Synthesis of 25-hydroxycholesterol from 3β-hydroxyandrost-5-en-17-one. A method for stereospecific construction of a sterol side-chain
Author:
Publisher
Royal Society of Chemistry (RSC)
Subject
Molecular Medicine
Link
http://pubs.rsc.org/en/content/articlepdf/1975/C3/C39750000968
Cited by 25 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. A Concise Account of Various Approaches for Stereoselective Construction of the C-20(H) Stereogenic Center in Steroid Side Chain;Chemical Reviews;2014-05-20
2. 24(R), 25-Dihydroxycholesterol; An Attempt for Side-Chain Stereocontrol Via Iodolactonization;Bulletin des Sociétés Chimiques Belges;2010-09-01
3. Synthesis of 17-epi-Calcitriol from a Common Androstane Derivative, Involving the Ring B Photochemical Opening and the Intermediate Triene Ozonolysis;The Journal of Organic Chemistry;2005-09-10
4. Introduction of 20-keto side chains in 17-oxosteroids: Wittig-Horner-Emmons reactions of (E)-17-[(diethylphosphino)isocyanomethylene]-3-methoxyandrosta-3,5-diene;The Journal of Organic Chemistry;1993-07
5. Stereoselective Synthesis of Vitamin D;Stereoselective Synthesis;1992
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