Issue 7, 2009

Stereocontrolled routes to β,β′-disubstituted α-amino acids

Abstract

Owing to their significant abundance in natural products, chiral β,β′-disubstituted α-amino acids remain an important synthetic objective. Emphasis has been focused in this critical review on the great diversity of enantio- and diastereoselective methodologies to reach these highly functionalized compounds. The oldest and cutting edge synthetic methods are described in parallel with the synthesis of many relevant biologically active targets (224 references).

Graphical abstract: Stereocontrolled routes to β,β′-disubstituted α-amino acids

Article information

Article type
Critical Review
Submitted
29 Oct 2008
First published
27 Apr 2009

Chem. Soc. Rev., 2009,38, 2093-2116

Stereocontrolled routes to β,β′-disubstituted α-amino acids

J. Michaux, G. Niel and J. Campagne, Chem. Soc. Rev., 2009, 38, 2093 DOI: 10.1039/B812116H

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