a CH (n-Pr) S (O) CFThree
D2-37a CH (n-Pr) S (O) CH2CFThree
D2-37a CH (n-Pr) S (O)2Me
D2-37a CH (n-Pr) S (O)2Et
D2-37a CH (n-Pr) S (O)2CFThree
D2-37a CH (n-Pr) S (O)2CH2CFThree
D2-37a CH (i-Pr) SMe
D2-37a CH (i-Pr) SEt
D2-37a CH (i-Pr) SCFThree
D2-37a CH (i-Pr) SCH2CFThree
D2-37a CH (i-Pr) S (O) Me
D2-37a CH (i-Pr) S (O) Et
D2-37a CH (i-Pr) S (O) CFThree
D2-37a CH (i-Pr) S (O) CH2CFThree
D2-37a CH (i-Pr) S (O)2Me
D2-37a CH (i-Pr) S (O)2Et
D2-37a CH (i-Pr) S (O)2CFThree
D2-37a CH (i-Pr) S (O)2CH2CFThree
D2-37a CH (n-Bu) SMe
D2-37a CH (n-Bu) SEt
D2-37a CH (n-Bu) SCFThree
D2-37a CH (n-Bu) SCH2CFThree
D2-37a CH (n-Bu) S (O) Me
D2-37a CH (n-Bu) S (O) Et
D2-37a CH (n-Bu) S (O) CFThree
D2-37a CH (n-Bu) S (O) CH2CFThree
D2-37a CH (n-Bu) S (O)2Me
D2-37a CH (n-Bu) S (O)2Et
D2-37a CH (n-Bu) S (O)2CFThree
D2-37a CH (n-Bu) S (O)2CH2CFThree
D2-37a CH (i-Bu) SMe
D2-37a CH (i-Bu) SEt
D2-37a CH (i-Bu) SCFThree
D2-37a CH (i-Bu) SCH2CFThree
D2-37a CH (i-Bu) S (O) Me
D2-37a CH (i-Bu) S (O) Et
D2-37a CH (i-Bu) S (O) CFThree
D2-37a CH (i-Bu) S (O) CH2CFThree
D2-37a CH (i-Bu) S (O)2Me
D2-37a CH (i-Bu) S (O)2Et
D2-37a CH (i-Bu) S (O)2CFThree
D2-37a CH (i-Bu) S (O)2CH2CFThree
D2-37a CH (s-Bu) SMe
D2-37a CH (s-Bu) SEt
D2-37a CH (s-Bu) SCFThree
D2-37a CH (s-Bu) SCH2CFThree
D2-37a CH (s-Bu) S (O) Me
D2-37a CH (s-Bu) S (O) Et
D2-37a CH (s-Bu) S (O) CFThree
D2-37a CH (s-Bu) S (O) CH2CFThree
D2-37a CH (s-Bu) S (O)2Me
D2-37a CH (s-Bu) S (O)2Et
D2-37a CH (s-Bu) S (O)2CFThree
D2-37a CH (s-Bu) S (O)2CH2CFThree
D2-37a CH (t-Bu) SMe
D2-37a CH (t-Bu) SEt
D2-37a CH (t-Bu) SCFThree
D2-37a CH (t-Bu) SCH2CFThree
D2-37a CH (t-Bu) S (O) Me
D2-37a CH (t-Bu) S (O) Et
D2-37a CH (t-Bu) S (O) CFThree
D2-37a CH (t-Bu) S (O) CH2CFThree
D2-37a CH (t-Bu) S (O)2Me
D2-37a CH (t-Bu) S (O)2Et
D2-37a CH (t-Bu) S (O)2CFThree
D2-37a CH (t-Bu) S (O)2CH2CFThree
D2-37a CH (CFThreeSMe
D2-37a CH (CFThree) SEt
D2-37a CH (CFThree) SCFThree
D2-37a CH (CFThree) SCH2CFThree
D2-37a CH (CFThree) S (O) Me
D2-37a CH (CFThree) S (O) Et
D2-37a CH (CFThree) S (O) CFThree
D2-37a CH (CFThree) S (O) CH2CFThree
D2-37a CH (CFThree) S (O)2Me
D2-37a CH (CFThree) S (O)2Et
D2-37a CH (CFThree) S (O)2CFThree
D2-37a CH (CFThree) S (O)2CH2CFThree
D2-37a CH2CH2SMe
D2-37a CH2CH2SEt
D2-37a CH2CH2SCFThree
D2-37a CH2CH2SCH2CFThree
D2-37a CH2CH2S (O) Me
D2-37a CH2CH2S (O) Et
D2-37a CH2CH2S (O) CFThree
D2-37a CH2CH2S (O) CH2CFThree
D2-37a CH2CH2S (O)2Me
D2-37a CH2CH2S (O)2Et
D2-37a CH2CH2S (O)2CFThree
D2-37a CH2CH2S (O)2CH2CFThree
D2-37a CH (Me) CH2SMe
D2-37a CH (Me) CH2SEt
D2-37a CH (Me) CH2SCFThree
D2-37a CH (Me) CH2SCH2CFThree
D2-37a CH (Me) CH2S (O) Me
D2-37a CH (Me) CH2S (O) Et
D2-37a CH (Me) CH2S (O) CFThree
D2-37a CH (Me) CH2S (O) CH2CFThree
D2-37a CH (Me) CH2S (O)2Me
D2-37a CH (Me) CH2S (O)2Et
D2-37a CH (Me) CH2S (O)2CFThree
D2-37a CH (Me) CH2S (O)2CH2CFThree
D2-37a CH (Et) CH2SMe
D2-37a CH (Et) CH2SEt
D2-37a CH (Et) CH2SCFThree
D2-37a CH (Et) CH2SCH2CFThree
D2-37a CH (Et) CH2S (O) Me
D2-37a CH (Et) CH2S (O) Et
D2-37a CH (Et) CH2S (O) CFThree
D2-37a CH (Et) CH2S (O) CH2CFThree
D2-37a CH (Et) CH2S (O)2Me
D2-37a CH (Et) CH2S (O)2Et
D2-37a CH (Et) CH2S (O)2CFThree
D2-37a CH (Et) CH2S (O)2CH2CFThree
D2-37a C (Me)2CH2SMe
D2-37a C (Me)2CH2SEt
D2-37a C (Me)2CH2SCFThree
D2-37a C (Me)2CH2SCH2CFThree
D2-37a C (Me)2CH2S (O) Me
D2-37a C (Me)2CH2S (O) Et
D2-37a C (Me)2CH2S (O) CFThree
D2-37a C (Me)2CH2S (O) CH2CFThree
D2-37a C (Me)2CH2S (O)2Me
D2-37a C (Me)2CH2S (O)2Et
D2-37a C (Me)2CH2S (O)2CFThree
D2-37a C (Me)2CH2S (O)2CH2CFThree
D2-37a CH2CH (Me) SMe
D2-37a CH2CH (Me) SEt
D2-37a CH2CH (Me) SCFThree
D2-37a CH2CH (Me) SCH2CFThree
D2-37a CH2CH (Me) S (O) Me
D2-37a CH2CH (Me) S (O) Et
D2-37a CH2CH (Me) S (O) CFThree
D2-37a CH2CH (Me) S (O) CH2CFThree
D2-37a CH2CH (Me) S (O)2Me
D2-37a CH2CH (Me) S (O)2Et
D2-37a CH2CH (Me) S (O)2CFThree
D2-37a CH2CH (Me) S (O)2CH2CFThree
D2-37a CH2CH (Et) SMe
D2-37a CH2CH (Et) SEt
D2-37a CH2CH (Et) SCFThree
D2-37a CH2CH (Et) SCH2CFThree
D2-37a CH2CH (Et) S (O) Me
D2-37a CH2CH (Et) S (O) Et
D2-37a CH2CH (Et) S (O) CFThree
D2-37a CH2CH (Et) S (O) CH2CFThree
D2-37a CH2CH (Et) S (O)2Me
D2-37a CH2CH (Et) S (O)2Et
D2-37a CH2CH (Et) S (O)2CFThree
D2-37a CH2CH (Et) S (O)2CH2CFThree
D2-37a CH (Me) CH (Me) SMe
D2-37a CH (Me) CH (Me) SEt
D2-37a CH (Me) CH (Me) SCFThree
D2-37a CH (Me) CH (Me) SCH2CFThree
D2-37a CH (Me) CH (Me) S (O) Me
D2-37a CH (Me) CH (Me) S (O) Et
D2-37a CH (Me) CH (Me) S (O) CFThree
D2-37a CH (Me) CH (Me) S (O) CH2CFThree
D2-37a CH (Me) CH (Me) S (O)2Me
D2-37a CH (Me) CH (Me) S (O)2Et
D2-37a CH (Me) CH (Me) S (O)2CFThree
D2-37a CH (Me) CH (Me) S (O)2CH2CFThree
D2-38a CH2SMe
D2-38a CH2SEt
D2-38a CH2SCFThree
D2-38a CH2SCH2CFThree
D2-38a CH2S (O) Me
D2-38a CH2S (O) Et
D2-38a CH2S (O) CFThree
D2-38a CH2S (O) CH2CFThree
D2-38a CH2S (O)2Me
D2-38a CH2S (O)2Et
D2-38a CH2S (O)2CFThree
D2-38a CH2S (O)2CH2CFThree
D2-38a CH (Me) SMe
D2-38a CH (Me) SEt
D2-38a CH (Me) SCFThree
D2-38a CH (Me) SCH2CFThree
D2-38a CH (Me) S (O) Me
D2-38a CH (Me) S (O) Et
D2-38a CH (Me) S (O) CFThree
D2-38a CH (Me) S (O) CH2CFThree
D2-38a CH (Me) S (O)2Me
D2-38a CH (Me) S (O)2Et
D2-38a CH (Me) S (O)2CFThree
D2-38a CH (Me) S (O)2CH2CFThree
D2-38a CH (Et) SMe
D2-38a CH (Et) SEt
D2-38a CH (Et) SCFThree
D2-38a CH (Et) SCH2CFThree
D2-38a CH (Et) S (O) Me
D2-38a CH (Et) S (O) Et
D2-38a CH (Et) S (O) CFThree
D2-38a CH (Et) S (O) CH2CFThree
D2-38a CH (Et) S (O)2Me
D2-38a CH (Et) S (O)2Et
D2-38a CH (Et) S (O)2CFThree
D2-38a CH (Et) S (O)2CH2CFThree
D2-38a CH (n-Pr) SMe
D2-38a CH (n-Pr) SEt
D2-38a CH (n-Pr) SCFThree
D2-38a CH (n-Pr) SCH2CFThree
D2-38a CH (n-Pr) S (O) Me
D2-38a CH (n-Pr) S (O) Et
D2-38a CH (n-Pr) S (O) CFThree
D2-38a CH (n-Pr) S (O) CH2CFThree
D2-38a CH (n-Pr) S (O)2Me
D2-38a CH (n-Pr) S (O)2Et
D2-38a CH (n-Pr) S (O)2CFThree
D2-38a CH (n-Pr) S (O)2CH2CFThree
D2-38a CH (i-Pr) SMe
D2-38a CH (i-Pr) SEt
D2-38a CH (i-Pr) SCFThree
D2-38a CH (i-Pr) SCH2CFThree
D2-38a CH (i-Pr) S (O) Me
D2-38a CH (i-Pr) S (O) Et
D2-38a CH (i-Pr) S (O) CFThree
D2-38a CH (i-Pr) S (O) CH2CFThree
D2-38a CH (i-Pr) S (O)2Me
D2-38a CH (i-Pr) S (O)2Et
D2-38a CH (i-Pr) S (O)2CFThree
D2-38a CH (i-Pr) S (O)2CH2CFThree
D2-38a CH (n-Bu) SMe
D2-38a CH (n-Bu) SEt
D2-38a CH (n-Bu) SCFThree
D2-38a CH (n-Bu) SCH2CFThree
D2-38a CH (n-Bu) S (O) Me
D2-38a CH (n-Bu) S (O) Et
D2-38a CH (n-Bu) S (O) CFThree
D2-38a CH (n-Bu) S (O) CH2CFThree
D2-38a CH (n-Bu) S (O)2Me
D2-38a CH (n-Bu) S (O)2Et
D2-38a CH (n-Bu) S (O)2CFThree
D2-38a CH (n-Bu) S (O)2CH2CFThree
D2-38a CH (i-Bu) SMe
D2-38a CH (i-Bu) SEt
D2-38a CH (i-Bu) SCFThree
D2-38a CH (i-Bu) SCH2CFThree
D2-38a CH (i-Bu) S (O) Me
D2-38a CH (i-Bu) S (O) Et
D2-38a CH (i-Bu) S (O) CFThree
D2-38a CH (i-Bu) S (O) CH2CFThree
D2-38a CH (i-Bu) S (O)2Me
D2-38a CH (i-Bu) S (O)2Et
D2-38a CH (i-Bu) S (O)2CFThree
D2-38a CH (i-Bu) S (O)2CH2CFThree
D2-38a CH (s-Bu) SMe
D2-38a CH (s-Bu) SEt
D2-38a CH (s-Bu) SCFThree
D2-38a CH (s-Bu) SCH2CFThree
D2-38a CH (s-Bu) S (O) Me
D2-38a CH (s-Bu) S (O) Et
D2-38a CH (s-Bu) S (O) CFThree
D2-38a CH (s-Bu) S (O) CH2CFThree
D2-38a CH (s-Bu) S (O)2Me
D2-38a CH (s-Bu) S (O)2Et
D2-38a CH (s-Bu) S (O)2CFThree
D2-38a CH (s-Bu) S (O)2CH2CFThree
D2-38a CH (t-Bu) SMe
D2-38a CH (t-Bu) SEt
D2-38a CH (t-Bu) SCFThree
D2-38a CH (t-Bu) SCH2CFThree
D2-38a CH (t-Bu) S (O) Me
D2-38a CH (t-Bu) S (O) Et
D2-38a CH (t-Bu) S (O) CFThree
D2-38a CH (t-Bu) S (O) CH2CFThree
D2-38a CH (t-Bu) S (O)2Me
D2-38a CH (t-Bu) S (O)2Et
D2-38a CH (t-Bu) S (O)2CFThree
D2-38a CH (t-Bu) S (O)2CH2CFThree
D2-38a CH (CFThreeSMe
D2-38a CH (CFThree) SEt
D2-38a CH (CFThree) SCFThree
D2-38a CH (CFThree) SCH2CFThree
D2-38a CH (CFThree) S (O) Me
D2-38a CH (CFThree) S (O) Et
D2-38a CH (CFThree) S (O) CFThree
D2-38a CH (CFThree) S (O) CH2CFThree
D2-38a CH (CFThree) S (O)2Me
D2-38a CH (CFThree) S (O)2Et
D2-38a CH (CFThree) S (O)2CFThree
D2-38a CH (CFThree) S (O)2CH2CFThree
D2-38a CH2CH2SMe
D2-38a CH2CH2SEt
D2-38a CH2CH2SCFThree
D2-38a CH2CH2SCH2CFThree
D2-38a CH2CH2S (O) Me
D2-38a CH2CH2S (O) Et
D2-38a CH2CH2S (O) CFThree
D2-38a CH2CH2S (O) CH2CFThree
D2-38a CH2CH2S (O)2Me
D2-38a CH2CH2S (O)2Et
D2-38a CH2CH2S (O)2CFThree
D2-38a CH2CH2S (O)2CH2CFThree
D2-38a CH (Me) CH2SMe
D2-38a CH (Me) CH2SEt
D2-38a CH (Me) CH2SCFThree
D2-38a CH (Me) CH2SCH2CFThree
D2-38a CH (Me) CH2S (O) Me
D2-38a CH (Me) CH2S (O) Et
D2-38a CH (Me) CH2S (O) CFThree
D2-38a CH (Me) CH2S (O) CH2CFThree
D2-38a CH (Me) CH2S (O)2Me
D2-38a CH (Me) CH2S (O)2Et
D2-38a CH (Me) CH2S (O)2CFThree
D2-38a CH (Me) CH2S (O)2CH2CFThree
D2-38a CH (Et) CH2SMe
D2-38a CH (Et) CH2SEt
D2-38a CH (Et) CH2SCFThree
D2-38a CH (Et) CH2SCH2CFThree
D2-38a CH (Et) CH2S (O) Me
D2-38a CH (Et) CH2S (O) Et
D2-38a CH (Et) CH2S (O) CFThree
D2-38a CH (Et) CH2S (O) CH2CFThree
D2-38a CH (Et) CH2S (O)2Me
D2-38a CH (Et) CH2S (O)2Et
D2-38a CH (Et) CH2S (O)2CFThree
D2-38a CH (Et) CH2S (O)2CH2CFThree
D2-38a C (Me)2CH2SMe
D2-38a C (Me)2CH2SEt
D2-38a C (Me)2CH2SCFThree
D2-38a C (Me)2CH2SCH2CFThree
D2-38a C (Me)2CH2S (O) Me
D2-38a C (Me)2CH2S (O) Et
D2-38a C (Me)2CH2S (O) CFThree
D2-38a C (Me)2CH2S (O) CH2CFThree
D2-38a C (Me)2CH2S (O)2Me
D2-38a C (Me)2CH2S (O)2Et
D2-38a C (Me)2CH2S (O)2CFThree
D2-38a C (Me)2CH2S (O)2CH2CFThree
D2-38a CH2CH (Me) SMe
D2-38a CH2CH (Me) SEt
D2-38a CH2CH (Me) SCFThree
D2-38a CH2CH (Me) SCH2CFThree
D2-38a CH2CH (Me) S (O) Me
D2-38a CH2CH (Me) S (O) Et
D2-38a CH2CH (Me) S (O) CFThree
D2-38a CH2CH (Me) S (O) CH2CFThree
D2-38a CH2CH (Me) S (O)2Me
D2-38a CH2CH (Me) S (O)2Et
D2-38a CH2CH (Me) S (O)2CFThree
D2-38a CH2CH (Me) S (O)2CH2CFThree
D2-38a CH2CH (Et) SMe
D2-38a CH2CH (Et) SEt
D2-38a CH2CH (Et) SCFThree
D2-38a CH2CH (Et) SCH2CFThree
D2-38a CH2CH (Et) S (O) Me
D2-38a CH2CH (Et) S (O) Et
D2-38a CH2CH (Et) S (O) CFThree
D2-38a CH2CH (Et) S (O) CH2CFThree
D2-38a CH2CH (Et) S (O)2Me
D2-38a CH2CH (Et) S (O)2Et
D2-38a CH2CH (Et) S (O)2CFThree
D2-38a CH2CH (Et) S (O)2CH2CFThree
D2-38a CH (Me) CH (Me) SMe
D2-38a CH (Me) CH (Me) SEt
D2-38a CH (Me) CH (Me) SCFThree
D2-38a CH (Me) CH (Me) SCH2CFThree
D2-38a CH (Me) CH (Me) S (O) Me
D2-38a CH (Me) CH (Me) S (O) Et
D2-38a CH (Me) CH (Me) S (O) CFThree
D2-38a CH (Me) CH (Me) S (O) CH2CFThree
D2-38a CH (Me) CH (Me) S (O)2Me
D2-38a CH (Me) CH (Me) S (O)2Et
D2-38a CH (Me) CH (Me) S (O)2CFThree
D2-38a CH (Me) CH (Me) S (O)2CH2CFThree
D2-92a CH2SMe
D2-92a CH2SEt
D2-92a CH2SCFThree
D2-92a CH2SCH2CFThree
D2-92a CH2S (O) Me
D2-92a CH2S (O) Et
D2-92a CH2S (O) CFThree
D2-92a CH2S (O) CH2CFThree
D2-92a CH2S (O)2Me
D2-92a CH2S (O)2Et
D2-92a CH2S (O)2CFThree
D2-92a CH2S (O)2CH2CFThree
D2-92a CH (Me) SMe
D2-92a CH (Me) SEt
D2-92a CH (Me) SCFThree
D2-92a CH (Me) SCH2CFThree
D2-92a CH (Me) S (O) Me
D2-92a CH (Me) S (O) Et
D2-92a CH (Me) S (O) CFThree
D2-92a CH (Me) S (O) CH2CFThree
D2-92a CH (Me) S (O)2Me
D2-92a CH (Me) S (O)2Et
D2-92a CH (Me) S (O)2CFThree
D2-92a CH (Me) S (O)2CH2CFThree
D2-92a CH (Et) SMe
D2-92a CH (Et) SEt
D2-92a CH (Et) SCFThree
D2-92a CH (Et) SCH2CFThree
D2-92a CH (Et) S (O) Me
D2-92a CH (Et) S (O) Et
D2-92a CH (Et) S (O) CFThree
D2-92a CH (Et) S (O) CH2CFThree
D2-92a CH (Et) S (O)2Me
D2-92a CH (Et) S (O)2Et
D2-92a CH (Et) S (O)2CFThree
D2-92a CH (Et) S (O)2CH2CFThree
D2-92a CH (n-Pr) SMe
D2-92a CH (n-Pr) SEt
D2-92a CH (n-Pr) SCFThree
D2-92a CH (n-Pr) SCH2CFThree
D2-92a CH (n-Pr) S (O) Me
D2-92a CH (n-Pr) S (O) Et
D2-92a CH (n-Pr) S (O) CFThree
D2-92a CH (n-Pr) S (O) CH2CFThree
D2-92a CH (n-Pr) S (O)2Me
D2-92a CH (n-Pr) S (O)2Et
D2-92a CH (n-Pr) S (O)2CFThree
D2-92a CH (n-Pr) S (O)2CH2CFThree
D2-92a CH (i-Pr) SMe
D2-92a CH (i-Pr) SEt
D2-92a CH (i-Pr) SCFThree
D2-92a CH (i-Pr) SCH2CFThree
D2-92a CH (i-Pr) S (O) Me
D2-92a CH (i-Pr) S (O) Et
D2-92a CH (i-Pr) S (O) CFThree
D2-92a CH (i-Pr) S (O) CH2CFThree
D2-92a CH (i-Pr) S (O)2Me
D2-92a CH (i-Pr) S (O)2Et
D2-92a CH (i-Pr) S (O)2CFThree
D2-92a CH (i-Pr) S (O)2CH2CFThree
D2-92a CH (n-Bu) SMe
D2-92a CH (n-Bu) SEt
D2-92a CH (n-Bu) SCFThree
D2-92a CH (n-Bu) SCH2CFThree
D2-92a CH (n-Bu) S (O) Me
D2-92a CH (n-Bu) S (O) Et
D2-92a CH (n-Bu) S (O) CFThree
D2-92a CH (n-Bu) S (O) CH2CFThree
D2-92a CH (n-Bu) S (O)2Me
D2-92a CH (n-Bu) S (O)2Et
D2-92a CH (n-Bu) S (O)2CFThree
D2-92a CH (n-Bu) S (O)2CH2CFThree
D2-92a CH (i-Bu) SMe
D2-92a CH (i-Bu) SEt
D2-92a CH (i-Bu) SCFThree
D2-92a CH (i-Bu) SCH2CFThree
D2-92a CH (i-Bu) S (O) Me
D2-92a CH (i-Bu) S (O) Et
D2-92a CH (i-Bu) S (O) CFThree
D2-92a CH (i-Bu) S (O) CH2CFThree
D2-92a CH (i-Bu) S (O)2Me
D2-92a CH (i-Bu) S (O)2Et
D2-92a CH (i-Bu) S (O)2CFThree
D2-92a CH (i-Bu) S (O)2CH2CFThree
D2-92a CH (s-Bu) SMe
D2-92a CH (s-Bu) SEt
D2-92a CH (s-Bu) SCFThree
D2-92a CH (s-Bu) SCH2CFThree
D2-92a CH (s-Bu) S (O) Me
D2-92a CH (s-Bu) S (O) Et
D2-92a CH (s-Bu) S (O) CFThree
D2-92a CH (s-Bu) S (O) CH2CFThree
D2-92a CH (s-Bu) S (O)2Me
D2-92a CH (s-Bu) S (O)2Et
D2-92a CH (s-Bu) S (O)2CFThree
D2-92a CH (s-Bu) S (O)2CH2CFThree
D2-92a CH (t-Bu) SMe
D2-92a CH (t-Bu) SEt
D2-92a CH (t-Bu) SCFThree
D2-92a CH (t-Bu) SCH2CFThree
D2-92a CH (t-Bu) S (O) Me
D2-92a CH (t-Bu) S (O) Et
D2-92a CH (t-Bu) S (O) CFThree
D2-92a CH (t-Bu) S (O) CH2CFThree
D2-92a CH (t-Bu) S (O)2Me
D2-92a CH (t-Bu) S (O)2Et
D2-92a CH (t-Bu) S (O)2CFThree
D2-92a CH (t-Bu) S (O)2CH2CFThree
D2-92a CH (CFThreeSMe
D2-92a CH (CFThree) SEt
D2-92a CH (CFThree) SCFThree
D2-92a CH (CFThree) SCH2CFThree
D2-92a CH (CFThree) S (O) Me
D2-92a CH (CFThree) S (O) Et
D2-92a CH (CFThree) S (O) CFThree
D2-92a CH (CFThree) S (O) CH2CFThree
D2-92a CH (CFThree) S (O)2Me
D2-92a CH (CFThree) S (O)2Et
D2-92a CH (CFThree) S (O)2CFThree
D2-92a CH (CFThree) S (O)2CH2CFThree
D2-92a CH2CH2SMe
D2-92a CH2CH2SEt
D2-92a CH2CH2SCFThree
D2-92a CH2CH2SCH2CFThree
D2-92a CH2CH2S (O) Me
D2-92a CH2CH2S (O) Et
D2-92a CH2CH2S (O) CFThree
D2-92a CH2CH2S (O) CH2CFThree
D2-92a CH2CH2S (O)2Me
D2-92a CH2CH2S (O)2Et
D2-92a CH2CH2S (O)2CFThree
D2-92a CH2CH2S (O)2CH2CFThree
D2-92a CH (Me) CH2SMe
D2-92a CH (Me) CH2SEt
D2-92a CH (Me) CH2SCFThree
D2-92a CH (Me) CH2SCH2CFThree
D2-92a CH (Me) CH2S (O) Me
D2-92a CH (Me) CH2S (O) Et
D2-92a CH (Me) CH2S (O) CFThree
D2-92a CH (Me) CH2S (O) CH2CFThree
D2-92a CH (Me) CH2S (O)2Me
D2-92a CH (Me) CH2S (O)2Et
D2-92a CH (Me) CH2S (O)2CFThree
D2-92a CH (Me) CH2S (O)2CH2CFThree
D2-92a CH (Et) CH2SMe
D2-92a CH (Et) CH2SEt
D2-92a CH (Et) CH2SCFThree
D2-92a CH (Et) CH2SCH2CFThree
D2-92a CH (Et) CH2S (O) Me
D2-92a CH (Et) CH2S (O) Et
D2-92a CH (Et) CH2S (O) CFThree
D2-92a CH (Et) CH2S (O) CH2CFThree
D2-92a CH (Et) CH2S (O)2Me
D2-92a CH (Et) CH2S (O)2Et
D2-92a CH (Et) CH2S (O)2CFThree
D2-92a CH (Et) CH2S (O)2CH2CFThree
D2-92a C (Me)2CH2SMe
D2-92a C (Me)2CH2SEt
D2-92a C (Me)2CH2SCFThree
D2-92a C (Me)2CH2SCH2CFThree
D2-92a C (Me)2CH2S (O) Me
D2-92a C (Me)2CH2S (O) Et
D2-92a C (Me)2CH2S (O) CFThree
D2-92a C (Me)2CH2S (O) CH2CFThree
D2-92a C (Me)2CH2S (O)2Me
D2-92a C (Me)2CH2S (O)2Et
D2-92a C (Me)2CH2S (O)2CFThree
D2-92a C (Me)2CH2S (O)2CH2CFThree
D2-92a CH2CH (Me) SMe
D2-92a CH2CH (Me) SEt
D2-92a CH2CH (Me) SCFThree
D2-92a CH2CH (Me) SCH2CFThree
D2-92a CH2CH (Me) S (O) Me
D2-92a CH2CH (Me) S (O) Et
D2-92a CH2CH (Me) S (O) CFThree
D2-92a CH2CH (Me) S (O) CH2CFThree
D2-92a CH2CH (Me) S (O)2Me
D2-92a CH2CH (Me) S (O)2Et
D2-92a CH2CH (Me) S (O)2CFThree
D2-92a CH2CH (Me) S (O)2CH2CFThree
D2-92a CH2CH (Et) SMe
D2-92a CH2CH (Et) SEt
D2-92a CH2CH (Et) SCFThree
D2-92a CH2CH (Et) SCH2CFThree
D2-92a CH2CH (Et) S (O) Me
D2-92a CH2CH (Et) S (O) Et
D2-92a CH2CH (Et) S (O) CFThree
D2-92a CH2CH (Et) S (O) CH2CFThree
D2-92a CH2CH (Et) S (O)2Me
D2-92a CH2CH (Et) S (O)2Et
D2-92a CH2CH (Et) S (O)2CFThree
D2-92a CH2CH (Et) S (O)2CH2CFThree
D2-92a CH (Me) CH (Me) SMe
D2-92a CH (Me) CH (Me) SEt
D2-92a CH (Me) CH (Me) SCFThree
D2-92a CH (Me) CH (Me) SCH2CFThree
D2-92a CH (Me) CH (Me) S (O) Me
D2-92a CH (Me) CH (Me) S (O) Et
D2-92a CH (Me) CH (Me) S (O) CFThree
D2-92a CH (Me) CH (Me) S (O) CH2CFThree
D2-92a CH (Me) CH (Me) S (O)2Me
D2-92a CH (Me) CH (Me) S (O)2Et
D2-92a CH (Me) CH (Me) S (O)2CFThree
D2-92a CH (Me) CH (Me) S (O)2CH2CFThree
CH (Me) SMe CH2SMe
CH (Me) SMe CH2SEt
CH (Me) SMe CH2SCFThree
CH (Me) SMe CH2SCH2CFThree
CH (Me) SMe CH2S (O) Me
CH (Me) SMe CH2S (O) Et
CH (Me) SMe CH2S (O) CFThree
CH (Me) SMe CH2S (O) CH2CFThree
CH (Me) SMe CH2S (O)2Me
CH (Me) SMe CH2S (O)2Et
CH (Me) SMe CH2S (O)2CFThree
CH (Me) SMe CH2S (O)2CH2CFThree
CH (Me) SMe CH (Me) SMe
CH (Me) SMe CH (Me) SEt
CH (Me) SMe CH (Me) SCFThree
CH (Me) SMe CH (Me) SCH2CFThree
CH (Me) SMe CH (Me) S (O) Me
CH (Me) SMe CH (Me) S (O) Et
CH (Me) SMe CH (Me) S (O) CFThree
CH (Me) SMe CH (Me) S (O) CH2CFThree
CH (Me) SMe CH (Me) S (O)2Me
CH (Me) SMe CH (Me) S (O)2Et
CH (Me) SMe CH (Me) S (O)2CFThree
CH (Me) SMe CH (Me) S (O)2CH2CFThree
CH (Me) SMe CH (Et) SMe
CH (Me) SMe CH (Et) SEt
CH (Me) SMe CH (Et) SCFThree
CH (Me) SMe CH (Et) SCH2CFThree
CH (Me) SMe CH (Et) S (O) Me
CH (Me) SMe CH (Et) S (O) Et
CH (Me) SMe CH (Et) S (O) CFThree
CH (Me) SMe CH (Et) S (O) CH2CFThree
CH (Me) SMe CH (Et) S (O)2Me
CH (Me) SMe CH (Et) S (O)2Et
CH (Me) SMe CH (Et) S (O)2CFThree
CH (Me) SMe CH (Et) S (O)2CH2CFThree
CH (Me) SMe CH (n-Pr) SMe
CH (Me) SMe CH (n-Pr) SEt
CH (Me) SMe CH (n-Pr) SCFThree
CH (Me) SMe CH (n-Pr) SCH2CFThree
CH (Me) SMe CH (n-Pr) S (O) Me
CH (Me) SMe CH (n-Pr) S (O) Et
CH (Me) SMe CH (n-Pr) S (O) CFThree
CH (Me) SMe CH (n-Pr) S (O) CH2CFThree
CH (Me) SMe CH (n-Pr) S (O)2Me
CH (Me) SMe CH (n-Pr) S (O)2Et
CH (Me) SMe CH (n-Pr) S (O)2CFThree
CH (Me) SMe CH (n-Pr) S (O)2CH2CFThree
CH (Me) SMe CH (i-Pr) SMe
CH (Me) SMe CH (i-Pr) SEt
CH (Me) SMe CH (i-Pr) SCFThree
CH (Me) SMe CH (i-Pr) SCH2CFThree
CH (Me) SMe CH (i-Pr) S (O) Me
CH (Me) SMe CH (i-Pr) S (O) Et
CH (Me) SMe CH (i-Pr) S (O) CFThree
CH (Me) SMe CH (i-Pr) S (O) CH2CFThree
CH (Me) SMe CH (i-Pr) S (O)2Me
CH (Me) SMe CH (i-Pr) S (O)2Et
CH (Me) SMe CH (i-Pr) S (O)2CFThree
CH (Me) SMe CH (i-Pr) S (O)2CH2CFThree
CH (Me) SMe CH (n-Bu) SMe
CH (Me) SMe CH (n-Bu) SEt
CH (Me) SMe CH (n-Bu) SCFThree
CH (Me) SMe CH (n-Bu) SCH2CFThree
CH (Me) SMe CH (n-Bu) S (O) Me
CH (Me) SMe CH (n-Bu) S (O) Et
CH (Me) SMe CH (n-Bu) S (O) CFThree
CH (Me) SMe CH (n-Bu) S (O) CH2CFThree
CH (Me) SMe CH (n-Bu) S (O)2Me
CH (Me) SMe CH (n-Bu) S (O)2Et
CH (Me) SMe CH (n-Bu) S (O)2CFThree
CH (Me) SMe CH (n-Bu) S (O)2CH2CFThree
CH (Me) SMe CH (i-Bu) SMe
CH (Me) SMe CH (i-Bu) SEt
CH (Me) SMe CH (i-Bu) SCFThree
CH (Me) SMe CH (i-Bu) SCH2CFThree
CH (Me) SMe CH (i-Bu) S (O) Me
CH (Me) SMe CH (i-Bu) S (O) Et
CH (Me) SMe CH (i-Bu) S (O) CFThree
CH (Me) SMe CH (i-Bu) S (O) CH2CFThree
CH (Me) SMe CH (i-Bu) S (O)2Me
CH (Me) SMe CH (i-Bu) S (O)2Et
CH (Me) SMe CH (i-Bu) S (O)2CFThree
CH (Me) SMe CH (i-Bu) S (O)2CH2CFThree
CH (Me) SMe CH (s-Bu) SMe
CH (Me) SMe CH (s-Bu) SEt
CH (Me) SMe CH (s-Bu) SCFThree
CH (Me) SMe CH (s-Bu) SCH2CFThree
CH (Me) SMe CH (s-Bu) S (O) Me
CH (Me) SMe CH (s-Bu) S (O) Et
CH (Me) SMe CH (s-Bu) S (O) CFThree
CH (Me) SMe CH (s-Bu) S (O) CH2CFThree
CH (Me) SMe CH (s-Bu) S (O)2Me
CH (Me) SMe CH (s-Bu) S (O)2Et
CH (Me) SMe CH (s-Bu) S (O)2CFThree
CH (Me) SMe CH (s-Bu) S (O)2CH2CFThree
CH (Me) SMe CH (t-Bu) SMe
CH (Me) SMe CH (t-Bu) SEt
CH (Me) SMe CH (t-Bu) SCFThree
CH (Me) SMe CH (t-Bu) SCH2CFThree
CH (Me) SMe CH (t-Bu) S (O) Me
CH (Me) SMe CH (t-Bu) S (O) Et
CH (Me) SMe CH (t-Bu) S (O) CFThree
CH (Me) SMe CH (t-Bu) S (O) CH2CFThree
CH (Me) SMe CH (t-Bu) S (O)2Me
CH (Me) SMe CH (t-Bu) S (O)2Et
CH (Me) SMe CH (t-Bu) S (O)2CFThree
CH (Me) SMe CH (t-Bu) S (O)2CH2CFThree
CH (Me) SMe CH (CFThreeSMe
CH (Me) SMe CH (CFThree) SEt
CH (Me) SMe CH (CFThree) SCFThree
CH (Me) SMe CH (CFThree) SCH2CFThree
CH (Me) SMe CH (CFThree) S (O) Me
CH (Me) SMe CH (CFThree) S (O) Et
CH (Me) SMe CH (CFThree) S (O) CFThree
CH (Me) SMe CH (CFThree) S (O) CH2CFThree
CH (Me) SMe CH (CFThree) S (O)2Me
CH (Me) SMe CH (CFThree) S (O)2Et
CH (Me) SMe CH (CFThree) S (O)2CFThree
CH (Me) SMe CH (CFThree) S (O)2CH2CFThree
CH (Me) SMe CH2CH2SMe
CH (Me) SMe CH2CH2SEt
CH (Me) SMe CH2CH2SCFThree
CH (Me) SMe CH2CH2SCH2CFThree
CH (Me) SMe CH2CH2S (O) Me
CH (Me) SMe CH2CH2S (O) Et
CH (Me) SMe CH2CH2S (O) CFThree
CH (Me) SMe CH2CH2S (O) CH2CFThree
CH (Me) SMe CH2CH2S (O)2Me
CH (Me) SMe CH2CH2S (O)2Et
CH (Me) SMe CH2CH2S (O)2CFThree
CH (Me) SMe CH2CH2S (O)2CH2CFThree
CH (Me) SMe CH (Me) CH2SMe
CH (Me) SMe CH (Me) CH2SEt
CH (Me) SMe CH (Me) CH2SCFThree
CH (Me) SMe CH (Me) CH2SCH2CFThree
CH (Me) SMe CH (Me) CH2S (O) Me
CH (Me) SMe CH (Me) CH2S (O) Et
CH (Me) SMe CH (Me) CH2S (O) CFThree
CH (Me) SMe CH (Me) CH2S (O) CH2CFThree
CH (Me) SMe CH (Me) CH2S (O)2Me
CH (Me) SMe CH (Me) CH2S (O)2Et
CH (Me) SMe CH (Me) CH2S (O)2CFThree
CH (Me) SMe CH (Me) CH2S (O)2CH2CFThree
CH (Me) SMe CH (Et) CH2SMe
CH (Me) SMe CH (Et) CH2SEt
CH (Me) SMe CH (Et) CH2SCFThree
CH (Me) SMe CH (Et) CH2SCH2CFThree
CH (Me) SMe CH (Et) CH2S (O) Me
CH (Me) SMe CH (Et) CH2S (O) Et
CH (Me) SMe CH (Et) CH2S (O) CFThree
CH (Me) SMe CH (Et) CH2S (O) CH2CFThree
CH (Me) SMe CH (Et) CH2S (O)2Me
CH (Me) SMe CH (Et) CH2S (O)2Et
CH (Me) SMe CH (Et) CH2S (O)2CFThree
CH (Me) SMe CH (Et) CH2S (O)2CH2CFThree
CH (Me) SMe C (Me)2CH2SMe
CH (Me) SMe C (Me)2CH2SEt
CH (Me) SMe C (Me)2CH2SCFThree
CH (Me) SMe C (Me)2CH2SCH2CFThree
CH (Me) SMe C (Me)2CH2S (O) Me
CH (Me) SMe C (Me)2CH2S (O) Et
CH (Me) SMe C (Me)2CH2S (O) CFThree
CH (Me) SMe C (Me)2CH2S (O) CH2CFThree
CH (Me) SMe C (Me)2CH2S (O)2Me
CH (Me) SMe C (Me)2CH2S (O)2Et
CH (Me) SMe C (Me)2CH2S (O)2CFThree
CH (Me) SMe C (Me)2CH2S (O)2CH2CFThree
CH (Me) SMe CH2CH (Me) SMe
CH (Me) SMe CH2CH (Me) SEt
CH (Me) SMe CH2CH (Me) SCFThree
CH (Me) SMe CH2CH (Me) SCH2CFThree
CH (Me) SMe CH2CH (Me) S (O) Me
CH (Me) SMe CH2CH (Me) S (O) Et
CH (Me) SMe CH2CH (Me) S (O) CFThree
CH (Me) SMe CH2CH (Me) S (O) CH2CFThree
CH (Me) SMe CH2CH (Me) S (O)2Me
CH (Me) SMe CH2CH (Me) S (O)2Et
CH (Me) SMe CH2CH (Me) S (O)2CFThree
CH (Me) SMe CH2CH (Me) S (O)2CH2CFThree
CH (Me) SMe CH2CH (Et) SMe
CH (Me) SMe CH2CH (Et) SEt
CH (Me) SMe CH2CH (Et) SCFThree
CH (Me) SMe CH2CH (Et) SCH2CFThree
CH (Me) SMe CH2CH (Et) S (O) Me
CH (Me) SMe CH2CH (Et) S (O) Et
CH (Me) SMe CH2CH (Et) S (O) CFThree
CH (Me) SMe CH2CH (Et) S (O) CH2CFThree
CH (Me) SMe CH2CH (Et) S (O)2Me
CH (Me) SMe CH2CH (Et) S (O)2Et
CH (Me) SMe CH2CH (Et) S (O)2CFThree
CH (Me) SMe CH2CH (Et) S (O)2CH2CFThree
CH (Me) SMe CH (Me) CH (Me) SMe
CH (Me) SMe CH (Me) CH (Me) SEt
CH (Me) SMe CH (Me) CH (Me) SCFThree
CH (Me) SMe CH (Me) CH (Me) SCH2CFThree
CH (Me) SMe CH (Me) CH (Me) S (O) Me
CH (Me) SMe CH (Me) CH (Me) S (O) Et
CH (Me) SMe CH (Me) CH (Me) S (O) CFThree
CH (Me) SMe CH (Me) CH (Me) S (O) CH2CFThree
CH (Me) SMe CH (Me) CH (Me) S (O)2Me
CH (Me) SMe CH (Me) CH (Me) S (O)2Et
CH (Me) SMe CH (Me) CH (Me) S (O)2CFThree
CH (Me) SMe CH (Me) CH (Me) S (O)2CH2CFThree
C (O) Me CH2SMe
C (O) Me CH2SEt
C (O) Me CH2SCFThree
C (O) Me CH2SCH2CFThree
C (O) Me CH2S (O) Me
C (O) Me CH2S (O) Et
C (O) Me CH2S (O) CFThree
C (O) Me CH2S (O) CH2CFThree
C (O) Me CH2S (O)2Me
C (O) Me CH2S (O)2Et
C (O) Me CH2S (O)2CFThree
C (O) Me CH2S (O)2CH2CFThree
C (O) Me CH (Me) SMe
C (O) Me CH (Me) SEt
C (O) Me CH (Me) SCFThree
C (O) Me CH (Me) SCH2CFThree
C (O) Me CH (Me) S (O) Me
C (O) Me CH (Me) S (O) Et
C (O) Me CH (Me) S (O) CFThree
C (O) Me CH (Me) S (O) CH2CFThree
C (O) Me CH (Me) S (O)2Me
C (O) Me CH (Me) S (O)2Et
C (O) Me CH (Me) S (O)2CFThree
C (O) Me CH (Me) S (O)2CH2CFThree
C (O) Me CH (Et) SMe
C (O) Me CH (Et) SEt
C (O) Me CH (Et) SCFThree
C (O) Me CH (Et) SCH2CFThree
C (O) Me CH (Et) S (O) Me
C (O) Me CH (Et) S (O) Et
C (O) Me CH (Et) S (O) CFThree
C (O) Me CH (Et) S (O) CH2CFThree
C (O) Me CH (Et) S (O)2Me
C (O) Me CH (Et) S (O)2Et
C (O) Me CH (Et) S (O)2CFThree
C (O) Me CH (Et) S (O)2CH2CFThree
C (O) Me CH (n-Pr) SMe
C (O) Me CH (n-Pr) SEt
C (O) Me CH (n-Pr) SCFThree
C (O) Me CH (n-Pr) SCH2CFThree
C (O) Me CH (n-Pr) S (O) Me
C (O) Me CH (n-Pr) S (O) Et
C (O) Me CH (n-Pr) S (O) CFThree
C (O) Me CH (n-Pr) S (O) CH2CFThree
C (O) Me CH (n-Pr) S (O)2Me
C (O) Me CH (n-Pr) S (O)2Et
C (O) Me CH (n-Pr) S (O)2CFThree
C (O) Me CH (n-Pr) S (O)2CH2CFThree
C (O) Me CH (i-Pr) SMe
C (O) Me CH (i-Pr) SEt
C (O) Me CH (i-Pr) SCFThree
C (O) Me CH (i-Pr) SCH2CFThree
C (O) Me CH (i-Pr) S (O) Me
C (O) Me CH (i-Pr) S (O) Et
C (O) Me CH (i-Pr) S (O) CFThree
C (O) Me CH (i-Pr) S (O) CH2CFThree
C (O) Me CH (i-Pr) S (O)2Me
C (O) Me CH (i-Pr) S (O)2Et
C (O) Me CH (i-Pr) S (O)2CFThree
C (O) Me CH (i-Pr) S (O)2CH2CFThree
C (O) Me CH (n-Bu) SMe
C (O) Me CH (n-Bu) SEt
C (O) Me CH (n-Bu) SCFThree
C (O) Me CH (n-Bu) SCH2CFThree
C (O) Me CH (n-Bu) S (O) Me
C (O) Me CH (n-Bu) S (O) Et
C (O) Me CH (n-Bu) S (O) CFThree
C (O) Me CH (n-Bu) S (O) CH2CFThree
C (O) Me CH (n-Bu) S (O)2Me
C (O) Me CH (n-Bu) S (O)2Et
C (O) Me CH (n-Bu) S (O)2CFThree
C (O) Me CH (n-Bu) S (O)2CH2CFThree
C (O) Me CH (i-Bu) SMe
C (O) Me CH (i-Bu) SEt
C (O) Me CH (i-Bu) SCFThree
C (O) Me CH (i-Bu) SCH2CFThree
C (O) Me CH (i-Bu) S (O) Me
C (O) Me CH (i-Bu) S (O) Et
C (O) Me CH (i-Bu) S (O) CFThree
C (O) Me CH (i-Bu) S (O) CH2CFThree
C (O) Me CH (i-Bu) S (O)2Me
C (O) Me CH (i-Bu) S (O)2Et
C (O) Me CH (i-Bu) S (O)2CFThree
C (O) Me CH (i-Bu) S (O)2CH2CFThree
C (O) Me CH (s-Bu) SMe
C (O) Me CH (s-Bu) SEt
C (O) Me CH (s-Bu) SCFThree
C (O) Me CH (s-Bu) SCH2CFThree
C (O) Me CH (s-Bu) S (O) Me
C (O) Me CH (s-Bu) S (O) Et
C (O) Me CH (s-Bu) S (O) CFThree
C (O) Me CH (s-Bu) S (O) CH2CFThree
C (O) Me CH (s-Bu) S (O)2Me
C (O) Me CH (s-Bu) S (O)2Et
C (O) Me CH (s-Bu) S (O)2CFThree
C (O) Me CH (s-Bu) S (O)2CH2CFThree
C (O) Me CH (t-Bu) SMe
C (O) Me CH (t-Bu) SEt
C (O) Me CH (t-Bu) SCFThree
C (O) Me CH (t-Bu) SCH2CFThree
C (O) Me CH (t-Bu) S (O) Me
C (O) Me CH (t-Bu) S (O) Et
C (O) Me CH (t-Bu) S (O) CFThree
C (O) Me CH (t-Bu) S (O) CH2CFThree
C (O) Me CH (t-Bu) S (O)2Me
C (O) Me CH (t-Bu) S (O)2Et
C (O) Me CH (t-Bu) S (O)2CFThree
C (O) Me CH (t-Bu) S (O)2CH2CFThree
C (O) Me CH (CFThreeSMe
C (O) Me CH (CFThree) SEt
C (O) Me CH (CFThree) SCFThree
C (O) Me CH (CFThree) SCH2CFThree
C (O) Me CH (CFThree) S (O) Me
C (O) Me CH (CFThree) S (O) Et
C (O) Me CH (CFThree) S (O) CFThree
C (O) Me CH (CFThree) S (O) CH2CFThree
C (O) Me CH (CFThree) S (O)2Me
C (O) Me CH (CFThree) S (O)2Et
C (O) Me CH (CFThree) S (O)2CFThree
C (O) Me CH (CFThree) S (O)2CH2CFThree
C (O) Me CH2CH2SMe
C (O) Me CH2CH2SEt
C (O) Me CH2CH2SCFThree
C (O) Me CH2CH2SCH2CFThree
C (O) Me CH2CH2S (O) Me
C (O) Me CH2CH2S (O) Et
C (O) Me CH2CH2S (O) CFThree
C (O) Me CH2CH2S (O) CH2CFThree
C (O) Me CH2CH2S (O)2Me
C (O) Me CH2CH2S (O)2Et
C (O) Me CH2CH2S (O)2CFThree
C (O) Me CH2CH2S (O)2CH2CFThree
C (O) Me CH (Me) CH2SMe
C (O) Me CH (Me) CH2SEt
C (O) Me CH (Me) CH2SCFThree
C (O) Me CH (Me) CH2SCH2CFThree
C (O) Me CH (Me) CH2S (O) Me
C (O) Me CH (Me) CH2S (O) Et
C (O) Me CH (Me) CH2S (O) CFThree
C (O) Me CH (Me) CH2S (O) CH2CFThree
C (O) Me CH (Me) CH2S (O)2Me
C (O) Me CH (Me) CH2S (O)2Et
C (O) Me CH (Me) CH2S (O)2CFThree
C (O) Me CH (Me) CH2S (O)2CH2CFThree
C (O) Me CH (Et) CH2SMe
C (O) Me CH (Et) CH2SEt
C (O) Me CH (Et) CH2SCFThree
C (O) Me CH (Et) CH2SCH2CFThree
C (O) Me CH (Et) CH2S (O) Me
C (O) Me CH (Et) CH2S (O) Et
C (O) Me CH (Et) CH2S (O) CFThree
C (O) Me CH (Et) CH2S (O) CH2CFThree
C (O) Me CH (Et) CH2S (O)2Me
C (O) Me CH (Et) CH2S (O)2Et
C (O) Me CH (Et) CH2S (O)2CFThree
C (O) Me CH (Et) CH2S (O)2CH2CFThree
C (O) Me C (Me)2CH2SMe
C (O) Me C (Me)2CH2SEt
C (O) Me C (Me)2CH2SCFThree
C (O) Me C (Me)2CH2SCH2CFThree
C (O) Me C (Me)2CH2S (O) Me
C (O) Me C (Me)2CH2S (O) Et
C (O) Me C (Me)2CH2S (O) CFThree
C (O) Me C (Me)2CH2S (O) CH2CFThree
C (O) Me C (Me)2CH2S (O)2Me
C (O) Me C (Me)2CH2S (O)2Et
C (O) Me C (Me)2CH2S (O)2CFThree
C (O) Me C (Me)2CH2S (O)2CH2CFThree
C (O) Me CH2CH (Me) SMe
C (O) Me CH2CH (Me) SEt
C (O) Me CH2CH (Me) SCFThree
C (O) Me CH2CH (Me) SCH2CFThree
C (O) Me CH2CH (Me) S (O) Me
C (O) Me CH2CH (Me) S (O) Et
C (O) Me CH2CH (Me) S (O) CFThree
C (O) Me CH2CH (Me) S (O) CH2CFThree
C (O) Me CH2CH (Me) S (O)2Me
C (O) Me CH2CH (Me) S (O)2Et
C (O) Me CH2CH (Me) S (O)2CFThree
C (O) Me CH2CH (Me) S (O)2CH2CFThree
C (O) Me CH2CH (Et) SMe
C (O) Me CH2CH (Et) SEt
C (O) Me CH2CH (Et) SCFThree
C (O) Me CH2CH (Et) SCH2CFThree
C (O) Me CH2CH (Et) S (O) Me
C (O) Me CH2CH (Et) S (O) Et
C (O) Me CH2CH (Et) S (O) CFThree
C (O) Me CH2CH (Et) S (O) CH2CFThree
C (O) Me CH2CH (Et) S (O)2Me
C (O) Me CH2CH (Et) S (O)2Et
C (O) Me CH2CH (Et) S (O)2CFThree
C (O) Me CH2CH (Et) S (O)2CH2CFThree
C (O) Me CH (Me) CH (Me) SMe
C (O) Me CH (Me) CH (Me) SEt
C (O) Me CH (Me) CH (Me) SCFThree
C (O) Me CH (Me) CH (Me) SCH2CFThree
C (O) Me CH (Me) CH (Me) S (O) Me
C (O) Me CH (Me) CH (Me) S (O) Et
C (O) Me CH (Me) CH (Me) S (O) CFThree
C (O) Me CH (Me) CH (Me) S (O) CH2CFThree
C (O) Me CH (Me) CH (Me) S (O)2Me
C (O) Me CH (Me) CH (Me) S (O)2Et
C (O) Me CH (Me) CH (Me) S (O)2CFThree
C (O) Me CH (Me) CH (Me) S (O)2CH2CFThree
C (O) OMe CH2SMe
C (O) OMe CH2SEt
C (O) OMe CH2SCFThree
C (O) OMe CH2SCH2CFThree
C (O) OMe CH2S (O) Me
C (O) OMe CH2S (O) Et
C (O) OMe CH2S (O) CFThree
C (O) OMe CH2S (O) CH2CFThree
C (O) OMe CH2S (O)2Me
C (O) OMe CH2S (O)2Et
C (O) OMe CH2S (O)2CFThree
C (O) OMe CH2S (O)2CH2CFThree
C (O) OMe CH (Me) SMe
C (O) OMe CH (Me) SEt
C (O) OMe CH (Me) SCFThree
C (O) OMe CH (Me) SCH2CFThree
C (O) OMe CH (Me) S (O) Me
C (O) OMe CH (Me) S (O) Et
C (O) OMe CH (Me) S (O) CFThree
C (O) OMe CH (Me) S (O) CH2CFThree
C (O) OMe CH (Me) S (O)2Me
C (O) OMe CH (Me) S (O)2Et
C (O) OMe CH (Me) S (O)2CFThree
C (O) OMe CH (Me) S (O)2CH2CFThree
C (O) OMe CH (Et) SMe
C (O) OMe CH (Et) SEt
C (O) OMe CH (Et) SCFThree
C (O) OMe CH (Et) SCH2CFThree
C (O) OMe CH (Et) S (O) Me
C (O) OMe CH (Et) S (O) Et
C (O) OMe CH (Et) S (O) CFThree
C (O) OMe CH (Et) S (O) CH2CFThree
C (O) OMe CH (Et) S (O)2Me
C (O) OMe CH (Et) S (O)2Et
C (O) OMe CH (Et) S (O)2CFThree
C (O) OMe CH (Et) S (O)2CH2CFThree
C (O) OMe CH (n-Pr) SMe
C (O) OMe CH (n-Pr) SEt
C (O) OMe CH (n-Pr) SCFThree
C (O) OMe CH (n-Pr) SCH2CFThree
C (O) OMe CH (n-Pr) S (O) Me
C (O) OMe CH (n-Pr) S (O) Et
C (O) OMe CH (n-Pr) S (O) CFThree
C (O) OMe CH (n-Pr) S (O) CH2CFThree
C (O) OMe CH (n-Pr) S (O)2Me
C (O) OMe CH (n-Pr) S (O)2Et
C (O) OMe CH (n-Pr) S (O)2CFThree
C (O) OMe CH (n-Pr) S (O)2CH2CFThree
C (O) OMe CH (i-Pr) SMe
C (O) OMe CH (i-Pr) SEt
C (O) OMe CH (i-Pr) SCFThree
C (O) OMe CH (i-Pr) SCH2CFThree
C (O) OMe CH (i-Pr) S (O) Me
C (O) OMe CH (i-Pr) S (O) Et
C (O) OMe CH (i-Pr) S (O) CFThree
C (O) OMe CH (i-Pr) S (O) CH2CFThree
C (O) OMe CH (i-Pr) S (O)2Me
C (O) OMe CH (i-Pr) S (O)2Et
C (O) OMe CH (i-Pr) S (O)2CFThree
C (O) OMe CH (i-Pr) S (O)2CH2CFThree
C (O) OMe CH (n-Bu) SMe
C (O) OMe CH (n-Bu) SEt
C (O) OMe CH (n-Bu) SCFThree
C (O) OMe CH (n-Bu) SCH2CFThree
C (O) OMe CH (n-Bu) S (O) Me
C (O) OMe CH (n-Bu) S (O) Et
C (O) OMe CH (n-Bu) S (O) CFThree
C (O) OMe CH (n-Bu) S (O) CH2CFThree
C (O) OMe CH (n-Bu) S (O)2Me
C (O) OMe CH (n-Bu) S (O)2Et
C (O) OMe CH (n-Bu) S (O)2CFThree
C (O) OMe CH (n-Bu) S (O)2CH2CFThree
C (O) OMe CH (i-Bu) SMe
C (O) OMe CH (i-Bu) SEt
C (O) OMe CH (i-Bu) SCFThree
C (O) OMe CH (i-Bu) SCH2CFThree
C (O) OMe CH (i-Bu) S (O) Me
C (O) OMe CH (i-Bu) S (O) Et
C (O) OMe CH (i-Bu) S (O) CFThree
C (O) OMe CH (i-Bu) S (O) CH2CFThree
C (O) OMe CH (i-Bu) S (O)2Me
C (O) OMe CH (i-Bu) S (O)2Et
C (O) OMe CH (i-Bu) S (O)2CFThree
C (O) OMe CH (i-Bu) S (O)2CH2CFThree
C (O) OMe CH (s-Bu) SMe
C (O) OMe CH (s-Bu) SEt
C (O) OMe CH (s-Bu) SCFThree
C (O) OMe CH (s-Bu) SCH2CFThree
C (O) OMe CH (s-Bu) S (O) Me
C (O) OMe CH (s-Bu) S (O) Et
C (O) OMe CH (s-Bu) S (O) CFThree
C (O) OMe CH (s-Bu) S (O) CH2CFThree
C (O) OMe CH (s-Bu) S (O)2Me
C (O) OMe CH (s-Bu) S (O)2Et
C (O) OMe CH (s-Bu) S (O)2CFThree
C (O) OMe CH (s-Bu) S (O)2CH2CFThree
C (O) OMe CH (t-Bu) SMe
C (O) OMe CH (t-Bu) SEt
C (O) OMe CH (t-Bu) SCFThree
C (O) OMe CH (t-Bu) SCH2CFThree
C (O) OMe CH (t-Bu) S (O) Me
C (O) OMe CH (t-Bu) S (O) Et
C (O) OMe CH (t-Bu) S (O) CFThree
C (O) OMe CH (t-Bu) S (O) CH2CFThree
C (O) OMe CH (t-Bu) S (O)2Me
C (O) OMe CH (t-Bu) S (O)2Et
C (O) OMe CH (t-Bu) S (O)2CFThree
C (O) OMe CH (t-Bu) S (O)2CH2CFThree
C (O) OMe CH (CFThreeSMe
C (O) OMe CH (CFThree) SEt
C (O) OMe CH (CFThree) SCFThree
C (O) OMe CH (CFThree) SCH2CFThree
C (O) OMe CH (CFThree) S (O) Me
C (O) OMe CH (CFThree) S (O) Et
C (O) OMe CH (CFThree) S (O) CFThree
C (O) OMe CH (CFThree) S (O) CH2CFThree
C (O) OMe CH (CFThree) S (O)2Me
C (O) OMe CH (CFThree) S (O)2Et
C (O) OMe CH (CFThree) S (O)2CFThree
C (O) OMe CH (CFThree) S (O)2CH2CFThree
C (O) OMe CH2CH2SMe
C (O) OMe CH2CH2SEt
C (O) OMe CH2CH2SCFThree
C (O) OMe CH2CH2SCH2CFThree
C (O) OMe CH2CH2S (O) Me
C (O) OMe CH2CH2S (O) Et
C (O) OMe CH2CH2S (O) CFThree
C (O) OMe CH2CH2S (O) CH2CFThree
C (O) OMe CH2CH2S (O)2Me
C (O) OMe CH2CH2S (O)2Et
C (O) OMe CH2CH2S (O)2CFThree
C (O) OMe CH2CH2S (O)2CH2CFThree
C (O) OMe CH (Me) CH2SMe
C (O) OMe CH (Me) CH2SEt
C (O) OMe CH (Me) CH2SCFThree
C (O) OMe CH (Me) CH2SCH2CFThree
C (O) OMe CH (Me) CH2S (O) Me
C (O) OMe CH (Me) CH2S (O) Et
C (O) OMe CH (Me) CH2S (O) CFThree
C (O) OMe CH (Me) CH2S (O) CH2CFThree
C (O) OMe CH (Me) CH2S (O)2Me
C (O) OMe CH (Me) CH2S (O)2Et
C (O) OMe CH (Me) CH2S (O)2CFThree
C (O) OMe CH (Me) CH2S (O)2CH2CFThree
C (O) OMe CH (Et) CH2SMe
C (O) OMe CH (Et) CH2SEt
C (O) OMe CH (Et) CH2SCFThree
C (O) OMe CH (Et) CH2SCH2CFThree
C (O) OMe CH (Et) CH2S (O) Me
C (O) OMe CH (Et) CH2S (O) Et
C (O) OMe CH (Et) CH2S (O) CFThree
C (O) OMe CH (Et) CH2S (O) CH2CFThree
C (O) OMe CH (Et) CH2S (O)2Me
C (O) OMe CH (Et) CH2S (O)2Et
C (O) OMe CH (Et) CH2S (O)2CFThree
C (O) OMe CH (Et) CH2S (O)2CH2CFThree
C (O) OMe C (Me)2CH2SMe
C (O) OMe C (Me)2CH2SEt
C (O) OMe C (Me)2CH2SCFThree
C (O) OMe C (Me)2CH2SCH2CFThree
C (O) OMe C (Me)2CH2S (O) Me
C (O) OMe C (Me)2CH2S (O) Et
C (O) OMe C (Me)2CH2S (O) CFThree
C (O) OMe C (Me)2CH2S (O) CH2CFThree
C (O) OMe C (Me)2CH2S (O)2Me
C (O) OMe C (Me)2CH2S (O)2Et
C (O) OMe C (Me)2CH2S (O)2CFThree
C (O) OMe C (Me)2CH2S (O)2CH2CFThree
C (O) OMe CH2CH (Me) SMe
C (O) OMe CH2CH (Me) SEt
C (O) OMe CH2CH (Me) SCFThree
C (O) OMe CH2CH (Me) SCH2CFThree
C (O) OMe CH2CH (Me) S (O) Me
C (O) OMe CH2CH (Me) S (O) Et
C (O) OMe CH2CH (Me) S (O) CFThree
C (O) OMe CH2CH (Me) S (O) CH2CFThree
C (O) OMe CH2CH (Me) S (O)2Me
C (O) OMe CH2CH (Me) S (O)2Et
C (O) OMe CH2CH (Me) S (O)2CFThree
C (O) OMe CH2CH (Me) S (O)2CH2CFThree
C (O) OMe CH2CH (Et) SMe
C (O) OMe CH2CH (Et) SEt
C (O) OMe CH2CH (Et) SCFThree
C (O) OMe CH2CH (Et) SCH2CFThree
C (O) OMe CH2CH (Et) S (O) Me
C (O) OMe CH2CH (Et) S (O) Et
C (O) OMe CH2CH (Et) S (O) CFThree
C (O) OMe CH2CH (Et) S (O) CH2CFThree
C (O) OMe CH2CH (Et) S (O)2Me
C (O) OMe CH2CH (Et) S (O)2Et
C (O) OMe CH2CH (Et) S (O)2CFThree
C (O) OMe CH2CH (Et) S (O)2CH2CFThree
C (O) OMe CH (Me) CH (Me) SMe
C (O) OMe CH (Me) CH (Me) SEt
C (O) OMe CH (Me) CH (Me) SCFThree
C (O) OMe CH (Me) CH (Me) SCH2CFThree
C (O) OMe CH (Me) CH (Me) S (O) Me
C (O) OMe CH (Me) CH (Me) S (O) Et
C (O) OMe CH (Me) CH (Me) S (O) CFThree
C (O) OMe CH (Me) CH (Me) S (O) CH2CFThree
C (O) OMe CH (Me) CH (Me) S (O)2Me
C (O) OMe CH (Me) CH (Me) S (O)2Et
C (O) OMe CH (Me) CH (Me) S (O)2CFThree
C (O) OMe CH (Me) CH (Me) S (O)2CH2CFThree
CH2OMe CH2SMe
CH2OMe CH2SEt
CH2OMe CH2SCFThree
CH2OMe CH2SCH2CFThree
CH2OMe CH2S (O) Me
CH2OMe CH2S (O) Et
CH2OMe CH2S (O) CFThree
CH2OMe CH2S (O) CH2CFThree
CH2OMe CH2S (O)2Me
CH2OMe CH2S (O)2Et
CH2OMe CH2S (O)2CFThree
CH2OMe CH2S (O)2CH2CFThree
CH2OMe CH (Me) SMe
CH2OMe CH (Me) SEt
CH2OMe CH (Me) SCFThree
CH2OMe CH (Me) SCH2CFThree
CH2OMe CH (Me) S (O) Me
CH2OMe CH (Me) S (O) Et
CH2OMe CH (Me) S (O) CFThree
CH2OMe CH (Me) S (O) CH2CFThree
CH2OMe CH (Me) S (O)2Me
CH2OMe CH (Me) S (O)2Et
CH2OMe CH (Me) S (O)2CFThree
CH2OMe CH (Me) S (O)2CH2CFThree
CH2OMe CH (Et) SMe
CH2OMe CH (Et) SEt
CH2OMe CH (Et) SCFThree
CH2OMe CH (Et) SCH2CFThree
CH2OMe CH (Et) S (O) Me
CH2OMe CH (Et) S (O) Et
CH2OMe CH (Et) S (O) CFThree
CH2OMe CH (Et) S (O) CH2CFThree
CH2OMe CH (Et) S (O)2Me
CH2OMe CH (Et) S (O)2Et
CH2OMe CH (Et) S (O)2CFThree
CH2OMe CH (Et) S (O)2CH2CFThree
CH2OMe CH (n-Pr) SMe
CH2OMe CH (n-Pr) SEt
CH2OMe CH (n-Pr) SCFThree
CH2OMe CH (n-Pr) SCH2CFThree
CH2OMe CH (n-Pr) S (O) Me
CH2OMe CH (n-Pr) S (O) Et
CH2OMe CH (n-Pr) S (O) CFThree
CH2OMe CH (n-Pr) S (O) CH2CFThree
CH2OMe CH (n-Pr) S (O)2Me
CH2OMe CH (n-Pr) S (O)2Et
CH2OMe CH (n-Pr) S (O)2CFThree
CH2OMe CH (n-Pr) S (O)2CH2CFThree
CH2OMe CH (i-Pr) SMe
CH2OMe CH (i-Pr) SEt
CH2OMe CH (i-Pr) SCFThree
CH2OMe CH (i-Pr) SCH2CFThree
CH2OMe CH (i-Pr) S (O) Me
CH2OMe CH (i-Pr) S (O) Et
CH2OMe CH (i-Pr) S (O) CFThree
CH2OMe CH (i-Pr) S (O) CH2CFThree
CH2OMe CH (i-Pr) S (O)2Me
CH2OMe CH (i-Pr) S (O)2Et
CH2OMe CH (i-Pr) S (O)2CFThree
CH2OMe CH (i-Pr) S (O)2CH2CFThree
CH2OMe CH (n-Bu) SMe
CH2OMe CH (n-Bu) SEt
CH2OMe CH (n-Bu) SCFThree
CH2OMe CH (n-Bu) SCH2CFThree
CH2OMe CH (n-Bu) S (O) Me
CH2OMe CH (n-Bu) S (O) Et
CH2OMe CH (n-Bu) S (O) CFThree
CH2OMe CH (n-Bu) S (O) CH2CFThree
CH2OMe CH (n-Bu) S (O)2Me
CH2OMe CH (n-Bu) S (O)2Et
CH2OMe CH (n-Bu) S (O)2CFThree
CH2OMe CH (n-Bu) S (O)2CH2CFThree
CH2OMe CH (i-Bu) SMe
CH2OMe CH (i-Bu) SEt
CH2OMe CH (i-Bu) SCFThree
CH2OMe CH (i-Bu) SCH2CFThree
CH2OMe CH (i-Bu) S (O) Me
CH2OMe CH (i-Bu) S (O) Et
CH2OMe CH (i-Bu) S (O) CFThree
CH2OMe CH (i-Bu) S (O) CH2CFThree
CH2OMe CH (i-Bu) S (O)2Me
CH2OMe CH (i-Bu) S (O)2Et
CH2OMe CH (i-Bu) S (O)2CFThree
CH2OMe CH (i-Bu) S (O)2CH2CFThree
CH2OMe CH (s-Bu) SMe
CH2OMe CH (s-Bu) SEt
CH2OMe CH (s-Bu) SCFThree
CH2OMe CH (s-Bu) SCH2CFThree
CH2OMe CH (s-Bu) S (O) Me
CH2OMe CH (s-Bu) S (O) Et
CH2OMe CH (s-Bu) S (O) CFThree
CH2OMe CH (s-Bu) S (O) CH2CFThree
CH2OMe CH (s-Bu) S (O)2Me
CH2OMe CH (s-Bu) S (O)2Et
CH2OMe CH (s-Bu) S (O)2CFThree
CH2OMe CH (s-Bu) S (O)2CH2CFThree
CH2OMe CH (t-Bu) SMe
CH2OMe CH (t-Bu) SEt
CH2OMe CH (t-Bu) SCFThree
CH2OMe CH (t-Bu) SCH2CFThree
CH2OMe CH (t-Bu) S (O) Me
CH2OMe CH (t-Bu) S (O) Et
CH2OMe CH (t-Bu) S (O) CFThree
CH2OMe CH (t-Bu) S (O) CH2CFThree
CH2OMe CH (t-Bu) S (O)2Me
CH2OMe CH (t-Bu) S (O)2Et
CH2OMe CH (t-Bu) S (O)2CFThree
CH2OMe CH (t-Bu) S (O)2CH2CFThree
CH2OMe CH (CFThreeSMe
CH2OMe CH (CFThree) SEt
CH2OMe CH (CFThree) SCFThree
CH2OMe CH (CFThree) SCH2CFThree
CH2OMe CH (CFThree) S (O) Me
CH2OMe CH (CFThree) S (O) Et
CH2OMe CH (CFThree) S (O) CFThree
CH2OMe CH (CFThree) S (O) CH2CFThree
CH2OMe CH (CFThree) S (O)2Me
CH2OMe CH (CFThree) S (O)2Et
CH2OMe CH (CFThree) S (O)2CFThree
CH2OMe CH (CFThree) S (O)2CH2CFThree
CH2OMe CH2CH2SMe
CH2OMe CH2CH2SEt
CH2OMe CH2CH2SCFThree
CH2OMe CH2CH2SCH2CFThree
CH2OMe CH2CH2S (O) Me
CH2OMe CH2CH2S (O) Et
CH2OMe CH2CH2S (O) CFThree
CH2OMe CH2CH2S (O) CH2CFThree
CH2OMe CH2CH2S (O)2Me
CH2OMe CH2CH2S (O)2Et
CH2OMe CH2CH2S (O)2CFThree
CH2OMe CH2CH2S (O)2CH2CFThree
CH2OMe CH (Me) CH2SMe
CH2OMe CH (Me) CH2SEt
CH2OMe CH (Me) CH2SCFThree
CH2OMe CH (Me) CH2SCH2CFThree
CH2OMe CH (Me) CH2S (O) Me
CH2OMe CH (Me) CH2S (O) Et
CH2OMe CH (Me) CH2S (O) CFThree
CH2OMe CH (Me) CH2S (O) CH2CFThree
CH2OMe CH (Me) CH2S (O)2Me
CH2OMe CH (Me) CH2S (O)2Et
CH2OMe CH (Me) CH2S (O)2CFThree
CH2OMe CH (Me) CH2S (O)2CH2CFThree
CH2OMe CH (Et) CH2SMe
CH2OMe CH (Et) CH2SEt
CH2OMe CH (Et) CH2SCFThree
CH2OMe CH (Et) CH2SCH2CFThree
CH2OMe CH (Et) CH2S (O) Me
CH2OMe CH (Et) CH2S (O) Et
CH2OMe CH (Et) CH2S (O) CFThree
CH2OMe CH (Et) CH2S (O) CH2CFThree
CH2OMe CH (Et) CH2S (O)2Me
CH2OMe CH (Et) CH2S (O)2Et
CH2OMe CH (Et) CH2S (O)2CFThree
CH2OMe CH (Et) CH2S (O)2CH2CFThree
CH2OMe C (Me)2CH2SMe
CH2OMe C (Me)2CH2SEt
CH2OMe C (Me)2CH2SCFThree
CH2OMe C (Me)2CH2SCH2CFThree
CH2OMe C (Me)2CH2S (O) Me
CH2OMe C (Me)2CH2S (O) Et
CH2OMe C (Me)2CH2S (O) CFThree
CH2OMe C (Me)2CH2S (O) CH2CFThree
CH2OMe C (Me)2CH2S (O)2Me
CH2OMe C (Me)2CH2S (O)2Et
CH2OMe C (Me)2CH2S (O)2CFThree
CH2OMe C (Me)2CH2S (O)2CH2CFThree
CH2OMe CH2CH (Me) SMe
CH2OMe CH2CH (Me) SEt
CH2OMe CH2CH (Me) SCFThree
CH2OMe CH2CH (Me) SCH2CFThree
CH2OMe CH2CH (Me) S (O) Me
CH2OMe CH2CH (Me) S (O) Et
CH2OMe CH2CH (Me) S (O) CFThree
CH2OMe CH2CH (Me) S (O) CH2CFThree
CH2OMe CH2CH (Me) S (O)2Me
CH2OMe CH2CH (Me) S (O)2Et
CH2OMe CH2CH (Me) S (O)2CFThree
CH2OMe CH2CH (Me) S (O)2CH2CFThree
CH2OMe CH2CH (Et) SMe
CH2OMe CH2CH (Et) SEt
CH2OMe CH2CH (Et) SCFThree
CH2OMe CH2CH (Et) SCH2CFThree
CH2OMe CH2CH (Et) S (O) Me
CH2OMe CH2CH (Et) S (O) Et
CH2OMe CH2CH (Et) S (O) CFThree
CH2OMe CH2CH (Et) S (O) CH2CFThree
CH2OMe CH2CH (Et) S (O)2Me
CH2OMe CH2CH (Et) S (O)2Et
CH2OMe CH2CH (Et) S (O)2CFThree
CH2OMe CH2CH (Et) S (O)2CH2CFThree
CH2OMe CH (Me) CH (Me) SMe
CH2OMe CH (Me) CH (Me) SEt
CH2OMe CH (Me) CH (Me) SCFThree
CH2OMe CH (Me) CH (Me) SCH2CFThree
CH2OMe CH (Me) CH (Me) S (O) Me
CH2OMe CH (Me) CH (Me) S (O) Et
CH2OMe CH (Me) CH (Me) S (O) CFThree
CH2OMe CH (Me) CH (Me) S (O) CH2CFThree
CH2OMe CH (Me) CH (Me) S (O)2Me
CH2OMe CH (Me) CH (Me) S (O)2Et
CH2OMe CH (Me) CH (Me) S (O)2CFThree
CH2OMe CH (Me) CH (Me) S (O)2CH2CFThree
CH2SMe CH2SMe
CH2SEt CH2SMe
CH2S (O) Me CH2SMe
CH2S (O) Et CH2SMe
CH2S (O)2Me CH2SMe
CH2S (O)2Et CH2SMe
CH (Me) SMe CH2SMe
CH (Me) SEt CH2SMe
CH (Me) S (O) Me CH2SMe
CH (Me) S (O) Et CH2SMe
CH (Me) S (O)2Me CH2SMe
CH (Me) S (O)2Et CH2SMe
CH (Et) SMe CH2SMe
CH (Et) SEt CH2SMe
CH (Et) S (O) Me CH2SMe
CH (Et) S (O) Et CH2SMe
CH (Et) S (O)2Me CH2SMe
CH (Et) S (O)2Et CH2SMe
CH (n-Pr) SMe CH2SMe
CH (n-Pr) SEt CH2SMe
CH (n-Pr) S (O) Me CH2SMe
CH (n-Pr) S (O) Et CH2SMe
CH (n-Pr) S (O)2Me CH2SMe
CH (n-Pr) S (O)2Et CH2SMe
CH (i-Pr) SMe CH2SMe
CH (i-Pr) SEt CH2SMe
CH (i-Pr) S (O) Me CH2SMe
CH (i-Pr) S (O) Et CH2SMe
CH (i-Pr) S (O)2Me CH2SMe
CH (i-Pr) S (O)2Et CH2SMe
CH (n-Bu) SMe CH2SMe
CH (n-Bu) SEt CH2SMe
CH (n-Bu) S (O) Me CH2SMe
CH (n-Bu) S (O) Et CH2SMe
CH (n-Bu) S (O)2Me CH2SMe
CH (n-Bu) S (O)2Et CH2SMe
CH (i-Bu) SMe CH2SMe
CH (i-Bu) SEt CH2SMe
CH (i-Bu) S (O) Me CH2SMe
CH (i-Bu) S (O) Et CH2SMe
CH (i-Bu) S (O)2Me CH2SMe
CH (i-Bu) S (O)2Et CH2SMe
CH (s-Bu) SMe CH2SMe
CH (s-Bu) SEt CH2SMe
CH (s-Bu) S (O) Me CH2SMe
CH (s-Bu) S (O) Et CH2SMe
CH (s-Bu) S (O)2Me CH2SMe
CH (s-Bu) S (O)2Et CH2SMe
CH (t-Bu) SMe CH2SMe
CH (t-Bu) SEt CH2SMe
CH (t-Bu) S (O) Me CH2SMe
CH (t-Bu) S (O) Et CH2SMe
CH (t-Bu) S (O)2Me CH2SMe
CH (t-Bu) S (O)2Et CH2SMe
CH2CH2SMe CH2SMe
CH2CH2SEt CH2SMe
CH2CH2S (O)2Me CH2SMe
CH2CH2S (O)2Et CH2SMe
CH (Me) CH2SMe CH2SMe
CH (Me) CH2SEt CH2SMe
CH (Me) CH2S (O) Me CH2SMe
CH (Me) CH2S (O) Et CH2SMe
CH (Me) CH2S (O)2Me CH2SMe
CH (Me) CH2S (O)2Et CH2SMe
CH (Et) CH2SMe CH2SMe
CH (Et) CH2SEt CH2SMe
CH (Et) CH2S (O) Me CH2SMe
CH (Et) CH2S (O) Et CH2SMe
CH (Et) CH2S (O)2Me CH2SMe
CH (Et) CH2S (O)2Et CH2SMe
C (Me)2CH2SMe CH2SMe
C (Me)2CH2SEt CH2SMe
C (Me)2CH2S (O) Me CH2SMe
C (Me)2CH2S (O) Et CH2SMe
C (Me)2CH2S (O)2Me CH2SMe
C (Me)2CH2S (O)2Et CH2SMe
CH2CH (Me) SMe CH2SMe
CH2CH (Me) SEt CH2SMe
CH2CH (Me) S (O) Me CH2SMe
CH2CH (Me) S (O) Et CH2SMe
CH2CH (Me) S (O)2Me CH2SMe
CH2CH (Me) S (O)2Et CH2SMe
CH2CH (Et) SMe CH2SMe
CH2CH (Et) SEt CH2SMe
CH2CH (Et) S (O) Me CH2SMe
CH2CH (Et) S (O) Et CH2SMe
CH2CH (Et) S (O)2Me CH2SMe
CH2CH (Et) S (O)2Et CH2SMe
CH (Me) CH (Me) SMe CH2SMe
CH (Me) CH (Me) SEt CH2SMe
CH (Me) CH (Me) S (O) Me CH2SMe
CH (Me) CH (Me) S (O) Et CH2SMe
CH (Me) CH (Me) S (O)2Me CH2SMe
CH (Me) CH (Me) S (O)2Et CH2SMe
CH2SMe CH2S (O) Me
CH2SEt CH2S (O) Me
CH2S (O) Me CH2S (O) Me
CH2S (O) Et CH2S (O) Me
CH2S (O)2Me CH2S (O) Me
CH2S (O)2Et CH2S (O) Me
CH (Me) SMe CH2S (O) Me
CH (Me) SEt CH2S (O) Me
CH (Me) S (O) Me CH2S (O) Me
CH (Me) S (O) Et CH2S (O) Me
CH (Me) S (O)2Me CH2S (O) Me
CH (Me) S (O)2Et CH2S (O) Me
CH (Et) SMe CH2S (O) Me
CH (Et) SEt CH2S (O) Me
CH (Et) S (O) Me CH2S (O) Me
CH (Et) S (O) Et CH2S (O) Me
CH (Et) S (O)2Me CH2S (O) Me
CH (Et) S (O)2Et CH2S (O) Me
CH (n-Pr) SMe CH2S (O) Me
CH (n-Pr) SEt CH2S (O) Me
CH (n-Pr) S (O) Me CH2S (O) Me
CH (n-Pr) S (O) Et CH2S (O) Me
CH (n-Pr) S (O)2Me CH2S (O) Me
CH (n-Pr) S (O)2Et CH2S (O) Me
CH (i-Pr) SMe CH2S (O) Me
CH (i-Pr) SEt CH2S (O) Me
CH (i-Pr) S (O) Me CH2S (O) Me
CH (i-Pr) S (O) Et CH2S (O) Me
CH (i-Pr) S (O)2Me CH2S (O) Me
CH (i-Pr) S (O)2Et CH2S (O) Me
CH (n-Bu) SMe CH2S (O) Me
CH (n-Bu) SEt CH2S (O) Me
CH (n-Bu) S (O) Me CH2S (O) Me
CH (n-Bu) S (O) Et CH2S (O) Me
CH (n-Bu) S (O)2Me CH2S (O) Me
CH (n-Bu) S (O)2Et CH2S (O) Me
CH (i-Bu) SMe CH2S (O) Me
CH (i-Bu) SEt CH2S (O) Me
CH (i-Bu) S (O) Me CH2S (O) Me
CH (i-Bu) S (O) Et CH2S (O) Me
CH (i-Bu) S (O)2Me CH2S (O) Me
CH (i-Bu) S (O)2Et CH2S (O) Me
CH (s-Bu) SMe CH2S (O) Me
CH (s-Bu) SEt CH2S (O) Me
CH (s-Bu) S (O) Me CH2S (O) Me
CH (s-Bu) S (O) Et CH2S (O) Me
CH (s-Bu) S (O)2Me CH2S (O) Me
CH (s-Bu) S (O)2Et CH2S (O) Me
CH (t-Bu) SMe CH2S (O) Me
CH (t-Bu) SEt CH2S (O) Me
CH (t-Bu) S (O) Me CH2S (O) Me
CH (t-Bu) S (O) Et CH2S (O) Me
CH (t-Bu) S (O)2Me CH2S (O) Me
CH (t-Bu) S (O)2Et CH2S (O) Me
CH2CH2SMe CH2S (O) Me
CH2CH2SEt CH2S (O) Me
CH2CH2S (O)2Me CH2S (O) Me
CH2CH2S (O)2Et CH2S (O) Me
CH (Me) CH2SMe CH2S (O) Me
CH (Me) CH2SEt CH2S (O) Me
CH (Me) CH2S (O) Me CH2S (O) Me
CH (Me) CH2S (O) Et CH2S (O) Me
CH (Me) CH2S (O)2Me CH2S (O) Me
CH (Me) CH2S (O)2Et CH2S (O) Me
CH (Et) CH2SMe CH2S (O) Me
CH (Et) CH2SEt CH2S (O) Me
CH (Et) CH2S (O) Me CH2S (O) Me
CH (Et) CH2S (O) Et CH2S (O) Me
CH (Et) CH2S (O)2Me CH2S (O) Me
CH (Et) CH2S (O)2Et CH2S (O) Me
C (Me)2CH2SMe CH2S (O) Me
C (Me)2CH2SEt CH2S (O) Me
C (Me)2CH2S (O) Me CH2S (O) Me
C (Me)2CH2S (O) Et CH2S (O) Me
C (Me)2CH2S (O)2Me CH2S (O) Me
C (Me)2CH2S (O)2Et CH2S (O) Me
CH2CH (Me) SMe CH2S (O) Me
CH2CH (Me) SEt CH2S (O) Me
CH2CH (Me) S (O) Me CH2S (O) Me
CH2CH (Me) S (O) Et CH2S (O) Me
CH2CH (Me) S (O)2Me CH2S (O) Me
CH2CH (Me) S (O)2Et CH2S (O) Me
CH2CH (Et) SMe CH2S (O) Me
CH2CH (Et) SEt CH2S (O) Me
CH2CH (Et) S (O) Me CH2S (O) Me
CH2CH (Et) S (O) Et CH2S (O) Me
CH2CH (Et) S (O)2Me CH2S (O) Me
CH2CH (Et) S (O)2Et CH2S (O) Me
CH (Me) CH (Me) SMe CH2S (O) Me
CH (Me) CH (Me) SEt CH2S (O) Me
CH (Me) CH (Me) S (O) Me CH2S (O) Me
CH (Me) CH (Me) S (O) Et CH2S (O) Me
CH (Me) CH (Me) S (O)2Me CH2S (O) Me
CH (Me) CH (Me) S (O)2Et CH2S (O) Me
CH2SMe CH2S (O)2Me
CH2SEt CH2S (O)2Me
CH2S (O) Me CH2S (O)2Me
CH2S (O) Et CH2S (O)2Me
CH2S (O)2Me CH2S (O)2Me
CH2S (O)2Et CH2S (O)2Me
CH (Me) SMe CH2S (O)2Me
CH (Me) SEt CH2S (O)2Me
CH (Me) S (O) Me CH2S (O)2Me
CH (Me) S (O) Et CH2S (O)2Me
CH (Me) S (O)2Me CH2S (O)2Me
CH (Me) S (O)2Et CH2S (O)2Me
CH (Et) SMe CH2S (O)2Me
CH (Et) SEt CH2S (O)2Me
CH (Et) S (O) Me CH2S (O)2Me
CH (Et) S (O) Et CH2S (O)2Me
CH (Et) S (O)2Me CH2S (O)2Me
CH (Et) S (O)2Et CH2S (O)2Me
CH (n-Pr) SMe CH2S (O)2Me
CH (n-Pr) SEt CH2S (O)2Me
CH (n-Pr) S (O) Me CH2S (O)2Me
CH (n-Pr) S (O) Et CH2S (O)2Me
CH (n-Pr) S (O)2Me CH2S (O)2Me
CH (n-Pr) S (O)2Et CH2S (O)2Me
CH (i-Pr) SMe CH2S (O)2Me
CH (i-Pr) SEt CH2S (O)2Me
CH (i-Pr) S (O) Me CH2S (O)2Me
CH (i-Pr) S (O) Et CH2S (O)2Me
CH (i-Pr) S (O)2Me CH2S (O)2Me
CH (i-Pr) S (O)2Et CH2S (O)2Me
CH (n-Bu) SMe CH2S (O)2Me
CH (n-Bu) SEt CH2S (O)2Me
CH (n-Bu) S (O) Me CH2S (O)2Me
CH (n-Bu) S (O) Et CH2S (O)2Me
CH (n-Bu) S (O)2Me CH2S (O)2Me
CH (n-Bu) S (O)2Et CH2S (O)2Me
CH (i-Bu) SMe CH2S (O)2Me
CH (i-Bu) SEt CH2S (O)2Me
CH (i-Bu) S (O) Me CH2S (O)2Me
CH (i-Bu) S (O) Et CH2S (O)2Me
CH (i-Bu) S (O)2Me CH2S (O)2Me
CH (i-Bu) S (O)2Et CH2S (O)2Me
CH (s-Bu) SMe CH2S (O)2Me
CH (s-Bu) SEt CH2S (O)2Me
CH (s-Bu) S (O) Me CH2S (O)2Me
CH (s-Bu) S (O) Et CH2S (O)2Me
CH (s-Bu) S (O)2Me CH2S (O)2Me
CH (s-Bu) S (O)2Et CH2S (O)2Me
CH (t-Bu) SMe CH2S (O)2Me
CH (t-Bu) SEt CH2S (O)2Me
CH (t-Bu) S (O) Me CH2S (O)2Me
CH (t-Bu) S (O) Et CH2S (O)2Me
CH (t-Bu) S (O)2Me CH2S (O)2Me
CH (t-Bu) S (O)2Et CH2S (O)2Me
CH2CH2SMe CH2S (O)2Me
CH2CH2SEt CH2S (O)2Me
CH2CH2S (O)2Me CH2S (O)2Me
CH2CH2S (O)2Et CH2S (O)2Me
CH (Me) CH2SMe CH2S (O)2Me
CH (Me) CH2SEt CH2S (O)2Me
CH (Me) CH2S (O) Me CH2S (O)2Me
CH (Me) CH2S (O) Et CH2S (O)2Me
CH (Me) CH2S (O)2Me CH2S (O)2Me
CH (Me) CH2S (O)2Et CH2S (O)2Me
CH (Et) CH2SMe CH2S (O)2Me
CH (Et) CH2SEt CH2S (O)2Me
CH (Et) CH2S (O) Me CH2S (O)2Me
CH (Et) CH2S (O) Et CH2S (O)2Me
CH (Et) CH2S (O)2Me CH2S (O)2Me
CH (Et) CH2S (O)2Et CH2S (O)2Me
C (Me)2CH2SMe CH2S (O)2Me
C (Me)2CH2SEt CH2S (O)2Me
C (Me)2CH2S (O) Me CH2S (O)2Me
C (Me)2CH2S (O) Et CH2S (O)2Me
C (Me)2CH2S (O)2Me CH2S (O)2Me
C (Me)2CH2S (O)2Et CH2S (O)2Me
CH2CH (Me) SMe CH2S (O)2Me
CH2CH (Me) SEt CH2S (O)2Me
CH2CH (Me) S (O) Me CH2S (O)2Me
CH2CH (Me) S (O) Et CH2S (O)2Me
CH2CH (Me) S (O)2Me CH2S (O)2Me
CH2CH (Me) S (O)2Et CH2S (O)2Me
CH2CH (Et) SMe CH2S (O)2Me
CH2CH (Et) SEt CH2S (O)2Me
CH2CH (Et) S (O) Me CH2S (O)2Me
CH2CH (Et) S (O) Et CH2S (O)2Me
CH2CH (Et) S (O)2Me CH2S (O)2Me
CH2CH (Et) S (O)2Et CH2S (O)2Me
CH (Me) CH (Me) SMe CH2S (O)2Me
CH (Me) CH (Me) SEt CH2S (O)2Me
CH (Me) CH (Me) S (O) Me CH2S (O)2Me
CH (Me) CH (Me) S (O) Et CH2S (O)2Me
CH (Me) CH (Me) S (O)2Me CH2S (O)2Me
CH (Me) CH (Me) S (O)2Et CH2S (O)2Me
CH2SMe SMe
CH2SEt SMe
CH2S (O) Me SMe
CH2S (O) Et SMe
CH2S (O)2Me SMe
CH2S (O)2Et SMe
CH (Me) SMe SMe
CH (Me) SEt SMe
CH (Me) S (O) Me SMe
CH (Me) S (O) Et SMe
CH (Me) S (O)2Me SMe
CH (Me) S (O)2Et SMe
CH (Et) SMe SMe
CH (Et) SEt SMe
CH (Et) S (O) Me SMe
CH (Et) S (O) Et SMe
CH (Et) S (O)2Me SMe
CH (Et) S (O)2Et SMe
CH (n-Pr) SMe SMe
CH (n-Pr) SEt SMe
CH (n-Pr) S (O) Me SMe
CH (n-Pr) S (O) Et SMe
CH (n-Pr) S (O)2Me SMe
CH (n-Pr) S (O)2Et SMe
CH (i-Pr) SMe SMe
CH (i-Pr) SEt SMe
CH (i-Pr) S (O) Me SMe
CH (i-Pr) S (O) Et SMe
CH (i-Pr) S (O)2Me SMe
CH (i-Pr) S (O)2Et SMe
CH (n-Bu) SMe SMe
CH (n-Bu) SEt SMe
CH (n-Bu) S (O) Me SMe
CH (n-Bu) S (O) Et SMe
CH (n-Bu) S (O)2Me SMe
CH (n-Bu) S (O)2Et SMe
CH (i-Bu) SMe SMe
CH (i-Bu) SEt SMe
CH (i-Bu) S (O) Me SMe
CH (i-Bu) S (O) Et SMe
CH (i-Bu) S (O)2Me SMe
CH (i-Bu) S (O)2Et SMe
CH (s-Bu) SMe SMe
CH (s-Bu) SEt SMe
CH (s-Bu) S (O) Me SMe
CH (s-Bu) S (O) Et SMe
CH (s-Bu) S (O)2Me SMe
CH (s-Bu) S (O)2Et SMe
CH (t-Bu) SMe SMe
CH (t-Bu) SEt SMe
CH (t-Bu) S (O) Me SMe
CH (t-Bu) S (O) Et SMe
CH (t-Bu) S (O)2Me SMe
CH (t-Bu) S (O)2Et SMe
CH2CH2SMe SMe
CH2CH2SEt SMe
CH2CH2S (O)2Me SMe
CH2CH2S (O)2Et SMe
CH (Me) CH2SMe SMe
CH (Me) CH2SEt SMe
CH (Me) CH2S (O) Me SMe
CH (Me) CH2S (O) Et SMe
CH (Me) CH2S (O)2Me SMe
CH (Me) CH2S (O)2Et SMe
CH (Et) CH2SMe SMe
CH (Et) CH2SEt SMe
CH (Et) CH2S (O) Me SMe
CH (Et) CH2S (O) Et SMe
CH (Et) CH2S (O)2Me SMe
CH (Et) CH2S (O)2Et SMe
C (Me)2CH2SMe SMe
C (Me)2CH2SEt SMe
C (Me)2CH2S (O) Me SMe
C (Me)2CH2S (O) Et SMe
C (Me)2CH2S (O)2Me SMe
C (Me)2CH2S (O)2Et SMe
CH2CH (Me) SMe SMe
CH2CH (Me) SEt SMe
CH2CH (Me) S (O) Me SMe
CH2CH (Me) S (O) Et SMe
CH2CH (Me) S (O)2Me SMe
CH2CH (Me) S (O)2Et SMe
CH2CH (Et) SMe SMe
CH2CH (Et) SEt SMe
CH2CH (Et) S (O) Me SMe
CH2CH (Et) S (O) Et SMe
CH2CH (Et) S (O)2Me SMe
CH2CH (Et) S (O)2Et SMe
CH (Me) CH (Me) SMe SMe
CH (Me) CH (Me) SEt SMe
CH (Me) CH (Me) S (O) Me SMe
CH (Me) CH (Me) S (O) Et SMe
CH (Me) CH (Me) S (O)2Me SMe
CH (Me) CH (Me) S (O)2Et SMe
CH2SMe S (O) Me
CH2SEt S (O) Me
CH2S (O) Me S (O) Me
CH2S (O) Et S (O) Me
CH2S (O)2Me S (O) Me
CH2S (O)2Et S (O) Me
CH (Me) SMe S (O) Me
CH (Me) SEt S (O) Me
CH (Me) S (O) Me S (O) Me
CH (Me) S (O) Et S (O) Me
CH (Me) S (O)2Me S (O) Me
CH (Me) S (O)2Et S (O) Me
CH (Et) SMe S (O) Me
CH (Et) SEt S (O) Me
CH (Et) S (O) Me S (O) Me
CH (Et) S (O) Et S (O) Me
CH (Et) S (O)2Me S (O) Me
CH (Et) S (O)2Et S (O) Me
CH (n-Pr) SMe S (O) Me
CH (n-Pr) SEt S (O) Me
CH (n-Pr) S (O) Me S (O) Me
CH (n-Pr) S (O) Et S (O) Me
CH (n-Pr) S (O)2Me S (O) Me
CH (n-Pr) S (O)2Et S (O) Me
CH (i-Pr) SMe S (O) Me
CH (i-Pr) SEt S (O) Me
CH (i-Pr) S (O) Me S (O) Me
CH (i-Pr) S (O) Et S (O) Me
CH (i-Pr) S (O)2Me S (O) Me
CH (i-Pr) S (O)2Et S (O) Me
CH (n-Bu) SMe S (O) Me
CH (n-Bu) SEt S (O) Me
CH (n-Bu) S (O) Me S (O) Me
CH (n-Bu) S (O) Et S (O) Me
CH (n-Bu) S (O)2Me S (O) Me
CH (n-Bu) S (O)2Et S (O) Me
CH (i-Bu) SMe S (O) Me
CH (i-Bu) SEt S (O) Me
CH (i-Bu) S (O) Me S (O) Me
CH (i-Bu) S (O) Et S (O) Me
CH (i-Bu) S (O)2Me S (O) Me
CH (i-Bu) S (O)2Et S (O) Me
CH (s-Bu) SMe S (O) Me
CH (s-Bu) SEt S (O) Me
CH (s-Bu) S (O) Me S (O) Me
CH (s-Bu) S (O) Et S (O) Me
CH (s-Bu) S (O)2Me S (O) Me
CH (s-Bu) S (O)2Et S (O) Me
CH (t-Bu) SMe S (O) Me
CH (t-Bu) SEt S (O) Me
CH (t-Bu) S (O) Me S (O) Me
CH (t-Bu) S (O) Et S (O) Me
CH (t-Bu) S (O)2Me S (O) Me
CH (t-Bu) S (O)2Et S (O) Me
CH2CH2SMe S (O) Me
CH2CH2SEt S (O) Me
CH2CH2S (O)2Me S (O) Me
CH2CH2S (O)2Et S (O) Me
CH (Me) CH2SMe S (O) Me
CH (Me) CH2SEt S (O) Me
CH (Me) CH2S (O) Me S (O) Me
CH (Me) CH2S (O) Et S (O) Me
CH (Me) CH2S (O)2Me S (O) Me
CH (Me) CH2S (O)2Et S (O) Me
CH (Et) CH2SMe S (O) Me
CH (Et) CH2SEt S (O) Me
CH (Et) CH2S (O) Me S (O) Me
CH (Et) CH2S (O) Et S (O) Me
CH (Et) CH2S (O)2Me S (O) Me
CH (Et) CH2S (O)2Et S (O) Me
C (Me)2CH2SMe S (O) Me
C (Me)2CH2SEt S (O) Me
C (Me)2CH2S (O) Me S (O) Me
C (Me)2CH2S (O) Et S (O) Me
C (Me)2CH2S (O)2Me S (O) Me
C (Me)2CH2S (O)2Et S (O) Me
CH2CH (Me) SMe S (O) Me
CH2CH (Me) SEt S (O) Me
CH2CH (Me) S (O) Me S (O) Me
CH2CH (Me) S (O) Et S (O) Me
CH2CH (Me) S (O)2Me S (O) Me
CH2CH (Me) S (O)2Et S (O) Me
CH2CH (Et) SMe S (O) Me
CH2CH (Et) SEt S (O) Me
CH2CH (Et) S (O) Me S (O) Me
CH2CH (Et) S (O) Et S (O) Me
CH2CH (Et) S (O)2Me S (O) Me
CH2CH (Et) S (O)2Et S (O) Me
CH (Me) CH (Me) SMe S (O) Me
CH (Me) CH (Me) SEt S (O) Me
CH (Me) CH (Me) S (O) Me S (O) Me
CH (Me) CH (Me) S (O) Et S (O) Me
CH (Me) CH (Me) S (O)2Me S (O) Me
CH (Me) CH (Me) S (O)2Et S (O) Me
CH2SMe S (O)2Me
CH2SEt S (O)2Me
CH2S (O) Me S (O)2Me
CH2S (O) Et S (O)2Me
CH2S (O)2Me S (O)2Me
CH2S (O)2Et S (O)2Me
CH (Me) SMe S (O)2Me
CH (Me) SEt S (O)2Me
CH (Me) S (O) Me S (O)2Me
CH (Me) S (O) Et S (O)2Me
CH (Me) S (O)2Me S (O)2Me
CH (Me) S (O)2Et S (O)2Me
CH (Et) SMe S (O)2Me
CH (Et) SEt S (O)2Me
CH (Et) S (O) Me S (O)2Me
CH (Et) S (O) Et S (O)2Me
CH (Et) S (O)2Me S (O)2Me
CH (Et) S (O)2Et S (O)2Me
CH (n-Pr) SMe S (O)2Me
CH (n-Pr) SEt S (O)2Me
CH (n-Pr) S (O) Me S (O)2Me
CH (n-Pr) S (O) Et S (O)2Me
CH (n-Pr) S (O)2Me S (O)2Me
CH (n-Pr) S (O)2Et S (O)2Me
CH (i-Pr) SMe S (O)2Me
CH (i-Pr) SEt S (O)2Me
CH (i-Pr) S (O) Me S (O)2Me
CH (i-Pr) S (O) Et S (O)2Me
CH (i-Pr) S (O)2Me S (O)2Me
CH (i-Pr) S (O)2Et S (O)2Me
CH (n-Bu) SMe S (O)2Me
CH (n-Bu) SEt S (O)2Me
CH (n-Bu) S (O) Me S (O)2Me
CH (n-Bu) S (O) Et S (O)2Me
CH (n-Bu) S (O)2Me S (O)2Me
CH (n-Bu) S (O)2Et S (O)2Me
CH (i-Bu) SMe S (O)2Me
CH (i-Bu) SEt S (O)2Me
CH (i-Bu) S (O) Me S (O)2Me
CH (i-Bu) S (O) Et S (O)2Me
CH (i-Bu) S (O)2Me S (O)2Me
CH (i-Bu) S (O)2Et S (O)2Me
CH (s-Bu) SMe S (O)2Me
CH (s-Bu) SEt S (O)2Me
CH (s-Bu) S (O) Me S (O)2Me
CH (s-Bu) S (O) Et S (O)2Me
CH (s-Bu) S (O)2Me S (O)2Me
CH (s-Bu) S (O)2Et S (O)2Me
CH (t-Bu) SMe S (O)2Me
CH (t-Bu) SEt S (O)2Me
CH (t-Bu) S (O) Me S (O)2Me
CH (t-Bu) S (O) Et S (O)2Me
CH (t-Bu) S (O)2Me S (O)2Me
CH (t-Bu) S (O)2Et S (O)2Me
CH2CH2SMe S (O)2Me
CH2CH2SEt S (O)2Me
CH2CH2S (O)2Me S (O)2Me
CH2CH2S (O)2Et S (O)2Me
CH (Me) CH2SMe S (O)2Me
CH (Me) CH2SEt S (O)2Me
CH (Me) CH2S (O) Me S (O)2Me
CH (Me) CH2S (O) Et S (O)2Me
CH (Me) CH2S (O)2Me S (O)2Me
CH (Me) CH2S (O)2Et S (O)2Me
CH (Et) CH2SMe S (O)2Me
CH (Et) CH2SEt S (O)2Me
CH (Et) CH2S (O) Me S (O)2Me
CH (Et) CH2S (O) Et S (O)2Me
CH (Et) CH2S (O)2Me S (O)2Me
CH (Et) CH2S (O)2Et S (O)2Me
C (Me)2CH2SMe S (O)2Me
C (Me)2CH2SEt S (O)2Me
C (Me)2CH2S (O) Me S (O)2Me
C (Me)2CH2S (O) Et S (O)2Me
C (Me)2CH2S (O)2Me S (O)2Me
C (Me)2CH2S (O)2Et S (O)2Me
CH2CH (Me) SMe S (O)2Me
CH2CH (Me) SEt S (O)2Me
CH2CH (Me) S (O) Me S (O)2Me
CH2CH (Me) S (O) Et S (O)2Me
CH2CH (Me) S (O)2Me S (O)2Me
CH2CH (Me) S (O)2Et S (O)2Me
CH2CH (Et) SMe S (O)2Me
CH2CH (Et) SEt S (O)2Me
CH2CH (Et) S (O) Me S (O)2Me
CH2CH (Et) S (O) Et S (O)2Me
CH2CH (Et) S (O)2Me S (O)2Me
CH2CH (Et) S (O)2Et S (O)2Me
CH (Me) CH (Me) SMe S (O)2Me
CH (Me) CH (Me) SEt S (O)2Me
CH (Me) CH (Me) S (O) Me S (O)2Me
CH (Me) CH (Me) S (O) Et S (O)2Me
CH (Me) CH (Me) S (O)2Me S (O)2Me
CH (Me) CH (Me) S (O)2Et S (O)2Me
CH2SMe H
CH2SEt H
CH2S (O) Me H
CH2S (O) Et H
CH2S (O)2Me H
CH2S (O)2Et H
CH (Me) SMe H
CH (Me) SEt H
CH (Me) S (O) Me H
CH (Me) S (O) Et H
CH (Me) S (O)2Me H
CH (Me) S (O)2Et H
CH (Et) SMe H
CH (Et) SEt H
CH (Et) S (O) Me H
CH (Et) S (O) Et H
CH (Et) S (O)2Me H
CH (Et) S (O)2Et H
CH (n-Pr) SMe H
CH (n-Pr) SEt H
CH (n-Pr) S (O) Me H
CH (n-Pr) S (O) Et H
CH (n-Pr) S (O)2Me H
CH (n-Pr) S (O)2Et H
CH (i-Pr) SMe H
CH (i-Pr) SEt H
CH (i-Pr) S (O) Me H
CH (i-Pr) S (O) Et H
CH (i-Pr) S (O)2Me H
CH (i-Pr) S (O)2Et H
CH (n-Bu) SMe H
CH (n-Bu) SEt H
CH (n-Bu) S (O) Me H
CH (n-Bu) S (O) Et H
CH (n-Bu) S (O)2Me H
CH (n-Bu) S (O)2Et H
CH (i-Bu) SMe H
CH (i-Bu) SEt H
CH (i-Bu) S (O) Me H
CH (i-Bu) S (O) Et H
CH (i-Bu) S (O)2Me H
CH (i-Bu) S (O)2Et H
CH (s-Bu) SMe H
CH (s-Bu) SEt H
CH (s-Bu) S (O) Me H
CH (s-Bu) S (O) Et H
CH (s-Bu) S (O)2Me H
CH (s-Bu) S (O)2Et H
CH (t-Bu) SMe H
CH (t-Bu) SEt H
CH (t-Bu) S (O) Me H
CH (t-Bu) S (O) Et H
CH (t-Bu) S (O)2Me H
CH (t-Bu) S (O)2Et H
CH2CH2SMe H
CH2CH2SEt H
CH2CH2S (O)2Me H
CH2CH2S (O)2Et H
CH (Me) CH2SMe H
CH (Me) CH2SEt H
CH (Me) CH2S (O) Me H
CH (Me) CH2S (O) Et H
CH (Me) CH2S (O)2Me H
CH (Me) CH2S (O)2Et H
CH (Et) CH2SMe H
CH (Et) CH2SEt H
CH (Et) CH2S (O) Me H
CH (Et) CH2S (O) Et H
CH (Et) CH2S (O)2Me H
CH (Et) CH2S (O)2Et H
C (Me)2CH2SMe H
C (Me)2CH2SEt H
C (Me)2CH2S (O) Me H
C (Me)2CH2S (O) Et H
C (Me)2CH2S (O)2Me H
C (Me)2CH2S (O)2Et H
CH2CH (Me) SMe H
CH2CH (Me) SEt H
CH2CH (Me) S (O) Me H
CH2CH (Me) S (O) Et H
CH2CH (Me) S (O)2Me H
CH2CH (Me) S (O)2Et H
CH2CH (Et) SMe H
CH2CH (Et) SEt H
CH2CH (Et) S (O) Me H
CH2CH (Et) S (O) Et H
CH2CH (Et) S (O)2Me H
CH2CH (Et) S (O)2Et H
CH (Me) CH (Me) SMe H
CH (Me) CH (Me) SEt H
CH (Me) CH (Me) S (O) Me H
CH (Me) CH (Me) S (O) Et H
CH (Me) CH (Me) S (O)2Me H
CH (Me) CH (Me) S (O)2Et H
CH2SMe Me
CH2SEt Me
CH2S (O) Me Me
CH2S (O) Et Me
CH2S (O)2Me Me
CH2S (O)2Et Me
CH (Me) SMe Me
CH (Me) SEt Me
CH (Me) S (O) Me Me
CH (Me) S (O) Et Me
CH (Me) S (O)2Me Me
CH (Me) S (O)2Et Me
CH (Et) SMe Me
CH (Et) SEt Me
CH (Et) S (O) Me Me
CH (Et) S (O) Et Me
CH (Et) S (O)2Me Me
CH (Et) S (O)2Et Me
CH (n-Pr) SMe Me
CH (n-Pr) SEt Me
CH (n-Pr) S (O) Me Me
CH (n-Pr) S (O) Et Me
CH (n-Pr) S (O)2Me Me
CH (n-Pr) S (O)2Et Me
CH (i-Pr) SMe Me
CH (i-Pr) SEt Me
CH (i-Pr) S (O) Me Me
CH (i-Pr) S (O) Et Me
CH (i-Pr) S (O)2Me Me
CH (i-Pr) S (O)2Et Me
CH (n-Bu) SMe Me
CH (n-Bu) SEt Me
CH (n-Bu) S (O) Me Me
CH (n-Bu) S (O) Et Me
CH (n-Bu) S (O)2Me Me
CH (n-Bu) S (O)2Et Me
CH (i-Bu) SMe Me
CH (i-Bu) SEt Me
CH (i-Bu) S (O) Me Me
CH (i-Bu) S (O) Et Me
CH (i-Bu) S (O)2Me Me
CH (i-Bu) S (O)2Et Me
CH (s-Bu) SMe Me
CH (s-Bu) SEt Me
CH (s-Bu) S (O) Me Me
CH (s-Bu) S (O) Et Me
CH (s-Bu) S (O)2Me Me
CH (s-Bu) S (O)2Et Me
CH (t-Bu) SMe Me
CH (t-Bu) SEt Me
CH (t-Bu) S (O) Me Me
CH (t-Bu) S (O) Et Me
CH (t-Bu) S (O)2Me Me
CH (t-Bu) S (O)2Et Me
CH2CH2SMe Me
CH2CH2SEt Me
CH2CH2S (O)2Me Me
CH2CH2S (O)2Et Me
CH (Me) CH2SMe Me
CH (Me) CH2SEt Me
CH (Me) CH2S (O) Me Me
CH (Me) CH2S (O) Et Me
CH (Me) CH2S (O)2Me Me
CH (Me) CH2S (O)2Et Me
CH (Et) CH2SMe Me
CH (Et) CH2SEt Me
CH (Et) CH2S (O) Me Me
CH (Et) CH2S (O) Et Me
CH (Et) CH2S (O)2Me Me
CH (Et) CH2S (O)2Et Me
C (Me)2CH2SMe Me
C (Me)2CH2SEt Me
C (Me)2CH2S (O) Me Me
C (Me)2CH2S (O) Et Me
C (Me)2CH2S (O)2Me Me
C (Me)2CH2S (O)2Et Me
CH2CH (Me) SMe Me
CH2CH (Me) SEt Me
CH2CH (Me) S (O) Me Me
CH2CH (Me) S (O) Et Me
CH2CH (Me) S (O)2Me Me
CH2CH (Me) S (O)2Et Me
CH2CH (Et) SMe Me
CH2CH (Et) SEt Me
CH2CH (Et) S (O) Me Me
CH2CH (Et) S (O) Et Me
CH2CH (Et) S (O)2Me Me
CH2CH (Et) S (O)2Et Me
CH (Me) CH (Me) SMe Me
CH (Me) CH (Me) SEt Me
CH (Me) CH (Me) S (O) Me Me
CH (Me) CH (Me) S (O) Et Me
CH (Me) CH (Me) S (O)2Me Me
CH (Me) CH (Me) S (O)2Et Me
CH2SMe CFThree
CH2SEt CFThree
CH2S (O) Me CFThree
CH2S (O) Et CFThree
CH2S (O)2Me CFThree
CH2S (O)2Et CFThree
CH (Me) SMe CFThree
CH (Me) SEt CFThree
CH (Me) S (O) Me CFThree
CH (Me) S (O) Et CFThree
CH (Me) S (O)2Me CFThree
CH (Me) S (O)2Et CFThree
CH (Et) SMe CFThree
CH (Et) SEt CFThree
CH (Et) S (O) Me CFThree
CH (Et) S (O) Et CFThree
CH (Et) S (O)2Me CFThree
CH (Et) S (O)2Et CFThree
CH (n-Pr) SMe CFThree
CH (n-Pr) SEt CFThree
CH (n-Pr) S (O) Me CFThree
CH (n-Pr) S (O) Et CFThree
CH (n-Pr) S (O)2Me CFThree
CH (n-Pr) S (O)2Et CFThree
CH (i-Pr) SMe CFThree
CH (i-Pr) SEt CFThree
CH (i-Pr) S (O) Me CFThree
CH (i-Pr) S (O) Et CFThree
CH (i-Pr) S (O)2Me CFThree
CH (i-Pr) S (O)2Et CFThree
CH (n-Bu) SMe CFThree
CH (n-Bu) SEt CFThree
CH (n-Bu) S (O) Me CFThree
CH (n-Bu) S (O) Et CFThree
CH (n-Bu) S (O)2Me CFThree
CH (n-Bu) S (O)2Et CFThree
CH (i-Bu) SMe CFThree
CH (i-Bu) SEt CFThree
CH (i-Bu) S (O) Me CFThree
CH (i-Bu) S (O) Et CFThree
CH (i-Bu) S (O)2Me CFThree
CH (i-Bu) S (O)2Et CFThree
CH (s-Bu) SMe CFThree
CH (s-Bu) SEt CFThree
CH (s-Bu) S (O) Me CFThree
CH (s-Bu) S (O) Et CFThree
CH (s-Bu) S (O)2Me CFThree
CH (s-Bu) S (O)2Et CFThree
CH (t-Bu) SMe CFThree
CH (t-Bu) SEt CFThree
CH (t-Bu) S (O) Me CFThree
CH (t-Bu) S (O) Et CFThree
CH (t-Bu) S (O)2Me CFThree
CH (t-Bu) S (O)2Et CFThree
CH2CH2SMe CFThree
CH2CH2SEt CFThree
CH2CH2S (O)2Me CFThree
CH2CH2S (O)2Et CFThree
CH (Me) CH2SMe CFThree
CH (Me) CH2SEt CFThree
CH (Me) CH2S (O) Me CFThree
CH (Me) CH2S (O) Et CFThree
CH (Me) CH2S (O)2Me CFThree
CH (Me) CH2S (O)2Et CFThree
CH (Et) CH2SMe CFThree
CH (Et) CH2SEt CFThree
CH (Et) CH2S (O) Me CFThree
CH (Et) CH2S (O) Et CFThree
CH (Et) CH2S (O)2Me CFThree
CH (Et) CH2S (O)2Et CFThree
C (Me)2CH2SMe CFThree
C (Me)2CH2SEt CFThree
C (Me)2CH2S (O) Me CFThree
C (Me)2CH2S (O) Et CFThree
C (Me)2CH2S (O)2Me CFThree
C (Me)2CH2S (O)2Et CFThree
CH2CH (Me) SMe CFThree
CH2CH (Me) SEt CFThree
CH2CH (Me) S (O) Me CFThree
CH2CH (Me) S (O) Et CFThree
CH2CH (Me) S (O)2Me CFThree
CH2CH (Me) S (O)2Et CFThree
CH2CH (Et) SMe CFThree
CH2CH (Et) SEt CFThree
CH2CH (Et) S (O) Me CFThree
CH2CH (Et) S (O) Et CFThree
CH2CH (Et) S (O)2Me CFThree
CH2CH (Et) S (O)2Et CFThree
CH (Me) CH (Me) SMe CFThree
CH (Me) CH (Me) SEt CFThree
CH (Me) CH (Me) S (O) Me CFThree
CH (Me) CH (Me) S (O) Et CFThree
CH (Me) CH (Me) S (O)2Me CFThree
CH (Me) CH (Me) S (O)2Et CFThree
CH2SMe CN
CH2SEt CN
CH2S (O) Me CN
CH2S (O) Et CN
CH2S (O)2Me CN
CH2S (O)2Et CN
CH (Me) SMe CN
CH (Me) SEt CN
CH (Me) S (O) Me CN
CH (Me) S (O) Et CN
CH (Me) S (O)2Me CN
CH (Me) S (O)2Et CN
CH (Et) SMe CN
CH (Et) SEt CN
CH (Et) S (O) Me CN
CH (Et) S (O) Et CN
CH (Et) S (O)2Me CN
CH (Et) S (O)2Et CN
CH (n-Pr) SMe CN
CH (n-Pr) SEt CN
CH (n-Pr) S (O) Me CN
CH (n-Pr) S (O) Et CN
CH (n-Pr) S (O)2Me CN
CH (n-Pr) S (O)2Et CN
CH (i-Pr) SMe CN
CH (i-Pr) SEt CN
CH (i-Pr) S (O) Me CN
CH (i-Pr) S (O) Et CN
CH (i-Pr) S (O)2Me CN
CH (i-Pr) S (O)2Et CN
CH (n-Bu) SMe CN
CH (n-Bu) SEt CN
CH (n-Bu) S (O) Me CN
CH (n-Bu) S (O) Et CN
CH (n-Bu) S (O)2Me CN
CH (n-Bu) S (O)2Et CN
CH (i-Bu) SMe CN
CH (i-Bu) SEt CN
CH (i-Bu) S (O) Me CN
CH (i-Bu) S (O) Et CN
CH (i-Bu) S (O)2Me CN
CH (i-Bu) S (O)2Et CN
CH (s-Bu) SMe CN
CH (s-Bu) SEt CN
CH (s-Bu) S (O) Me CN
CH (s-Bu) S (O) Et CN
CH (s-Bu) S (O)2Me CN
CH (s-Bu) S (O)2Et CN
CH (t-Bu) SMe CN
CH (t-Bu) SEt CN
CH (t-Bu) S (O) Me CN
CH (t-Bu) S (O) Et CN
CH (t-Bu) S (O)2Me CN
CH (t-Bu) S (O)2Et CN
CH2CH2SMe CN
CH2CH2SEt CN
CH2CH2S (O)2Me CN
CH2CH2S (O)2Et CN
CH (Me) CH2SMe CN
CH (Me) CH2SEt CN
CH (Me) CH2S (O) Me CN
CH (Me) CH2S (O) Et CN
CH (Me) CH2S (O)2Me CN
CH (Me) CH2S (O)2Et CN
CH (Et) CH2SMe CN
CH (Et) CH2SEt CN
CH (Et) CH2S (O) Me CN
CH (Et) CH2S (O) Et CN
CH (Et) CH2S (O)2Me CN
CH (Et) CH2S (O)2Et CN
C (Me)2CH2SMe CN
C (Me)2CH2SEt CN
C (Me)2CH2S (O) Me CN
C (Me)2CH2S (O) Et CN
C (Me)2CH2S (O)2Me CN
C (Me)2CH2S (O)2Et CN
CH2CH (Me) SMe CN
CH2CH (Me) SEt CN
CH2CH (Me) S (O) Me CN
CH2CH (Me) S (O) Et CN
CH2CH (Me) S (O)2Me CN
CH2CH (Me) S (O)2Et CN
CH2CH (Et) SMe CN
CH2CH (Et) SEt CN
CH2CH (Et) S (O) Me CN
CH2CH (Et) S (O) Et CN
CH2CH (Et) S (O)2Me CN
CH2CH (Et) S (O)2Et CN
CH (Me) CH (Me) SMe CN
CH (Me) CH (Me) SEt CN
CH (Me) CH (Me) S (O) Me CN
CH (Me) CH (Me) S (O) Et CN
CH (Me) CH (Me) S (O)2Me CN
CH (Me) CH (Me) S (O)2Et CN
CH2SMe Cl
CH2SEt Cl
CH2S (O) Me Cl
CH2S (O) Et Cl
CH2S (O)2Me Cl
CH2S (O)2Et Cl
CH (Me) SMe Cl
CH (Me) SEt Cl
CH (Me) S (O) Me Cl
CH (Me) S (O) Et Cl
CH (Me) S (O)2Me Cl
CH (Me) S (O)2Et Cl
CH (Et) SMe Cl
CH (Et) SEt Cl
CH (Et) S (O) Me Cl
CH (Et) S (O) Et Cl
CH (Et) S (O)2Me Cl
CH (Et) S (O)2Et Cl
CH (n-Pr) SMe Cl
CH (n-Pr) SEt Cl
CH (n-Pr) S (O) Me Cl
CH (n-Pr) S (O) Et Cl
CH (n-Pr) S (O)2Me Cl
CH (n-Pr) S (O)2Et Cl
CH (i-Pr) SMe Cl
CH (i-Pr) SEt Cl
CH (i-Pr) S (O) Me Cl
CH (i-Pr) S (O) Et Cl
CH (i-Pr) S (O)2Me Cl
CH (i-Pr) S (O)2Et Cl
CH (n-Bu) SMe Cl
CH (n-Bu) SEt Cl
CH (n-Bu) S (O) Me Cl
CH (n-Bu) S (O) Et Cl
CH (n-Bu) S (O)2Me Cl
CH (n-Bu) S (O)2Et Cl
CH (i-Bu) SMe Cl
CH (i-Bu) SEt Cl
CH (i-Bu) S (O) Me Cl
CH (i-Bu) S (O) Et Cl
CH (i-Bu) S (O)2Me Cl
CH (i-Bu) S (O)2Et Cl
CH (s-Bu) SMe Cl
CH (s-Bu) SEt Cl
CH (s-Bu) S (O) Me Cl
CH (s-Bu) S (O) Et Cl
CH (s-Bu) S (O)2Me Cl
CH (s-Bu) S (O)2Et Cl
CH (t-Bu) SMe Cl
CH (t-Bu) SEt Cl
CH (t-Bu) S (O) Me Cl
CH (t-Bu) S (O) Et Cl
CH (t-Bu) S (O)2Me Cl
CH (t-Bu) S (O)2Et Cl
CH2CH2SMe Cl
CH2CH2SEt Cl
CH2CH2S (O)2Me Cl
CH2CH2S (O)2Et Cl
CH (Me) CH2SMe Cl
CH (Me) CH2SEt Cl
CH (Me) CH2S (O) Me Cl
CH (Me) CH2S (O) Et Cl
CH (Me) CH2S (O)2Me Cl
CH (Me) CH2S (O)2Et Cl
CH (Et) CH2SMe Cl
CH (Et) CH2SEt Cl
CH (Et) CH2S (O) Me Cl
CH (Et) CH2S (O) Et Cl
CH (Et) CH2S (O)2Me Cl
CH (Et) CH2S (O)2Et Cl
C (Me)2CH2SMe Cl
C (Me)2CH2SEt Cl
C (Me)2CH2S (O) Me Cl
C (Me)2CH2S (O) Et Cl
C (Me)2CH2S (O)2Me Cl
C (Me)2CH2S (O)2Et Cl
CH2CH (Me) SMe Cl
CH2CH (Me) SEt Cl
CH2CH (Me) S (O) Me Cl
CH2CH (Me) S (O) Et Cl
CH2CH (Me) S (O)2Me Cl
CH2CH (Me) S (O)2Et Cl
CH2CH (Et) SMe Cl
CH2CH (Et) SEt Cl
CH2CH (Et) S (O) Me Cl
CH2CH (Et) S (O) Et Cl
CH2CH (Et) S (O)2Me Cl
CH2CH (Et) S (O)2Et Cl
CH (Me) CH (Me) SMe Cl
CH (Me) CH (Me) SEt Cl
CH (Me) CH (Me) S (O) Me Cl
CH (Me) CH (Me) S (O) Et Cl
CH (Me) CH (Me) S (O)2Me Cl
CH (Me) CH (Me) S (O)2Et Cl
CH2SMe C (O) OMe
CH2SEt C (O) OMe
CH2S (O) Me C (O) OMe
CH2S (O) Et C (O) OMe
CH2S (O)2Me C (O) OMe
CH2S (O)2Et C (O) OMe
CH (Me) SMe C (O) OMe
CH (Me) SEt C (O) OMe
CH (Me) S (O) Me C (O) OMe
CH (Me) S (O) Et C (O) OMe
CH (Me) S (O)2Me C (O) OMe
CH (Me) S (O)2Et C (O) OMe
CH (Et) SMe C (O) OMe
CH (Et) SEt C (O) OMe
CH (Et) S (O) Me C (O) OMe
CH (Et) S (O) Et C (O) OMe
CH (Et) S (O)2Me C (O) OMe
CH (Et) S (O)2Et C (O) OMe
CH (n-Pr) SMe C (O) OMe
CH (n-Pr) SEt C (O) OMe
CH (n-Pr) S (O) Me C (O) OMe
CH (n-Pr) S (O) Et C (O) OMe
CH (n-Pr) S (O)2Me C (O) OMe
CH (n-Pr) S (O)2Et C (O) OMe
CH (i-Pr) SMe C (O) OMe
CH (i-Pr) SEt C (O) OMe
CH (i-Pr) S (O) Me C (O) OMe
CH (i-Pr) S (O) Et C (O) OMe
CH (i-Pr) S (O)2Me C (O) OMe
CH (i-Pr) S (O)2Et C (O) OMe
CH (n-Bu) SMe C (O) OMe
CH (n-Bu) SEt C (O) OMe
CH (n-Bu) S (O) Me C (O) OMe
CH (n-Bu) S (O) Et C (O) OMe
CH (n-Bu) S (O)2Me C (O) OMe
CH (n-Bu) S (O)2Et C (O) OMe
CH (i-Bu) SMe C (O) OMe
CH (i-Bu) SEt C (O) OMe
CH (i-Bu) S (O) Me C (O) OMe
CH (i-Bu) S (O) Et C (O) OMe
CH (i-Bu) S (O)2Me C (O) OMe
CH (i-Bu) S (O)2Et C (O) OMe
CH (s-Bu) SMe C (O) OMe
CH (s-Bu) SEt C (O) OMe
CH (s-Bu) S (O) Me C (O) OMe
CH (s-Bu) S (O) Et C (O) OMe
CH (s-Bu) S (O)2Me C (O) OMe
CH (s-Bu) S (O)2Et C (O) OMe
CH (t-Bu) SMe C (O) OMe
CH (t-Bu) SEt C (O) OMe
CH (t-Bu) S (O) Me C (O) OMe
CH (t-Bu) S (O) Et C (O) OMe
CH (t-Bu) S (O)2Me C (O) OMe
CH (t-Bu) S (O)2Et C (O) OMe
CH2CH2SMe C (O) OMe
CH2CH2SEt C (O) OMe
CH2CH2S (O)2Me C (O) OMe
CH2CH2S (O)2Et C (O) OMe
CH (Me) CH2SMe C (O) OMe
CH (Me) CH2SEt C (O) OMe
CH (Me) CH2S (O) Me C (O) OMe
CH (Me) CH2S (O) Et C (O) OMe
CH (Me) CH2S (O)2Me C (O) OMe
CH (Me) CH2S (O)2Et C (O) OMe
CH (Et) CH2SMe C (O) OMe
CH (Et) CH2SEt C (O) OMe
CH (Et) CH2S (O) Me C (O) OMe
CH (Et) CH2S (O) Et C (O) OMe
CH (Et) CH2S (O)2Me C (O) OMe
CH (Et) CH2S (O)2Et C (O) OMe
C (Me)2CH2SMe C (O) OMe
C (Me)2CH2SEt C (O) OMe
C (Me)2CH2S (O) Me C (O) OMe
C (Me)2CH2S (O) Et C (O) OMe
C (Me)2CH2S (O)2Me C (O) OMe
C (Me)2CH2S (O)2Et C (O) OMe
CH2CH (Me) SMe C (O) OMe
CH2CH (Me) SEt C (O) OMe
CH2CH (Me) S (O) Me C (O) OMe
CH2CH (Me) S (O) Et C (O) OMe
CH2CH (Me) S (O)2Me C (O) OMe
CH2CH (Me) S (O)2Et C (O) OMe
CH2CH (Et) SMe C (O) OMe
CH2CH (Et) SEt C (O) OMe
CH2CH (Et) S (O) Me C (O) OMe
CH2CH (Et) S (O) Et C (O) OMe
CH2CH (Et) S (O)2Me C (O) OMe
CH2CH (Et) S (O)2Et C (O) OMe
CH (Me) CH (Me) SMe C (O) OMe
CH (Me) CH (Me) SEt C (O) OMe
CH (Me) CH (Me) S (O) Me C (O) OMe
CH (Me) CH (Me) S (O) Et C (O) OMe
CH (Me) CH (Me) S (O)2Me C (O) OMe
CH (Me) CH (Me) S (O)2Et C (O) OMe
CH2OMe CH2SMe
CH2OMe CH2SEt
CH2OMe CH2SCFThree
CH2OMe CH2SCH2CFThree
CH2OMe CH2S (O) Me
CH2OMe CH2S (O) Et
CH2OMe CH2S (O) CFThree
CH2OMe CH2S (O) CH2CFThree
CH2OMe CH2S (O)2Me
CH2OMe CH2S (O)2Et
CH2OMe CH2S (O)2CFThree
CH2OMe CH2S (O)2CH2CFThree
CH2OMe CH (Me) SMe
CH2OMe CH (Me) SEt
CH2OMe CH (Me) SCFThree
CH2OMe CH (Me) SCH2CFThree
CH2OMe CH (Me) S (O) Me
CH2OMe CH (Me) S (O) Et
CH2OMe CH (Me) S (O) CFThree
CH2OMe CH (Me) S (O) CH2CFThree
CH2OMe CH (Me) S (O)2Me
CH2OMe CH (Me) S (O)2Et
CH2OMe CH (Me) S (O)2CFThree
CH2OMe CH (Me) S (O)2CH2CFThree
CH2OMe CH (Et) SMe
CH2OMe CH (Et) SEt
CH2OMe CH (Et) SCFThree
CH2OMe CH (Et) SCH2CFThree
CH2OMe CH (Et) S (O) Me
CH2OMe CH (Et) S (O) Et
CH2OMe CH (Et) S (O) CFThree
CH2OMe CH (Et) S (O) CH2CFThree
CH2OMe CH (Et) S (O)2Me
CH2OMe CH (Et) S (O)2Et
CH2OMe CH (Et) S (O)2CFThree
CH2OMe CH (Et) S (O)2CH2CFThree
CH2OMe CH (n-Pr) SMe
CH2OMe CH (n-Pr) SEt
CH2OMe CH (n-Pr) SCFThree
CH2OMe CH (n-Pr) SCH2CFThree
CH2OMe CH (n-Pr) S (O) Me
CH2OMe CH (n-Pr) S (O) Et
CH2OMe CH (n-Pr) S (O) CFThree
CH2OMe CH (n-Pr) S (O) CH2CFThree
CH2OMe CH (n-Pr) S (O)2Me
CH2OMe CH (n-Pr) S (O)2Et
CH2OMe CH (n-Pr) S (O)2CFThree
CH2OMe CH (n-Pr) S (O)2CH2CFThree
CH2OMe CH (i-Pr) SMe
CH2OMe CH (i-Pr) SEt
CH2OMe CH (i-Pr) SCFThree
CH2OMe CH (i-Pr) SCH2CFThree
CH2OMe CH (i-Pr) S (O) Me
CH2OMe CH (i-Pr) S (O) Et
CH2OMe CH (i-Pr) S (O) CFThree
CH2OMe CH (i-Pr) S (O) CH2CFThree
CH2OMe CH (i-Pr) S (O)2Me
CH2OMe CH (i-Pr) S (O)2Et
CH2OMe CH (i-Pr) S (O)2CFThree
CH2OMe CH (i-Pr) S (O)2CH2CFThree
CH2OMe CH (n-Bu) SMe
CH2OMe CH (n-Bu) SEt
CH2OMe CH (n-Bu) SCFThree
CH2OMe CH (n-Bu) SCH2CFThree
CH2OMe CH (n-Bu) S (O) Me
CH2OMe CH (n-Bu) S (O) Et
CH2OMe CH (n-Bu) S (O) CFThree
CH2OMe CH (n-Bu) S (O) CH2CFThree
CH2OMe CH (n-Bu) S (O)2Me
CH2OMe CH (n-Bu) S (O)2Et
CH2OMe CH (n-Bu) S (O)2CFThree
CH2OMe CH (n-Bu) S (O)2CH2CFThree
CH2OMe CH (i-Bu) SMe
CH2OMe CH (i-Bu) SEt
CH2OMe CH (i-Bu) SCFThree
CH2OMe CH (i-Bu) SCH2CFThree
CH2OMe CH (i-Bu) S (O) Me
CH2OMe CH (i-Bu) S (O) Et
CH2OMe CH (i-Bu) S (O) CFThree
CH2OMe CH (i-Bu) S (O) CH2CFThree
CH2OMe CH (i-Bu) S (O)2Me
CH2OMe CH (i-Bu) S (O)2Et
CH2OMe CH (i-Bu) S (O)2CFThree
CH2OMe CH (i-Bu) S (O)2CH2CFThree
CH2OMe CH (s-Bu) SMe
CH2OMe CH (s-Bu) SEt
CH2OMe CH (s-Bu) SCFThree
CH2OMe CH (s-Bu) SCH2CFThree
CH2OMe CH (s-Bu) S (O) Me
CH2OMe CH (s-Bu) S (O) Et
CH2OMe CH (s-Bu) S (O) CFThree
CH2OMe CH (s-Bu) S (O) CH2CFThree
CH2OMe CH (s-Bu) S (O)2Me
CH2OMe CH (s-Bu) S (O)2Et
CH2OMe CH (s-Bu) S (O)2CFThree
CH2OMe CH (s-Bu) S (O)2CH2CFThree
CH2OMe CH (t-Bu) SMe
CH2OMe CH (t-Bu) SEt
CH2OMe CH (t-Bu) SCFThree
CH2OMe CH (t-Bu) SCH2CFThree
CH2OMe CH (t-Bu) S (O) Me
CH2OMe CH (t-Bu) S (O) Et
CH2OMe CH (t-Bu) S (O) CFThree
CH2OMe CH (t-Bu) S (O) CH2CFThree
CH2OMe CH (t-Bu) S (O)2Me
CH2OMe CH (t-Bu) S (O)2Et
CH2OMe CH (t-Bu) S (O)2CFThree
CH2OMe CH (t-Bu) S (O)2CH2CFThree
CH2OMe CH (CFThreeSMe
CH2OMe CH (CFThree) SEt
CH2OMe CH (CFThree) SCFThree
CH2OMe CH (CFThree) SCH2CFThree
CH2OMe CH (CFThree) S (O) Me
CH2OMe CH (CFThree) S (O) Et
CH2OMe CH (CFThree) S (O) CFThree
CH2OMe CH (CFThree) S (O) CH2CFThree
CH2OMe CH (CFThree) S (O)2Me
CH2OMe CH (CFThree) S (O)2Et
CH2OMe CH (CFThree) S (O)2CFThree
CH2OMe CH (CFThree) S (O)2CH2CFThree
CH2OMe CH2CH2SMe
CH2OMe CH2CH2SEt
CH2OMe CH2CH2SCFThree
CH2OMe CH2CH2SCH2CFThree
CH2OMe CH2CH2S (O) Me
CH2OMe CH2CH2S (O) Et
CH2OMe CH2CH2S (O) CFThree
CH2OMe CH2CH2S (O) CH2CFThree
CH2OMe CH2CH2S (O)2Me
CH2OMe CH2CH2S (O)2Et
CH2OMe CH2CH2S (O)2CFThree
CH2OMe CH2CH2S (O)2CH2CFThree
CH2OMe CH (Me) CH2SMe
CH2OMe CH (Me) CH2SEt
CH2OMe CH (Me) CH2SCFThree
CH2OMe CH (Me) CH2SCH2CFThree
CH2OMe CH (Me) CH2S (O) Me
CH2OMe CH (Me) CH2S (O) Et
CH2OMe CH (Me) CH2S (O) CFThree
CH2OMe CH (Me) CH2S (O) CH2CFThree
CH2OMe CH (Me) CH2S (O)2Me
CH2OMe CH (Me) CH2S (O)2Et
CH2OMe CH (Me) CH2S (O)2CFThree
CH2OMe CH (Me) CH2S (O)2CH2CFThree
CH2OMe CH (Et) CH2SMe
CH2OMe CH (Et) CH2SEt
CH2OMe CH (Et) CH2SCFThree
CH2OMe CH (Et) CH2SCH2CFThree
CH2OMe CH (Et) CH2S (O) Me
CH2OMe CH (Et) CH2S (O) Et
CH2OMe CH (Et) CH2S (O) CFThree
CH2OMe CH (Et) CH2S (O) CH2CFThree
CH2OMe CH (Et) CH2S (O)2Me
CH2OMe CH (Et) CH2S (O)2Et
CH2OMe CH (Et) CH2S (O)2CFThree
CH2OMe CH (Et) CH2S (O)2CH2CFThree
CH2OMe C (Me)2CH2SMe
CH2OMe C (Me)2CH2SEt
CH2OMe C (Me)2CH2SCFThree
CH2OMe C (Me)2CH2SCH2CFThree
CH2OMe C (Me)2CH2S (O) Me
CH2OMe C (Me)2CH2S (O) Et
CH2OMe C (Me)2CH2S (O) CFThree
CH2OMe C (Me)2CH2S (O) CH2CFThree
CH2OMe C (Me)2CH2S (O)2Me
CH2OMe C (Me)2CH2S (O)2Et
CH2OMe C (Me)2CH2S (O)2CFThree
CH2OMe C (Me)2CH2S (O)2CH2CFThree
CH2OMe CH2CH (Me) SMe
CH2OMe CH2CH (Me) SEt
CH2OMe CH2CH (Me) SCFThree
CH2OMe CH2CH (Me) SCH2CFThree
CH2OMe CH2CH (Me) S (O) Me
CH2OMe CH2CH (Me) S (O) Et
CH2OMe CH2CH (Me) S (O) CFThree
CH2OMe CH2CH (Me) S (O) CH2CFThree
CH2OMe CH2CH (Me) S (O)2Me
CH2OMe CH2CH (Me) S (O)2Et
CH2OMe CH2CH (Me) S (O)2CFThree
CH2OMe CH2CH (Me) S (O)2CH2CFThree
CH2OMe CH2CH (Et) SMe
CH2OMe CH2CH (Et) SEt
CH2OMe CH2CH (Et) SCFThree
CH2OMe CH2CH (Et) SCH2CFThree
CH2OMe CH2CH (Et) S (O) Me
CH2OMe CH2CH (Et) S (O) Et
CH2OMe CH2CH (Et) S (O) CFThree
CH2OMe CH2CH (Et) S (O) CH2CFThree
CH2OMe CH2CH (Et) S (O)2Me
CH2OMe CH2CH (Et) S (O)2Et
CH2OMe CH2CH (Et) S (O)2CFThree
CH2OMe CH2CH (Et) S (O)2CH2CFThree
CH2OMe CH (Me) CH (Me) SMe
CH2OMe CH (Me) CH (Me) SEt
CH2OMe CH (Me) CH (Me) SCFThree
CH2OMe CH (Me) CH (Me) SCH2CFThree
CH2OMe CH (Me) CH (Me) S (O) Me
CH2OMe CH (Me) CH (Me) S (O) Et
CH2OMe CH (Me) CH (Me) S (O) CFThree
CH2OMe CH (Me) CH (Me) S (O) CH2CFThree
CH2OMe CH (Me) CH (Me) S (O)2Me
CH2OMe CH (Me) CH (Me) S (O)2Et
CH2OMe CH (Me) CH (Me) S (O)2CFThree
CH2OMe CH (Me) CH (Me) S (O)2CH2CFThree
CH2C (= NOMe) Me CH2SMe
CH2C (= NOMe) Me CH2SEt
CH2C (= NOMe) Me CH2SCFThree
CH2C (= NOMe) Me CH2SCH2CFThree
CH2C (= NOMe) Me CH2S (O) Me
CH2C (= NOMe) Me CH2S (O) Et
CH2C (= NOMe) Me CH2S (O) CFThree
CH2C (= NOMe) Me CH2S (O) CH2CFThree
CH2C (= NOMe) Me CH2S (O)2Me
CH2C (= NOMe) Me CH2S (O)2Et
CH2C (= NOMe) Me CH2S (O)2CFThree
CH2C (= NOMe) Me CH2S (O)2CH2CFThree
CH2C (= NOMe) Me CH (Me) SMe
CH2C (= NOMe) Me CH (Me) SEt
CH2C (= NOMe) Me CH (Me) SCFThree
CH2C (= NOMe) Me CH (Me) SCH2CFThree
CH2C (= NOMe) Me CH (Me) S (O) Me
CH2C (= NOMe) Me CH (Me) S (O) Et
CH2C (= NOMe) Me CH (Me) S (O) CFThree
CH2C (= NOMe) Me CH (Me) S (O) CH2CFThree
CH2C (= NOMe) Me CH (Me) S (O)2Me
CH2C (= NOMe) Me CH (Me) S (O)2Et
CH2C (= NOMe) Me CH (Me) S (O)2CFThree
CH2C (= NOMe) Me CH (Me) S (O)2CH2CFThree
CH2C (= NOMe) Me CH (Et) SMe
CH2C (= NOMe) Me CH (Et) SEt
CH2C (= NOMe) Me CH (Et) SCFThree
CH2C (= NOMe) Me CH (Et) SCH2CFThree
CH2C (= NOMe) Me CH (Et) S (O) Me
CH2C (= NOMe) Me CH (Et) S (O) Et
CH2C (= NOMe) Me CH (Et) S (O) CFThree
CH2C (= NOMe) Me CH (Et) S (O) CH2CFThree
CH2C (= NOMe) Me CH (Et) S (O)2Me
CH2C (= NOMe) Me CH (Et) S (O)2Et
CH2C (= NOMe) Me CH (Et) S (O)2CFThree
CH2C (= NOMe) Me CH (Et) S (O)2CH2CFThree
CH2C (= NOMe) Me CH (n-Pr) SMe
CH2C (= NOMe) Me CH (n-Pr) SEt
CH2C (= NOMe) Me CH (n-Pr) SCFThree
CH2C (= NOMe) Me CH (n-Pr) SCH2CFThree
CH2C (= NOMe) Me CH (n-Pr) S (O) Me
CH2C (= NOMe) Me CH (n-Pr) S (O) Et
CH2C (= NOMe) Me CH (n-Pr) S (O) CFThree
CH2C (= NOMe) Me CH (n-Pr) S (O) CH2CFThree
CH2C (= NOMe) Me CH (n-Pr) S (O)2Me
CH2C (= NOMe) Me CH (n-Pr) S (O)2Et
CH2C (= NOMe) Me CH (n-Pr) S (O)2CFThree
CH2C (= NOMe) Me CH (n-Pr) S (O)2CH2CFThree
CH2C (= NOMe) Me CH (i-Pr) SMe
CH2C (= NOMe) Me CH (i-Pr) SEt
CH2C (= NOMe) Me CH (i-Pr) SCFThree
CH2C (= NOMe) Me CH (i-Pr) SCH2CFThree
CH2C (= NOMe) Me CH (i-Pr) S (O) Me
CH2C (= NOMe) Me CH (i-Pr) S (O) Et
CH2C (= NOMe) Me CH (i-Pr) S (O) CFThree
CH2C (= NOMe) Me CH (i-Pr) S (O) CH2CFThree
CH2C (= NOMe) Me CH (i-Pr) S (O)2Me
CH2C (= NOMe) Me CH (i-Pr) S (O)2Et
CH2C (= NOMe) Me CH (i-Pr) S (O)2CFThree
CH2C (= NOMe) Me CH (i-Pr) S (O)2CH2CFThree
CH2C (= NOMe) Me CH (n-Bu) SMe
CH2C (= NOMe) Me CH (n-Bu) SEt
CH2C (= NOMe) Me CH (n-Bu) SCFThree
CH2C (= NOMe) Me CH (n-Bu) SCH2CFThree
CH2C (= NOMe) Me CH (n-Bu) S (O) Me
CH2C (= NOMe) Me CH (n-Bu) S (O) Et
CH2C (= NOMe) Me CH (n-Bu) S (O) CFThree
CH2C (= NOMe) Me CH (n-Bu) S (O) CH2CFThree
CH2C (= NOMe) Me CH (n-Bu) S (O)2Me
CH2C (= NOMe) Me CH (n-Bu) S (O)2Et
CH2C (= NOMe) Me CH (n-Bu) S (O)2CFThree
CH2C (= NOMe) Me CH (n-Bu) S (O)2CH2CFThree
CH2C (= NOMe) Me CH (i-Bu) SMe
CH2C (= NOMe) Me CH (i-Bu) SEt
CH2C (= NOMe) Me CH (i-Bu) SCFThree
CH2C (= NOMe) Me CH (i-Bu) SCH2CFThree
CH2C (= NOMe) Me CH (i-Bu) S (O) Me
CH2C (= NOMe) Me CH (i-Bu) S (O) Et
CH2C (= NOMe) Me CH (i-Bu) S (O) CFThree
CH2C (= NOMe) Me CH (i-Bu) S (O) CH2CFThree
CH2C (= NOMe) Me CH (i-Bu) S (O)2Me
CH2C (= NOMe) Me CH (i-Bu) S (O)2Et
CH2C (= NOMe) Me CH (i-Bu) S (O)2CFThree
CH2C (= NOMe) Me CH (i-Bu) S (O)2CH2CFThree
CH2C (= NOMe) Me CH (s-Bu) SMe
CH2C (= NOMe) Me CH (s-Bu) SEt
CH2C (= NOMe) Me CH (s-Bu) SCFThree
CH2C (= NOMe) Me CH (s-Bu) SCH2CFThree
CH2C (= NOMe) Me CH (s-Bu) S (O) Me
CH2C (= NOMe) Me CH (s-Bu) S (O) Et
CH2C (= NOMe) Me CH (s-Bu) S (O) CFThree
CH2C (= NOMe) Me CH (s-Bu) S (O) CH2CFThree
CH2C (= NOMe) Me CH (s-Bu) S (O)2Me
CH2C (= NOMe) Me CH (s-Bu) S (O)2Et
CH2C (= NOMe) Me CH (s-Bu) S (O)2CFThree
CH2C (= NOMe) Me CH (s-Bu) S (O)2CH2CFThree
CH2C (= NOMe) Me CH (t-Bu) SMe
CH2C (= NOMe) Me CH (t-Bu) SEt
CH2C (= NOMe) Me CH (t-Bu) SCFThree
CH2C (= NOMe) Me CH (t-Bu) SCH2CFThree
CH2C (= NOMe) Me CH (t-Bu) S (O) Me
CH2C (= NOMe) Me CH (t-Bu) S (O) Et
CH2C (= NOMe) Me CH (t-Bu) S (O) CFThree
CH2C (= NOMe) Me CH (t-Bu) S (O) CH2CFThree
CH2C (= NOMe) Me CH (t-Bu) S (O)2Me
CH2C (= NOMe) Me CH (t-Bu) S (O)2Et
CH2C (= NOMe) Me CH (t-Bu) S (O)2CFThree
CH2C (= NOMe) Me CH (t-Bu) S (O)2CH2CFThree
CH2C (= NOMe) Me CH (CFThreeSMe
CH2C (= NOMe) Me CH (CFThree) SEt
CH2C (= NOMe) Me CH (CFThree) SCFThree
CH2C (= NOMe) Me CH (CFThree) SCH2CFThree
CH2C (= NOMe) Me CH (CFThree) S (O) Me
CH2C (= NOMe) Me CH (CFThree) S (O) Et
CH2C (= NOMe) Me CH (CFThree) S (O) CFThree
CH2C (= NOMe) Me CH (CFThree) S (O) CH2CFThree
CH2C (= NOMe) Me CH (CFThree) S (O)2Me
CH2C (= NOMe) Me CH (CFThree) S (O)2Et
CH2C (= NOMe) Me CH (CFThree) S (O)2CFThree
CH2C (= NOMe) Me CH (CFThree) S (O)2CH2CFThree
CH2C (= NOMe) Me CH2CH2SMe
CH2C (= NOMe) Me CH2CH2SEt
CH2C (= NOMe) Me CH2CH2SCFThree
CH2C (= NOMe) Me CH2CH2SCH2CFThree
CH2C (= NOMe) Me CH2CH2S (O) Me
CH2C (= NOMe) Me CH2CH2S (O) Et
CH2C (= NOMe) Me CH2CH2S (O) CFThree
CH2C (= NOMe) Me CH2CH2S (O) CH2CFThree
CH2C (= NOMe) Me CH2CH2S (O)2Me
CH2C (= NOMe) Me CH2CH2S (O)2Et
CH2C (= NOMe) Me CH2CH2S (O)2CFThree
CH2C (= NOMe) Me CH2CH2S (O)2CH2CFThree
CH2C (= NOMe) Me CH (Me) CH2SMe
CH2C (= NOMe) Me CH (Me) CH2SEt
CH2C (= NOMe) Me CH (Me) CH2SCFThree
CH2C (= NOMe) Me CH (Me) CH2SCH2CFThree
CH2C (= NOMe) Me CH (Me) CH2S (O) Me
CH2C (= NOMe) Me CH (Me) CH2S (O) Et
CH2C (= NOMe) Me CH (Me) CH2S (O) CFThree
CH2C (= NOMe) Me CH (Me) CH2S (O) CH2CFThree
CH2C (= NOMe) Me CH (Me) CH2S (O)2Me
CH2C (= NOMe) Me CH (Me) CH2S (O)2Et
CH2C (= NOMe) Me CH (Me) CH2S (O)2CFThree
CH2C (= NOMe) Me CH (Me) CH2S (O)2CH2CFThree
CH2C (= NOMe) Me CH (Et) CH2SMe
CH2C (= NOMe) Me CH (Et) CH2SEt
CH2C (= NOMe) Me CH (Et) CH2SCFThree
CH2C (= NOMe) Me CH (Et) CH2SCH2CFThree
CH2C (= NOMe) Me CH (Et) CH2S (O) Me
CH2C (= NOMe) Me CH (Et) CH2S (O) Et
CH2C (= NOMe) Me CH (Et) CH2S (O) CFThree
CH2C (= NOMe) Me CH (Et) CH2S (O) CH2CFThree
CH2C (= NOMe) Me CH (Et) CH2S (O)2Me
CH2C (= NOMe) Me CH (Et) CH2S (O)2Et
CH2C (= NOMe) Me CH (Et) CH2S (O)2CFThree
CH2C (= NOMe) Me CH (Et) CH2S (O)2CH2CFThree
CH2C (= NOMe) Me C (Me)2CH2SMe
CH2C (= NOMe) Me C (Me)2CH2SEt
CH2C (= NOMe) Me C (Me)2CH2SCFThree
CH2C (= NOMe) Me C (Me)2CH2SCH2CFThree
CH2C (= NOMe) Me C (Me)2CH2S (O) Me
CH2C (= NOMe) Me C (Me)2CH2S (O) Et
CH2C (= NOMe) Me C (Me)2CH2S (O) CFThree
CH2C (= NOMe) Me C (Me)2CH2S (O) CH2CFThree
CH2C (= NOMe) Me C (Me)2CH2S (O)2Me
CH2C (= NOMe) Me C (Me)2CH2S (O)2Et
CH2C (= NOMe) Me C (Me)2CH2S (O)2CFThree
CH2C (= NOMe) Me C (Me)2CH2S (O)2CH2CFThree
CH2C (= NOMe) Me CH2CH (Me) SMe
CH2C (= NOMe) Me CH2CH (Me) SEt
CH2C (= NOMe) Me CH2CH (Me) SCFThree
CH2C (= NOMe) Me CH2CH (Me) SCH2CFThree
CH2C (= NOMe) Me CH2CH (Me) S (O) Me
CH2C (= NOMe) Me CH2CH (Me) S (O) Et
CH2C (= NOMe) Me CH2CH (Me) S (O) CFThree
CH2C (= NOMe) Me CH2CH (Me) S (O) CH2CFThree
CH2C (= NOMe) Me CH2CH (Me) S (O)2Me
CH2C (= NOMe) Me CH2CH (Me) S (O)2Et
CH2C (= NOMe) Me CH2CH (Me) S (O)2CFThree
CH2C (= NOMe) Me CH2CH (Me) S (O)2CH2CFThree
CH2C (= NOMe) Me CH2CH (Et) SMe
CH2C (= NOMe) Me CH2CH (Et) SEt
CH2C (= NOMe) Me CH2CH (Et) SCFThree
CH2C (= NOMe) Me CH2CH (Et) SCH2CFThree
CH2C (= NOMe) Me CH2CH (Et) S (O) Me
CH2C (= NOMe) Me CH2CH (Et) S (O) Et
CH2C (= NOMe) Me CH2CH (Et) S (O) CFThree
CH2C (= NOMe) Me CH2CH (Et) S (O) CH2CFThree
CH2C (= NOMe) Me CH2CH (Et) S (O)2Me
CH2C (= NOMe) Me CH2CH (Et) S (O)2Et
CH2C (= NOMe) Me CH2CH (Et) S (O)2CFThree
CH2C (= NOMe) Me CH2CH (Et) S (O)2CH2CFThree
CH2C (= NOMe) Me CH (Me) CH (Me) SMe
CH2C (= NOMe) Me CH (Me) CH (Me) SEt
CH2C (= NOMe) Me CH (Me) CH (Me) SCFThree
CH2C (= NOMe) Me CH (Me) CH (Me) SCH2CFThree
CH2C (= NOMe) Me CH (Me) CH (Me) S (O) Me
CH2C (= NOMe) Me CH (Me) CH (Me) S (O) Et
CH2C (= NOMe) Me CH (Me) CH (Me) S (O) CFThree
CH2C (= NOMe) Me CH (Me) CH (Me) S (O) CH2CFThree
CH2C (= NOMe) Me CH (Me) CH (Me) S (O)2Me
CH2C (= NOMe) Me CH (Me) CH (Me) S (O)2Et
CH2C (= NOMe) Me CH (Me) CH (Me) S (O)2CFThree
CH2C (= NOMe) Me CH (Me) CH (Me) S (O)2CH2CFThree
――――――――――――――――――
The compounds of the present invention are stored in warehouses, so-called agricultural pests that harm agricultural and horticultural crops and trees, so-called livestock pests that parasitize livestock and poultry, so-called sanitary pests that cause various adverse effects in the human living environment such as houses. It is possible to effectively control insects such as so-called stored grain pests that harm cereals and the like, and pests such as mites, crustaceans, molluscs, and nematodes that occur and harm in similar situations at low concentrations.
本発明化合物を用いて防除しうる昆虫類、ダニ類、甲殻類、軟体動物及び線虫類には具体的に、例えば、下記の生物が挙げられるが、本発明はこれらのみに限定されるものではない。 Specific examples of insects, mites, crustaceans, molluscs and nematodes that can be controlled using the compounds of the present invention include the following organisms, but the present invention is not limited to these. is not.
チャノコカクモンハマキ(Adoxophyes honmai)、リンゴコカクモンハマキ(Adoxophyes orana faciata)、リンゴモンハマキ(Archips breviplicanus)、ミダレカクモンハマキ(Archips fuscocupreanus)、ナシヒメシンクイ(Grapholita molesta)、チャハマキ(Homona magnanima)、マメシンクイガ(Leguminivora glycinivorella)、マメヒメサヤムシガ(Matsumuraeses phaseoli)、トビハマキ(Pandemis heparana)、ナシチビガ(Bucculatrix pyrivorella)、モモハモグリガ(Lyonetia clerkella)、ギンモンハモグリガ(Lyonetia prunifoliella malinella)、チャノホソガ(Caloptilia theivora)、キンモンホソガ(Phyllonorycter ringoniella)、ミカンハモグリガ(Phyllocnistis citrella)、ネギコガ(Acrolepiopsis sapporensis)、ヤマノイモコガ(Acrolepiopsis suzukiella)、コナガ(Plutella xylostella)、カキノヘタムシガ(Stathmopoda masinissa)、イモキバガ(Helcystogramma triannulella)、ワタアカミムシ(Pectinophora gossypiella)、モモシンクイガ(Carposina sasakii)、コドリンガ(Cydla pomonella)、ニカメイガ(Chilo suppressalis)、コブノメイガ(Cnaphalocrocis medinalis)、モモノゴマダラノメイガ(Conogethes punctiferalis)、ワタヘリクロノメイガ(Diaphania indica)、シロイチモジマダラメイガ(Etiella zinckenella)、クワノメイガ(Glyphodes pyloalis)、ハイマダラノメイガ(Hellula undalis)、アワノメイガ(Ostrinia furnacalis)、アズキノメイガ(Ostrinia scapulalis)、ヨーロピアンコーンボーラー(Ostrinia nubilalis)、シバツトガ(Parapediasia teterrella)、イチモンジセセリ(Parnara guttata)、オオモンシロチョウ(Pieris brassicae)、モンシロチョウ(Pieris rapae crucivora)、ヨモギエダシャク(Ascotis selenaria)、ソイビーンルーパー(Pseudoplusia includens)、チャドクガ(Euproctis pseudoconspersa)、マイマイガ(Lymantria dispar)、ヒメシロモンドクガ(Orgyia thyellina)、アメリカシロヒトリ(Hyphantria cunea)、クワゴマダラヒトリ(Lemyra imparilis)、アケビコノハ(Adris tyrannus)、ナカジロシタバ(Aedia leucomelas)、タマナヤガ(Agrotis ipsilon)、カブラヤガ(Agrotis segetum)、タマナギンウワバ(Autographa nigrisigna)、ミツモンキンウワバ(Ctenoplusia agnata)、オオタバコガ(Helicoverpa armigera)、タバコガ(Helicoverpa assulta)、コットンボールワーム(Helicoverpa zea)、タバコバッドワーム(Heliothis virescens)、ヨトウガ(Mamestra brassicae)、アワヨトウ(Mythimna separata)、フタオビコヤガ(Naranga aenescens)、サザンアーミーワーム(Spodoptera eridania)、シロイチモジヨトウ(Spodoptera exigua)、フォールアーミーワーム(Spodoptera frugiperda)、コットンリーフワーム(Spodoptera littoralis)、ハスモンヨトウ(Spodoptera litura)、スジキリヨトウ(Spodoptera depravata)、イラクサギンウワバ(Trichoplusia ni)、グレープベリーモス(Endopiza viteana)、トマトホーンワーム(Manduca quinquemaculata)、タバコホーンワーム(Manduca sexta)等の鱗翅目昆虫。 Adoxophyes honmai, Adoxophyes orana faciata, Archips breviplicanus, Archips fuscocupreanus, Grapholita molesta, Chama magnan Leguminivora glycinivorella), Matsumuraeses phaseoli, Pandemis heparana, Bucculatrix pyrivorella, Lyonetia clerkella, Lyonetia prunifal ringoniella), mandarin leaf moth (Phyllocnistis citrella), green moth (Acrolepiopsis sapporensis), wild moth (Acrolepiopsis suzukiella), black moth (Plutella xylostella), oyster leaf moth (Stathmopoda masinissa), cystogram tria ora gossypiella), peach sinker moth (Carposina sasakii), codling moth (Cydla pomonella), green moth (Chilo suppressalis), corn borer (Cnaphalocrocis medinalis), peach moth (Conogethes punctiferalis), cotton moth (Dia) (Etiella zinckenella), Glyphodes pyloalis, Hellula undalis, Ostrinia furnacalis, Ostrinia scapulalis, European corn borer (Ostrinia nubilaliseter, Pesta pal) ), White-tailed butterfly (Pieris brassicae), white-tailed butterfly (Pieris rapae crucivora), mugwort (Ascotis selenaria), soy bean looper (Pseudoplusia includens), chadokuga (Euproctis pseudoconspersa), maimaiga (Lymantria disparia), thymeina ), White-spotted starfish (Hyphantria cunea), white-spotted starfish (Lemyra imparilis), Akebiko-no-ha (Adris tyrannus), red-footed butterfly (Aedia leucomelas), red-footed squirrel (Agrotis ipsilon), red-tailed squirrel (Agrotis segetum) Uwaba (Ctenoplusia agnata), Helicoverpa armigera, Tobacco moth (Helicoverpa assulta), Cotton ball worm (Helicoverpa zea), Tobacco bad worm (Heliothis virescens), Mamestra brassicae, Mythimna naa ), Southern army worm (Spodoptera eridania), Spodoptera exigua, Fall army worm (Spodoptera frugiperda), Cotton leaf worm (Spodoptera littoralis), Spodoptera litura, Spodoptera litura, Spodoptera era ), Leeb Berry Moss (Endopiza viteana), tomato horn worm (Manduca quinquemaculata), tobacco horn worm (Manduca sexta) lepidopteran insects such as.
ヒラズハナアザミウマ(Frankliniella intonsa)、ミカンキイロアザミウマ(Frankliniella occidentalis)、クロトンアザミウマ(Heliothrips haemorrhoidalis)、チャノキイロアザミウマ(Scirtothrips dorsalis)、ミナミキイロアザミウマ(Thrips palmi)、ネギアザミウマ(Thrips tabaci)、カキクダアザミウマ(Ponticulothrips diospyrosi)等の総翅目昆虫。 Thrips thrips (Frankliniella intonsa), Citrus thrips (Frankliniella occidentalis), Croton thrips (Prithia thrips) Moths in total.
ブチヒゲカメムシ(Dolycoris baccarum)、ナガメ(Eurydema rugosum)、トゲシラホシカメムシ(Eysarcoris aeneus)、オオトゲシラホシカメムシ(Eysarcoris lewisi)、シラホシカメムシ(Eysarcoris ventralis)、ツヤアオカメムシ(Glaucias subpunctatus)、クサギカメムシ(Halyomorpha halys)、アオクサカメムシ(Nezara antennata)、ミナミアオカメムシ(Nezara viridula)、イチモンジカメムシ(Piezodorus hybneri)、チャバネアオカメムシ(Plautia crossota)、イネクロカメムシ(Scotinophora lurida)、ホソハリカメムシ(Cletus punctiger)、クモヘリカメムシ(Leptocorisa chinensis)、ホソヘリカメムシ(Riptortus clavatus)、アカヒメヘリカメムシ(Rhopalus msculatus)、カンシャコバネナガカメムシ(Cavelerius saccharivorus)、コバネヒョウタンナガカメムシ(Togo hemipterus)、アカホシカメムシ(Dysdercus cingulatus)、ツツジグンバイ(Stephanitis pyrioides)、クロトビカスミカメ(Halticus insularis)、ターニッシュドプラントバグ(Lygus lineolaris)、ナガムギカスミカメ(Stenodema sibiricum)、アカスジカスミカメ(Stenotus rubrovittatus)、イネホソミドリカスミカメ(Trigonotylus caelestialium)、フタテンヒメヨコバイ(Arboridia apicalis)、ミドリナガヨコバイ(Balclutha saltuella)、フタテンオオヨコバイ(Epiacanthus stramineus)、ポテトリーフホッパー(Empoasca fabae)、カキノヒメヨコバイ(Empoasca nipponica)、チャノミドリヒメヨコバイ(Empoasca onukii)、マメノミドリヒメヨコバイ(Empoasca sakaii)、ヒメフタテンヨコバイ(Macrosteles striifrons)、ツマグロヨコバイ(Nephotettix cinctinceps)、コットンフリーホッパー(Psuedatomoscelis seriatus)、ヒメトビウンカ(Laodelphax striatella)、トビイロウンカ(Nilaparvata lugens)、セジロウンカ(Sogatella furcifera)、ミカンキジラミ(Diaphorina citri)、ナシキジラミ(Psylla pyrisuga)、ミカントゲコナジラミ(Aleurocanthus spiniferus)、シルバーリーフコナジラミ(Bemisia argentifolii)、タバココナジラミ(Bemisia tabaci)、ミカンコナジラミ(Dialeurodes citri)、オンシツコナジラミ(Trialeurodes vaporariorum)、ブドウネアブラムシ(Viteus vitifolii)、ワタアブラムシ(Aphis gossypii)、ユキヤナギアブラムシ(Aphis spiraecola)、モモアカアブラムシ(Myzus persicae)、コミカンアブラムシ(Toxoptera aurantii)、オオワラジカイガラムシ(Drosicha corpulenta)、イセリアカイガラムシ(Icerya purchasi)、ナスコナカイガラムシ(Phenacoccus solani)、ミカンコナカイガラムシ(Planococcus citri)、フジコナカイガラムシ(Planococcus kuraunhiae)、クワコナカイガラムシ(Pseudococcus comstocki)、ツノロウムシ(Ceroplastes ceriferus)、ルビーロウムシ(Ceroplastes rubens)、アカマルカイガラムシ(Aonidiella aurantii)、ナシマルカイガラムシ(Comstockaspis perniciosa)、ティースケール(Fiorinia theae)、チャノマルカイガラムシ(Pseudaonidia paeoniae)、クワシロカイガラムシ(Pseudaulacaspis pentagona)、ウメシロカイガラムシ(Pseudaulacaspis prunicola)、マサキナガカイガラムシ(Unaspis euonymi)、ヤノネカイガラムシ(Unaspis yanonensis)、トコジラミ(Cimex lectularius)等の半翅目昆虫。 Spotted beetle (Dolycoris baccarum), sea turtle (Eurydema rugosum), bark beetle (Eysarcoris aeneus), horseshoe beetle (Eysarcoris lewisi), white-headed beetle (Eysarcoris ventralis), subtilus , Nezara antennata, Nezara viridula, Piezodorus hybneri, Plautia crossota, Scotinophora lurida, tiger C Stink bug (Leptocorisa chinensis), Hoso-heli beetle (Riptortus clavatus), Red-headed beetle (Rhopalus msculatus), Cavelerius saccharivorus, Toba hemipterus cus, Togo hemipterus (Stephanitis pyrioides), Kuroto Bikasumi turtle (Halticus insularis), Turned plant bug (Lygus lineolaris), Nagamu sika turtle (Stenodema sibiricum), Akasika sika turtle (Stenotus rubrovittatus), Rice moss turtle (Trigonotylus caelestialium), ical Arisbori dia Green leafhopper (Balclutha saltuella), butterfly leafhopper (Epiacanthus stramineus), potato leaf hopper (Empoasca fabae), oyster leafhopper (Empoasca nipponica), Chanomidorimempei (Empoasca onukii), omenosaka ), Leafhopper leafhopper (Macrosteles striifrons), leafhopper leafhopper (Nephotettix cinctinceps), cotton-free hopper (Psuedatomoscelis seriatus), leafhopper (Laodelphax striatella), leafhopper (Nilaparvata lugens) Psylla pyrisuga, Aleurocanthus spiniferus, Silver leaf whitefly (Bemisia argentifolii), Tobacco whitefly (Bemisia tabaci), Citrus whitefly (Dialeurodes citri), Onsitsuna whitefly (trialeurous grape rum, Trialeurodes vapor Cotton Aphid (Aphis gossypii), Snowy Aphid (Aphis spiraecola), Peach Aphid (Myzus persicae), Komikan Aphid (Toxoptera aurantii), Alaska Scale Aphid (Drosicha corpulenta), Iceria scale P solani), citrus scale insect (Planococcus citri), stag beetle scale (Planococcus kuraunhiae), stag beetle scale (Pseudococcus comstocki), horn beetle (Ceroplastes ceriferus), ruby rotum (Ceroplastes rubens), red scallop Nymphalidae (Comstockaspis perniciosa), tea scale (Fiorinia theae), chanomarine scale insect (Pseudaonidia paeoniae), stag beetle (Pseudaulacaspis pentagona), scallop scale (Pseudaulacaspis prunicola), euglena (Unaspis yanonensis), Hemiptera (Cimex lectularius) and other Hemiptera insects.
ドウガネブイブイ(Anomala cuprea)、ヒメコガネ(Anomala rufocuprea)、コアオハナムグリ(Gametis jucunda)、ナガチャコガネ(Heptophylla picea)、マメコガネ(Popillia japonica)、コロラドポテトビートル(Lepinotarsa decemlineata)、マルクビクシコメツキ(Melanotus fortnumi)、カンシャクシコメツキ(Melanotus tamsuyensis)、タバコシバンムシ(Lasioderma serricorne)、ヒメヒラタケシキスイ(Epuraea domina)、インゲンテントウ(Epilachna varivestis)、ニジュウヤホシテントウ(Epilachna vigintioctopunctata)、チャイロコメノゴミムシダマシ(Tenebrio molitor)、コクヌストモドキ(Tribolium castaneum)、ゴマダラカミキリ(Anoplophora malasiaca)、マツノマダラカミキリ(Monochamus alternatus)、キボシカミキリ(Psacothea hilaris)、ブドウトラカミキリ(Xylotrechus pyrrhoderus)、アズキゾウムシ(Callosobruchus chinensis)、ウリハムシ(Aulacophora femoralis)、テンサイトビハムシ(Chaetocnema concinna)、サザンコーンルートワーム(Diabrotica undecimpunctata)、ウエスタンコーンルートワーム(Diabrotica virgifera)、ノーザンコーンルートワーム(Diabrotica barberi)、イネドロオイムシ(Oulema oryzae)、キスジノミハムシ(Phyllotreta striolata)、ナスナガスネトビハムシ(Psylliodes angusticollis)、モモチョッキリゾウムシ(Rhynchites heros)、アリモドキゾウムシ(Cylas formicarius)、ワタミゾウムシ(Anthonomus grandis)、イネゾウムシ(Echinocnemus squameus)、イモゾウムシ(Euscepes postfasciatus)、アルファルファタコゾウムシ(Hypera postica)、イネミズゾウムシ(Lissohoptrus oryzophilus)、キンケクチブトゾウムシ(Otiorhynchus sulcatus)、グラナリーウィービル(Sitophilus granarius)、コクゾウムシ(Sitophilus zeamais)、シバオサゾウムシ(Sphenophorus venatus vestitus)、アオバアリガタハネカクシ(Paederus fuscipes)等の鞘翅目昆虫。 Douganebubui (Anomala cuprea), Japanese common squirrel (Anomala rufocuprea), Core ohanamuri (Gametis jucunda), Nagachakogane (Heptophylla picea), Japanese beetle (Popillia japonica), Colorado potato beetle (Lepinotarsa decemlineata) White-footed beetle (Melanotus tamsuyensis), Tobacco beetle (Lasioderma serricorne), Himetaketakekisui (Epuraea domina), Green beetle (Epilachna varivestis), Nijuya-hoshi-tento (Epilachna vigintioctopunctata), T. Tribolium castaneum, Anoplophora malasiaca, Monochamus alternatus, Psacothea hilaris, Xylotrechus pyrrhoderus, callosobruchus, Callosobruchus Western Root beetle (Chaetocnema concinna), Southern corn root worm (Diabrotica undecimpunctata), Western corn root worm (Diabrotica virgifera), Northern corn root worm (Diabrotica barberi), Inedro beetle (Oulema oryzae), Phyllotreta nastriatum, Phyllotreta striol Tobet beetle (Psylliodes angusticollis), peach weevil (Rhynchites heros), aphid weevil (Cylas formicarius), cotton weevil (Anthonomus grandis), weevil (Echinocnemus squameus), weevil (Euscepes postfasciatus) Rice weevil (Lissohoptrus oryzophilus), horned weevil (Otiorhynchus sulcatus), granary weevil (Sitophilus granarius), hornet weevil (Sitophilus zeamais), bark weevil (Sphenophorus venatus vestitus moth) erus fuscipes).
ダイズサヤタマバエ(Asphondylia yushimai)、ムギアカタマバエ(Sitodiplosis mosellana)、ウリミバエ(Bactrocera cucurbitae)、ミカンコミバエ(Bactrocera dorsalis)、チチュウカイミバエ(Ceratitis capitata)、イネヒメハモグリバエ(Hydrellia griseola)、オウトウショウジョウバエ(Drosophila suzukii)、イネハモグリバエ(Agromyza oryzae)、ナモグリバエ(Chromatomyia horticola)、ナスハモグリバエ(Liriomyza bryoniae)、ネギハモグリバエ(Liriomyza chinensis)、トマトハモグリバエ(Liriomyza sativae)、マメハモグリバエ(Liriomyza trifolii)、タネバエ(Delia platura)、テンサイモグリハナバエ(Pegomya cunicularia)、アップルマゴット(Rhagoletis pomonella)、ヘシアンフライ(Mayetiola destructor)、イエバエ(Musca domestica)、サシバエ(Stomoxys calcitrans)、ヒツジシラミバエ(Melophagus ovinus)、ウシバエ(Hypoderma bovis)、キスジウシバエ(Hypoderma lineatum)、ヒツジバエ(Oestrus ovis)、ツェツェバエ(Glossina palpalis, Glossina morsitans)、キアシオオブユ(Prosimulium yezoensis)、ウシアブ(Tabanus trigonus)、オオチョウバエ(Telmatoscopus albipunctatus)、トクナガヌカカ(Leptoconops nipponensis)、アカイエカ(Culex pipiens pallens)、ネッタイシマカ(Aedes aegypti)、ヒトスジシマカ(Aedes albopicutus)、シナハマダラカ(Anopheles hyracanus sinesis)等の双翅目昆虫。 Soybean flies (Asphondylia yushimai), mud wings (Sitodiplosis mosellana), fruit flies (Bactrocera cucurbitae), citrus fruit flies (Bactrocera dorsalis), citrus fruit flies (Ceratitis capitata), rice moth flies Leafhopper (Agromyza oryzae), Leafworm (Chromatomyia horticola), Eggplant leaffly (Liriomyza bryoniae), Leafhopper (Liriomyza chinensis), Tomato leaffly (Liriomyza sativae), Beanworm (Liriomyza trifoli), Liriomyza trifoli (Pegomya cunicularia), apple haggot (Rhagoletis pomonella), hessian fly (Mayetiola destructor), housefly (Musca domestica), barn fly (Stomoxys calcitrans), sheep flies (Melophagus ovinus), bullflies (Hypoderma bovisma), , Sheep flies (Oestrus ovis), tsetse flies (Glossina palpalis, Glossina morsitans), black-headed ayu (Prosimulium yezoensis), bullfly (Tabanus trigonus), giant fly (Telmatoscopus albipunctatus), nipponen sip (Leptocons) Diptera, such as Aedes aegypti, Aedes albopicutus, Anopheles hyracanus sinesis.
クリハバチ(Apethymus kuri)、カブラハバチ(Athalia rosae)、チュウレンジハバチ(Arge pagana)、マツノキハバチ(Neodiprion sertifer)、クリタマバチ(Dryocosmus kuriphilus)、グンタイアリ(Eciton burchelli, Eciton schmitti)、クロオオアリ(Camponotus japonicus)、オオスズメバチ(Vespa mandarina)、ブルドックアント(Myrmecia spp.)、ファイヤーアント類(Solenopsis spp.)、ファラオアント(Monomorium pharaonis)等の膜翅目昆虫。 Bumblebee (Apethymus kuri), Bumblebee (Athalia rosae), Bumblebee (Arge pagana), Bumblebee (Neodiprion sertifer), Bumblebee (Dryocosmus kuriphilus), Gantai (Eciton burchelli, Eciton schmitus), Eciton burchelli, Eciton schmitus Hymenoptera insects such as mandarina, bulldog ant (Myrmecia spp.), fire ant (Solenopsis spp.), pharaoh ant (Monomorium pharaonis).
エンマコオロギ(Teleogryllus emma)、ケラ(Gryllotalpa orientalis)、トノサマバッタ(Locusta migratoria)、コバネイナゴ(Oxya yezoensis)、サバクワタリバッタ(Schistocerca gregaria)等の直翅目昆虫。 Straight-legged insects such as Teleogryllus emma, Gryllotalpa orientalis, Locusta migratoria, Oxya yezoensis, Schistocerca gregaria and others.
トゲナシシロトビムシ(Onychiurus folsomi)、シベリアシロトビムシ(Onychiurus sibiricus)、キボシマルトビムシ(Bourletiella hortensis)等の粘管目昆虫。 Coleoptera insects such as Onychiurus folsomi, Onychiurus sibiricus and Bourletiella hortensis.
クロゴキブリ(Periplaneta fuliginosa)、ヤマトゴキブリ(Periplaneta japonica)、チャバネゴキブリ(Blattella germanica)等の網翅目昆虫。 Reticulate insects such as black cockroach (Periplaneta fuliginosa), cockroach (Periplaneta japonica), German cockroach (Blattella germanica).
イエシロアリ(Coptotermes formosanus)、ヤマトシロアリ(Reticulitermes speratus)、タイワンシロアリ(Odontotermes formosanus)等のシロアリ目昆虫。 Termite insects such as termites (Coptotermes formosanus), Yamato termites (Reticulitermes speratus), Taiwan termites (Odontotermes formosanus).
ネコノミ(Ctenocephalidae felis)、イヌノミ(Ctenocephalides canis)、ニワトリノミ(Echidnophaga gallinacea)、ヒトノミ(Pulex irritans)、ケオプスネズミノミ(Xenopsylla cheopis)等の等翅目昆虫。 Coleoptera insects such as cat fleas (Ctenocephalidae felis), dog fleas (Ctenocephalides canis), chicken fleas (Echidnophaga gallinacea), human fleas (Pulex irritans), keops rat fleas (Xenopsylla cheopis) and the like.
ニワトリオオハジラミ(Menacanthus stramineus)、ウシハジラミ(Bovicola bovis)等のハジラミ目昆虫。 White-headed insects such as chicken lice (Menacanthus stramineus) and bovine lice (Bovicola bovis).
ウシジラミ(Haematopinus eurysternus)、ブタジラミ(Haematopinus suis)、ウシホソジラミ(Linognathus vituli)、ケブカウシジラミ(Solenopotes capillatus)等のシラミ目昆虫。 Louse insects such as cattle lice (Haematopinus eurysternus), pig lice (Haematopinus suis), cattle white lice (Linognathus vituli), horned lice (Solenopotes capillatus) and the like.
シクラメンホコリダニ(Phytonemus pallidus)、チャノホコリダニ(Polyphagotarsonemus latus)、スジブトホコリダニ(Tarsonemus bilobatus)等のホコリダニ類、
ハクサイダニ(Penthaleus erythrocephalus)、ムギダニ(Penthaleus major)等のハシリダニ類。
Dust mites such as cyclamen dust mite (Phytonemus pallidus), chano dust mite (Polyphagotarsonemus latus), red mite dust mite (Tarsonemus bilobatus),
Spider mites such as cabbage mite (Penthaleus erythrocephalus) and wheat mite (Penthaleus major).
イネハダニ(Oligonychus shinkajii)、ミカンハダニ(Panonychus citri)、クワオオハダニ(Panonychus mori)、リンゴハダニ(Panonychus ulmi)、カンザワハダニ(Tetranychus kanzawai)、ナミハダニ(Tetranychus urticae)等のハダニ類。 Spider mites such as rice spider mite (Oligonychus shinkajii), citrus spider mite (Panonychus citri), blue spider mite (Panonychus mori), apple spider mite (Panonychus ulmi), Kanzawa spider mite (Tetranychus kanzawai), spider mite (Tetranychus urticae), etc.
チャノナガサビダニ(Acaphylla theavagrans)、チューリップサビダニ(Aceria tulipae)、トマトサビダニ(Aculops lycopersici)、ミカンサビダニ(Aculops pelekassi)、リンゴサビダニ(Aculus schlechtendali)、ニセナシサビダニ(Eriophyes chibaensis)、シトラスラストマイト(Phyllocoptruta oleivora)等のフシダニ類。 Chinese cabbage mite (Acaphylla theavagrans), tulip rust mite (Aceria tulipae), tomato rust mite (Aculops lycopersici), citrus red mite (Aculops pelekassi), apple rust mite (Aculus schlechtendali), black rust mite (Eriophyes chitrastrostrum) ) Etc.
ロビンネダニ(Rhizoglyphus robini)、ケナガコナダニ(Tyrophagus putrescentiae)、ホウレンソウケナガコナダニ(Tyrophagus similis)等のコナダニ類、
ミツバチヘギイタダニ(Varroa jacobsoni)等のハチダニ類。
Acarids such as robin mite (Rhizoglyphus robini), mushroom mite (Tyrophagus putrescentiae), spinach mushroom mite (Tyrophagus similis),
Bee mites such as honeybee mite (Varroa jacobsoni).
オウシマダニ(Boophilus microplus)、クリイロコイタマダニ(Rhipicephalus sanguineus)、フタトゲチマダニ(Haemaphysalis longicornis)、キチマダニ(Haemophysalis flava)、ツリガネチマダニ(Haemophysalis campanulata)、ヤマトマダニ(Ixodes ovatus)、シュルツェマダニ(Ixodes persulcatus)、オオマダニ(Amblyomma spp.)、アミメマダニ(Dermacentor spp.)等のマダニ類。 Tick tick (Boophilus microplus), Rhipicephalus sanguineus, Tick tick (Haemaphysalis longicornis), Tick tick (Haemophysalis flava), Tick tick (Haemophysalis campanulata), Tick tick (Ixo tus tick) Tick such as Amblyomma spp.), Dermacentor spp.
イヌツメダニ(Cheyletiella yasguri)、ネコツメダニ(Cheyletiella blakei)等のツメダニ類。 Crawling ticks, such as the crayfish tick (Cheyletiella yasguri) and the cat crawfish tick (Cheyletiella blakei).
イヌニキビダニ(Demodex canis)、ネコニキビダニ(Demodex cati)などのニキビダニ類。 Acne mites, such as Inodex canis and Demodex cati.
ヒツジキュウセンダニ(Psoroptes ovis)等のキュウセンダニ類。 Cucumber mites such as sheep cucumber mites (Psoroptes ovis).
センコウヒゼンダニ(Sarcoptes scabiei)、ネコショウセンコウヒゼンダニ(Notoedres cati)、ニワトリヒゼンダニ(Knemidocoptes spp.)等のヒゼンダニ類。 Spider mites, such as Sarcoptes scabiei, Notoedres cati, and Knemidocoptes spp.
オカダンゴムシ(Armadillidium vulgare)等の甲殻類。 Crustacea such as Armadillidium vulgare.
スクミリンゴガイ(Pomacea canaliculata)、アフリカマイマイ(Achatina fulica)、ナメクジ(Meghimatium bilineatum)、チャコウラナメクジ(Limax Valentiana)、ウスカワマイマイ(Acusta despecta sieboldiana)、ミスジマイマイ(Euhadra peliomphala)等の腹足類。 Gastropods such as Pomacea canaliculata, African mussel (Achatina fulica), Slug (Meghimatium bilineatum), Chaukoura slug (Limax Valentiana), Uskawamai (Acusta despecta sieboldiana), Mishamai mai (Euhadra peliomphala).
ミナミネグサレセンチュウ(Prathylenchus coffeae)、キタネグサレセンチュウ(Prathylenchus penetrans)、クルミネグサレセンチュウ(Prathylenchus vulnus)、ジャガイモシストセンチュウ(Globodera rostochiensis)、ダイズシストセンチュウ(Heterodera glycines)、キタネコブセンチュウ(Meloidogyne hapla)、サツマイモネコブセンチュウ(Meloidogyne incognita)、イネシンガレセンチュウ(Aphelenchoides besseyi)、マツノザイセンチュウ(Bursaphelenchus xylophilus)等の線虫類。 Southern nematode nematode (Prathylenchus coffeae), Kitane-negususa nematode (Prathylenchus penetrans), Kurume rushes nematode (Prathylenchus vulnus), potato cyst nematode (Globodera rostochiensis), soybean cyst nematode (Heterodera lypter Nematodes such as root-knot nematodes (Meloidogyne incognita), rice-spotted nematodes (Aphelenchoides besseyi), and pine wood nematodes (Bursaphelenchus xylophilus).
また、本発明化合物を用いて防除しうる家畜、家禽、愛玩動物等の内部寄生虫としては具体的に、例えば、下記の生物が挙げられるが、本発明はこれらのみに限定されるものではない。 In addition, specific examples of endoparasites such as livestock, poultry, and pet animals that can be controlled using the compounds of the present invention include the following organisms, but the present invention is not limited to these. .
ヘモンクス属(Haemonchus)、トリコストロンギルス属(Trichostrongylus)、オステルターギヤ属(Ostertagia)、ネマトディルス属(Nematodirus)、クーペリア属(Cooperia)、アスカリス属(Ascaris)、ブノストムーム属(Bunostomum)、エスファゴストムーム属(Oesophagostomum)、チャベルチア属(Chabertia)、トリキュリス属(Trichuris)、ストロンギルス属(Storongylus)、トリコネマ属(Trichonema)、ディクチオカウルス属(Dictyocaulus)、キャピラリア属(Capillaria)、ヘテラキス属(Heterakis)、トキソカラ属(Toxocara)、アスカリディア属(Ascaridia)、オキシウリス属(Oxyuris)、アンキロストーマ属(Ancylostoma)、ウンシナリア属(Uncinaria)、トキサスカリス属(Toxascaris)、パラスカリス属(Parascaris)などの線虫類。 Haemonchus, Trichostrongylus, Ostertagia, Nematodirus, Cooperia, Ascaris, Bunostomum, Esphagostomum Genus (Oesophagostomum), Chabertia, Trichuris, Strongylus, Trichonema, Dictyocaulus, Capillaria, Heterakis ), Toxocara, Ascaridia, Oxyuris, Ancylostoma, Uncinaria, Toxacaris, Parascaris, and other nematodes .
ブツヘレリア属(Wuchereria)、ブルージア属(Brugia)、オンコセルカ属(Onchoceca)、ディロフィラリア属(Dirofilaria)、ロア糸状虫属(Loa)などのフィラリア科(Filariidae)線虫類。 Filariidae nematodes such as Wuchereria, Brugia, Onchoceca, Dirofilaria and Loa.
ドラクンクルス属(Deacunculus)などの蛇状線虫科(Dracunculidae)線虫類。 Dracunculidae nematodes, such as the genus Deacunculus.
犬条虫(Dipylidium caninum)、猫条虫(Taenia taeniaeformis)、有鉤条虫(Taenia solium)、無鉤条虫(Taenia saginata)、縮小条虫(Hymenolepis diminuta)、ベネデン条虫(Moniezia benedeni)、広節裂頭条虫(Diphyllobothrium latum)、マンソン裂頭条虫(Diphyllobothrium erinacei)、単包条虫(Echinococcus granulosus)、多包条虫(Echinococcus multilocularis)などの条虫類。 Dogworms (Dipylidium caninum), caterpillars (Taenia taeniaeformis), rodents (Taenia solium), striped tapeworms (Taenia saginata), contracted tapeworms (Hymenolepis diminuta), Beneden tapeworms (Moniezia benedeni), Tapeworms such as Diphyllobothrium latum, Manson cleftworm (Diphyllobothrium erinacei), Echinococcus granulosus, Echinococcus multilocularis.
肝蛭(Fasciola hepatica,F.gigantica)、ウエステルマン肺吸虫(Paragonimus westermanii)、肥大吸虫(Fasciolopsic bruski)、膵吸虫(Eurytrema pancreaticum,E.coelomaticum)、肝吸虫(Clonorchis sinensis)、日本住血吸虫(Schistosoma japonicum)、ビルハルツ住血吸虫(Schistosoma haematobium)、マンソン住血吸虫(Schistosoma mansoni)などの吸虫類。 Fasciola hepatica (F. gigantica), Westermann lung fluke (Paragonimus westermanii), hypertrophic fluke (Fasciolopsic bruski), pancreatic fluke (Eurytrema pancreaticum, E. coelomaticum), liver fluke (Clonorchis sinensis), Schistosoma Schistosoma japonicum), Schistosoma haematobium, Schistosoma mansoni, etc.
エイメリア・テネラ(Eimeria tenella)、エイメリア・アセルブリナ(Eimeria acervulina)、エイメリア・ブルネッチ(Eimeria brunetti)、エイメリア・マクシマ(Eimeria maxima)、エイメリア・ネカトリクス(Eimeria necatrix)、エイメリア・ボビス(Eimeria bovis)、エイメリア・オビノイダリス(Eimeria ovinoidalis)のようなエイメリア類(Eimeria spp.)。 Eimeria tenella, Eimeria acervulina, Eimeria brunetti, Eimeria maxima, Eimeria necatrix, Eimeria bovis, Eimeria bovis Eimeria spp., Such as Eimeria ovinoidalis.
クルーズトリパノソーマ(Trypanosomsa cruzi)、リーシュマニア類(Leishmania spp.)、マラリア原虫(Plasmodium spp.)、バベシア類(Babesis spp.)、トリコモナス類(Trichomonadidae spp.)、ヒストモナス類(Histomanas spp.)、ジアルディア類(Giardia spp.)、トキソプラズマ類(Toxoplasma spp.)、赤痢アメーバ(Entamoeba histolytica)、タイレリア類(Theileria spp.)。 Trypanosomsa cruzi, Leishmania spp., Plasmodium spp., Babesis spp., Trichomonadidae spp., Histomanas spp., Giardia (Giardia spp.), Toxoplasma spp., Entamoeba histolytica, Theileria spp.
さらに、本発明化合物は、有機燐系化合物、カーバメート系化合物又はピレスロイド系化合物等の既存の殺虫剤に対して抵抗性の発達した有害生物に対しても有効である。 Furthermore, the compound of the present invention is also effective against pests that have developed resistance to existing insecticides such as organophosphorus compounds, carbamate compounds, and pyrethroid compounds.
すなわち、本発明化合物は、粘管目(トビムシ目)、網翅目(ゴキブリ目)、直翅目(バッタ目)、シロアリ目、総翅目(アザミウマ目)、半翅目(カメムシ目及びヨコバイ目)、鱗翅目(チョウ目)、鞘翅目(コウチュウ目)、膜翅目(ハチ目)、双翅目(ハエ目)、等翅目(ノミ目)及びシラミ目等の昆虫類、ダニ類、腹足類及び線虫類等に属する有害生物を低濃度で有効に防除することが出来る。一方、本発明化合物はホ乳類、魚類、甲殻類及び益虫(ミツバチ、マルハナバチ等の有用昆虫やツヤコバチ、アブラバチ、ヤドリバエ、ヒメハナカメムシ、カブリダニ等の天敵)に対してほとんど悪影響の無い極めて有用な特長を有している。 That is, the compound of the present invention is composed of the order of mucous eyes (Coleoptera), reticulates (Roaches), straight moths (Grasshoppers), termites, common moths (Thrips), hemimorphs (stink bugs and leafhoppers). Eyes), Lepidoptera (Lepidoptera), Coleoptera (Coleoptera), Hymenoptera (Hymenoptera), Diptera (Flyidae), Islamic (Flea), Liceid, and other insects, ticks In addition, pests belonging to gastropods and nematodes can be effectively controlled at low concentrations. On the other hand, the compounds of the present invention are extremely useful with little adverse effect on mammals, fish, crustaceans and beneficial insects (beneficial insects such as bees and bumblebees, natural enemies such as honeybees, wasps, mistletoe flies, mosquitoes, and mites). Has features.
本発明化合物を使用するにあたっては、通常適当な固体担体又は液体担体と混合し、更に所望により界面活性剤、浸透剤、展着剤、増粘剤、凍結防止剤、結合剤、固結防止剤、崩壊剤、消泡剤、防腐剤及び分解防止剤等を添加して、液剤(soluble concentrate)、乳剤(emulsifiable concentrate)、水和剤(wettable powder)、水溶剤(water soluble powder)、顆粒水和剤(water dispersible granule)、顆粒水溶剤(water soluble granule)、懸濁剤(suspension concentrate)、乳濁剤(concentrated emulsion)、サスポエマルジョン(suspoemulsion)、マイクロエマルジョン(microemulsion)、粉剤(dustable powder)、粒剤(granule)錠剤(tablet)及び乳化性ゲル剤(emulsifiable gel)等任意の剤型の製剤にて実用に供することができる。また、省力化及び安全性向上の観点から、上記任意の剤型の製剤を、水溶性カプセル及び水溶性フィルムの袋等の水溶性包装体に封入して供することもできる。 When using the compound of the present invention, it is usually mixed with a suitable solid carrier or liquid carrier, and if desired, a surfactant, penetrant, spreading agent, thickener, antifreezing agent, binder, anti-caking agent. , Disintegrating agents, antifoaming agents, preservatives and anti-decomposition agents, etc., and soluble concentrate, emulsion (emulsifiable concentrate), wettable powder, water-soluble solvent, granular water Water dispersible granule, water soluble granule, suspension concentrate, concentrated emulsion, suspoemulsion, microemulsion, dustable powder ), Granule tablets and emulsifiable gels, and can be put to practical use. In addition, from the viewpoint of labor saving and safety improvement, the preparations of the above arbitrary dosage forms can be provided by being enclosed in a water-soluble package such as a water-soluble capsule and a bag of a water-soluble film.
固体担体としては、例えば石英、方解石、海泡石、ドロマイト、チョーク、カオリナイト、パイロフィライト、セリサイト、ハロサイト、メタハロサイト、木節粘土、蛙目粘土、陶石、ジークライト、アロフェン、シラス、きら、タルク、ベントナイト、活性白土、酸性白土、軽石、アタパルジャイト、ゼオライト及び珪藻土等の天然鉱物質、例えば焼成クレー、パーライト、シラスバルーン、バーミキュライト、アタパルガスクレー及び焼成珪藻土等の天然鉱物質の焼成品、例えば炭酸マグネシウム、炭酸カルシウム、炭酸ナトリウム、炭酸水素ナトリウム、硫酸アンモニウム、硫酸ナトリウム、硫酸マグネシウム、リン酸水素二アンモニウム、リン酸二水素アンモニウム及び塩化カリウム等の無機塩類、例えばブドウ糖、果糖、しょ糖及び乳糖などの糖類、例えば澱粉、粉末セルロース及びデキストリン等の多糖類、例えば尿素、尿素誘導体、安息香酸及び安息香酸の塩等の有機物、例えば木粉、コルク粉、トウモロコシ穂軸、クルミ殻及びタバコ茎等の植物類、フライアッシュ、ホワイトカーボン(例えば、含水合成シリカ、無水合成シリカ及び含水合成シリケート等)ならびに肥料等が挙げられる。 Examples of the solid carrier include quartz, calcite, gypsum, dolomite, chalk, kaolinite, pyrophyllite, sericite, halosite, metahalosite, kibushi clay, glazed clay, porcelain stone, siegrite, allophane , Shirasu, Kira, Talc, Bentonite, Activated clay, Acid clay, Pumice, Attapulgite, Zeolite and diatomite Baked products, such as magnesium carbonate, calcium carbonate, sodium carbonate, sodium bicarbonate, ammonium sulfate, sodium sulfate, magnesium sulfate, diammonium hydrogen phosphate, ammonium dihydrogen phosphate and potassium chloride, such as glucose, fructose , Sucrose and Sugars such as lactose, polysaccharides such as starch, powdered cellulose and dextrin, organic substances such as urea, urea derivatives, benzoic acid and benzoic acid salts, such as wood flour, cork powder, corn cob, walnut shell and tobacco stem And the like, fly ash, white carbon (for example, hydrous synthetic silica, anhydrous synthetic silica, hydrous synthetic silicate, etc.) and fertilizer.
液体担体としては、例えばキシレン、アルキル(C9又はC10等)ベンゼン、フェニルキシリルエタン及びアルキル(C1又はC3等)ナフタレン等の芳香族炭化水素類、マシン油、ノルマルパラフィン、イソパラフィン及びナフテン等の脂肪族炭化水素類、ケロシン等の芳香族炭化水素と脂肪族炭化水素の混合物、エタノール、イソプロパノール、シクロヘキサノール、フェノキシエタノール及びベンジルアルコール等のアルコール、エチレングリコール、プロピレングリコール、ジエチレングリコール、ヘキシレングリコール、ポリエチレングリコール及びポリプロピレングリコール等の多価アルコール、プロピルセロソルブ、ブチルセロソルブ、フェニルセロソルブ、プロピレングリコールモノメチルエーテル、プロピレングリコールモノエチルエーテル、プロピレングリコールモノプロピルエーテル、プロピレングリコールモノブチルエーテル及びプロピレングリコールモノフェニルエーテル等のエーテル、アセトフェノン、シクロヘキサノン及びγ−ブチロラクトン等のケトン、脂肪酸メチルエステル、コハク酸ジアルキルエステル、グルタミン酸ジアルキルエステル、アジピン酸ジアルキルエステル及びフタル酸ジアルキルエステル等のエステル、N−アルキル(C1、C8又はC12等)ピロリドン等の酸アミド、大豆油、アマニ油、ナタネ油、ヤシ油、綿実油及びヒマシ油等の油脂、ジメチルスルホキシドならびに水が挙げられる。 Examples of the liquid carrier include aromatic hydrocarbons such as xylene, alkyl (C 9 or C 10 ) benzene, phenylxylylethane and alkyl (C 1 or C 3 ) naphthalene, machine oil, normal paraffin, isoparaffin, and the like. Aliphatic hydrocarbons such as naphthene, mixtures of aromatic and aliphatic hydrocarbons such as kerosene, alcohols such as ethanol, isopropanol, cyclohexanol, phenoxyethanol and benzyl alcohol, ethylene glycol, propylene glycol, diethylene glycol, hexylene glycol , Polyhydric alcohols such as polyethylene glycol and polypropylene glycol, propyl cellosolve, butyl cellosolve, phenyl cellosolve, propylene glycol monomethyl ether, propylene glycol Ethers such as ethyl ether, propylene glycol monopropyl ether, propylene glycol monobutyl ether and propylene glycol monophenyl ether, ketones such as acetophenone, cyclohexanone and γ-butyrolactone, fatty acid methyl esters, dialkyl esters of succinic acid, dialkyl esters of glutamic acid, dialkyl adipates Esters such as esters and dialkyl phthalates, acid amides such as N-alkyl (C 1 , C 8 or C 12 ) pyrrolidone, soybean oil, linseed oil, rapeseed oil, oils and fats such as coconut oil, cottonseed oil and castor oil, Examples include dimethyl sulfoxide as well as water.
これら固体及び液体担体は、単独で用いても2種以上を併用してもよい。 These solid and liquid carriers may be used alone or in combination of two or more.
界面活性剤としては、例えばポリオキシエチレンアルキルエーテル、ポリオキシエチレンアルキル(モノ又はジ)フェニルエーテル、ポリオキシエチレン(モノ、ジ又はトリ)スチリルフェニルエーテル、ポリオキシエチレンポリオキシプロピレンブロックコポリマー、ポリオキシエチレン脂肪酸(モノ又はジ)エステル、ソルビタン脂肪酸エステル、ポリオキシエチレンソルビタン脂肪酸エステル、ヒマシ油エチレンオキサイド付加物、アセチレングリコール、アセチレンアルコール、アセチレングリコールのエチレンオキサイド付加物、アセチレンアルコールのエチレンオキサイド付加物及びアルキルグリコシド等のノニオン性界面活性剤、アルキル硫酸エステル塩、アルキルベンゼンスルホン酸塩、リグニンスルホン酸塩、アルキルスルホコハク酸塩、ナフタレンスルホン酸塩、アルキルナフタレンスルホン酸塩、ナフタレンスルホン酸のホルマリン縮合物の塩、アルキルナフタレンスルホン酸のホルマリン縮合物の塩、ポリオキシエチレンアルキルエーテル硫酸又は燐酸エステル塩、ポリオキシエチレン(モノ又はジ)アルキルフェニルエーテル硫酸又は燐酸エステル塩、ポリオキシエチレン(モノ、ジ又はトリ)スチリルフェニルエーテル硫酸又は燐酸エステル塩、ポリカルボン酸塩(例えば、ポリアクリル酸塩、ポリマレイン酸塩及びマレイン酸とオレフィンとの共重合物等)及びポリスチレンスルホン酸塩等のアニオン性界面活性剤、アルキルアミン塩及びアルキル4級アンモニウム塩等のカチオン性界面活性剤、アミノ酸型及びベタイン型等の両性界面活性剤、シリコーン系界面活性剤ならびにフッ素系界面活性剤が挙げられる。 Examples of the surfactant include polyoxyethylene alkyl ether, polyoxyethylene alkyl (mono or di) phenyl ether, polyoxyethylene (mono, di or tri) styryl phenyl ether, polyoxyethylene polyoxypropylene block copolymer, polyoxyethylene Ethylene fatty acid (mono or di) ester, sorbitan fatty acid ester, polyoxyethylene sorbitan fatty acid ester, castor oil ethylene oxide adduct, acetylene glycol, acetylene alcohol, ethylene oxide adduct of acetylene glycol, ethylene oxide adduct of acetylene alcohol and alkyl Nonionic surfactants such as glycosides, alkyl sulfate esters, alkylbenzene sulfonates, lignin sulfonates, alkyls Succinate, naphthalenesulfonate, alkylnaphthalenesulfonate, salt of formalin condensate of naphthalenesulfonic acid, salt of formalin condensate of alkylnaphthalenesulfonic acid, polyoxyethylene alkyl ether sulfate or phosphate ester salt, polyoxyethylene (Mono or di) alkyl phenyl ether sulfate or phosphate ester salt, polyoxyethylene (mono, di or tri) styryl phenyl ether sulfate or phosphate ester salt, polycarboxylate (eg, polyacrylate, polymaleate and maleate) Copolymers of acid and olefins) and anionic surfactants such as polystyrene sulfonates, cationic surfactants such as alkylamine salts and alkyl quaternary ammonium salts, and amphoteric surfactants such as amino acid types and betaine types Agent Corn-based surfactants and fluorine-based surfactants.
これら界面活性剤の含有量は、特に限定されるものではないが、本発明の製剤100重量部に対し、通常0.05〜20重量部の範囲が望ましい。また、これら界面活性剤は、単独で用いても2種以上を併用してもよい。 The content of these surfactants is not particularly limited, but is usually preferably in the range of 0.05 to 20 parts by weight with respect to 100 parts by weight of the preparation of the present invention. These surfactants may be used alone or in combination of two or more.
本発明化合物の施用薬量は適用場面、施用時期、施用方法、栽培作物等により差異は有るが、一般には有効成分量としてヘクタール(ha)当たり0.005〜50kg程度が適当である。 The application amount of the compound of the present invention varies depending on the application scene, application time, application method, cultivated crops, etc., but generally 0.005 to 50 kg per hectare (ha) is appropriate as the amount of active ingredient.
一方、家畜及び愛玩動物としての哺乳動物及び鳥類の外部又は内部寄生虫の防除に本発明化合物を使用するにあたっては、有効量の本発明化合物を製剤用添加物とともに経口投与、注射(筋肉内、皮下、静脈内、腹腔内)などの非経口投与;浸漬、スプレー、入浴、洗浄、滴下(pouring-on)及びスポッティング(spotting-on)並びにダスティング(dusting)などの経皮投与;経鼻投与により投与することができる。本発明化合物はまた、細片、プレート、バンド、カラー、イヤー・マーク(ear mark)、リム(limb)・バンド、標識装置などを用いた成形製品により投与することができる。投与にあたっては本発明化合物を投与経路に適した任意の剤型とすることができる。 On the other hand, when using the compound of the present invention for the control of the ectoparasites of mammals and birds as domestic animals and pets, an effective amount of the compound of the present invention is administered orally together with injections (intramuscular, Parenteral administration such as subcutaneous, intravenous, intraperitoneal); transdermal administration such as immersion, spraying, bathing, washing, pouring-on and spotting-on and dusting; nasal administration Can be administered. The compounds of the present invention can also be administered by molded products using strips, plates, bands, collars, ear marks, limb bands, labeling devices and the like. In administration, the compound of the present invention can be in any dosage form suitable for the administration route.
調製される任意の剤型としては、粉剤、粒剤、水和剤、ペレット、錠剤、大丸薬、カプセル剤、活性化合物を含む成形製品などの固体調製物;注射用液剤、経口用液剤、皮膚上又は体腔中に用いる液剤;滴下(Pour-on)剤、点下(Spot-on)剤、フロアブル剤、乳剤などの溶液調製物;軟膏剤、ゲルなどの半固体調製物などが挙げられる。 Arbitrary forms to be prepared include solid preparations such as powders, granules, wettable powders, pellets, tablets, large pills, capsules, molded products containing active compounds; injection solutions, oral solutions, skin Liquid preparations used above or in body cavities; solution preparations such as Pour-on agents, spot-on agents, flowable agents and emulsions; semi-solid preparations such as ointments and gels.
固体調製物は、主に経口投与あるいは水などで希釈して経皮投与にあるいは環境処理にて用いることができる。固体調製物は、活性化合物を必要ならば補助剤を加えて適当な賦形剤と共に混合し、そして所望の形状に変えることにより調製できる。適当な賦形剤としては、例えば炭酸塩、炭酸水素塩、リン酸塩、酸化アルミニウム、シリカ、粘土などの無機物質、糖、セルロース、粉砕された穀物、澱粉などの有機物質がある。 The solid preparation can be used mainly for oral administration or diluted with water for transdermal administration or environmental treatment. Solid preparations can be prepared by adding the active compound, if necessary, with adjuncts, mixing with appropriate excipients, and converting to the desired shape. Suitable excipients include, for example, inorganic substances such as carbonates, bicarbonates, phosphates, aluminum oxides, silicas, clays, and organic substances such as sugars, cellulose, crushed grains, and starches.
注射用液剤は、静脈内、筋肉内及び皮下に投与できる、注射用液剤は、活性化合物を適当な溶媒に溶解させ、そして必要ならば可溶化剤、酸、塩基、緩衝用塩、酸化防止剤及び保護剤などの添加剤を加えることにより調製できる。適当な溶媒としては、水、エタノール、ブタノール、ベンジルアルコール、グリセリン、プロピレングリコール、ポリエチレングリコール、N−メチルピロリドン並びにこれらの混合物、生理学的に許容しうる植物油、注射に適する合成油などがあげられる。可溶化剤としては、ポリビニルピロリドン、ポリオキシエチル化されたヒマシ油及びポリオキシエチル化されたソルビタンエステルなどがあげられる。保護剤には、ベンジルアルコール、トリクロロブタノール、p−ヒドロキシ安息香酸エステル及びn−ブタノールなどがある。 Injection solutions can be administered intravenously, intramuscularly and subcutaneously. Injection solutions dissolve the active compound in a suitable solvent and, if necessary, solubilizers, acids, bases, buffer salts, antioxidants. And an additive such as a protective agent. Suitable solvents include water, ethanol, butanol, benzyl alcohol, glycerin, propylene glycol, polyethylene glycol, N-methylpyrrolidone and mixtures thereof, physiologically acceptable vegetable oils, synthetic oils suitable for injection, and the like. Examples of the solubilizer include polyvinylpyrrolidone, polyoxyethylated castor oil, polyoxyethylated sorbitan ester, and the like. Protecting agents include benzyl alcohol, trichlorobutanol, p-hydroxybenzoic acid ester and n-butanol.
経口液剤は直接又は希釈して投与することができる。注射用液剤と同様に調製することができる。 Oral solutions can be administered directly or diluted. It can be prepared in the same manner as an injectable solution.
フロアブル剤、乳剤、などは直接又は希釈して経皮的に、又は環境処理にて投与できる。 Flowables, emulsions, etc. can be administered directly or diluted transdermally or by environmental treatment.
皮膚上で用いる液剤は、滴下し、広げ、すり込み、噴霧し、散布するか、又は浸漬(浸漬、入浴又は洗浄)により塗布することにより投与できる。これらの液剤は注射用液剤と同様に調製できる。 Solutions used on the skin can be administered by dripping, spreading, rubbing, spraying, spraying or applying by dipping (immersion, bathing or washing). These solutions can be prepared in the same manner as injection solutions.
滴下(Pour-on)剤及び点下(Spot-on)剤は皮膚の限定された場所に滴下するか、又は噴霧し、これにより活性化合物を皮膚に浸漬させそして全身的に作用させることができる。滴下剤及び点下剤は、有効成分を適当な皮膚適合性溶媒又は溶媒混合物に溶解するか、懸濁させるか又は乳化することにより調製できる。必要ならば、界面活性剤、着色剤、吸収促進物質、酸化防止剤、光安定剤及び接着剤などの補助剤を加えてもよい。 Pour-on and spot-on agents can be dripped or sprayed onto a limited area of the skin, so that the active compound can be immersed in the skin and act systemically . Drops and drop preparations can be prepared by dissolving, suspending or emulsifying the active ingredient in suitable skin-compatible solvents or solvent mixtures. If necessary, auxiliary agents such as surfactants, colorants, absorption promoting substances, antioxidants, light stabilizers and adhesives may be added.
適当な溶媒としては、水、アルカノール、グリコール、ポリエチレングリコール、ポリプロピレングリコール、グリセリン、ベンジルアルコール、フェニルエタノール、フェノキシエタノール、酢酸エチル、酢酸ブチル、安息香酸ベンジル、ジプロピレングリコールモノメチルエーテル、ジエチレングリコールモノブチルエーテル、アセトン、メチルエチルケトン、芳香族及び/又は脂肪族炭化水素、植物又は合成油、DMF、流動パラフィン、軽質流動パラフィン、シリコーン、ジメチルアセトアミド、N−メチルピロリドン又は2,2−ジメチル−4−オキシ−メチレン−1,3−ジオキソランが挙げられる。吸収促進物質には、DMSO、ミリスチン酸イソプロピル、ペラルゴン酸ジプロピレングリコール、シリコーン油、脂肪族エステル、トリグリセリド及び脂肪アルコールが挙げられる。酸化防止剤には、亜硫酸塩、メタ重亜硫酸塩、アスコルビン酸、ブチルヒドロキシトルエン、ブチルヒドロキシアニソール及びトコフェロールが挙げられる。 Suitable solvents include water, alkanol, glycol, polyethylene glycol, polypropylene glycol, glycerin, benzyl alcohol, phenylethanol, phenoxyethanol, ethyl acetate, butyl acetate, benzyl benzoate, dipropylene glycol monomethyl ether, diethylene glycol monobutyl ether, acetone, Methyl ethyl ketone, aromatic and / or aliphatic hydrocarbons, vegetable or synthetic oil, DMF, liquid paraffin, light liquid paraffin, silicone, dimethylacetamide, N-methylpyrrolidone or 2,2-dimethyl-4-oxy-methylene-1, 3-dioxolane is mentioned. Absorption enhancers include DMSO, isopropyl myristate, dipropylene glycol pelargonate, silicone oil, aliphatic esters, triglycerides and fatty alcohols. Antioxidants include sulfites, metabisulfites, ascorbic acid, butylhydroxytoluene, butylhydroxyanisole and tocopherol.
乳剤は、経口投与、経皮投与又は注射として投与できる。乳剤は、有効成分を疎水性相又は親水性相に溶解させ、このものを適当な乳化剤により、必要ならばさらに着色剤、吸収促進物質、保護剤、酸化防止剤、遮光剤及び増粘物質などの補助剤と共に他の相の溶媒と均質化することにより調製できる。 The emulsion can be administered orally, transdermally or as an injection. In the emulsion, the active ingredient is dissolved in a hydrophobic phase or a hydrophilic phase, and this is added with a suitable emulsifier, and if necessary, a colorant, an absorption promoting substance, a protective agent, an antioxidant, a light-shielding agent, a thickening substance, etc. Can be prepared by homogenizing with other phase solvents together with other auxiliary agents.
疎水性相(油)としては、パラフィン油、シリコーン油、ゴマ油、アーモンド油、ヒマシ油、合成トリグリセリド、ステアリン酸エチル、アジピン酸ジーn−ブチリル、ラウリル酸ヘキシル、ペラルゴン酸ジプロピレングリコール、分枝鎖状の短鎖長脂肪酸と鎖長C16〜C18の飽和脂肪酸とのエステル、ミリスチン酸イソプロピル、パルミチン酸イソプロピル、鎖長C12〜C18の飽和脂肪アルコールのカプリル/カプリン酸エステル、ステアリン酸イソプロピル、オレイン酸オレイル、オレイン酸デシル、オレイン酸エチル、乳酸エチル、ワックス状脂肪酸エステル、フタル酸ジブチル、アジピン酸ジイソプロピル、イソトリデシルアルコール、2−オクチルドデカノール、セチルステアリルアルコール、オレイルアルコールが挙げられる。 As hydrophobic phase (oil), paraffin oil, silicone oil, sesame oil, almond oil, castor oil, synthetic triglyceride, ethyl stearate, di-n-butyryl adipate, hexyl laurate, dipropylene glycol pelargonate, branched chain Of a short fatty acid having a chain length and a saturated fatty acid having a chain length of C16 to C18, isopropyl myristate, isopropyl palmitate, capryl / caprate of a saturated fatty alcohol having a chain length of C12 to C18, isopropyl stearate, oleyl oleate Decyl oleate, ethyl oleate, ethyl lactate, waxy fatty acid ester, dibutyl phthalate, diisopropyl adipate, isotridecyl alcohol, 2-octyldodecanol, cetyl stearyl alcohol, oleyl alcohol It is.
親水性相としては、水、プロピレングリコール、グリセリン、ソルビトールが挙げられる。 Examples of the hydrophilic phase include water, propylene glycol, glycerin, and sorbitol.
乳化剤としては、ポリオキシエチル化されたヒマシ油、ポリオキシエチル化されたモノオレフィン酸ソルビタン、モノステアリン酸ソルビタン、モノステアリン酸グリセリン、ステアリン酸ポリオキシエチル、アルキルフェノールポリグリコールエーテルなどの非イオン性界面活性剤;N−ラウリル−β−イミノジプロピオン酸二ナトリウム、レシチンなどの両性界面活性剤;ラウリル硫酸ナトリウム、脂肪アルコール硫酸エーテル、モノ/ジアルキルポリグリコールオルトリン酸エステルのモノエタノールアミン塩などの陰イオン性界面活性剤;塩化セチルトリメチルアンモニウムなどの陽イオン性界面活性剤などが挙げられる。 Emulsifiers include nonionic interfaces such as polyoxyethylated castor oil, polyoxyethylated sorbitan monoolefin acid, sorbitan monostearate, glyceryl monostearate, polyoxyethyl stearate, alkylphenol polyglycol ether, etc. Activators; amphoteric surfactants such as disodium N-lauryl-β-iminodipropionate and lecithin; anions such as sodium lauryl sulfate, fatty alcohol sulfate ether, monoethanolamine salt of mono / dialkyl polyglycol orthophosphate Surfactants; cationic surfactants such as cetyltrimethylammonium chloride.
他の補助剤として、カルボキシメチルセルロース、メチルセルロース、ポリアクリレート、アルギネート、ゼラチン、アラビアゴム、ポリビニルピロリドン、ポリビニルアルコール、メチルビニルエーテル、無水マレイン酸の共重合体、ポリエチレングリコール、ワックス、コロイド状シリカが挙げられる。 Other adjuvants include carboxymethyl cellulose, methyl cellulose, polyacrylate, alginate, gelatin, gum arabic, polyvinyl pyrrolidone, polyvinyl alcohol, methyl vinyl ether, a copolymer of maleic anhydride, polyethylene glycol, wax, colloidal silica.
半固体調製物は皮膚上に塗布するか、もしくは広げるか、又は体腔中に導入することにより投与できる。ゲルは注射用液剤について上記したように調製した溶液に、軟膏状の粘稠性を有する透明な物質を生じさせるに十分なシックナーを加えることにより調製できる。 Semi-solid preparations can be administered by application on the skin or spreading or introduction into body cavities. Gels can be prepared by adding sufficient thickener to a solution prepared as described above for an injectable solution to produce a clear material having an ointment-like consistency.
次に本発明化合物を用いる場合の製剤の配合例を示す。但し本発明の配合例は、これらのみに限定されるものではない。なお、以下の配合例において「部」は重量部を意味する。 Next, formulation examples of the preparation when using the compound of the present invention are shown. However, the formulation examples of the present invention are not limited to these. In the following formulation examples, “parts” means parts by weight.
〔水和剤〕
本発明化合物 0.1〜80部
固体担体 5〜98.9部
界面活性剤 1〜10部
その他 0〜5部
その他として、例えば固結防止剤、分解防止剤等があげれらる。
[Wettable powder]
Compound of the present invention 0.1 to 80 parts Solid carrier 5 to 98.9 parts Surfactant 1 to 10 parts Others 0 to 5 parts Other examples include anti-caking agents and decomposition inhibitors.
〔乳剤〕
本発明化合物 0.1〜30部
液体担体 45〜95部
界面活性剤 4.9〜15部
その他 0〜10部
その他として、例えば展着剤、分解防止剤等が挙げられる。
〔emulsion〕
Compound of the present invention 0.1-30 parts Liquid carrier 45-95 parts Surfactant 4.9-15 parts Others 0-10 parts Others include, for example, spreading agents, decomposition inhibitors, and the like.
〔懸濁剤〕
本発明化合物 0.1〜70部
液体担体 15〜98.89部
界面活性剤 1〜12部
その他 0.01〜30部
その他として、例えば凍結防止剤、増粘剤等が挙げられる。
[Suspension]
Compound of the present invention 0.1 to 70 parts Liquid carrier 15 to 98.89 parts Surfactant 1 to 12 parts Others 0.01 to 30 parts Others include, for example, antifreezing agents and thickeners.
〔顆粒水和剤〕
本発明化合物 0.1〜90部
固体担体 0〜98.9部
界面活性剤 1〜20部
その他 0〜10部
その他として、例えば結合剤、分解防止剤等が挙げられる。
[Granule wettable powder]
Compound of the present invention 0.1 to 90 parts Solid carrier 0 to 98.9 parts Surfactant 1 to 20 parts Others 0 to 10 parts Others include, for example, binders and decomposition inhibitors.
〔液剤〕
本発明化合物 0.01〜70部
液体担体 20〜99.99部
その他 0〜10部
その他として、例えば凍結防止剤、展着剤等が挙げられる。
[Liquid]
Compound of the present invention 0.01 to 70 parts Liquid carrier 20 to 99.99 parts Others 0 to 10 parts Other examples include antifreezing agents and spreading agents.
〔粒剤〕
本発明化合物 0.01〜80部
固体担体 10〜99.99部
その他 0〜10部
その他として、例えば結合剤、分解防止剤等が挙げられる。
[Granule]
Compound of the present invention 0.01 to 80 parts Solid carrier 10 to 99.99 parts Others 0 to 10 parts Others include, for example, binders, decomposition inhibitors and the like.
〔粉剤〕
本発明化合物 0.01〜30部
固体担体 65〜99.99部
その他 0〜5部
その他として、例えばドリフト防止剤、分解防止剤等が挙げられる。
[Dust]
Compound of the present invention 0.01 to 30 parts Solid support 65 to 99.99 parts Others 0 to 5 parts Other examples include a drift inhibitor and a decomposition inhibitor.
次に、本発明化合物を有効成分とする製剤例をより具体的に示すが、本発明はこれらに限定されるものではない。 Next, although the formulation example which uses this invention compound as an active ingredient is shown more concretely, this invention is not limited to these.
尚、以下の配合例において、「部」は重量部を意味する。 In the following formulation examples, “parts” means parts by weight.
〔配合例1〕水和剤
本発明化合物No.1-001 20部
パイロフィライト 74部
ソルポール5039 4部
(非イオン性界面活性剤とアニオン性界面活性剤との混合物:東邦化学工業(株)商品名)
カープレックス#80D 2部
(合成含水珪酸:塩野義製薬(株)商品名)
以上を均一に混合粉砕して水和剤とする。
[Formulation Example 1] wettable powder Compound No.1-001 20 parts pyrophyllite 74 parts Solpol 5039 4 parts (mixture of nonionic surfactant and anionic surfactant: Toho Chemical Co., Ltd.) Product name)
Carplex # 80D 2 parts (Synthetic hydrous silicic acid: Shionogi & Co., Ltd. trade name)
The above is uniformly mixed and ground to obtain a wettable powder.
〔配合例2〕乳 剤
本発明化合物No.1-001 5部
キシレン 75部
N−メチルピロリドン 15部
ソルポール2680 5部
(非イオン性界面活性剤とアニオン性界面活性剤との混合物:東邦化学工業(株)商品名)
以上を均一に混合して乳剤とする。
[Formulation Example 2] Milk Compound of the present invention No.1-001 5 parts Xylene 75 parts N-methylpyrrolidone 15 parts Solpol 2680 5 parts (mixture of nonionic surfactant and anionic surfactant: Toho Chemical Industry (Product name)
The above is uniformly mixed to obtain an emulsion.
〔配合例3〕懸濁剤
本発明化合物No.1-001 25部
アグリゾールS−710 10部
(非イオン性界面活性剤:花王(株)商品名)
ルノックス1000C 0.5部
(アニオン性界面活性剤:東邦化学工業(株)商品名)
キサンタンガム 0.2部
水 64.3部
以上を均一に混合した後、湿式粉砕して懸濁剤とする。
[Formulation Example 3] Suspension Agent Compound No.1-001 25 parts Agrisol S-710 10 parts (Nonionic Surfactant: Kao Corporation trade name)
LUNOX 1000C 0.5 part (anionic surfactant: Toho Chemical Industries, Ltd. trade name)
Xanthan gum 0.2 parts water 64.3 parts After uniformly mixing the above, wet pulverize to make a suspension.
〔配合例4〕顆粒水和剤
本発明化合物No.1-001 75部
ハイテノールNE-15 5部
(アニオン性界面活性剤:第一工業製薬(株)商品名)
バニレックスN 10部
(アニオン性界面活性剤:日本製紙(株)商品名)
カープレックス#80D 10部
(合成含水珪酸:塩野義製薬(株)商品名)
以上を均一に混合粉砕した後、少量の水を加えて攪拌混合し、押出式造粒機で造粒し、乾燥して顆粒水和剤とする。
[Composition Example 4] Granule wettable powder Compound No.1-001 of the present invention 75 parts Hytenol NE-15 5 parts (anionic surfactant: Daiichi Kogyo Seiyaku Co., Ltd. trade name)
Vanillex N 10 parts (anionic surfactant: Nippon Paper Industries Co., Ltd. trade name)
Carplex # 80D 10 parts (Synthetic hydrous silicic acid: Shionogi Pharmaceutical Co., Ltd. trade name)
After uniformly mixing and pulverizing the above, a small amount of water is added, stirred and mixed, granulated with an extrusion granulator, and dried to obtain a granulated wettable powder.
〔配合例5〕粒剤
本発明化合物No.1-001 5部
ベントナイト 50部
タルク 45部
以上を均一に混合粉砕した後、少量の水を加えて攪拌混合し、押出式造粒機で造粒し、乾燥して粒剤とする。
[Formulation Example 5] Granules Present compound No.1-001 5 parts Bentonite 50 parts Talc 45 parts After uniformly mixing and pulverizing the above, a small amount of water is added and mixed with stirring, and granulated with an extrusion granulator. And dried into granules.
〔配合例6〕粉剤
本発明化合物No.1-001 3部
カープレックス#80D 0.5部
(合成含水珪酸:塩野義製薬(株)商品名)
カオリナイト 95部
リン酸ジイソプロピル 1.5部
以上を均一に混合粉砕して粉剤とする。
[Formulation Example 6] Powder Compound of the present invention No.1-001 3 parts Carplex # 80D 0.5 part (Synthetic hydrous silicic acid: Shionogi Pharmaceutical Co., Ltd. trade name)
Kaolinite 95 parts Diisopropyl phosphate 1.5 parts The above is uniformly mixed and ground to obtain a powder.
使用に際しては、上記製剤を水で1〜10000倍に希釈して、又は希釈せずに直接散布する。 In use, the above preparation is diluted 1 to 10000 times with water or sprayed directly without dilution.
〔配合例7〕水和剤調製物
本発明化合物No.1-001 25部
ジイソブチルナフタレンスルホン酸ナトリウム 1部
n−ドデシルベンゼンスルホン酸カルシウム 10部
アルキルアリール ポリグリコールエーテル 12部
ナフタレンスルホン酸ホルマリン縮合物のナトリウム塩 3部
エマルジョン型シリコーン 1部
二酸化ケイ素 3部
カオリン 45部
〔配合例8〕水溶性濃厚剤調製物
本発明化合物No.1-001 20部
ポリオキシエチレンラウリルエーテル 3部
ジオクチルスルホコハク酸ナトリウム 3.5部
ジメチルスルホキシド 37部
2−プロパノール 36.5部
〔配合例9〕噴霧用液剤
本発明化合物No.1-001 2部
ジメチルスルホキシド 10部
2−プロパノール 35部
アセトン 53部
〔配合例10〕経皮投与用液剤
本発明化合物No.1-001 5部
ヘキシレングリコール 50部
イソプロパノール 45部
〔配合例11〕経皮投与用液剤
本発明化合物No.1-001 5部
プロピレングリコールモノメチルエーテル 50部
ジプロピレングリコール 45部
〔配合例12〕経皮投与(滴下)用液剤
本発明化合物No.1-001 2部
軽質流動パラフィン 98部
〔配合例13〕経皮投与(滴下)用液剤
本発明化合物No.1-001 2部
軽質流動パラフィン 58部
オリーブ油 30部
ODO−H 9部
信越シリコーン 1部
また、本発明化合物を農薬として使用する場合には、必要に応じて製剤時又は散布時に他種の除草剤、各種殺虫剤、殺ダニ剤、殺線虫剤、殺菌剤、植物生長調節剤、共力剤、肥料、土壌改良剤等と混合施用しても良い。
[Formulation Example 7] wettable powder preparation Compound No. 1-001 of the present invention 25 parts sodium diisobutylnaphthalenesulfonate 1 part calcium n-dodecylbenzenesulfonate 10 parts alkylaryl polyglycol ether 12 parts naphthalenesulfonic acid formalin condensate Sodium salt 3 parts Emulsion type silicone 1 part Silicon dioxide 3 parts Kaolin 45 parts [Formulation Example 8] Water-soluble thickener preparation Compound No.1-001 20 parts Polyoxyethylene lauryl ether 3 parts Sodium dioctyl sulfosuccinate 3. 5 parts dimethyl sulfoxide 37 parts 2-propanol 36.5 parts [Formulation Example 9] Solution for spraying the present compound No.1-001 2 parts dimethyl sulfoxide 10 parts 2-propanol 35 parts acetone 53 parts [Formulation Example 10] transdermal Solution for administration The present compound No.1-001 5 Parts hexylene glycol 50 parts isopropanol 45 parts [Formulation Example 11] Solution for transdermal administration Compound No. 1-001 5 parts propylene glycol monomethyl ether 50 parts Dipropylene glycol 45 parts [Formulation example 12] transdermal administration (instillation) ) Solution for the Invention Compound No.1-001 2 parts Light Liquid Paraffin 98 parts [Formulation Example 13] Solution for the transdermal administration (drip) Compound No.1-001 2 parts Light Liquid Paraffin 58 parts Olive Oil 30 parts ODO -H 9 parts Shin-Etsu Silicone 1 part In addition, when the compound of the present invention is used as an agrochemical, other types of herbicides, various insecticides, acaricides, nematicides, You may mix and apply with a disinfectant, a plant growth regulator, a synergist, a fertilizer, a soil conditioner, etc.
特に他の農薬あるいは植物ホルモンと混合施用することにより、施用薬量の低減による低コスト化、混合薬剤の相乗作用による殺虫スペクトラムの拡大やより高い有害生物防除効果が期待できる。この際、同時に複数の公知農薬との組み合わせも可能である。本発明化合物と混合使用する農薬の種類としては、例えばザ・ペスティサイド・マニュアル(The Pesticide Manual)15版、2009年に記載されている化合物等が挙げられる。具体的にその一般名を例示すれば次の通りであるが、必ずしもこれらのみに限定されるものではない。 In particular, when mixed with other pesticides or plant hormones, the cost can be reduced by reducing the amount of applied medicine, the insecticidal spectrum can be expanded by the synergistic action of the mixed drugs, and higher pest control effects can be expected. At this time, a combination with a plurality of known agricultural chemicals is also possible. Examples of the type of agricultural chemical used in combination with the compound of the present invention include compounds described in The Pesticide Manual 15th edition, 2009, and the like. Specific examples of common names are as follows, but the general names are not necessarily limited to these.
殺菌剤:アシベンゾラルーS−メチル(acibenzolar-S-methyl)、アシルアミノベンザミド(acylaminobenzamide)、アシペタックス(acypetacs)、アルジモルフ(aldimorph)、アミスルブロム(amisulbrom)、アンバム(amobam)、アムプロピルホス(ampropyfos)、アニラジン(anilazine)、アザコナゾール(azaconazole)、アジチラム(azithiram)、アゾキシストロビン(azoxystrobin)、バリウムポリサルファイド(barium polysulfide)、ベナラキシル(benalaxyl)、ベノダニル(benodanil)、ベノミル(benomyl)、ベンキノックス(benquinox)、ベンタルロン(bentaluron)、ベンチアバリカルブ(benthiavalicarb)、ベンチアゾール(benthiazole)、ベンザマクリル(benzamacril)、ベンズアモルフ(benzamorf)、ベトキサジン(bethoxazine)、ビナパクリル(binapacryl)、ビフェニル(biphenyl)、ビテルタノール(bitertanol)、ブラストサイジン−S(blasticidin-S)、ボルドー液(bordeaux mixture)、ボスカリド(boscalid)、ブロモコナゾール(bromoconazole)、ブピリメート(bupirimate)、ブチオベート(buthiobate)、カルシウムポリスルフィド(calcium polysulfide)、キャプタフォール(captafol)、キャプタン(captan)、カルプロパミド(carpropamid)、カルバモルフ(carbamorph)、カルベンダジン(carbendazim)、カルボキシン(carboxin)、カルボン(carvone)、チェシュントミクスチャ(cheshunt mixture)、キノメチオネート(chinomethionat)、クロベンチアゾン(chlobenthiazone)、クロラニフォルメタン(chloraniformethane)、クロラニル(chloranil)、クロルフェナゾール(chlorfenazol)、クロロネブ(chloroneb)、クロロピクリン(chloropicrin)、クロロタロニル(chlorothalonil)、クロロキノックス(chlorquinox)、クロゾリネート(chlozolinate)、クリムバゾール(climbazole)、クロトリマゾール(clotrimazole)、カッパーアセテイト(copper acetate)、塩基性炭酸銅(copper carbonate, basic)、水酸化第二銅(copper hydroxide)、カッパーナフタレン(copper naphthenate)、カッパーオルアイト(copper oleate)、カッパーオキシクロリド(copper oxychloride)、硫酸銅(copper sulfate)、塩基性硫酸銅(copper sulfate, basic)、カッパージンククロメイト(copper zinc chromate)、クフラネブ(cufraneb)、クプロバム(cuprobam)、シアゾファミド(cyazofamid)、シクラフルアミド(cyclafuramid)、シクロヘキシミド(cycloheximide)、シフルフェナミド(cyflufenamid)、シモキサニル(cymoxanil)、サイペンダゾール(cypendazole)、シプロコナゾール(cyproconazol)、シプロジニル(cyprodinil)、シプロフラム(cyprofuram)、ダゾメット(dazomet)、デバカルブ(debacarb)、デカフェンチン(decafentin)、デハイドロアセテイト(dehydroacetic acid)、ジクロフルアニド(dichlofluanid)、ジクロン(dichlone)、ジクロロフェン(dichlorophen)、ジクロゾリン(dichlozoline)、ジクロブトラゾール(diclobutrazol)、ジクロシメット(diclocymet)、ジクロメジン(diclomedine)、ジクロラン(dicloran)など。 Bactericides: acibenzolar-S-methyl, acylaminobenzamide, acypetacs, aldimorph, amisulbrom, amobam, ampropyfos, Anilazine, azaconazole, azithiram, azoxystrobin, barium polysulfide, benalaxyl, benodanil, benomyl, benquinox , Benthaluron, benthiavalicarb, benthiazole, benzamacril, benzamorf, bethoxazine, binapacryl, biphenyl, bitertanol ,blast Idin-S (blasticidin-S), Bordeaux mixture, boscalid, bromoconazole, bupirimate, buthiobate, calcium polysulfide, captafol , Captan, carpropamid, carbamorph, carbendazim, carboxin, carvone, carvone, cheshunt mixture, chinomethionat, clobenazone (Chlobenthiazone), chloraniformethane, chloranil, chlorfenazol, chloroneb, chloropicrin, chlorothalonil, chlorquinox, clozolinate linate), climbazole, clotrimazole, copper acetate, basic carbonate, copper carbonate, copper hydroxide, copper naphthenate , Copper oleate, copper oxychloride, copper sulfate, copper sulfate, basic, copper zinc chromate, cufraneb, Cuprobam, cyazofamid, cyclafuramid, cycloheximide, cyflufenamid, cymoxanil, cypendazole, cyproconazol, din , Cyprofuram, dazomet, debacarb, decafenci Decafentin, dehydroacetic acid, dichlofluanid, dichlone, dichlorophen, dichlorophenoline, diclobutrazol, diclocymet, diclocymet, Diclomedine, dicloran, etc.
殺菌剤(続き):ジエトフェンカルブ(diethofencarb)、ジフェノコナゾール(difenoconazole)、ジフルメトリン(diflumetorim)、ジメチリモール(dimethirimol)、ジメトモルフ(dimethomorph)、ジモキシストロビン(dimoxystrobin)、ジニコナゾール(diniconazole)、ジニコナゾール−M(diniconazole-M)、ジノブトン(dinobuton)、ジノカップ(dinocap)、ジノカップ−4(dinocap-4)、ジノカップ−6(dinocap-6)、ジノクトン(dinocton)、ジノスルフォン(dinosulfon)、ジノテルボン(dinoterbon)、ジフェニルアミン(diphenylamine)、ジピリチオン(dipyrithione)、ジタリムホス(ditalimfos)、ジチアノン(dithianon)、ドデモルフ(dodemorph)、ドジン(dodine)、ドラゾクソロン(drazoxolon)、エデフェノホス(edifenphos)、エポキシコナゾール(epoxiconazole)、エタコナゾール(etaconazole)、エテム(etem)、エチリモル(ethirimol)、エトキシキン(ethoxyquin)、エトリジアノール(etridiazole)、ファモキサゾン(famoxadone)、フェナリモル(fenarimol)、フェブコナゾール(febuconazole)、フェナミドン(fenamidone)、フェナミノスルフ(fenaminosulf)、フェナパニル(fenapanil)、フェンダゾスラム(fendazosulam)、フェンフラム(fenfuram)、フェンヘキサミド(fenhexamid)、フェニトロパン(fenitropan)、フェノキサニル(fenoxanil)、フェンピクロニル(fenpiclonil)、フェンプロピジン(fenpropidin)、フェンプロピモルフ(fenpropimorph)、フェンチン(fentin)、フェルバン(ferbam)、フェリムゾン(ferimzone)、フルアジナム(fluazinam)、フルジオキソニル(fludioxonil)、フルメトベル(flumetover)、フルモルフ(flumorph)、フルオピコリド(fluopicolide)、フルオロイミド(fluoroimide)、フルオトリマゾール(fluotrimazole)、フルオキサストロビン(fluoxastrobin)、フルキンコナゾール(fluquinconazole)、フルシラゾール(flusilazole)、フルスルファミド(flusulfamide)、フルトラニル(flutolanil)、フルトリアフォール(flutriafol)、フォルペット(folpet)、フォセチル−アルミニウム(fosetyl-aluminium)、フベリダゾール(fuberidazole)、フララキシル(furalaxyl)、フラメトピル(furametpyr)、フルカルバニル(furcarbanil)、フルコナゾール(furconazole)、フルコナゾール−シス(furconazole-cis)、フルメシクロックス(furmecyclox)、フルファネート(furphanate)、グリオジン(glyodin)、グリセオフルビン(griseofulvin)、グアザチン(guazatine)、ハラクリネイト(halacrinate)、ヘキサクロロベンゼン(hexachlorobenzene)、ヘキサコナゾール(hexaconazole)、ヘキシルチオフォス(hexylthiofos)、ハイドロキシキノリン サルフェイト(8-hydroxyquinoline sulfate)、ヒメキサゾール(hymexazol)、イマザリル(imazalil)、イミベンコナゾール(imibenconazole)、イミノクタジン(iminoctadine)、イプコナゾール(ipconazole)、イプロベンホス(iprobenfos)、イプロジオン(iprodione)、イプロバリカルブ(iprovalicarb)、イソプロチオラン(isoprothiolane)、イソバレジオン(isovaledione)など。 Bactericides (continued): diethofencarb, difenoconazole, diflumetorim, dimethirimol, dimethomorph, dimoxystrobin, diniconazole-M, diniconazole-M, diniconazole-M M), dinobuton, dinocap, dinocap-4, dinocap-6, dinoton, dinosulfon, dinoterbon, diphenylamine ), Dipyrithione, ditalimfos, dithianon, dodemorph, dodine, drazoxolone, edifenphos, epoxiconazole, etaconazole, etaconazole (etem), ethirimol, ethoxyquin, etridiazole, famoxadone, fenarimol, febuconazole, fenamidone, fenaminosulf, fenapanil , Fendazosulam, fenfuram, fenhexamid, fenitropan, phenoxanil, fenpiclonil, fenpropidin, fenpropimorph, Fentin, ferbam, ferimzone, fluazinam, fludioxonil, flumetover, flumorph, fluopicolide, fluoroimide, Fluotrimazole, fluoxastrobin, fluquinconazole, flusilazole, flusulfamide, flutolanil, flutriafol, folpet, fosetyl- Aluminum (fosetyl-aluminium), fuberidazole, furalaxyl, furametpyr, furcarbanil, furconazole, furconazole, fluconazole-cis, furmecyclox, furphanate ( furphanate), glyodin, griseofulvin, guazatine, halacrinate, hexachlorobenzene, hexaconazole, hexylthiofos , Hydroxyquinoline sulfate, hymexazol, imazalil, imibenconazole, iminoctadine, ipconazole, iprobenfos, iprobenfos, proprobion (Iprovalicarb), isoprothiolane, and isovaledione.
殺菌剤(続き):カスガマイシン(kasugamycin)、クレソキシム−メチル(kresoxim-methyl)、マンカッパー(mancopper)、マンコゼブ(mancozeb)、マンジプロパミド(mandipropamid)、マンネブ(maneb)、メベニル(mebenil)、メカルビンジド(mecarbinzid)、メパニピリム(mepanipyrim)、メプロニル(mepronil)、メタラキシル(metalaxyl)、メタラキシル−M(metalaxyl-M)、メタム(metam)、メタゾキソロン(metazoxolon)、メトコナゾール(metconazole)、メタスルホカルブ(methasulfocarb)、メトフロキサム(methfuroxam)、メチルイソチオシアネイト(methyl isothiocyanate)、メチラム(metiram)、メトミノストロビン(metominostrobin)、メトラフェノン(metrafenone)、メトスルフォバックス(metsulfovax)、ミルネブ(milneb)、ミクロブタニル(myclobutanil)、ミクロゾリン(myclozolin)、ナバム(nabam)、ナタマイシン(natamycin)、ニッケルビス(ジメチルジチオカーバメート)(nickel bis(dimethyldithiocarbamate))、ニトロスチレン(nitrostyrene)、ニトロタール−イソプロピル(nitrothal-isopropyl)、ヌアリモル(nuarimol)、オーシーエイチ(OCH)、オクチリノン(octhilinone)、オフレース(ofurace)、オリサストロビン(orysastrobin)、オキサジキシル(oxadixyl)、有機銅(oxine copper)、オキシカルボキシン(oxycarboxin)、オキスポコナゾールフマール酸塩(oxpoconazole fumarate)、ペフラゾエート(pefurzoate)、ペンコナゾール(penconazole)、ペンシクロン(pencycuron)、ペンチオピラド(penthiopyrad)、オルソフェニルフェノール(o-phenylphenol)、フォスジフェン(phosdiphen)、フタライド(phthalide)、ピコキシストロビン(picoxystrobin)、ピペラリン(piperalin)、ポリカーバメート(polycarbamate)、ポリオキシン(polyoxins)、ポリオクソリム(polyoxorim)、ポタシウムアザイド(potassium azide)、炭酸水素カリウム(potassium hydrogen carbonate)、プロキナジド(proquinazid)、プロベナゾール(probenazole)、プロクロラズ(prochloraz)、プロシミドン(procymidone)、プロパモカルブ塩酸塩(propamocarb hydrochloride)、プロピコナゾール(propiconazole)、プロピネブ(propineb)、プロチオカルブ(prothiocarb)、プロチオコナゾール(prothioconazole)、ピラカルボリド(pyracarbolid)、ピラクロストロビン(pyraclostrobin)、ピラゾホス(pyrazophos)、ピリジニトリル(pyridinitril)、ピリフェノックス(pyrifenox)、ピリメタニル(pyrimethanil)、ピロキュロン(pyroquilon)、ピロキシクロル(pyroxychlor)、ピロキシフル(pyroxyfur)、キノメチオネート(quinomethionate)、キノキシフェン(quinoxyfen)、キントゼン(quintozene)、キナセトール・スルフェート(quinacetol-sulfate)、キナザミド(quinazamid)、キンコナゾール(quinconazole)、ラベンザゾール(rabenzazole)など。 Fungicide (continued): kasugamycin, kresoxim-methyl, mancopper, mancozeb, mandipropamid, maneb, mebenil, mecarbinzid , Mepanipyrim, mepronil, metalaxyl, metalaxyl-M, metam, metazoxolon, metconazole, metasulfocarb, metoxasulfocarb, metoxafloxam ), Methyl isothiocyanate, metiram, metinominostrobin, metrafenone, metsulfovax, milneb, microbutanil, microzoline (myclozo) lin), nabam, natamycin, nickel bis (dimethyldithiocarbamate), nitrostyrene, nitrothal-isopropyl, nuarimol, OH (OCH), octhilinone, offurace, orysastrobin, oxadixyl, oxine copper, oxycarboxin, oxpoconazole fumarate , Pefurzoate, penconazole, penconcuron, penthiopyrad, ortho-phenylphenol, phosdiphen, phthalide, picoxystrobin, pipette Laparin (piperalin), polycarbamate, polyoxins, polyoxorim, polyoxorim, potassium azide, potassium hydrogen carbonate, proquinazid, probenazole, prochloraz ( prochloraz, procymidone, propamocarb hydrochloride, propiconazole, propineb, propinecarb, prothiocarb, prothioconazole, pyracarbolid, pyraclostrobin ), Pyrazophos, pyridinitril, pyrifenox, pyrimethanil, pyroquilon, pyroxychlor, pyroxifl (pyroxyf) ur), quinomethionate, quinoxyfen, quintozene, quinacetol-sulfate, quinazamid, quinconazole, rabenzazole and the like.
殺菌剤(続き):アジ化ナトリウム(sodium azide)、炭酸水素ナトリウム(sodium hydrogen carbonate)、次亜塩素酸ナトリウム(sodium hypochlorite)、硫黄(sulfur)、スピロキサミン(spiroxamine)、サリチルアニリド(salycylanilide)、シルチオファム(silthiofam)、シメコナゾール(simeconazole)、テブコナゾール(tebuconazole)、テクナゼン(tecnazene)、テコラム(tecoram)、テトラコナゾール(tetraconazole)、チアベンダゾール(thiabendazole)、チアジフルオール(thiadifluor)、チシオフェン(thicyofen)、チフルザミド(thifluzamide)、チオクロルフェンフィム(thiochlorfenphim)、チオファネート(thiophanate)、チオファネート−メチル(thiophanate-methyl)、チオキノックス(thioquinox)、チラム(thiram)、チアジニル(tiadinil)、チオキシミド(tioxymid)、トルクロホス−メチル(tolclofos-methyl)、トリルフラニド(tolylfluanid)、トリアジメホン(triadimefon)、トリアジメノール(toriadimenol)、トリアミフォス(triamiphos)、トリアリモル(triarimol)、トリアゾキシド(triazoxide)、トリアズブチル(triazbutil)、トリブチルチンオキサイド(tributyltin oxide)、トリクラミド(trichlamide)、トリシクラゾール(tricyclazole)、トリデモルフ(tridemorph)、トリフロキシストロビン(trifloxystrobin)、トリフルミゾール(triflumizole)、トリホリン(triforine)、トリチコナゾール(triticonazole)、バリダマイシン(validamycin)、ビンクロゾリン(vinclozolin)、ザリルアミド(zarilamide)、硫酸亜鉛(zinc sulfate)、ジネブ(zineb)、ジラム(ziram)、ゾキサミド(zoxamide)及びシイタケ菌糸体抽出物など。 Fungicide (continued): sodium azide, sodium hydrogen carbonate, sodium hypochlorite, sulfur, spiroxamine, salicylanilide, silthiofam (Silthiofam), simeconazole, tebuconazole, tecnazene, tecoram, tetraconazole, thiabendazole, thiadifluor, thicyofen, thifluzamide thifluzamide, thiochlorfenphim, thiophanate, thiophanate-methyl, thioquinox, thiram, thiadinyl, tioxymid, tolcrophos-me Tolclofos-methyl, tolylfluanid, triadimefon, triadimenol, triamiphos, triarimol, triazoxide, triazbutil, tributyltin oxide ), Trichlamide, tricyclazole, triridemorph, trifloxystrobin, triflumizole, triforine, triticonazole, validamycin, vinclozoline (Vinclozolin), zalilamide, zinc sulfate, zineb, ziram, zoxamide, shiitake mycelium extract and the like.
殺バクテリア剤:ベンザルコニウムクロライド(benzalkonium chloride)、ビチオノール(bithionol)、ブロノポール(bronopol)、クレゾール(cresol)、ホルムアルデヒド(formaldehyde)、ニトラピリン(nitrapyrin)、オキソリニックアシド(oxolinic acid)、オキシテトラサイクリン(oxyterracycline)、ストレプトマイシン(streptomycin)及びテクロフタラム(tecloftalam)など。 Bactericides: benzalkonium chloride, bithionol, bronopol, cresol, formaldehyde, nitrapyrin, oxolinic acid, oxyterracycline , Streptomycin and tecloftalam.
殺線虫剤:アルドキシカルブ(aldoxycarb)、カズサホス(cadusafos)、デービーシーピー(DBCP)、ジクロフェンチオン(dichlofenthion)、デーエスピー(DSP)、エトプロホス(ethoprophos)、フェナミホス(fenamiphos)、フェンスルホチオン(fensulfothion)、フォスチアゼート(fosthiazate)、フォスチエタン(fosthietan)、イミシアホス(imicyafos)、イサミドホス(isamidofos)、イサゾホス(isazofos)、オキサミル(oxamyl)及びチオナジン(thionazin)など。 Nematicides: aldoxycarb, cadusafos, DDBCP, dichlofenthion, DSP (DSP), etoprophos, fenamiphos, fensulfothion, fostiazeto (Fosthiazate), fosthietan, imiciafos, isamifos, isazofos, oxamyl and thionazin.
殺ダニ剤:アセキノシル(acequinocyl)、アクリナトリン(acrinathrin)、アミトラズ(amitraz)、BCI−033(試験名)、ビフェナゼート(bifenazate)、ブロモプロピレート(bromopropylate)、チノメチオネート(chinomethionat)、クロロベンジラート(chlorobezilate)、クロフェンテジン(clofentezine)、シエノピラフェン(cyenopyrafen)、シフルメトフェン(cyflumetofen)、サイヘキサチン(cyhexatine)、ジコフォール(dicofol)、ジエノクロール(dienochlor)、デーエヌオーシー(DNOC)、エトキサゾール(etoxazole)、フェナザキン(fenazaquin)、フェンブタチンオキシド(fenbutatin oxide)、フェノチオカルブ(fenothiocarb)、フェンプロパトリン(fenpropathrin)、フェンピロキシメート(fenpyroximate)、フルアクリピリム(fluacrypyrim)、ハルフェンプロックス(halfenprox)、ヘキシチアゾックス(hexythiazox)、ミルベメクチン(milbemectin)、プロパルギット(propargite)、ピリダベン(pyridaben)、ピリミジフェン(pyrimidifen)、S−1870(試験名)、スピロジクロフェン(spirodiclofen)、スピロメシフェン(spyromesifen)及びテブフェンピラド(tebufenpyrad)など。 Acaricide: acequinocyl, acrinathrin, amitraz, BCI-033 (test name), bifenazate, bromopropylate, chinomethionat, chlorobezilate , Clofentezine, cyenopyrafen, cyflumetofen, cyhexatine, dicofol, dienochlor, denochlor (DNOC), etoxazole, quinazaquin (fenaza) Fenbutatin oxide, fenothiocarb, fenpropathrin, fenpyroximate, fluacrypyrim, halfenprox (halfenpro) x), hexythiazox, milbemectin, propargite, pyridaben, pyrimidifen, S-1870 (test name), spirodiclofen, spiromesifen ( spyromesifen) and tebufenpyrad.
殺虫剤:アバメクチン(abamectin)、アセフェート(acephate)、アセタミピリド(acetamipirid)、アラニカルブ(alanycarb)、アルディカルブ(aldicarb)、アレスリン(allethrin)、アジンホス−メチル(azinphos-methyl)、バチルスチューリンゲシス(bacillus thuringiensis)、ベンジオカルブ(bendiocarb)、ベンフラカルブ(benfuracarb)、ベンスルタップ(bensultap)、ビフェントリン(bifenthrin)、ブプロフェジン(buprofezin)、ブトカルボキシン(butocarboxim)、カルバリル(carbaryl)、カルボフラン(carbofuran)、カルボスルファン(carbosulfan)、カルタップ(cartap)、クロルアントラニリプロール(chlorantraniliprole)、クロルフェナピル(chlorfenapyr)、クロルフェンビンホス(chlorfenvinphos)、クロルフルアズロン(chlorfluazuron)、クロルピリホス(chlorpyrifos)、クロピリホス−メチル(chlorpyrifos-methyl)、クロマフェノジド(chromafenozide)、クロチアニジン(clothianidin)、シクロプロトリン(cycloprothrin)、シフルメトフェン(cyflumetofen)、シフルトリン(cyfluthrin)、ベータ−シフルトリン(beta-cyfluthrin)、シハロトリン(cyhalothrin)、ラムダ−シハロトリン(lambda-cyhalothrin)、シペルメトリン(cypermethrin)、シロマジン(cyromazine)、デルタメトリン(deltamethrin)、ジアクロデン(diacloden)、ジアフェンチウロン(diafenthiuron)、ダイアジノン(diazinon)、ジクロルボス(dichlorvos)、ジフルベンズロン(diflubenzuron)、ジメチルビンホス(dimethylvinphos)、ジノテフラン(dinotefuran)、ジオフェノラン(diofenolan)、ジスルフォトン(disulfoton)、ジメトエート(dimethoate)、エマメクチンベンゾエート(emamectin-benzoate)、イーピーエヌ(EPN)、エスフェンバレレート(esfenvalerate)、エチオフェンカルブ(ethiofencarb)、エチプロール(ethiprole)、エトフェンプロックス(etofenprox)、エトリムホス(etrimfos)、フェニトロチオン(fenitrothion)、フェノブカルブ(fenobucarb)、フェノキシカーブ(fenoxycarb)、フェンプロパトリン(fenpropathrin)、フェンチオン(fenthion)、フェンバレレート(fenvalerate)、フィプロニル(fipronil)、フロニカミド(flonicamid)、フルベンジアミド(flubendiamide)、フルシトリネート(flucythrinate)、フルフェネリム(flufenerim)、フルフェノクスウロン(flufenoxuron)、フルフェンプロックス(flufenprox)、フルバリネート(fluvalinate)、タウ−フルバリネート(tau-fluvalinate)、ホノホス(fonophos)、フォルメタネート(formetanate)、フォルモチオン(formothion)、フラチオカルブ(furathiocarb)など。 Insecticides: abamectin, acephate, acetamipirid, alanycarb, aldicarb, allethrin, azinphos-methyl, bacillus thuringiensis ), Bendiocarb, benfuracarb, bensultap, bifenthrin, buprofezin, butocarboxim, carbaryl, carbofuran, carbosulfan , Cartap, chlorantraniliprole, chlorfenapyr, chlorfenvinphos, chlorfluazuron, chlorpyrifos, chlorpyrifos, chlorpyrifos, chlorpyrifos Pyrifos-methyl, chromafenozide, clothianidin, cycloprothrin, cyflumetofen, cyfluthrin, beta-cyfluthrin, cyhalothrin, cyhalothrin Lambda-cyhalothrin, cypermethrin, cyromazine, deltamethrin, diacloden, diafenthiuron, diazinon, dichlorvos, diflubenzuron diflubenzuron, dimethylvinphos, dinotefuran, diofenolan, disulfoton, dimethoate, emamectin-benzoat e), EPN, esfenvalerate, ethiofencarb, ethiprole, etofenprox, etrimfos, fenitrothion, fenobucarb, phenoxy curve fenoxycarb), fenpropathrin, fenthion, fenvalerate, fipronil, flonicamid, flubendiamide, flucythrinate, flufenerim, flufenerim Flufenoxuron, flufenprox, fluvalinate, tau-fluvalinate, fonophos, formetanate, formoti On (formothion), furathiocarb (furathiocarb), etc.
殺虫剤(続き):ハロフェノジド(halofenozide)、ヘキサフルムロン(hexaflumuron)、ヒドラメチルノン(hydramethylnon)、イミダクロプリド(imidacloprid)、イソフェンホス(isofenphos)、インドキサカルブ(indoxacarb)、イソプロカルブ(isoprocarb)、イソキサチオン(isoxathion)、レピメクチン(lepimectin)、ルフェヌウロン(lufenuron)、マラチオン(malathion)、メタルデヒド(metaldehyde)、メタミドホス(methamidophos)、メチダチオン(methidathion)、メタクリホス(methacrifos)、メタフルミゾン(metaflumizone)、メタルカルブ(metalcarb)、メソミル(methomyl)、メソプレン(methoprene)、メトキシクロール(methoxychlor)、メトキシフェノジド(methoxyfenozide)、メチルブロマイド(methyl bromide)、モノクロトホス(monocrotophos)、ムスカルーレ(muscalure)、ニテンピラム(nitenpyram)、ノバルロン(novaluron)、オメトエート(omethoate)、オキサミル(oxamyl)、オキシデメトン−メチル(oxydemeton-methyl)、オキシデプロホス(oxydeprofos)、パラチオン(parathion)、パラチオン−メチル(parathion-methyl)、ペンタクロロフェノール(pentachlorophenol(PCP))、ペルメトリン(permethrin)、フェントエート(phenthoate)、フォキシム(phoxim)、ホレート(phorate)、ホサロン(phosalone)、ホスメット(phosmet)、ホスファミドン(phosphamidon)、ピリミカルブ(pirimicarb)、ピリミホス−メチル(pirimiphos-methyl)、プロフェノホス(profenofos)、プロチオホス(prothiofos)、プロパホス(propaphos)、プロトリフェンブト(protrifenbute)、ピメトロジン(pymetrozine)、ピラクロホス(pyraclofos)、ピリダリル(pyridalyl)、ピリフルキナゾン(pyrifluquinazon)、ピリプロキシフェン(pyriproxyfen)、ロテノン(rotenone)、SI−0405(試験名)、スルプロホス(sulprofos)、シラフルオフェン(silafluofen)、スピネトラム(spinetoram)、スピノサド(spinosad)、スピロテトラマート(spirotetramat)、スルホテップ(sulfotep)、SYJ−159(試験名)、テブフェノジド(tebfenozide)、テフルベンズロン(teflubenzuron)、テフルトリン(tefluthorin)、テルブホス(terbufos)、テトラクロロビンホス(tetrachlorvinphos)、チアクロプリド(thiacloprid)、チオシクラム(thiocyclam)、チオジカルブ(thiodicarb)、チアメトキサム(thiamethoxam)、チオファノックス(thiofanox)、チオメトン(thiometon)、トルフェンピラド(tolfenpyrad)、トラロメスリン(tralomethrin)、トリクロルホン(trichlorfon)、トリアズロン(triazuron)、トリフルムロン(triflumuron)及びバミドチオン(vamidothion)など。 Insecticides (continued): halofenozide, hexaflumuron, hydramethylnon, imidacloprid, isofenphos, indoxacarb, isoprocarb, isoxathion ), Lepimectin, lufenuron, malathion, metaldehyde, methamidophos, metidathion, methacrifos, metaflumizone, metalcarb, methmeth ), Methoprene, methoxychlor, methoxyfenozide, methyl bromide, monocrotophos, muscalure, mite Nitepyram, novaluron, omethoate, oxamyl, oxydemeton-methyl, oxydeprofos, parathion, parathion-methyl, Pentachlorophenol (PCP), permethrin, phenthoate, phoxim, phorate, phosalone, phosmet, phosphamidon, pirimicarb, Pirimiphos-methyl, profenofos, prothiofos, propaphos, protrifenbute, pymetrozine, pyraclofos, pyridalyl, pyrifylquinazo (Pyrifluquinazon), pyriproxyfen, rotenone, SI-0405 (study name), sulprofos, silafluofen, spinetoram, spinosad, spirotetramat , Sulfotep, SYJ-159 (test name), tebfenozide, teflubenzuron, tefluthorin, terbufos, tetrachlorvinphos, thiacloprid, thioam ), Thiodicarb, thiamethoxam, thiofanox, thiometon, tolfenpyrad, tralomethrin, trichlorfon, triazulo Such as triazuron, triflumuron and vamidothion.
以下に本発明化合物の合成例、試験例を実施例として具体的に述べることで、本発明をさらに詳しく説明するが、本発明はこれらによって限定されるものではない。 Hereinafter, the present invention will be described in more detail by specifically describing synthesis examples and test examples of the compounds of the present invention as examples, but the present invention is not limited thereto.
合成例に記載した中圧分取液体クロマトグラフィーは、山善株式会社中圧分取装置;YFLC−Wprep(流速18ml/min、シリカゲル40μmのカラム)を使用した。また、高速分取液体クロマトグラフィーは、島津製作所製;10AVPシステム{オーブン温度:40℃、移動相:アセトニトリル7ml/min,水4ml/min、カラム:GLサイエンス Inertsil−ODS3(内径20mm、長さ250mm、粒子径5μm)}を使用した。 The medium pressure preparative liquid chromatography described in the synthesis example used an intermediate pressure preparative apparatus (Yamazen Co., Ltd.); Further, high performance preparative liquid chromatography is manufactured by Shimadzu Corporation; 10AVP system {oven temperature: 40 ° C., mobile phase: acetonitrile 7 ml / min, water 4 ml / min, column: GL Science Inertsil-ODS3 (inner diameter 20 mm, length 250 mm) , Particle diameter 5 μm)}.
合成例に記載したプロトン核磁気共鳴(1H NMR)ケミカルシフト値は、基準物質としてMe4Si(テトラメチルシラン)を用い、300MHzにて測定した。またケミカルシフト値中の記号は下記の意味を表す。
s:シングレット、d:ダブレット、t:トリプレット、m:マルチプレット。
The proton nuclear magnetic resonance ( 1 H NMR) chemical shift value described in the synthesis example was measured at 300 MHz using Me 4 Si (tetramethylsilane) as a reference substance. Moreover, the symbol in a chemical shift value represents the following meaning.
s: singlet, d: doublet, t: triplet, m: multiplet.
[合成例]
合成例1
エチル 2−メチル−8−(ピリジン−3−イル)−6,8−ジヒドロ−5H−ピラゾロ[3,4−h]キノリン−3−カルボキシレートの製造(本発明化合物4−001)
工程1
2−(ピリジン−3−イル)−6,7−ジヒドロ−2H−インダゾ−ル−4(5H)−オンの製造
3−ヨードピリジン11.9gのN,N−ジメチルホルムアミド80ml溶液に、6,7−ジヒドロ−1H−インダゾ−ル−4(5H)−オン5.2g及び炭酸セシウム29.0gを添加した。反応容器中を窒素ガスで置換した後に、ヨウ化銅(1価)1.5gを添加し、室温にて30分攪拌した。攪拌終了後、120℃にて15時間攪拌を継続した。反応終了後、該反応混合物を室温まで放冷した。放冷後に該反応混合物中に析出した不溶物をセライトろ過により除去した後、ろ液に酢酸エチル200mlを添加した。得られた有機層を飽和食塩水次いで無水硫酸ナトリウムの順で洗浄・乾燥し、減圧下にて溶媒を留去した。得られた残渣をn−ヘキサン−酢酸エチル{1:1(体積比、以下同じである)}にて溶出するシリカゲルカラムクロマトグラフィーで精製し、目的物2.1gを白色固体として得た。
1H NMR(CDCl3,Me4Si,300MHz)δ9.00(d,J=2.4Hz,1H),8.61(dd,J=1.8,4.8Hz,1H),8.38(s,1H),8.03(ddd,J=1.8,2.4,8.1Hz,1H),7.43(dd,J=4.8,8.1Hz,1H),2.95(t,J=6.6Hz,2H),2.57(dd,J=6.3,6.9Hz,2H),2.19(dtd,J=6.3,6.6,6.9Hz,2H)。
[Synthesis example]
Synthesis example 1
Preparation of ethyl 2-methyl-8- (pyridin-3-yl) -6,8-dihydro-5H-pyrazolo [3,4-h] quinoline-3-carboxylate (present compound 4-001)
Process 1
Preparation of 2- (pyridin-3-yl) -6,7-dihydro-2H-indazol-4 (5H) -one To a solution of 11.9 g of 3-iodopyridine in 80 ml of N, N-dimethylformamide, 5.2 g of 7-dihydro-1H-indazol-4 (5H) -one and 29.0 g of cesium carbonate were added. After replacing the inside of the reaction vessel with nitrogen gas, 1.5 g of copper iodide (monovalent) was added and stirred at room temperature for 30 minutes. After completion of stirring, stirring was continued at 120 ° C. for 15 hours. After completion of the reaction, the reaction mixture was allowed to cool to room temperature. After standing to cool, insoluble matter precipitated in the reaction mixture was removed by Celite filtration, and 200 ml of ethyl acetate was added to the filtrate. The obtained organic layer was washed and dried in the order of saturated brine and then anhydrous sodium sulfate, and the solvent was distilled off under reduced pressure. The obtained residue was purified by silica gel column chromatography eluting with n-hexane-ethyl acetate {1: 1 (volume ratio, the same shall apply hereinafter)} to obtain 2.1 g of the desired product as a white solid.
1 H NMR (CDCl 3 , Me 4 Si, 300 MHz) δ 9.00 (d, J = 2.4 Hz, 1H), 8.61 (dd, J = 1.8, 4.8 Hz, 1H), 8.38 (S, 1H), 8.03 (ddd, J = 1.8, 2.4, 8.1 Hz, 1H), 7.43 (dd, J = 4.8, 8.1 Hz, 1H), 2. 95 (t, J = 6.6 Hz, 2H), 2.57 (dd, J = 6.3, 6.9 Hz, 2H), 2.19 (dtd, J = 6.3, 6.6, 6. 9Hz, 2H).
工程2
5−{(ジメチルアミノ)メチレン}2−(ピリジン−3−イル)−6,7−ジヒドロ−2H−インダゾ−ル−4(5H)−オンの製造
2−(ピリジン−3−イル)−6,7−ジヒドロ−2H−インダゾ−ル−4(5H)−オン1.0gのN,N−ジメチルホルムアミド5ml溶液に、t−ブトキシビス(ジメチルアミノ)メタン0.98gを添加し、室温にて一晩攪拌した。攪拌終了後、t−ブトキシビス(ジメチルアミノ)メタン0.98gを添加し、室温にて一晩攪拌を継続した。反応終了後、減圧下にて溶媒を留去した。得られた固体をジイソプロピルエーテルで洗浄し、目的物1.1gを桃色固体として得た。
1H NMR(CDCl3,Me4Si,300MHz)δ9.03−8.99(m,1H),8.55(dd,J=1.2,4.8Hz,1H),8.35(s,1H),8.01(ddd,J=1.2,2.7,8.1Hz,1H),7.60(s,1H),7.40(ddd,J=0.6,4.8,8.1Hz,1H),3.14(s,6H),3.03(t,J=7.2Hz,2H),2.90(t,J=7.2Hz,2H)。
Process 2
Preparation of 5-{(dimethylamino) methylene} 2- (pyridin-3-yl) -6,7-dihydro-2H-indazol-4 (5H) -one 2- (Pyridin-3-yl) -6 , 7-dihydro-2H-indazol-4 (5H) -one To a solution of 1.0 g of N, N-dimethylformamide in 5 ml was added 0.98 g of t-butoxybis (dimethylamino) methane, and the mixture was stirred at room temperature. Stir overnight. After completion of stirring, 0.98 g of t-butoxybis (dimethylamino) methane was added, and stirring was continued overnight at room temperature. After completion of the reaction, the solvent was distilled off under reduced pressure. The obtained solid was washed with diisopropyl ether to obtain 1.1 g of the desired product as a pink solid.
1 H NMR (CDCl 3 , Me 4 Si, 300 MHz) δ 9.03-8.99 (m, 1H), 8.55 (dd, J = 1.2, 4.8 Hz, 1H), 8.35 (s , 1H), 8.01 (ddd, J = 1.2, 2.7, 8.1 Hz, 1H), 7.60 (s, 1H), 7.40 (ddd, J = 0.6, 4. 8, 8.1 Hz, 1H), 3.14 (s, 6H), 3.03 (t, J = 7.2 Hz, 2H), 2.90 (t, J = 7.2 Hz, 2H).
工程3
エチル 2−メチル−8−(ピリジン−3−イル)−6,8−ジヒドロ−5H−ピラゾロ[3,4−h]キノリン−3−カルボキシレートの製造
5−{(ジメチルアミノ)メチレン}−2−(ピリジン−3−イル)−6,7−ジヒドロ−2H−インダゾ−ル−4(5H)−オン0.5gの酢酸10ml溶液に、アセト酢酸エチル0.27g及び酢酸アンモニウム1.4gを添加した。反応容器中を窒素ガスで置換した後に、100℃にて3時間攪拌した。反応終了後、減圧下にて溶媒を留去した。得られた残渣に、飽和炭酸水素ナトリウム水溶液10mlを添加し、析出した不溶物を減圧下でろ過することにより取り除いた。得られたろ液を酢酸エチル10mlにて抽出した。得られた有機層を無水硫酸ナトリウムで脱水・乾燥し、減圧下にて溶媒を留去した。得られた固体をジイソプロピルエーテルにて洗浄し、目的物0.36gをの黄土色固体として得た。
融点;150−160℃
合成例2
2,7−ジ(ピリジン−3−イル)−5,7−ジヒドロ−4H−チアゾロ[4,5−e]インダゾ−ルの製造(本発明化合物3−001)
工程1
5−ブロモ−2−(ピリジン−3−イル)−6,7−ジヒドロ−2H−インダゾ−ル−4(5H)−オンの製造
2−(ピリジン−3−イル)−6,7−ジヒドロ−2H−インダゾ−ル−4(5H)−オン0.5gの47%臭化水素酸10ml溶液に、室温にて臭素0.41gを添加し、70℃にて4時間撹拌した。反応終了後、該反応混合物を室温まで放冷した後、ジイソプロピルエーテルを添加した。該反応混合物中に析出した固体を濾別し、目的物0.52gを桃色固体として得た。
融点;235℃(235℃で分解した)
工程2
2,7−ジ(ピリジン−3−イル)−5,7−ジヒドロ−4H−チアゾロ[4,5−e]インダゾ−ルの製造
5−ブロモ−2−(ピリジン−3−イル)−6,7−ジヒドロ−2H−インダゾ−ル−4(5H)−オン200mgのエタノール5ml溶液に、チオニコチンアミド82mgを添加し、溶媒の還流温度にて10時間撹拌した。反応終了後、減圧下にて溶媒を留去し、得られた残渣に、飽和炭酸水素ナトリウム水溶液10mlを添加した後、酢酸エチル10mlで抽出した。得られた有機層を無水硫酸ナトリウムで脱水・乾燥し、減圧下にて溶媒を留去した。得られた固体をジイソプロピルエーテルにて洗浄し、目的物89mgをの黄土色固体として得た。
融点;188−195℃
合成例3
3−{(メチルチオ)メチル}−7−(ピリジン−3−イル)−2,4,5,7−テトラヒドロピラゾロ[3,4−e]インダゾールの製造(本発明化合物1−002)
工程1
5−{2−(メチルチオ)アセチル}−2−(ピリジン−3−イル)−6,7−ジヒドロ−2H−インダゾール−4(5H)−オンの製造
2−(ピリジン−3−イル)−6,7−ジヒドロ−2H−インダゾ−ル−4(5H)−オン300mgのテトラヒドロフラン20ml溶液を、0℃に冷却した後、同温度にてリチウムビス(トリメチルシリル)アミド1.84mlを滴下した。滴下終了後、同温度にて1時間撹拌した後、2−(メチルチオ)−1−(1H−ピラゾール−1−イル)エタノン287mg添加した。添加終了後、室温にて15時間撹拌を継続した。反応終了後、該反応溶液を水50mlに注ぎ、酢酸エチル50mlにて抽出した。得られた有機層を飽和食塩水次いで無水硫酸ナトリウムの順で洗浄・乾燥し、減圧下にて溶媒を留去した。得られた残渣をn−ヘキサン−酢酸エチル(7:3〜1:9のグラジエント)にて溶出する中圧分取液体クロマトグラフィーにて精製し、目的物73mgを白色固体として得た。
融点;111−113℃
工程2
3−{(メチルチオ)メチル}−7−(ピリジン−3−イル)−2,4,5,7−テトラヒドロピラゾロ[3,4−e]インダゾールの製造
5−{2−(メチルチオ)アセチル}−2−(ピリジン−3−イル)−6,7−ジヒドロ−2H−インダゾール−4(5H)−オン300mgのエタノール10ml溶液に、ヒドラジン1水和物55mgを添加し、エタノールの還流温度で7時間撹拌した。反応終了後、該反応混合物の溶媒を減圧下で留去し、目的物300mgを白色結晶として得た。
融点;240−241℃
合成例4
3−{(メチルチオ)メチル}−7−(ピリジン−3−イル)−2−(2,2,2−トリフルオロエチル)−2,4,5,7−テトラヒドロピラゾロ[3,4−e]インダゾール(本発明化合物1−003)及び3−{(メチルチオ)メチル}−7−(ピリジン−3−イル)−1−(2,2,2−トリフルオロエチル)−1,4,5,7−テトラヒドロピラゾロ[3,4−e]インダゾール(本発明化合物2−001)の製造
3−{(メチルチオ)メチル}−7−(ピリジン−3−イル)−2,4,5,7−テトラヒドロピラゾロ[3,4−e]インダゾール280mgのN,N−ジメチルホルムアミド5ml溶液を0℃に冷却し、60重量%水素化ナトリウム(鉱油中に分散)57mgを添加した。添加終了後、同温度にて5分間撹拌した後、該反応混合物にトリフルオロメタンスルホン酸2,2,2−トリフルオロエチル325mgを添加した。添加終了後、室温にて15時間撹拌を継続した。反応終了後、該反応溶液を水20mlに注ぎ、酢酸エチル40mlにて抽出した。得られた有機層を飽和食塩水次いで無水硫酸ナトリウムの順で洗浄・乾燥し、減圧下にて溶媒を留去した。得られた残渣を高速分取液体クロマトグラフィーにて精製し、3−{(メチルチオ)メチル}−7−(ピリジン−3−イル)−2−(2,2,2−トリフルオロエチル)−2,4,5,7−テトラヒドロピラゾロ[3,4−e]インダゾールを110mgの白色固体として、3−{(メチルチオ)メチル}−7−(ピリジン−3−イル)−1−(2,2,2−トリフルオロエチル)−1,4,5,7−テトラヒドロピラゾロ[3,4−e]インダゾールを90mgの白色固体として得た。
融点;
3−{(メチルチオ)メチル}−7−(ピリジン−3−イル)−2−(2,2,2−トリフルオロエチル)−2,4,5,7−テトラヒドロピラゾロ[3,4−e]インダゾール;137−139℃
3−{(メチルチオ)メチル}−7−(ピリジン−3−イル)−1−(2,2,2−トリフルオロエチル)−1,4,5,7−テトラヒドロピラゾロ[3,4−e]インダゾール;173−174℃
本発明化合物は、前記製造法及び実施例に準じて製造することができる。合成例1〜4と同様に製造した本発明化合物の例を第4表乃至第9表に示すが、本発明はこれらのみに限定されるものではない。また、表中「m.p.」は融点を表す。なお、表中D2−33aで表される構造は下記の構造を表す。
Process 3
Preparation of ethyl 2-methyl-8- (pyridin-3-yl) -6,8-dihydro-5H-pyrazolo [3,4-h] quinoline-3-carboxylate 5-{(dimethylamino) methylene} -2 To a solution of 0.5 g of-(pyridin-3-yl) -6,7-dihydro-2H-indazol-4 (5H) -one in 10 ml of acetic acid was added 0.27 g of ethyl acetoacetate and 1.4 g of ammonium acetate. did. After replacing the inside of the reaction vessel with nitrogen gas, the mixture was stirred at 100 ° C. for 3 hours. After completion of the reaction, the solvent was distilled off under reduced pressure. To the obtained residue, 10 ml of a saturated aqueous sodium hydrogen carbonate solution was added, and the precipitated insoluble matter was removed by filtration under reduced pressure. The obtained filtrate was extracted with 10 ml of ethyl acetate. The obtained organic layer was dehydrated and dried over anhydrous sodium sulfate, and the solvent was distilled off under reduced pressure. The obtained solid was washed with diisopropyl ether to obtain 0.36 g of the desired product as an ocherous solid.
Melting point: 150-160 ° C
Synthesis example 2
Production of 2,7-di (pyridin-3-yl) -5,7-dihydro-4H-thiazolo [4,5-e] indazole (Compound 3-001 of the present invention)
Process 1
Preparation of 5-bromo-2- (pyridin-3-yl) -6,7-dihydro-2H-indazol-4 (5H) -one 2- (pyridin-3-yl) -6,7-dihydro- To a solution of 0.5 g of 2H-indazol-4 (5H) -one in 10 ml of 47% hydrobromic acid, 0.41 g of bromine was added at room temperature and stirred at 70 ° C. for 4 hours. After completion of the reaction, the reaction mixture was allowed to cool to room temperature, and diisopropyl ether was added. The solid precipitated in the reaction mixture was separated by filtration to obtain 0.52 g of the desired product as a pink solid.
Melting point: 235 ° C. (decomposed at 235 ° C.)
Process 2
Preparation of 2,7-di (pyridin-3-yl) -5,7-dihydro-4H-thiazolo [4,5-e] indazole 5-Bromo-2- (pyridin-3-yl) -6, To a solution of 7-dihydro-2H-indazol-4 (5H) -one 200 mg in ethanol 5 ml was added thionicotinamide 82 mg and stirred at the reflux temperature of the solvent for 10 hours. After completion of the reaction, the solvent was distilled off under reduced pressure, and 10 ml of a saturated aqueous sodium hydrogen carbonate solution was added to the resulting residue, followed by extraction with 10 ml of ethyl acetate. The obtained organic layer was dehydrated and dried over anhydrous sodium sulfate, and the solvent was distilled off under reduced pressure. The obtained solid was washed with diisopropyl ether to obtain 89 mg of the desired product as an ocherous solid.
Melting point: 188-195 ° C
Synthesis example 3
Production of 3-{(methylthio) methyl} -7- (pyridin-3-yl) -2,4,5,7-tetrahydropyrazolo [3,4-e] indazole (present compound 1-002)
Process 1
Preparation of 5- {2- (methylthio) acetyl} -2- (pyridin-3-yl) -6,7-dihydro-2H-indazol-4 (5H) -one 2- (Pyridin-3-yl) -6 , 7-dihydro-2H-indazol-4 (5H) -one A solution of 300 mg of tetrahydrofuran in 20 ml of tetrahydrofuran was cooled to 0 ° C., and 1.84 ml of lithium bis (trimethylsilyl) amide was added dropwise at the same temperature. After completion of the dropwise addition, the mixture was stirred at the same temperature for 1 hour, and then 287 mg of 2- (methylthio) -1- (1H-pyrazol-1-yl) ethanone was added. After completion of the addition, stirring was continued at room temperature for 15 hours. After completion of the reaction, the reaction solution was poured into 50 ml of water and extracted with 50 ml of ethyl acetate. The obtained organic layer was washed and dried in the order of saturated brine and then anhydrous sodium sulfate, and the solvent was distilled off under reduced pressure. The obtained residue was purified by medium pressure preparative liquid chromatography eluting with n-hexane-ethyl acetate (gradient 7: 3 to 1: 9) to obtain 73 mg of the desired product as a white solid.
Melting point: 111-113 ° C
Process 2
Preparation of 3-{(methylthio) methyl} -7- (pyridin-3-yl) -2,4,5,7-tetrahydropyrazolo [3,4-e] indazole 5- {2- (methylthio) acetyl} 2- (Pyridin-3-yl) -6,7-dihydro-2H-indazol-4 (5H) -one To a solution of 300 mg of ethanol in 10 ml of ethanol was added 55 mg of hydrazine monohydrate, and the ethanol was refluxed at 7 ° C. Stir for hours. After completion of the reaction, the solvent of the reaction mixture was distilled off under reduced pressure to obtain 300 mg of the desired product as white crystals.
Melting point: 240-241 ° C
Synthesis example 4
3-{(methylthio) methyl} -7- (pyridin-3-yl) -2- (2,2,2-trifluoroethyl) -2,4,5,7-tetrahydropyrazolo [3,4-e Indazole (present compound 1-003) and 3-{(methylthio) methyl} -7- (pyridin-3-yl) -1- (2,2,2-trifluoroethyl) -1,4,5 Preparation of 7-tetrahydropyrazolo [3,4-e] indazole (present compound 2-001) 3-{(methylthio) methyl} -7- (pyridin-3-yl) -2,4,5,7- A solution of 280 mg of tetrahydropyrazolo [3,4-e] indazole in 5 ml of N, N-dimethylformamide was cooled to 0 ° C., and 57 mg of 60 wt% sodium hydride (dispersed in mineral oil) was added. After completion of the addition, the mixture was stirred at the same temperature for 5 minutes, and then 325 mg of 2,2,2-trifluoroethyl trifluoromethanesulfonate was added to the reaction mixture. After completion of the addition, stirring was continued at room temperature for 15 hours. After completion of the reaction, the reaction solution was poured into 20 ml of water and extracted with 40 ml of ethyl acetate. The obtained organic layer was washed and dried in the order of saturated brine and then anhydrous sodium sulfate, and the solvent was distilled off under reduced pressure. The obtained residue was purified by high performance preparative liquid chromatography, and 3-{(methylthio) methyl} -7- (pyridin-3-yl) -2- (2,2,2-trifluoroethyl) -2. , 4,5,7-tetrahydropyrazolo [3,4-e] indazole as 110 mg of white solid as 3-{(methylthio) methyl} -7- (pyridin-3-yl) -1- (2,2 , 2-trifluoroethyl) -1,4,5,7-tetrahydropyrazolo [3,4-e] indazole was obtained as 90 mg of a white solid.
Melting point;
3-{(methylthio) methyl} -7- (pyridin-3-yl) -2- (2,2,2-trifluoroethyl) -2,4,5,7-tetrahydropyrazolo [3,4-e Indazole; 137-139 ° C
3-{(methylthio) methyl} -7- (pyridin-3-yl) -1- (2,2,2-trifluoroethyl) -1,4,5,7-tetrahydropyrazolo [3,4-e Indazole; 173-174 ° C
This invention compound can be manufactured according to the said manufacturing method and an Example. Although the example of this invention compound manufactured similarly to the synthesis examples 1-4 is shown in Table 4 thru | or Table 9, this invention is not limited only to these. In the table, “mp” represents the melting point. In addition, the structure represented by D2-33a in the table represents the following structure.
第4表 Table 4
〔第4表〕
――――――――――――――――――――――――――――――――――
No. R4 A3 X1 X1a m.p.(℃)
――――――――――――――――――――――――――――――――――
1-001 H CH2 H C(O)C(=NOCH3)CH2SCH3 155-160
1-002 H CH2 CH2SCH3 H 240-241
1-003 H CH2 CH2SCH3 CH2CF3 137-139
1-004 H CH2 CH2S(O)CH3 CH2CF3 246-247
1-005 H CH2 SCH3 H 253-256
1-006 H CH2 SCH3 CH2SCH3 164-165
1-007 H CH2 SCH3 CH2CF3 190-192
――――――――――――――――――――――――――――――――――
第5表
[Table 4]
――――――――――――――――――――――――――――――――――
No. R 4 A 3 X 1 X 1a mp (℃)
――――――――――――――――――――――――――――――――――
1-001 H CH 2 HC (O) C (= NOCH 3 ) CH 2 SCH 3 155-160
1-002 H CH 2 CH 2 SCH 3 H 240-241
1-003 H CH 2 CH 2 SCH 3 CH 2 CF 3 137-139
1-004 H CH 2 CH 2 S (O) CH 3 CH 2 CF 3 246-247
1-005 H CH 2 SCH 3 H 253-256
1-006 H CH 2 SCH 3 CH 2 SCH 3 164-165
1-007 H CH 2 SCH 3 CH 2 CF 3 190-192
――――――――――――――――――――――――――――――――――
Table 5
〔第5表〕
―――――――――――――――――――――――――――――――
No. R4 A3 X1 X1a m.p.(℃)
―――――――――――――――――――――――――――――――
2-001 H CH2 CH2SCH3 CH2CF3 173-174
2-002 H CH2 H C(O)C(=NOCH3)CH2SCH3116-118
2-003 H CH2 SCH3 CH2SCH3 154-156
2-004 H CH2 SCH3 CH2CF3 181-183
―――――――――――――――――――――――――――――――
第6表
[Table 5]
―――――――――――――――――――――――――――――――
No. R 4 A 3 X 1 X 1a mp (℃)
―――――――――――――――――――――――――――――――
2-001 H CH 2 CH 2 SCH 3 CH 2 CF 3 173-174
2-002 H CH 2 HC (O) C (= NOCH 3 ) CH 2 SCH 3 116-118
2-003 H CH 2 SCH 3 CH 2 SCH 3 154-156
2-004 H CH 2 SCH 3 CH 2 CF 3 181-183
―――――――――――――――――――――――――――――――
Table 6
〔第6表〕
―――――――――――――――――――――
No. R4 X1 m.p.(℃)
―――――――――――――――――――――
3-001 H D2-33a 188-195
3-002 H CH2SCH3 128-134
3-003 H CH2S(O)CH3 200-207
3-004 H CH2S(O)2CH3 214-218
―――――――――――――――――――――
第7表
[Table 6]
―――――――――――――――――――――
No. R 4 X 1 mp (℃)
―――――――――――――――――――――
3-001 H D2-33a 188-195
3-002 H CH 2 SCH 3 128-134
3-003 H CH 2 S (O) CH 3 200-207
3-004 H CH 2 S (O) 2 CH 3 214-218
―――――――――――――――――――――
Table 7
〔第7表〕
――――――――――――――――――――――――――――――――――
No. R4 X1-1 X1-2 m.p.(℃)
――――――――――――――――――――――――――――――――――
4-001 H CH3 C(O)OCH2CH3 150-160
4-002 H CH3 C(O)OH >280
4-003 H CH2SCH3 C(O)OCH2CH3 155-165
――――――――――――――――――――――――――――――――――
第8表
[Table 7]
――――――――――――――――――――――――――――――――――
No. R 4 X 1-1 X 1-2 mp (℃)
――――――――――――――――――――――――――――――――――
4-001 H CH 3 C (O) OCH 2 CH 3 150-160
4-002 H CH 3 C (O) OH> 280
4-003 H CH 2 SCH 3 C (O) OCH 2 CH 3 155-165
――――――――――――――――――――――――――――――――――
Table 8
〔第8表〕
―――――――――――――――――――
No. R4 X1 m.p.(℃)
―――――――――――――――――――
5-001 H SCH3 178-185
―――――――――――――――――――
第9表
[Table 8]
―――――――――――――――――――
No. R 4 X 1 mp (℃)
―――――――――――――――――――
5-001 H SCH 3 178-185
―――――――――――――――――――
Table 9
〔第9表〕
―――――――――――――――――――
No. R4 X1 m.p.(℃)
―――――――――――――――――――
6-001 H NHC(O)CH3 >285
―――――――――――――――――――
[試験例]
次に、本発明化合物の有害生物防除剤としての有用性について、以下の試験例において具体的に説明するが、本発明はこれらのみに限定されるものではない。
試験例1 トビイロウンカに対する殺虫試験
本発明化合物の10%乳剤(化合物によっては10%水和剤を供試)を展着剤の入った水で希釈して、500ppm濃度の薬液を調製した。この薬液中にイネの葉鞘を約10秒間浸漬し、風乾後試験管に入れ、この中にトビイロウンカ(Nilaparvata lugens)の2齢幼虫を試験管当たり5頭放虫し、スポンジで蓋をして25℃恒温室に収容した。6日後の死虫数を調査し、死虫率(%)(死虫数÷供試虫数×100)を算出した。尚、試験は2連制で行なった。
[Table 9]
―――――――――――――――――――
No. R 4 X 1 mp (℃)
―――――――――――――――――――
6-001 H NHC (O) CH 3 > 285
―――――――――――――――――――
[Test example]
Next, the usefulness of the compound of the present invention as a pest control agent will be specifically described in the following test examples, but the present invention is not limited to these.
Test Example 1 Insecticidal test against brown planthopper A 10% emulsion of the compound of the present invention (depending on the compound, 10% wettable powder) was diluted with water containing a spreading agent to prepare a chemical solution having a concentration of 500 ppm. Rice leaf sheaths are immersed in this chemical solution for about 10 seconds, air-dried and placed in a test tube, and 5 second-instar larvae of Nilaparvata lugens are released per test tube, covered with a sponge and 25 Housed in a constant temperature room. The number of dead insects after 6 days was investigated, and the death rate (%) (number of dead insects ÷ number of test insects × 100) was calculated. In addition, the test was performed by 2 continuous systems.
その結果、供試した化合物の内、下記の化合物が90%以上の死虫率を示した。
本発明化合物:1−001〜1−004、1−006、1−007、2−001〜2−004、3−001〜3−004、4−001〜4−003、5−001
試験例2 シルバーリーフコナジラミに対する殺虫試験
内径7cmのスチロールカップに湿った濾紙を敷き、その上に3cmに切り取ったインゲンの葉を置いた。本発明化合物の10%乳剤(化合物によっては10%水和剤を供試)を展着剤の入った水で希釈して、500ppm濃度の薬液を調製し、回転式散布塔を用いて薬液をスチロールカップ当たり2.5mlずつ散布した(2.5mg/cm2)。葉を風乾後、シルバーリーフコナジラミ(Bemisia argentifolii)の成虫を放虫し、蓋をして25℃恒温室に収容した。5日後の死虫数を調査し、試験例1と同様の計算式から死虫率を算出した。尚、試験は2連制で行なった。
As a result, among the compounds tested, the following compounds showed a death rate of 90% or more.
Compounds of the present invention: 1-001 to 1-004, 1-006, 1-007, 2-001 to 2-004, 3-001 to 3-004, 4-001 to 4-003, 5-001
Test Example 2 Insecticidal test for silver leaf whitefly A moist filter paper was laid on a styrene cup having an inner diameter of 7 cm, and a green leaf cut into 3 cm was placed thereon. A 10% emulsion of a compound of the present invention (depending on the compound, 10% wettable powder) is diluted with water containing a spreading agent to prepare a chemical solution with a concentration of 500 ppm, and the chemical solution is prepared using a rotary spray tower. 2.5 ml was sprayed per styrene cup (2.5 mg / cm 2 ). After the leaves were air-dried, adults of silver leaf whiteflies (Bemisia argentifolii) were released, covered, and housed in a thermostatic chamber at 25 ° C. The number of dead insects after 5 days was investigated, and the dead insect rate was calculated from the same calculation formula as in Test Example 1. In addition, the test was performed by 2 continuous systems.
その結果、供試した化合物の内、下記の化合物が90%以上の死虫率を示した。
本発明化合物:1−003、1−004、2−002、3−001〜3−004、4−003
試験例3 モモアカアブラムシに対する殺虫試験
内径3cmのガラスシャーレに湿った脱脂綿を敷き、その上に同径に切り取ったカンランの葉を置き、モモアカアブラムシ(Myzus persicae)無翅成虫を4頭放虫した。1日後、本発明化合物の10%乳剤(化合物によっては10%水和剤を供試)を展着剤の入った水で希釈して、500ppm濃度の薬液を調製し、回転式散布塔にて薬液を散布(2.5mg/cm2)、蓋をして25℃恒温室に収容した。6日後の死虫数を調査し、試験例1と同様の計算式から死虫率を算出した。尚、試験は2連制で行なった。
As a result, among the compounds tested, the following compounds showed a death rate of 90% or more.
Compound of the present invention: 1-003, 1-004, 2-002, 3-001 to 3-004, 4-003
Test Example 3 Insecticidal test against peach aphid A moist absorbent cotton was laid on a glass petri dish with an inner diameter of 3 cm, and kanran leaves cut out to the same diameter were placed on it. did. One day later, a 10% emulsion of the compound of the present invention (depending on the compound, 10% wettable powder was tested) was diluted with water containing a spreading agent to prepare a chemical solution with a concentration of 500 ppm, and then in a rotary spray tower. The chemical solution was sprayed (2.5 mg / cm 2 ), covered, and stored in a constant temperature room at 25 ° C. The number of dead insects after 6 days was investigated, and the death rate was calculated from the same calculation formula as in Test Example 1. In addition, the test was performed by 2 continuous systems.
その結果、供試した化合物の内、下記の化合物が90%以上の死虫率を示した。
本発明化合物:1−001〜1−004、1−006、1−007、2−001〜2−003、3−001〜3−004、4−001、4−003、5−001、6−001
試験例4 ワタアブラムシに対する殺虫試験
内径3cmのガラスシャーレに湿った脱脂綿を敷き、その上に同径に切り取ったキュウリの葉を置き、ワタアブラムシ(Aphis gossypii)無翅成虫を4頭放虫した。1日後、本発明化合物の10%乳剤(化合物によっては10%水和剤を供試)を展着剤の入った水で希釈して、500ppm濃度の薬液を調製し、回転式散布塔にて薬液を散布(2.5mg/cm2)、蓋をして25℃恒温室に収容した。6日後の死虫数を調査し、試験例1と同様の計算式から死虫率を算出した。尚、試験は2連制で行なった。
As a result, among the compounds tested, the following compounds showed a death rate of 90% or more.
Compounds of the present invention: 1-001 to 1-004, 1-006, 1-007, 2-001 to 2-003, 3-001 to 3-004, 4-001, 4-003, 5-001, 6- 001
Test Example 4 Insecticidal test for cotton aphids Wet cotton wool with a 3 cm inner diameter petri dish and a cucumber leaf cut out to the same diameter was placed on the cotton aphid, and four cotton aphids (Aphis gossypi) adults were released. One day later, a 10% emulsion of the compound of the present invention (depending on the compound, 10% wettable powder was tested) was diluted with water containing a spreading agent to prepare a chemical solution with a concentration of 500 ppm. The chemical solution was sprayed (2.5 mg / cm 2), covered, and stored in a constant temperature room at 25 ° C. The number of dead insects after 6 days was investigated, and the death rate was calculated from the same calculation formula as in Test Example 1. In addition, the test was performed by 2 continuous systems.
その結果、供試した化合物の内、下記の化合物が90%以上の死虫率を示した。
本発明化合物:1−001、1−003、1−004、1−007、2−001、2−002、3−001〜3−003、4−001、4−003、5−001、6−001
試験例5 モモアカアブラムシに対する土壌潅注処理試験
本発明化合物の10%乳剤を水道水で希釈して、濃度が100ppmの薬液を調製した。
As a result, among the compounds tested, the following compounds showed a death rate of 90% or more.
Compounds of the present invention: 1-001, 1-003, 1-004, 1-007, 2-001, 2-002, 3-001 to 3-003, 4-001, 4-003, 5-001, 6- 001
Test Example 5 Soil irrigation treatment test for peach aphid A 10% emulsion of the compound of the present invention was diluted with tap water to prepare a chemical solution having a concentration of 100 ppm.
プラスチックカップ植えキャベツ苗(2.5本葉期)の株元土壌部分に10mlの薬液を潅注処理し、温室内に放置した。潅注処理1日後にモモアカアブラムシ(Myzus persicae)の成虫を20頭/株で放虫し、その後温室内に放置した。放虫6日後の生存虫数を調査し、下記の計算式から対照値を算出した。
対照値(%)={1−(Cb×Tai)/(Cai×Tb)}×100
式中の文字は下記を表している。
Cb:無処理区における処理前の虫の数
Cai:無処理区における最終調査時の生存虫数
Tb:処理区における処理前の虫の数
Tai:処理区における最終調査時の生存虫数
その結果、供試した化合物の内、下記の化合物が90%以上の対照値を示した。
本発明化合物:1−003、1−004、3−002、3−003
10 ml of the chemical solution was irrigated to the stock soil portion of the plastic cup planted cabbage seedling (2.5 true leaf stage) and left in the greenhouse. One day after the irrigation treatment, 20 mosquitoes / strain of adult peach aphid (Myzus persicae) were released and then left in the greenhouse. The number of surviving insects 6 days after the release was examined, and a control value was calculated from the following formula.
Control value (%) = {1- (Cb × Tai) / (Cai × Tb)} × 100
The characters in the formula represent the following:
Cb: number of insects before treatment in the untreated group Cai: number of live insects at the time of final survey in the untreated group Tb: number of insects before treatment in the treated group Tai: number of live insects at the time of final survey in the treated group Among the compounds tested, the following compounds showed a control value of 90% or more.
Compounds of the present invention: 1-003, 1-004, 3-002, 3-003
本発明における新規なピラゾール誘導体は、優れた有害生物防除活性、特に殺虫・殺ダニ活性を示し、且つ、ホ乳動物、魚類及び益虫等の非標的生物に対してほとんど悪影響の無い、極めて有用な化合物である。 The novel pyrazole derivative in the present invention exhibits excellent pest control activity, particularly insecticidal / miticidal activity, and is extremely useful with little adverse effect on non-target organisms such as mammals, fish and beneficial insects. A compound.
Claims (9)
[式中、Bは、下記の構造式で表されるピラゾール環を表し、
A1は、−N(−O)m2又は−CR1を表し、
A2はD1−8、D1−15、D1−17、D1−22、D1−52又はD1−106を表し、
R1は、水素原子、ハロゲン原子、シアノ、ニトロ、C1〜C6アルキル、C1〜C6ハロアルキル、C1〜C6アルコキシ、C1〜C6ハロアルコキシ、C1〜C6アルキルチオ、C1〜C6アルキルスルフィニル、C1〜C6アルキルスルホニル、C1〜C6ハロアルキルチオ、C1〜C6ハロアルキルスルフィニル又はC1〜C6ハロアルキルスルホニルを表し、
R2は、ハロゲン原子、シアノ、ニトロ、C1〜C6アルキル、C1〜C6ハロアルキル、C1〜C6アルコキシ、C1〜C6ハロアルコキシ、C1〜C6アルキルチオ、C1〜C6アルキルスルフィニル、C1〜C6アルキルスルホニル、C1〜C6ハロアルキルチオ、C1〜C6ハロアルキルスルフィニル又はC1〜C6ハロアルキルスルホニルを表し、n1が2以上の整数を表すとき、各々のR2は互いに同一であっても又は互いに相異なってもよく、
R4は、水素原子、ハロゲン原子、C1〜C6アルキル、C3〜C6シクロアルキル、C2〜C6アルケニル、C2〜C6アルキニル、C1〜C6ハロアルキル、C1〜C6アルコキシ、C1〜C6ハロアルコキシ、C1〜C6アルキルチオ、C1〜C6アルキルスルフィニル、C1〜C6アルキルスルホニル、C1〜C6ハロアルキルチオ、C1〜C6ハロアルキルスルフィニル、C1〜C6ハロアルキルスルホニル、シアノ、C1〜C6アルコキシカルボニル、C1〜C6アルキルカルボニル、C1〜C6アルキルアミノカルボニル又はジ(C1〜C6アルキル)アミノカルボニルを表し、
D1−8、D1−15、D1−17、D1−22、D1−52及びD1−106は、それぞれ下記の構造式で表される環を表し、
X及びR3は、一緒になってC2〜C4アルキレン鎖又はC2〜C4アルケニレン鎖を形成することにより、Xの結合する炭素原子とR3の結合する炭素原子及びA2の結合する炭素原子と共に6〜8員環を形成し、このときアルキレン鎖又はアルケニレン鎖は、酸素原子又は硫黄原子を含んでもよく、
X1は、C1〜C12アルキル、R5によって任意に置換された(C1〜C12)アルキル、−OH、−OR6、−SH、−S(O)rR6、−N(R8)R9、−C(O)R7、−C(O)OH、−C(O)OR6、−C(O)N(R8)R9、−C(S)N(R8)R9、D2−32、D2−33、D2−34、D2−36、D2−37又はD2−38を表し、p2又はp3が2以上の整数を表すとき、各々のX1は互いに同一であっても又は互いに相異なってもよく、
X1aは、水素原子、C1〜C12アルキル、R5aによって任意に置換された(C1〜C12)アルキル又は−C(O)R7aを表し、
D2−32、D2−33、D2−34、D2−36、D2−37及びD2−38は、それぞれ下記の構造式で表される環を表し、
R5は、ハロゲン原子、−OH、−OR11、−SH、−S(O)rR11を表し、
R5aは、ハロゲン原子、シアノ、−OH,−OR11a、−SH又は−S(O)rR11aを表し、
R6は、C1〜C6アルキル又はC1〜C6ハロアルキルを表し、
R7は、水素原子、C1〜C6アルキル又はR14によって任意に置換された(C1〜C6)アルキルを表し、
R7aは、水素原子、C1〜C6アルキル、−C(R12a)=NOH又は−C(R12a)=NOR11aを表し、
R8及びR9は、各々独立して水素原子、C1〜C6アルキル又は−C(O)R12を表し、
R11は、C1〜C6アルキル又はR14によって任意に置換された(C1〜C6)アルキルを表し、
R11aは、C1〜C6アルキル又はR14aによって任意に置換された(C1〜C6)アルキルを表し、
R12は、水素原子又はC1〜C6アルキルを表し、
R12aは、水素原子、C1〜C6アルキル又はR14aによって任意に置換された(C1〜C6)アルキルを表し、
R14は、ハロゲン原子、C3〜C6シクロアルキル、−OH,−OR15、−SH又は−S(O)rR15
R14aは、ハロゲン原子、C3〜C6シクロアルキル、−OH,−OR15a、−SH又は−S(O)rR15aを表し、
R15及びR15aは、各々独立してC1〜C6アルキルを表し、
X2は、ハロゲン原子、シアノ、ニトロ、−OH、−SH、−NH2、C1〜C6アルキル、C2〜C6アルケニル、C2〜C6アルキニル、C3〜C8シクロアルキルを表し、
n1、p3及びt1は、各々独立して0〜3の整数を表し、
p1は、0〜1の整数を表し、
p2は、0〜2の整数を表し、
t4は、0〜4の整数を表し、
m1及びm2は、各々独立して0又は1の整数を表し、
rは、0〜2の整数を表す。]で表されるピラゾール誘導体又はその塩。 Formula (1):
[In the formula, B represents a pyrazole ring represented by the following structural formula;
A 1 represents —N (—O) m 2 or —CR 1 ,
A 2 represents D1-8, D1-15, D1-17, D1-22, D1-52 or D1-106,
R 1 is a hydrogen atom, a halogen atom, cyano, nitro, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 alkoxy, C 1 -C 6 haloalkoxy, C 1 -C 6 alkylthio, C 1 -C 6 alkylsulfinyl, C 1 -C 6 represent alkylsulfonyl, C 1 -C 6 haloalkylthio, a C 1 -C 6 haloalkylsulfinyl or C 1 -C 6 haloalkylsulfonyl,
R 2 is a halogen atom, cyano, nitro, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 alkoxy, C 1 -C 6 haloalkoxy, C 1 -C 6 alkylthio, C 1- C 6 alkylsulfinyl, C 1 -C 6 alkylsulfonyl, C 1 -C 6 haloalkylthio, represents C 1 -C 6 haloalkylsulfinyl or C 1 -C 6 haloalkylsulfonyl, when n1 represents an integer of 2 or more, each R 2 may be the same as or different from each other.
R 4 is a hydrogen atom, a halogen atom, C 1 -C 6 alkyl, C 3 -C 6 cycloalkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 1 -C 6 haloalkyl, C 1 -C 6 alkoxy, C 1 -C 6 haloalkoxy, C 1 -C 6 alkylthio, C 1 -C 6 alkylsulfinyl, C 1 -C 6 alkylsulfonyl, C 1 -C 6 haloalkylthio, C 1 -C 6 haloalkylsulfinyl, C 1 -C 6 haloalkylsulfonyl, represents cyano, C 1 -C 6 alkoxycarbonyl, C 1 -C 6 alkylcarbonyl, a C 1 -C 6 alkylaminocarbonyl or di (C 1 -C 6 alkyl) aminocarbonyl,
D1-8, D1-15, D1-17, D1-22, D1-52 and D1-106 each represent a ring represented by the following structural formula;
X and R 3 together form a C 2 to C 4 alkylene chain or a C 2 to C 4 alkenylene chain, whereby the carbon atom to which X is bonded to the carbon atom to which R 3 is bonded and the bond of A 2 Together with the carbon atom to form a 6-8 membered ring, wherein the alkylene chain or alkenylene chain may contain an oxygen atom or a sulfur atom,
X 1 is C 1 -C 12 alkyl, (C 1 -C 12 ) alkyl optionally substituted with R 5 , —OH, —OR 6 , —SH, —S (O) r R 6 , —N ( R 8) R 9, -C ( O) R 7, -C (O) OH, -C (O) OR 6, -C (O) N (R 8) R 9, -C (S) N (R 8 ) R 9 , D2-32, D2-33, D2-34, D2-36, D2-37 or D2-38, and when p2 or p3 represents an integer of 2 or more, each X 1 is the same as each other Or may be different from each other,
X 1a represents a hydrogen atom, C 1 -C 12 alkyl, (C 1 -C 12 ) alkyl optionally substituted with R 5a or —C (O) R 7a ,
D2-32, D2-33, D2-34, D2-36, D2-37 and D2-38 each represent a ring represented by the following structural formula;
R 5 represents a halogen atom, —OH, —OR 11 , —SH, —S (O) r R 11 ,
R 5a represents a halogen atom, cyano, —OH, —OR 11a , —SH or —S (O) r R 11a ,
R 6 represents C 1 -C 6 alkyl or C 1 -C 6 haloalkyl,
R 7 represents a hydrogen atom, C 1 -C 6 alkyl or (C 1 -C 6 ) alkyl optionally substituted with R 14 ,
R 7a represents a hydrogen atom, C 1 -C 6 alkyl, —C (R 12a ) ═NOH or —C (R 12a ) = NOR 11a ,
R 8 and R 9 each independently represents a hydrogen atom, C 1 -C 6 alkyl or —C (O) R 12 ;
R 11 represents C 1 -C 6 alkyl or (C 1 -C 6 ) alkyl optionally substituted by R 14 ,
R 11a represents C 1 -C 6 alkyl or (C 1 -C 6 ) alkyl optionally substituted with R 14a ,
R 12 represents a hydrogen atom or C 1 -C 6 alkyl;
R 12a represents a hydrogen atom, C 1 -C 6 alkyl or (C 1 -C 6 ) alkyl optionally substituted with R 14a ,
R 14 is a halogen atom, C 3 -C 6 cycloalkyl, —OH, —OR 15 , —SH or —S (O) r R 15.
R 14a represents a halogen atom, C 3 -C 6 cycloalkyl, —OH, —OR 15a , —SH or —S (O) r R 15a ,
R 15 and R 15a each independently represent C 1 -C 6 alkyl;
X 2 represents a halogen atom, cyano, nitro, —OH, —SH, —NH 2 , C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 3 -C 8 cycloalkyl. Represent,
n1, p3 and t1 each independently represents an integer of 0 to 3,
p1 represents an integer of 0 to 1,
p2 represents an integer of 0 to 2,
t4 represents an integer of 0 to 4,
m1 and m2 each independently represent an integer of 0 or 1,
r represents an integer of 0-2. ] The pyrazole derivative represented by these, or its salt.
R1及びR4は、各々独立して水素原子、ハロゲン原子又はC1〜C6アルキルを表し、
R2は、ハロゲン原子又はC1〜C6アルキルを表す請求項1記載のピラゾール誘導体又はその塩。 A 1 represents -CR 1
R 1 and R 4 each independently represent a hydrogen atom, a halogen atom or C 1 -C 6 alkyl;
The pyrazole derivative or a salt thereof according to claim 1 , wherein R 2 represents a halogen atom or C 1 -C 6 alkyl.
Bは、B−1a、B−2a、B−3a、B−4a、B−5a乃至B−6aのいずれかで表される環を表し、
X1は、C1〜C6アルキル、R5によって任意に置換された(C1〜C6)アルキル、−S(O)rR6、−N(R8)R9、−C(O)OH、−C(O)OR6又はD2−33を表し、p3が2の整数を表すとき、各々のX1は互いに同一であっても又は互いに相異なってもよく、
X1aは、水素原子、R5aによって任意に置換された(C1〜C6)アルキル又は−C(O)R7aを表し、
R5は、−S(O)rR11を表し、
R5aは、ハロゲン原子、又は−S(O)rR11aを表し、
R6は、C1〜C6アルキルを表し、
R7aは、−C(R12a)=NOR11aを表し、
R8は、水素原子を表し、
R9は、−C(O)R12を表し、
R11、R11a及びR12は、各々独立してC1〜C6アルキルを表し、
R12aは、R14aによって任意に置換された(C1〜C6)アルキルを表し、
R14aは、−S(O)rR15aを表し、
R15aは、C1〜C6アルキルを表し、
n1及びt4は、0を表し、
p1は、0〜1の整数を表し、
p2は、1の整数を表し、
p3は、2の整数を表し、
rは、0〜2の整数を表す請求項2記載のピラゾール誘導体又はその塩。 R 1 and R 4 represent a hydrogen atom,
B represents a ring represented by any of B-1a, B-2a, B-3a, B-4a, B-5a to B-6a,
X 1 is C 1 -C 6 alkyl, (C 1 -C 6 ) alkyl optionally substituted by R 5 , —S (O) r R 6 , —N (R 8 ) R 9 , —C (O ) Represents OH, —C (O) OR 6 or D2-33, and p3 represents an integer of 2, each X 1 may be the same as or different from each other;
X 1a represents a hydrogen atom, (C 1 -C 6 ) alkyl or —C (O) R 7a optionally substituted with R 5a ,
R 5 represents —S (O) r R 11 ,
R 5a represents a halogen atom or —S (O) r R 11a ,
R 6 represents C 1 -C 6 alkyl,
R 7a represents -C (R 12a ) = NOR 11a ,
R 8 represents a hydrogen atom,
R 9 represents —C (O) R 12 ,
R 11 , R 11a and R 12 each independently represent C 1 -C 6 alkyl;
R 12a represents (C 1 -C 6 ) alkyl optionally substituted with R 14a ,
R 14a represents -S (O) r R 15a ;
R 15a represents C 1 -C 6 alkyl;
n1 and t4 represent 0;
p1 represents an integer of 0 to 1,
p2 represents an integer of 1,
p3 represents an integer of 2,
The pyrazole derivative or a salt thereof according to claim 2, wherein r represents an integer of 0 to 2.
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