Issue 30, 2005
From the journal:

Chemical Communications

Highly enantioselective organocatalysis of the Hajos–Parrish–Eder–Sauer–Wiechert reaction by the β-amino acid cispentacin

Stephen G. Davies,*a   Ruth L. Sheppard,a   Andrew D. Smith*a  and  James E. Thomsona  

* Corresponding authors

a Department of Organic Chemistry, University of Oxford, Chemistry Research Laboratory, Mansfield Road, Oxford, UK
E-mail: steve.davies@chem.ox.ac.uk, andrew.smith@chem.ox.ac.uk

Abstract

The β-amino acid cispentacin promotes the Hajos–Parrish–Eder–Sauer–Wiechert reaction with levels of enantioselectivity comparable to or higher than proline.

Graphical abstract: Highly enantioselective organocatalysis of the Hajos–Parrish–Eder–Sauer–Wiechert reaction by the β-amino acid cispentacin

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Article information

DOI
https://doi.org/10.1039/B506780B
Article type
Communication
Submitted
12 May 2005
Accepted
01 Jun 2005
First published
30 Jun 2005

Chem. Commun., 2005, 3802-3804

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Highly enantioselective organocatalysis of the Hajos–Parrish–Eder–Sauer–Wiechert reaction by the β-amino acid cispentacin

S. G. Davies, R. L. Sheppard, A. D. Smith and J. E. Thomson, Chem. Commun., 2005, 3802 DOI: 10.1039/B506780B

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