Issue 2, 2014

Asymmetric organocatalysis mediated by primary amines derived from cinchona alkaloids: recent advances

Abstract

Primary amine catalysts derived from cinchona alkaloids have emerged as readily available, highly versatile and extremely powerful catalysts in asymmetric synthesis. In particular, they exhibit superior catalytic efficacy for successfully tackling major challenges in a variety of sterically hindered carbonyl compounds, which traditional approaches have not been able to address. This review aims to once again draw attention to this relatively underutilised process by highlighting the recent developments in the application of cinchona-based primary amine catalysts in asymmetric organocatalytic reactions.

Graphical abstract: Asymmetric organocatalysis mediated by primary amines derived from cinchona alkaloids: recent advances

Article information

Article type
Minireview
Submitted
29 Sep 2013
Accepted
27 Oct 2013
First published
29 Oct 2013

Catal. Sci. Technol., 2014,4, 311-320

Asymmetric organocatalysis mediated by primary amines derived from cinchona alkaloids: recent advances

J. Duan and P. Li, Catal. Sci. Technol., 2014, 4, 311 DOI: 10.1039/C3CY00739A

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