Issue 4, 1975

Epoxidation of 3α,5-cyclo-5α-androst-6-en-17-one

Abstract

Treatment of 3α,5-cyclo-5α-androst-6-en-17-one with m-chloroperbenzoic acid affords 3β,7α-dihydroxyandrost-5-en-17-one, 6β,7α-dihydroxy-3α,5-cyclo-5α-androstan-17-one, their 3β- and 6β-m-chlorobenzoates, and the 6β-methoxy-7α-hydroxy-cyclo-steroid. The unstable 6α,7α-epoxy-3α,5-cyclo-5α-androstan-17-one was obtained by epoxidation in ether. A similar range of solvent-dependent produts was obtained in the cholestane series.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1975, 323-326

Epoxidation of 3α,5-cyclo-5α-androst-6-en-17-one

R. C. Cambie, P. W. Thomas and J. R. Hanson, J. Chem. Soc., Perkin Trans. 1, 1975, 323 DOI: 10.1039/P19750000323

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Spotlight

Advertisements