First Synthesis of N-Acylated Photoactivatable Analogues of Glutathione Bearing an Aryl Azide Moiety

Dan Bernardi; Lalla Aïcha Ba; Gilbert Kirsch

doi:10.1055/s-2006-950374

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Synthesis 2007(1): 140-144
DOI: 10.1055/s-2006-950374

PAPER

First Synthesis of N-Acylated Photoactivatable Analogues of Glutathione Bearing an Aryl Azide Moiety

Dan Bernardi*, Lalla Aïcha Ba, Gilbert Kirsch*
Laboratoire d’Ingénierie Moléculaire et Biochimie Pharmacologique, Université Paul Verlaine, 1 Boulevard Arago, 57078 Metz Cedex 03, France
Fax: +33(38)7315801; e-Mail: kirsch@sciences.univ-metz.fr;

Further Information

Publication History

Received 24 July 2006
Publication Date:
21 November 2006 (online)

Abstract
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Abstract

N-Acylated photoactivatable analogues of glutathione bearing an aryl azide moiety were synthesized for the first time starting from S-tritylglutathione.

Key words

glutathione - photoactivatable - aryl azide - trityl group - N-acylation

References

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1

Current address, postdoctoral fellow: Institut de Chimie Organique et Analytique, Université d’Orléans, UMR CNRS 6005, B.P. 6759, 45067 Orléans Cedex 2, France, email: danbernardi@netcourrier.com.