An unusual stereochemical outcome of a peroxyacid epoxidation reaction: stereospecific synthesis of (4'R)-spiro[oxirane-2,4'-5'.alpha.-cholestan-3'.beta.-ol]
- 1 May 1988
- journal article
- research article
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 53 (10) , 2180-2183
- https://doi.org/10.1021/jo00245a010
Abstract
No abstract availableThis publication has 2 references indexed in Scilit:
- Sterols in marine invertebrates. 22. Isolation and structure elucidation of conicasterol and theonellasterol, two new 4-methylene sterols from the Red Sea sponges Theonella conica and Theonella swinhoeiThe Journal of Organic Chemistry, 1981
- Synthesis of 4-spiro[cyclopropanecholestan-3.beta.-ol]The Journal of Organic Chemistry, 1977