Issue 20, 1977

β-Asymmetric induction in the reduction of n-alkylidenesulphinamides. Synthesis of optically active amines

Abstract

Asymmetric synthesis occurs in the reduction by LiAlH4 of optically active N-alkylidenesulphinamides; the sulphinamides thus obtained can be oxidized to optically active sulphonamides or cleaved to optically active amines of high optical purity.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1977, 723-724

β-Asymmetric induction in the reduction of n-alkylidenesulphinamides. Synthesis of optically active amines

M. Cinquini and F. Cozzi, J. Chem. Soc., Chem. Commun., 1977, 723 DOI: 10.1039/C39770000723

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