JPH09501685A - 抗有害生物剤（殺菌・殺カビ剤）としての２−オキシイミノ−２−ピリジル−酢酸誘導体 - Google Patents

抗有害生物剤（殺菌・殺カビ剤）としての２−オキシイミノ−２−ピリジル−酢酸誘導体

Info

Publication number: JPH09501685A
Authority: JP; Japan
Prior art keywords: formula; branched; carbon atoms; chain; straight
Prior art date: 1993-08-24
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.): Pending

Application number

JP7507317A

Other languages

English (en)

Japanese (ja)

Inventor

クーント，デイートマー

ガイアー，ヘルベルト

ゲルデス，ペーター

ドウツツマン，シユテフアン

デーネ，ハインツ−ビルヘルム

ヘンスラー，ゲルト

Original Assignee

バイエル・アクチエンゲゼルシヤフト

Priority date (The priority date 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 date listed.)

1993-08-24

Filing date

1994-08-11

Publication date

1997-02-18

1994-08-11 Application filed by バイエル・アクチエンゲゼルシヤフト filed Critical バイエル・アクチエンゲゼルシヤフト

1997-02-18 Publication of JPH09501685A publication Critical patent/JPH09501685A/ja

Status Pending legal-status Critical Current

Links

239000003795 chemical substances by application Substances 0.000 title claims abstract description 13
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238000004519 manufacturing process Methods 0.000 claims abstract description 15
241000607479 Yersinia pestis Species 0.000 claims abstract description 6
150000001875 compounds Chemical class 0.000 claims description 170
-1 hydroxyimino Chemical group 0.000 claims description 147
125000004432 carbon atom Chemical group C* 0.000 claims description 126
125000000217 alkyl group Chemical group 0.000 claims description 70
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238000006243 chemical reaction Methods 0.000 claims description 43
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125000001424 substituent group Chemical group 0.000 claims description 34
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 31
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 27
229910052799 carbon Inorganic materials 0.000 claims description 27
239000000203 mixture Substances 0.000 claims description 27
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QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 22
239000001301 oxygen Substances 0.000 claims description 22
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238000002360 preparation method Methods 0.000 claims description 21
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239000012038 nucleophile Substances 0.000 claims description 6
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239000012433 hydrogen halide Substances 0.000 claims description 4
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125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 4
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125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 4
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GUJOJGAPFQRJSV-UHFFFAOYSA-N dialuminum;dioxosilane;oxygen(2-);hydrate Chemical compound O.[O-2].[O-2].[O-2].[Al+3].[Al+3].O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O GUJOJGAPFQRJSV-UHFFFAOYSA-N 0.000 description 1
125000003963 dichloro group Chemical group Cl* 0.000 description 1
235000014113 dietary fatty acids Nutrition 0.000 description 1
239000010459 dolomite Substances 0.000 description 1
229910000514 dolomite Inorganic materials 0.000 description 1
229940079593 drug Drugs 0.000 description 1
239000003814 drug Substances 0.000 description 1
238000010410 dusting Methods 0.000 description 1
238000004945 emulsification Methods 0.000 description 1
239000000839 emulsion Substances 0.000 description 1
239000008393 encapsulating agent Substances 0.000 description 1
125000004705 ethylthio group Chemical group C(C)S* 0.000 description 1
239000000194 fatty acid Substances 0.000 description 1
229930195729 fatty acid Natural products 0.000 description 1
150000002191 fatty alcohols Chemical class 0.000 description 1
239000003337 fertilizer Substances 0.000 description 1
125000004216 fluoromethyl group Chemical group [H]C([H])(F)* 0.000 description 1
239000004088 foaming agent Substances 0.000 description 1
235000012055 fruits and vegetables Nutrition 0.000 description 1
230000002538 fungal effect Effects 0.000 description 1
150000002334 glycols Chemical class 0.000 description 1
150000008282 halocarbons Chemical class 0.000 description 1
IXCSERBJSXMMFS-UHFFFAOYSA-N hcl hcl Chemical compound Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 1
BICAGYDGRXJYGD-UHFFFAOYSA-N hydrobromide;hydrochloride Chemical compound Cl.Br BICAGYDGRXJYGD-UHFFFAOYSA-N 0.000 description 1
229960000443 hydrochloric acid Drugs 0.000 description 1
230000007062 hydrolysis Effects 0.000 description 1
238000006460 hydrolysis reaction Methods 0.000 description 1
208000015181 infectious disease Diseases 0.000 description 1
239000001023 inorganic pigment Substances 0.000 description 1
239000002917 insecticide Substances 0.000 description 1
239000000543 intermediate Substances 0.000 description 1
239000011630 iodine Chemical group 0.000 description 1
229910052740 iodine Inorganic materials 0.000 description 1
229910052742 iron Inorganic materials 0.000 description 1
238000002955 isolation Methods 0.000 description 1
NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
239000004816 latex Substances 0.000 description 1
229920000126 latex Polymers 0.000 description 1
239000000787 lecithin Substances 0.000 description 1
235000010445 lecithin Nutrition 0.000 description 1
229940067606 lecithin Drugs 0.000 description 1
STJUJXONQFLCOP-UHFFFAOYSA-L lithium;sodium;carbonate Chemical compound [Li+].[Na+].[O-]C([O-])=O STJUJXONQFLCOP-UHFFFAOYSA-L 0.000 description 1
239000006166 lysate Substances 0.000 description 1
WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
239000004579 marble Substances 0.000 description 1
229940098779 methanesulfonic acid Drugs 0.000 description 1
TWUDAGNOZGNEIT-UHFFFAOYSA-N methyl 2-(2-chloropyridin-3-yl)-2-methoxyiminoacetate Chemical compound COC(C(=NOC)C=1C(=NC=CC=1)Cl)=O TWUDAGNOZGNEIT-UHFFFAOYSA-N 0.000 description 1
ORZVCJSOSLXCOE-UHFFFAOYSA-N methyl 2-(2-chloropyridin-3-yl)-2-oxoacetate Chemical compound COC(=O)C(=O)C1=CC=CN=C1Cl ORZVCJSOSLXCOE-UHFFFAOYSA-N 0.000 description 1
229920000609 methyl cellulose Polymers 0.000 description 1
BLLFVUPNHCTMSV-UHFFFAOYSA-N methyl nitrite Chemical compound CON=O BLLFVUPNHCTMSV-UHFFFAOYSA-N 0.000 description 1
239000001923 methylcellulose Substances 0.000 description 1
125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 1
MHQIMVYNMHGQSF-UHFFFAOYSA-N methylphosphanium;bromide Chemical compound [Br-].[PH3+]C MHQIMVYNMHGQSF-UHFFFAOYSA-N 0.000 description 1
125000004170 methylsulfonyl group Chemical group [H]C([H])([H])S(*)(=O)=O 0.000 description 1
XKBGEWXEAPTVCK-UHFFFAOYSA-M methyltrioctylammonium chloride Chemical compound [Cl-].CCCCCCCC[N+](C)(CCCCCCCC)CCCCCCCC XKBGEWXEAPTVCK-UHFFFAOYSA-M 0.000 description 1
230000003641 microbiacidal effect Effects 0.000 description 1
235000010446 mineral oil Nutrition 0.000 description 1
150000007522 mineralic acids Chemical class 0.000 description 1
229910052750 molybdenum Inorganic materials 0.000 description 1
239000011733 molybdenum Substances 0.000 description 1
229910052901 montmorillonite Inorganic materials 0.000 description 1
MLACQEBQGUBHKX-UHFFFAOYSA-N n,n-dimethylpiperidin-1-amine Chemical compound CN(C)N1CCCCC1 MLACQEBQGUBHKX-UHFFFAOYSA-N 0.000 description 1
SYSQUGFVNFXIIT-UHFFFAOYSA-N n-[4-(1,3-benzoxazol-2-yl)phenyl]-4-nitrobenzenesulfonamide Chemical class C1=CC([N+](=O)[O-])=CC=C1S(=O)(=O)NC1=CC=C(C=2OC3=CC=CC=C3N=2)C=C1 SYSQUGFVNFXIIT-UHFFFAOYSA-N 0.000 description 1
229940042880 natural phospholipid Drugs 0.000 description 1
229920005615 natural polymer Polymers 0.000 description 1
JCXJVPUVTGWSNB-UHFFFAOYSA-N nitrogen dioxide Inorganic materials O=[N]=O JCXJVPUVTGWSNB-UHFFFAOYSA-N 0.000 description 1
VPCDQGACGWYTMC-UHFFFAOYSA-N nitrosyl chloride Chemical compound ClN=O VPCDQGACGWYTMC-UHFFFAOYSA-N 0.000 description 1
235000019392 nitrosyl chloride Nutrition 0.000 description 1
235000015097 nutrients Nutrition 0.000 description 1
238000005580 one pot reaction Methods 0.000 description 1
150000007524 organic acids Chemical class 0.000 description 1
235000005985 organic acids Nutrition 0.000 description 1
239000007800 oxidant agent Substances 0.000 description 1
150000002923 oximes Chemical class 0.000 description 1
125000005646 oximino group Chemical group 0.000 description 1
229910052625 palygorskite Inorganic materials 0.000 description 1
239000012188 paraffin wax Substances 0.000 description 1
239000003444 phase transfer catalyst Substances 0.000 description 1
150000003904 phospholipids Chemical class 0.000 description 1
239000001007 phthalocyanine dye Substances 0.000 description 1
239000002798 polar solvent Substances 0.000 description 1
229940098458 powder spray Drugs 0.000 description 1
239000001294 propane Substances 0.000 description 1
239000003380 propellant Substances 0.000 description 1
239000011814 protection agent Substances 0.000 description 1
239000008262 pumice Substances 0.000 description 1
208000029561 pustule Diseases 0.000 description 1
238000001953 recrystallisation Methods 0.000 description 1
235000009566 rice Nutrition 0.000 description 1
239000011435 rock Substances 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
229910052624 sepiolite Inorganic materials 0.000 description 1
235000019355 sepiolite Nutrition 0.000 description 1
239000000741 silica gel Substances 0.000 description 1
229910002027 silica gel Inorganic materials 0.000 description 1
150000004760 silicates Chemical class 0.000 description 1
239000000377 silicon dioxide Substances 0.000 description 1
ODZPKZBBUMBTMG-UHFFFAOYSA-N sodium amide Chemical compound [NH2-].[Na+] ODZPKZBBUMBTMG-UHFFFAOYSA-N 0.000 description 1
PGSZYKMIHRQVPD-UHFFFAOYSA-M sodium;2-hydroxy-5-methylbenzoate Chemical compound [Na+].CC1=CC=C(O)C(C([O-])=O)=C1 PGSZYKMIHRQVPD-UHFFFAOYSA-M 0.000 description 1
238000003756 stirring Methods 0.000 description 1
239000004575 stone Substances 0.000 description 1
229940032330 sulfuric acid Drugs 0.000 description 1
238000003786 synthesis reaction Methods 0.000 description 1
229920001059 synthetic polymer Polymers 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
IOGXOCVLYRDXLW-UHFFFAOYSA-N tert-butyl nitrite Chemical compound CC(C)(C)ON=O IOGXOCVLYRDXLW-UHFFFAOYSA-N 0.000 description 1
JRMUNVKIHCOMHV-UHFFFAOYSA-M tetrabutylammonium bromide Chemical compound [Br-].CCCC[N+](CCCC)(CCCC)CCCC JRMUNVKIHCOMHV-UHFFFAOYSA-M 0.000 description 1
DPKBAXPHAYBPRL-UHFFFAOYSA-M tetrabutylazanium;iodide Chemical compound [I-].CCCC[N+](CCCC)(CCCC)CCCC DPKBAXPHAYBPRL-UHFFFAOYSA-M 0.000 description 1
OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
125000003652 trifluoroethoxy group Chemical group FC(CO*)(F)F 0.000 description 1
235000015112 vegetable and seed oil Nutrition 0.000 description 1
239000008158 vegetable oil Substances 0.000 description 1
235000021419 vinegar Nutrition 0.000 description 1
239000002699 waste material Substances 0.000 description 1
239000011701 zinc Substances 0.000 description 1
229910052725 zinc Inorganic materials 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/62—Oxygen or sulfur atoms
- C07D213/63—One oxygen atom
- C07D213/64—One oxygen atom attached in position 2 or 6
- C07D213/643—2-Phenoxypyridines; Derivatives thereof
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
- A01N43/40—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/61—Halogen atoms or nitro radicals

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Life Sciences & Earth Sciences (AREA)
Agronomy & Crop Science (AREA)
Pest Control & Pesticides (AREA)
Plant Pathology (AREA)
Health & Medical Sciences (AREA)
Engineering & Computer Science (AREA)
Dentistry (AREA)
General Health & Medical Sciences (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Environmental Sciences (AREA)
Pyridine Compounds (AREA)
Plural Heterocyclic Compounds (AREA)

JP7507317A 1993-08-24 1994-08-11 抗有害生物剤（殺菌・殺カビ剤）としての２−オキシイミノ−２−ピリジル−酢酸誘導体 Pending JPH09501685A (ja)

Applications Claiming Priority (3)

Application Number	Priority Date	Filing Date	Title
DE19934328385 DE4328385A1 (de)	1993-08-24	1993-08-24	2-Oximino-2-pyridyl-essigsäurederivate
DE4328385.3		1993-08-24
PCT/EP1994/002689 WO1995006033A1 (fr)	1993-08-24	1994-08-11	Derives d'acide 2-oximino-2-pyridylacetique utilises comme agents de lutte contre les parasites (fongicides)

Publications (1)

Publication Number	Publication Date
JPH09501685A true JPH09501685A (ja)	1997-02-18

Family

ID=6495856

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP7507317A Pending JPH09501685A (ja)	1993-08-24	1994-08-11	抗有害生物剤（殺菌・殺カビ剤）としての２−オキシイミノ−２−ピリジル−酢酸誘導体

Country Status (6)

Country	Link
EP (1)	EP0715621A1 (fr)
JP (1)	JPH09501685A (fr)
CN (1)	CN1133036A (fr)
AU (1)	AU7653094A (fr)
DE (1)	DE4328385A1 (fr)
WO (1)	WO1995006033A1 (fr)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
GB9412672D0 (en) *	1994-06-23	1994-08-10	Celltech Ltd	Chemical compounds
WO1998012179A1 (fr) *	1996-09-18	1998-03-26	Basf Aktiengesellschaft	Derives de pyridine, leur procede de preparation et leur utilisation pour lutter contre les parasites animaux et les champignons nuisibles
DE19804486A1 (de) *	1998-02-05	1999-08-12	Basf Ag	2-(Pyrazolyloxy)-pyridin-3-ylessigsäure- Derivate, sie enthaltende Mittel und ihr

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE3904931A1 (de) *	1989-02-17	1990-08-23	Bayer Ag	Pyridyl-substituierte acrylsaeureester
GB9018408D0 (en) *	1990-08-22	1990-10-03	Ici Plc	Fungicides
DE4030038A1 (de) *	1990-09-22	1992-03-26	Basf Ag	Ortho-substituierte phenylessigsaeureamide
DK0569384T4 (da) *	1991-01-30	2000-12-04	Zeneca Ltd	Fungicider
JPH05201980A (ja) *	1992-01-30	1993-08-10	Mitsubishi Kasei Corp	メトキシイミノ酢酸誘導体およびこれを有効成分とする農園芸用殺菌剤

1993
- 1993-08-24 DE DE19934328385 patent/DE4328385A1/de not_active Withdrawn
1994
- 1994-08-11 WO PCT/EP1994/002689 patent/WO1995006033A1/fr not_active Application Discontinuation
- 1994-08-11 JP JP7507317A patent/JPH09501685A/ja active Pending
- 1994-08-11 CN CN 94193763 patent/CN1133036A/zh active Pending
- 1994-08-11 AU AU76530/94A patent/AU7653094A/en not_active Abandoned
- 1994-08-11 EP EP94926831A patent/EP0715621A1/fr not_active Withdrawn

Also Published As

Publication number	Publication date
DE4328385A1 (de)	1995-03-02
CN1133036A (zh)	1996-10-09
AU7653094A (en)	1995-03-21
WO1995006033A1 (fr)	1995-03-02
EP0715621A1 (fr)	1996-06-12

Publication	Publication Date	Title
JP3472245B2 (ja)	2003-12-02	カーバメート誘導体及び農園芸用殺菌剤
JPH10507998A (ja)	1998-08-04	置換アザジオキサシクロアルケン及びその殺菌・殺カビ剤としての使用
PL183585B1 (pl)	2002-06-28	Amidy kwasu alkoksyiminooctowego, środek do zwalczania szkodników, sposób zwalczania szkodników i sposób wytwarzania amidów kwasu alkoksyiminooctowego
CZ176196A3 (en)	1997-03-12	Derivatives of arylacetic acid, process of their preparation and their use as fungicides
JPH11500103A (ja)	1999-01-06	置換されたカルボン酸アミド及びその殺菌・殺カビ剤としての使用
JPH05112541A (ja)	1993-05-07	トリアジニル置換アクリル酸エステル
JPH072750A (ja)	1995-01-06	２−オキシイミノ−２−フエニル−アセトアミド
JPH04230252A (ja)	1992-08-19	２−メトキシイミノカルボン酸エステル
JPH06199795A (ja)	1994-07-19	ピリジロキシ−アクリル酸エステル
JPH11505814A (ja)	1999-05-25	ピリジル−チアゾールおよび微生物による感染に対して植物を保護するためのそれらの使用
JPH09505315A (ja)	1997-05-27	３−メトキシ−２−フエニル−アクリル酸メチル
JPH09501685A (ja)	1997-02-18	抗有害生物剤（殺菌・殺カビ剤）としての２−オキシイミノ−２−ピリジル−酢酸誘導体
EP0617014B1 (fr)	1997-10-29	Composés d'oximéthers, procédé de leur préparation et fongicides les contenant
JPH06329649A (ja)	1994-11-29	オキサ（チア）−ジアゾル−オキシ−フエニルアクリレート
JPH06220043A (ja)	1994-08-09	置換されたチオフエンカルボキシアミド
JPH11509218A (ja)	1999-08-17	オキシムエーテル及びアクリル酸誘導体並びにその殺菌・殺カビ剤としての使用
JP3535556B2 (ja)	2004-06-07	シクロアルキルカルボキシアニリド
JPH10512868A (ja)	1998-12-08	置換アリールアザジオキサシクロアルケン殺菌・殺カビ剤
JPH10505075A (ja)	1998-05-19	イミジン酸誘導体及びその有害生物防除剤としての使用
JPH01249753A (ja)	1989-10-05	複素環で置換されたアクリル酸エステル
JP3162530B2 (ja)	2001-05-08	置換されたピリジルピリミジン
JPH08512295A (ja)	1996-12-24	２−オキシイミノ−２−チエニル−酢酸誘導体
EP0608862A1 (fr)	1994-08-03	Dérivés estérifiés de l'acide 6-chloro-2-(4,6-diméthoxypyrimidin-2-yl)-oxybenzoique, procédés pour leur production et méthode pour leur application comme herbicides
JP3083032B2 (ja)	2000-09-04	４−アミノピリミジン誘導体、その製法及び有害生物防除剤
JPH11503134A (ja)	1999-03-23	ヒドラゾノ酢酸アミド及びその有害生物防除剤としての使用