The reaction of some substituted 2α,3α-epoxy-5α-hydroxyandrostanes with hydrogen bromide in acetic acid
Author:
Publisher
Royal Society of Chemistry (RSC)
Link
http://pubs.rsc.org/en/content/articlepdf/1991/P1/P19910002177
Reference11 articles.
1. The aromatization of some 2α,3α-epoxy-5α-hydroxy-steroids
2. A2H n.m.r. study of the dienol–benzene and related steroid aromatization reactions
3. D. N. Kirk and M. P.Hartshorn, Steroid Reaction Mechanisms, Elsevier, Amsterdam, 1968.
4. Syntheses of 2α- and 2β-deuterio-testosterones and -androst-4-ene-3,17-diones
5. An unusual oxidation of some 5α-hydroxyandrost-2-enes
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1. Ionic Liquid-Promoted Wagner–Meerwein Rearrangement of 16α,17α-Epoxyandrostanes and 16α,17α-Epoxyestranes;The Journal of Organic Chemistry;2011-07-05
2. ChemInform Abstract: The Reaction of Some Substituted 2α,3α-Epoxy-5α- hydroxyandrostanes with Hydrogen Bromide in Acetic Acid.;ChemInform;2010-08-22
3. The General Dienol: Benzene Rearrangement of Ring a of the Steroids;Journal of Chemical Research;2005-03
4. The Formation and Structure of Some Androstane 4- and 6-Ketones;Journal of Chemical Research;1999-04
5. Steroid reactions and partial synthesis;Natural Product Reports;1993
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