Issue 0, 1967

6-Phenylazocholestane derivatives: reassignment of the structures of products from phenylhydrazine and ozonised cholesterol derivatives

Abstract

The reaction of phenylhydrazine with ozonised cholesteryl acetate has been reported to yield a product in which ring B is expanded to an eight-membered ring. This structure is shown to be incorrect, the true structure being 3β-acetoxy-6α-phenylazocholestan-5α-ol. Comparisons are made with related reactions in the carbohydrate field.

Article information

Article type
Paper

J. Chem. Soc. C, 1967, 1703-1706

6-Phenylazocholestane derivatives: reassignment of the structures of products from phenylhydrazine and ozonised cholesterol derivatives

J. Buckingham, G. J. F. Chittenden and R. D. Guthrie, J. Chem. Soc. C, 1967, 1703 DOI: 10.1039/J39670001703

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