Issue 6, 1975

Stereospecificity of oxidation at C-19 in oestrogen biosynthesis

Abstract

A method has been devised for determining the configuration of samples of 19-acetoxy-Δ5-androgens stereospecifically labelled at C-19; with the help of such samples it is shown that in the biological conversion of 19-hydroxyandrogens into oestrogen the pro-R hydrogen atom from C-19 is removed as a proton and the pro-S hydrogen atom is incor porated into formic acid.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1975, 185-186

Stereospecificity of oxidation at C-19 in oestrogen biosynthesis

D. Arigoni, R. Battaglia, M. Akhtar and T. Smith, J. Chem. Soc., Chem. Commun., 1975, 185 DOI: 10.1039/C39750000185

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