Issue 17, 1980

Asymmetric reduction with L-proline amide derivatives of 1,4-dihydronicotinamide

Abstract

The magnesium perchlorate-, zinc chloride-, and cobalt chloride-catalysed asymmetric reduction of ethyl benzoylformate with 1,4-dihydronicotinamides carrying an L-proline amide in the 3-carbamoyl side-chain afforded R-mandelate, the asymmetric yields being greatly affected by the catalyst metal species (5–83%).

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1980, 815-817

Asymmetric reduction with L-proline amide derivatives of 1,4-dihydronicotinamide

N. Baba, J. Oda and Y. Inouye, J. Chem. Soc., Chem. Commun., 1980, 815 DOI: 10.1039/C39800000815

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