An epoxidation cis to two allylic benzoyloxy-groups
- 1 January 1981
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Journal of the Chemical Society, Perkin Transactions 1
- No. 2,p. 401-402
- https://doi.org/10.1039/p19810000401
Abstract
Direct epoxidation of tri-O-benzoylcyclopentene-3,5/4-triol proceeds in the same stereochemical sense as that of the parent triol, which yields 1,2-anhydrocyclopentane-1,2,3,5/4-pentol.This publication has 1 reference indexed in Scilit:
- External yeast β-fructosidase: Stereospecific labeling by [3H]conduritol-B-epoxide and isolation of labeled peptides from the active siteBiochimica et Biophysica Acta (BBA) - Enzymology, 1977