Using click chemistry to access mono- and ditopic β-cyclodextrin hosts substituted by chiral amino acids

被引：19

作者：

Tran, Diem Ngan ^{[1
,2
]}

Blaszkiewicz, Claire ^{[1
,2
]}

Menuel, Stephane ^{[1
,2
]}

Roucoux, Alain ^{[3
]}

Philippot, Karine ^{[4
]}

Hapiot, Frederic ^{[1
,2
]}

Monflier, Eric ^{[1
,2
]}

机构：

[1] Univ Lille Nord France, F-59000 Lille, France

[2] UArtois, UCCS, CNRS, UMR 8181, F-62300 Lens, France

[3] Univ Europeenne Bretagne, Ecole Natl Super Chim Rennes, CNRS, UMR 6226, F-35708 Rennes 7, France

[4] Univ Toulouse, UPS, INPT, CNRS,LCC, F-31077 Toulouse, France

来源：

CARBOHYDRATE RESEARCH | 2011年 / 346卷 / 02期

关键词：

Cyclodextrins; Azides; Amino acids; Cycloaddition; Chirality; DERIVATIVES; MICROWAVES; COMPLEXES;

D O I：

10.1016/j.carres.2010.11.024

中图分类号：

Q5 [生物化学]; Q7 [分子生物学];

学科分类号：

071010 ; 081704 ;

摘要：

A wide range of chiral mono- and ditopic cyclodextrin-based receptors have been synthesized by Cul-catalyzed azide-alkyne cycloaddition starting from mono-6-azido-beta-cyclodextrin and chiral amino acids. Of interest, microwaves proved very efficient to access a wide range of ditopic p-cyclodextrin receptors with quantitative yields. (C) 2010 Elsevier Ltd. All rights reserved.

引用

页码：210 / 218

页数：9

共 42 条

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