[go: up one dir, main page]

King et al., 1970 - Google Patents

Remarkable stereoselectivity in the hydrolysis of dioxolenium ions and orthoesters fused to anchored six-membered rings

King et al., 1970

View PDF
Document ID
2700204084494514455
Author
King J
Allbutt A
Publication year
Publication venue
Canadian Journal of Chemistry

External Links

Snippet

Hydrolysis of dioxolenium (acyloxonium) ions fused to anchored six-membered rings gives almost exclusively that hydroxyester in which the ester function is axial (and the hydroxyl group equatorial). With the exception of the orthoformate, a group of related orthoesters …
Continue reading at cdnsciencepub.com (PDF) (other versions)

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07JSTEROIDS
    • C07J71/00Steroids in which the cyclopenta(a)hydrophenanthrene skeleton is condensed with a heterocyclic ring
    • C07J71/0005Oxygen-containing hetero ring
    • C07J71/001Oxiranes
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D493/00Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system
    • C07D493/02Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system in which the condensed system contains two hetero rings
    • C07D493/04Ortho-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07JSTEROIDS
    • C07J71/00Steroids in which the cyclopenta(a)hydrophenanthrene skeleton is condensed with a heterocyclic ring
    • C07J71/0036Nitrogen-containing hetero ring
    • C07J71/0042Nitrogen only
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07JSTEROIDS
    • C07J5/00Normal steroids containing carbon, hydrogen, halogen or oxygen, substituted in position 17 beta by a chain of two carbon atoms, e.g. pregnane and substituted in position 21 by only one singly bound oxygen atom, i.e. only one oxygen bound to position 21 by a single bond
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07JSTEROIDS
    • C07J17/00Normal steroids containing carbon, hydrogen, halogen or oxygen, having an oxygen-containing hetero ring not condensed with the cyclopenta(a)hydrophenanthrene skeleton
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07JSTEROIDS
    • C07J75/00Processes for the preparation of steroids in general
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07JSTEROIDS
    • C07J13/00Normal steroids containing carbon, hydrogen, halogen or oxygen having a carbon-to-carbon double bond from or to position 17
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2103/00Systems containing at least three condensed rings
    • C07C2103/02Ortho- or ortho- and peri-condensed systems
    • C07C2103/04Ortho- or ortho- and peri-condensed systems containing three rings
    • C07C2103/06Ortho- or ortho- and peri-condensed systems containing three rings containing at least one ring with less than six ring members
    • C07C2103/10Ortho- or ortho- and peri-condensed systems containing three rings containing at least one ring with less than six ring members containing five-membered rings
    • C07C2103/12Ortho- or ortho- and peri-condensed systems containing three rings containing at least one ring with less than six ring members containing five-membered rings only one five-membered ring
    • C07C2103/16(Hydrogenated) benz[e]indenes
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07JSTEROIDS
    • C07J63/00Steroids in which the cyclopenta(a)hydrophenanthrene skeleton has been modified by expansion of only one ring by one or two atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D311/00Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings
    • C07D311/02Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings ortho- or peri-condensed with carbocyclic rings or ring systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07JSTEROIDS
    • C07J1/00Normal steroids containing carbon, hydrogen, halogen or oxygen, not substituted in position 17 beta by a carbon atom, e.g. estrane, androstane
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C69/00Esters of carboxylic acids; Esters of carbonic or haloformic acids
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D317/00Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms
    • C07D317/08Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3
    • C07D317/10Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 not condensed with other rings
    • C07D317/14Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 not condensed with other rings with substituted hydrocarbon radicals attached to ring carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D303/00Compounds containing three-membered rings having one oxygen atom as the only ring heteroatom
    • C07D303/02Compounds containing oxirane rings
    • C07D303/12Compounds containing oxirane rings with hydrocarbon radicals substituted by singly or doubly bound oxygen atoms

Similar Documents

Publication Publication Date Title
King et al. Remarkable stereoselectivity in the hydrolysis of dioxolenium ions and orthoesters fused to anchored six-membered rings
Kokke et al. Minor and Trace Sterols in Marine Invertebrates. XII. Occurrence of 24 (R+ S)‐isopropenylcholesterol, 24 (R+ S)‐methylcholesta‐5, 25‐dien‐3β‐ol, and 24 (R+ S)‐methylcholesta‐7, 25‐dien‐3β‐ol in the caribbean sponge, Verongia cauliformis
Bagli et al. Synthetic studies on C-19 oxygenated pregnanes
Barton et al. Biosynthesis of terpenes and steroids. Part V. The synthesis of ergosta-5, 7, 22, 24 (28)-tetraen-3β-ol, a biosynthetic precursor of ergosterol
Andre et al. Direct Introduction of Oxygen into the Steroid Nucleus. I. Studies on the Chromic Anhydride Oxidation of Dehydroisoandrosterone Acetate Dibromide1
Galbraith et al. Moretenol and other triterpenes from Ficus macrophylla Desf
Angyal et al. Glycol Fission in Rigid Systems. II. The Cholestane-3β, 6, 7-triols. Existence of a Cyclic Intermediate1
Burrows et al. Reassignment of configuration to the 22-hydroxycholesterols. Synthesis of (22S)-and (22R)-3H-cholesterols
US4193921A (en) Pregnane derivatives
Berti et al. Preparation and stereochemical characterization of the diastereoisomeric 1-phenyl-4-t-butylcyclohexene oxides and 1-phenyl-4-t-butylcyclohexane-1, 2-diols
ISHIGURO et al. Studies on steroids. LI. Stereoselective introduction of 22-and 24-hydroxyl function in the steroidal side chain
IIDA et al. Potential Bile Acid Metabolites. XV.: Synthesis of 4β-Hydroxylated Bile Acids; Unique Bile Acids in Human Fetal Bile
Anderson et al. Metabolic intermediates in the biological oxidation of lanosterol to eburicoic acid
Kingston et al. Marine natural products. Novel C 21 Δ 20 pregnanes from the sea raspberry (Gersemia rubiformis)
Loozen et al. Ring enlargement of geminal dibromocyclopropanes with silver tosylate. Approach to medium sized rings
BECKER et al. MOLECULAR REARRANGEMENTS IN THE STEROLS. X. THE REARRANGEMENTS OF EPICHOLESTERYL p-TOLUENESULFONATE AND THE CHEMISTRY OF SOME ISOMERIC CHOLESTEROLS
MIYAHARA et al. Structure of tokoronin
US2318105A (en) Hydrated acetylene derivatives of the cyclopentanopolyhydrophenanthrene series and process of preparing same
Pradhan et al. Studies on oxidation of triterpenoids: part vii. Transformation of oleanane and ursane skeletons to 11α, 12α-oxidotriterpenoids with hydrogen perox
KAWATA et al. A new product of cholesterol by metal-free autoxidation in aqueous dispersion
Hayakawa et al. Microbiological Transformation of Diosgenin1
Warnhoff et al. TREIBS'119° GLYCOL; TRANSANNULAR ATTACK AT THE TERTIARY CARBON OF A SECONDARY–TERTIARY EPOXIDE
Musumeci et al. The oxidation of Δ2, Δ2, 4 and Δ4, 6 steroids with RuO4
KITAGAWA et al. Saponin and sapogenol. XXII. Structure of spergulatriol, a new bisnorhopane-type genuine sapogenol of isoanhydrospergulatriol, from the root of Mollugo spergula L.
Cross et al. Steroids CCLXXX. biologically-active labile ethers v. substituted tetrahydropyran-2-yl ethers of 17β-hydroxy-2α-methyi,-5α-androstan-3-one