Issue 0, 1986

Functionalisation of saturated hydrocarbons. Part 6. Selective oxidation of steroids and related compounds

Abstract

The oxidation of a series of steroids by the Gif system gives, almost without exception, the 20-ketone as major isolated product. The side-chain cleavage is made more selective by modification of rings A or B. The oxidation of oleana-1,12-diene-3,11-dione has also been studied and the two principal products have been identified.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1986, 1797-1804

Functionalisation of saturated hydrocarbons. Part 6. Selective oxidation of steroids and related compounds

D. H. R. Barton, J. Boivin and C. H. Hill, J. Chem. Soc., Perkin Trans. 1, 1986, 1797 DOI: 10.1039/P19860001797

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