Issue 0, 1972

Brominative cleavage of α-ketols

Abstract

Bromination of some α-ketols resulted in cleavage of the carbonyl–carbinol bond; 1-hydroxy-1,1 -diphenylacetone, for example, gave benzophenone. Bromination of diphenyl-substituted tertiary alcohols does not cause degradation and the products are bromohydrins and/or substituted alkenes.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1972, 1875-1876

Brominative cleavage of α-ketols

J. A. Donnelly and R. O'Donnell, J. Chem. Soc., Perkin Trans. 1, 1972, 1875 DOI: 10.1039/P19720001875

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