Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/22275
Title: Temperature controlled stereospecific epoxidation of 5-adrosten-3β, 17β-diol diacetate. Preparation of 6α-and 6β-substituted androstane derivatives
Authors: Srivastava, Brijesh Kumar
Kumar, Atul
Dwivedy, I
Ray, Suprabhat
Issue Date: May-2001
Publisher: NISCAIR-CSIR, India
Abstract: Reaction of 5-adrosten-3β, 17β-diol diacetate with m-chloroperbenzoic acid at different temperatures and pH in a biphasic system with NaHCO3 as a phase transfer catalyst yields corresponding 5α, 6α- and 5β, 6β-epoxides, which could be separated by column chromatography. Exclusive formation of 5a, 6a-epoxide could be obtained at a low temperature (-20°C). Epoxides on treatment with different amines lead to stereospecific opening, the amino substituent entering from the opposite side at C-6.
Page(s): 410-413
ISSN: 0975-0983(Online); 0376-4699(Print)
Appears in Collections:IJC-B Vol.40B(05) [May 2001]

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