BIOMAT Database Logo BIOMAT Database Logo

Stereospecific synthesis of the four 20,22-epoxycholesterols and of (Z)-20(22)-dehydrocholesterol. 1976

C Byon, and M Gut

UI MeSH Term Description Entries
D002784 Cholesterol The principal sterol of all higher animals, distributed in body tissues, especially the brain and spinal cord, and in animal fats and oils. Epicholesterol
D004852 Epoxy Compounds Organic compounds that include a cyclic ether with three ring atoms in their structure. They are commonly used as precursors for POLYMERS such as EPOXY RESINS. Epoxide,Epoxides,Epoxy Compound,Oxiranes,Compound, Epoxy,Compounds, Epoxy
D013237 Stereoisomerism The phenomenon whereby compounds whose molecules have the same number and kind of atoms and the same atomic arrangement, but differ in their spatial relationships. (From McGraw-Hill Dictionary of Scientific and Technical Terms, 5th ed) Molecular Stereochemistry,Stereoisomers,Stereochemistry, Molecular,Stereoisomer

Related Publications

C Byon, and M Gut
Stereospecific synthesis of (20S,22R)-17 ,20,22-trihydroxycholesterol and (20S,22S)-17 ,20,22-trihydroxycholesterol.
June 1972, The Journal of organic chemistry,
C Byon, and M Gut
(Z)-17(20)-dehydrocholesterol. A new sterol with C-21 and C-22 spatially fixed.
October 1976, The Journal of organic chemistry,
C Byon, and M Gut
Studies on steroids. Part 37. Synthesis of the four stereoisomers of 20,22-epoxycholesterol.
January 1976, Journal of the Chemical Society. Perkin transactions 1,
C Byon, and M Gut
The synthesis and stereochemistry of (22R)-20 alpha, 22- and (22S)-20 alpha, 22-dihydroxycholesterol.
April 1970, Steroids,
C Byon, and M Gut
ISOLATION OF 22-DEHYDROCHOLESTEROL FROM SCALLOP.
September 1964, Canadian journal of biochemistry,
C Byon, and M Gut
Stereospecific synthesis of (22R)-22-hydroxycholesterol and (22R)-cholesta-5,24-diene-3beta,22-diol.
January 1974, Journal of the Chemical Society. Perkin transactions 1,
C Byon, and M Gut
Stereospecific synthesis of (Z,Z)-3,5-tetradecadienoic acid, a component ofAttagenus elongatulus (Casey) pheromone.
January 1987, Journal of chemical ecology,
C Byon, and M Gut
Steroidal alkaloids. CLXI. Stereospecific synthesis of (22R)-and (22S)-22-aminocholesterol.
April 1974, The Journal of organic chemistry,
C Byon, and M Gut
Harnessing the Peterson Reaction for the Stereospecific Synthesis of Z-Vinyl Ethers.
January 2024, Chemistry (Weinheim an der Bergstrasse, Germany),
C Byon, and M Gut
Rearrangement of propargylic esters: metal-based stereospecific synthesis of (E)- and (Z)-knoevenagel derivatives.
June 2007, Journal of the American Chemical Society,
Copied contents to your clipboard!