Stereochemical effects in cyclopropane ring openings: synthesis and isomerization of petrosterol and all three of its trans cyclopropane diastereomers
- 1 September 1984
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 106 (19) , 5613-5622
- https://doi.org/10.1021/ja00331a035
Abstract
No abstract availableThis publication has 6 references indexed in Scilit:
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- Stereochemical Aspects of Acid‐Catalyzed Cyclopropane Ring‐Opening Reactions. A Stereospecific Pathway to Crinosterol and BrassicasterolHelvetica Chimica Acta, 1982
- Minor and trace sterols in marine invertebrates XVII. 1 (24R)-24,26-dimethylcholesta-5,26-dien-3β-01, a new sterol from the sponge Petrosia ficiformisSteroids, 1980
- Minor and trace sterols in marine invertebrates. 8. Isolation, structure elucidation, and partial synthesis of two novel sterols - stelliferasterol and isostelliferasterolJournal of the American Chemical Society, 1978