CHEMICAL SYNTHESIS OF P-NITROPHENYL BETA-SOPHOROSIDE AND P-NITROPHENYL BETA-LAMINARABIOSIDE

被引：7

作者：

IYER, RN

GOLDSTEIN, IJ

机构：

[1] Department of Biological Chemistry, The University of Michigan, Ann Arbor

来源：

CARBOHYDRATE RESEARCH | 1969年 / 11卷 / 02期

关键词：

D O I：

10.1016/S0008-6215(00)80080-4

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：

Condensation of tetra-O-acetyl-α-d-glucopyranosyl bromide with p-nitrophenyl 4,6-O-benzylidene-β-d-glucopyranoside followed by appropriate deblocking reactions gives rise to an approximately equimolar mixture of p-nitrophenyl β-sophoroside and p-nitrophenyl β-laminarabioside. The two glycosides are readily separated and isolated in pure form by cellulose-column chromatography. © 1969.

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页码：241 / +

页数：1

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