Stereocontrolled synthesis of steroid side chain; stereoselective syntheses of cholesterol and 25-hydroxycholesterol
- 1 January 1982
- journal article
- research article
- Published by Elsevier in Tetrahedron Letters
- Vol. 23 (45) , 4709-4712
- https://doi.org/10.1016/s0040-4039(00)85693-2
Abstract
No abstract availableThis publication has 15 references indexed in Scilit:
- A new synthesis of 25-hydroxycholesterolTetrahedron Letters, 1981
- Stereoselective synthesis of (25S)-25-hydroxyvitamin D3 26,23-lactoneTetrahedron Letters, 1981
- Simple synthesis of de-AB-cholesta-8(14),22-dien-9-one by highly stereoselective double Michael addition involving alkenylcopper-phosphine complex, vinyl ketone, and 2-methyl-2-cyclopentenone followed by Claisen rearrangement and rhodium-promoted decarbonylationJournal of the American Chemical Society, 1981
- Stereoselective synthesis of steroid side chains: a route to de-AB-cholestan-9-oneJournal of the American Chemical Society, 1981
- New stereospecific approach to steroid side chains: conversion of dehydroepiandrosterone to cholesterol, isocholesterol, and their 15.beta.-hydroxy derivativesJournal of the American Chemical Society, 1981
- C-20 Stereospecific introduction of a steroid side chainJournal of the American Chemical Society, 1981
- Stereoselective synthesis and structure proof of a metabolite of vitamin D3, (23S,25R)-25-hydroxyvitamin D3 26,23-lactone (calcidiol lactone).CHEMICAL & PHARMACEUTICAL BULLETIN, 1981
- Stereocontrolled synthesis of steroidal side chainsJournal of the American Chemical Society, 1981
- Stereocontrolled synthesis of a steroid side chainThe Journal of Organic Chemistry, 1981
- Facile, stereoselective synthesis of (24R)-24,25-dihydroxyvitamin D3 using D-glyceric acid as a chiral synthonTetrahedron Letters, 1980