Issue 11, 2008
From the journal:

Organic & Biomolecular Chemistry

Phenylenediamine catalysis of “click glycosylations” in water: practical and direct access to unprotected neoglycoconjugates†‡

Aurélie Baron,a   Yves Blériot,b   Matthieu Sollogoubb  and  Boris Vauzeilles*a  

* Corresponding authors

a CNRS and Univ Paris Sud, Glycochimie Moléculaire et Macromoléculaire, ICMMO, UMR 8182, Orsay, France
E-mail: bvauzeil@icmo.u-psud.fr
Fax: +33 1 69 15 47 15
Tel: +33 1 69 15 68 36

b Université Pierre et Marie Curie-Paris 6, Institut de Chimie Moléculaire (FR 2769), Laboratoire de Chimie Organique (UMR CNRS 7611), 4 place Jussieu, C. 181, Paris, France
Fax: + 33 1 44 27 55 04

Abstract

Phenylenediamine-catalyzed click chemistry leads to the efficient, practical, and column-free preparation of neoglycoconjugates from unprotected glucosyl azide, in pure water when aglycon solubility permits.

Graphical abstract: Phenylenediamine catalysis of “click glycosylations” in water: practical and direct access to unprotected neoglycoconjugates

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Article information

DOI
https://doi.org/10.1039/B805528A
Article type
Communication
Submitted
01 Apr 2008
Accepted
10 Apr 2008
First published
24 Apr 2008

Org. Biomol. Chem., 2008,6, 1898-1901

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Phenylenediamine catalysis of “click glycosylations” in water: practical and direct access to unprotected neoglycoconjugates

A. Baron, Y. Blériot, M. Sollogoub and B. Vauzeilles, Org. Biomol. Chem., 2008, 6, 1898 DOI: 10.1039/B805528A

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