Regioselective synthesis of sucrose monoesters as surfactants

被引：58

作者：

Vlahov, IR

Vlahova, PI

Linhardt, RJ

机构：

[1] UNIV IOWA,DIV MED & NAT PROD CHEM,IOWA CITY,IA 52240

[2] UNIV IOWA,DEPT CHEM & BIOCHEM ENGN,IOWA CITY,IA 52240

来源：

JOURNAL OF CARBOHYDRATE CHEMISTRY | 1997年 / 16卷 / 01期

关键词：

D O I：

10.1080/07328309708006506

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 highly regioselective conversion of sucrose into 6-O-acyl derivatives is reported. First sucrose was transformed into the dibutyltin acetal, thus enhancing the nucleophilicity at the C-6 oxygen and restricting the subsequent acylation reaction. The surface activity properties of the sucrose monoesters obtained were determined and compared with those of commercially available ionic and non-ionic surfactants.

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页码：1 / 10

页数：10

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