SYNTHESIS, NMR AND CONFORMATIONAL STUDIES OF SOME 1,4-LINKED DISACCHARIDES

被引：7

作者：

BACKMAN, I ^{[1
]}

JANSSON, PE ^{[1
]}

KENNE, L ^{[1
]}

机构：

[1] UNIV STOCKHOLM,ARRHENIUS LAB,DEPT ORGAN CHEM,S-10691 STOCKHOLM,SWEDEN

来源：

JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1 | 1990年 / 05期

关键词：

D O I：

10.1039/p19900001383

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Synthesis of, and NMR and conformational studies on the methyl glycosides of some 1,4-linked disaccharides, containing rhamnose and fucose in the methyl glycoside residue, have been performed. The glycosylation shifts were correlated with inter-residue atomic distances found in the calculated minimum energy conformations. It is concluded that a typical set of glycosylation shifts are obtained for the disaccharides thus making it possible to use these in the analysis of complex carbohydrates.

引用

页码：1383 / 1388

页数：6

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