SYNTHESIS OF A SERIES OF METHYL BETA-GLYCOSIDES OF (1-]6)-BETA-D-GALACTO-OLIGOSACCHARIDES HAVING ONE RESIDUE DEOXYGENATED AT POSITION-3

被引：11

作者：

KOVAC, P ^{[1
]}

EDGAR, KJ ^{[1
]}

机构：

[1] EASTMAN KODAK CO, RES LABS, EASTMAN CHEM DIV, KINGSPORT, TN 37662 USA

来源：

CARBOHYDRATE RESEARCH | 1990年 / 201卷 / 01期

关键词：

D O I：

10.1016/0008-6215(90)84226-K

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：

Methyl β-glycosides of β-(1→6)-linked d-galactobioses (13 and 16) and -galactotrioses (21, 24, and 26) containing a 3-deoxy-β-d-xylo-hexopyranosyl moiety either as one of the end units or the internal unit have been synthesized. The extension of the oligosaccharide chain was achieved, inter alia, by the use of two newly synthesized glycosyl donors derived from 3-deoxy-d-xylo-hexopyranose, namely, 2,4,6-tri-O-benzoyl-3-deoxy-α-d-xylo-hexopyranosyl chloride (8) and 2,4-di-O-benzoyl-6-O-bromoacetyl-3-deoxy-α-d-xylo-hexopyranosyl chloride (10). Glycosylation reactions were mediated by silver triflate under base-deficient conditions. © 1990.

引用

页码：79 / 93

页数：15

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