A versatile synthesis of linked cyclodextrins

被引：53

作者：

Easton, CJ ^{[1
]}

vanEyk, SJ ^{[1
]}

Lincoln, SF ^{[1
]}

May, BL ^{[1
]}

Papageorgiou, J ^{[1
]}

Williams, ML ^{[1
]}

机构：

[1] UNIV ADELAIDE,DEPT CHEM,ADELAIDE,SA 5005,AUSTRALIA

来源：

AUSTRALIAN JOURNAL OF CHEMISTRY | 1997年 / 50卷 / 01期

基金：

澳大利亚研究理事会;

关键词：

D O I：

10.1071/C96168

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

Reactions of amino-substituted cyclodextrins with bis(3-nitrophenyl) oxalate: malonate, succinate and glutarate, and with diphenyl carbonate, afford a range of linked cyclodextrins. These include alpha-and beta-cyclodextrin dimers, joined by substitution at either C6 or C3, and asymmetric species with a beta-cyclodextrin bonded to an beta-cyclodextrin and a C3-substituted cyclodextrin attached to a C6-substituted moiety.

引用

收藏

页码：9 / 12

页数：4

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