Issue 8, 2007

Organocatalytic asymmetric 5-hydroxyisoxazolidine synthesis: A highly enantioselective route to β-amino acids

Abstract

The highly chemo- and enantioselective organocatalytic tandem reaction between N-protected hydroxyl amines and α,β-unsaturated aldehydes is presented; the reaction provides access to 5-hydroxyisoxazolidines and β-amino acids in high yields and with 90–99% ee.

Graphical abstract: Organocatalytic asymmetric 5-hydroxyisoxazolidine synthesis: A highly enantioselective route to β-amino acids

Supplementary files

Article information

Article type
Communication
Submitted
14 Sep 2006
Accepted
01 Nov 2006
First published
23 Nov 2006

Chem. Commun., 2007, 849-851

Organocatalytic asymmetric 5-hydroxyisoxazolidine synthesis: A highly enantioselective route to β-amino acids

I. Ibrahem, R. Rios, J. Vesely, G. Zhao and A. Córdova, Chem. Commun., 2007, 849 DOI: 10.1039/B613410F

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