Issue 0, 1972

The aromatization of some 2α,3α-epoxy-5α-hydroxy-steroids

Abstract

2α,3α-Epoxy-5α-hydroxyandrostan-17-one and the corresponding 17β-acetate rearrange in hydrogen bromide-glacial acetic acid to form 4-methyloestra-1,3,5(10)-trien-17-one and the corresponding 17β-acetate. The related 6,17-diones afford 1-methyloestra-1,3,5(10)-triene-6,17-dione and the corresponding 17β-acetate.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1972, 1445-1447

The aromatization of some 2α,3α-epoxy-5α-hydroxy-steroids

J. R. Hanson and H. J. Shapter, J. Chem. Soc., Perkin Trans. 1, 1972, 1445 DOI: 10.1039/P19720001445

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