Issue 3, 1971

The tritylone protecting group: ether cleavage by Wolff–Kishner reduction

Abstract

Alcohols react readily with 9-phenyl-9-hydroxy-anthrone to form substituted trityl ethers which can be readily cleaved by a specific base-catalysed reaction, the Wolff–Kishner reduction.

Article information

Article type
Paper

J. Chem. Soc. D, 1971, 170-171

The tritylone protecting group: ether cleavage by Wolff–Kishner reduction

W. E. Barnett and L. L. Needham, J. Chem. Soc. D, 1971, 170 DOI: 10.1039/C29710000170

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