Issue 15, 2009

Enantioselective Henry reaction catalyzed by C2-symmetric chiral diamine–copper(II) complex

Abstract

A copper(II) complex of C2-symmetric diamine has been proved to be an efficient catalyst for the enantioselective Henry reaction between nitroalkanes and various aldehydes to provide β-hydroxy nitroalkanes in high yields (up to 97%), moderate diastereoselectivities (up to 71:29) and excellent enantiomeric excesses (up to 96%). The chiral nitroaldol adduct obtained has been further converted into chiral aziridine in few steps.

Graphical abstract: Enantioselective Henry reaction catalyzed by C2-symmetric chiral diamine–copper(II) complex

Supplementary files

Article information

Article type
Paper
Submitted
02 Mar 2009
Accepted
13 May 2009
First published
11 Jun 2009

Org. Biomol. Chem., 2009,7, 3156-3162

Enantioselective Henry reaction catalyzed by C2-symmetric chiral diamine–copper(II) complex

S. Selvakumar, D. Sivasankaran and V. K. Singh, Org. Biomol. Chem., 2009, 7, 3156 DOI: 10.1039/B904254G

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