Biohydrogenation of unsaturated compounds by Saccharomyces cerevisiae. Part 2: (S)-(–)-Ethyl 4-hydroxy-3-methylbutanoate as a chiral synthon for the preparation of (25S)-26-hydroxycholesterol
- 1 January 1987
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Journal of the Chemical Society, Perkin Transactions 1
- No. 8,p. 1749-1752
- https://doi.org/10.1039/p19870001749
Abstract
(25S)-26-Hydroxycholesterol (1b) has been synthesized from stigmasterol (4a) and (S)-(–)-ethyl 4-hydroxy-3-methylbutanoate (2a), the latter having the necessary chirality for the synthesis of the steroidal side-chain.This publication has 5 references indexed in Scilit:
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