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

被引：42

作者：

Baron, Aurelie ^{[1
,2
]}

Bleriot, Yves ^{[3
]}

Sollogoub, Matthieu ^{[3
]}

Vauzeilles, Boris ^{[1
,2
]}

机构：

[1] CNRS, F-91405 Orsay, France

[2] Univ Paris 11, ICMMO, UMR 8182, F-91405 Orsay, France

[3] Univ Paris 06, Inst Chim Mol FR 2769, Chim Organ Lab, UMR CNRS 7611, F-75005 Paris, France

来源：

ORGANIC & BIOMOLECULAR CHEMISTRY | 2008年 / 6卷 / 11期

关键词：

D O I：

10.1039/b805528a

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

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.

引用

页码：1898 / 1901

页数：4

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