Reactions of 5α-hydroxy-steroids: the mechanism of backbone rearrangement in sulphuric acid–acetic acid–acetic anhydride-Reference-Cited by-同舟云学术

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Reactions of 5α-hydroxy-steroids: the mechanism of backbone rearrangement in sulphuric acid–acetic acid–acetic anhydride

Published:1974 Issue:4 Volume: Page:131-132
ISSN:0022-4936
Container-title:J. Chem. Soc., Chem. Commun.
language:en
Short-container-title:J. Chem. Soc., Chem. Commun.

Author:

Bathurst E. T. John,Coxon James M.

Publisher

Royal Society of Chemistry (RSC)

Subject

Molecular Medicine

Link

http://pubs.rsc.org/en/content/articlepdf/1974/C3/C39740000131

Cited by 8 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 stereospecific tandem Wagner-Meerwein rearrangement in the solvolysis of 19-mesyloxy steroids;The Journal of Organic Chemistry;1986-12

2. Rearrangement spinal du dimethyl-4,4 epoxy-6α,20α (5α)androstane avec le trichlorure de bore;Tetrahedron;1981-01

3. A trapped derivative in steroid backbone rearrangement;Tetrahedron Letters;1977-01

4. Regiospecific syn-elimination from the acid-catalysed reactions of 9-hydroxy-10-methyldecahydronaphthalenes;Journal of the Chemical Society, Chemical Communications;1976

5. Dehydration studies of 8a-Methyldecahydronaphthalen-4a-ols;Australian Journal of Chemistry;1976

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