Issue 16, 2009

Diastereoselective Ritter reactions of chiral secondary benzylicalcohols

Abstract

An acid-catalysed Ritter reaction of chiral secondary benzylicalcohols enables diastereoselective access to chiral amides, which represent inter alia valuable intermediates for the synthesis of chiral 1,2-diamines and β-amino acids.

Graphical abstract: Diastereoselective Ritter reactions of chiral secondary benzylicalcohols

Supplementary files

Article information

Article type
Communication
Submitted
29 Jan 2009
Accepted
27 Feb 2009
First published
17 Mar 2009

Chem. Commun., 2009, 2130-2132

Diastereoselective Ritter reactions of chiral secondary benzylicalcohols

P. Rubenbauer and T. Bach, Chem. Commun., 2009, 2130 DOI: 10.1039/B901937E

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.

Social activity

Spotlight

Advertisements