Issue 15, 1994

A simple and efficient way to substituted 3-halogenopyruvamides from substituted α-carbamoyl-α-cyanooxiranes

Abstract

Regioselective ring opening of the readily accessible α-carbamoyl-α-cyanooxiranes with hydrogen halides gives β-halogeno-α-cyanohydrins which on being decyanated give, quantitatively, the corresponding substituted 3-halogenopyruvamides.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1994, 2045-2046

A simple and efficient way to substituted 3-halogenopyruvamides from substituted α-carbamoyl-α-cyanooxiranes

A. M. Maréchal, J. Pavc, A. Robert and P. Le Grel, J. Chem. Soc., Perkin Trans. 1, 1994, 2045 DOI: 10.1039/P19940002045

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