Issue 1, 2016

Enantioselective synthesis of (−)-chloramphenicol via silver-catalysed asymmetric isocyanoacetate aldol reaction

Abstract

The highly enantio- and diastereoselective aldol reaction of isocyanoacetates catalysed by Ag2O and cinchona-derived amino phosphines applied to the synthesis of (−)- and (+)-chloramphenicol is described. The concise synthesis showcases the utility of this catalytic asymmetric methodology for the preparation of bioactive compounds possessing α-amino-β-hydroxy motifs.

Graphical abstract: Enantioselective synthesis of (−)-chloramphenicol via silver-catalysed asymmetric isocyanoacetate aldol reaction

Supplementary files

Article information

Article type
Paper
Submitted
22 Sep 2015
Accepted
19 Oct 2015
First published
29 Oct 2015
This article is Open Access
Creative Commons BY license

Org. Biomol. Chem., 2016,14, 93-96

Enantioselective synthesis of (−)-chloramphenicol via silver-catalysed asymmetric isocyanoacetate aldol reaction

A. Franchino, P. Jakubec and D. J. Dixon, Org. Biomol. Chem., 2016, 14, 93 DOI: 10.1039/C5OB02141C

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