Issue 11, 2003
From the journal:

Chemical Communications

Enantioselective recognition of a chiral quaternary ammonium ion by C3 symmetric cyclic hexapeptides

Guido Heinrichs,a   Laurent Vial,b   Jérôme Lacourb  and  Stefan Kubik*a  

* Corresponding authors

a Institut für Organische Chemie und Makromolekulare Chemie, Heinrich-Heine-Universität, D-40225 Düsseldorf, Germany
E-mail: kubik@uni-duesseldorf.de
Fax: +49-211-81-15840
Tel: +49-211-81-13630

b Département de Chimie Organique, Université de Genève, Quai Ernest Ansermet 30, CH-1211 Geneve 4, Switzerland

Abstract

C 3 Symmetric cyclic hexapeptides containing alternating L-proline and 3-aminobenzoic acid derivatives as subunits possess different affinities towards the two enantiomers of the N,N,N-trimethyl-1-phenylethyl ammonium cation.

Graphical abstract: Enantioselective recognition of a chiral quaternary ammonium ion by C3 symmetric cyclic hexapeptides

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Article information

DOI
https://doi.org/10.1039/B302092D
Article type
Communication
Submitted
25 Feb 2003
Accepted
24 Mar 2003
First published
23 Apr 2003

Chem. Commun., 2003, 1252-1253

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Enantioselective recognition of a chiral quaternary ammonium ion by C3 symmetric cyclic hexapeptides

G. Heinrichs, L. Vial, J. Lacour and S. Kubik, Chem. Commun., 2003, 1252 DOI: 10.1039/B302092D

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