CHAIN ELONGATION OF ALDONOLACTONES

被引：19

作者：

CSUK, R ^{[1
]}

GLANZER, BI ^{[1
]}

机构：

[1] UNIV HEIDELBERG,INST ORGAN CHEM,W-6900 HEIDELBERG,GERMANY

来源：

JOURNAL OF CARBOHYDRATE CHEMISTRY | 1990年 / 9卷 / 06期

关键词：

D O I：

10.1080/07328309008543876

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：

As an alternative to the classical Reformatsky-type branching reaction of aldonolactones, ethyl trimethylsilylacetate, methyl 2-trimethylsilyl-propionate, trimethylsilylacetonitrile or alkyl 2-(trimethylsilylmethyl)-acrylates in the presence of catalytic amounts of tetra-n-butyl-ammonium fluoride can be used. The corresponding chain elongated monosaccharides are obtained in high yields. © 1990, Taylor & Francis Group, LLC. All rights reserved.

引用

页码：809 / 822

页数：14

共 38 条

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