Issue 16, 1990

Diastereoselective radical addition to derivatives of dehydroalanine and of dehydrolactic acid

Abstract

The cyclic methylene compounds (1)–(3) undergo diastereoselective free radical addition when treated with alkylmercury hydride or alkyl iodide/tributylstannane to give products useful for the enantioselective synthesis of α-amino and α-hydroxy acids.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1990, 1087-1088

Diastereoselective radical addition to derivatives of dehydroalanine and of dehydrolactic acid

A. L. J. Beckwith and C. L. L. Chai, J. Chem. Soc., Chem. Commun., 1990, 1087 DOI: 10.1039/C39900001087

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