USE OF C-13-NMR SPECTROSCOPY FOR THE QUANTITATIVE ESTIMATION OF 3-O-SUBSTITUTED AND 3,6-DI-O-SUBSTITUTED D-GLUCOPYRANOSYL RESIDUES IN ALPHA-D-GLUCANS FORMED BY THE D-GLUCOSYLTRANSFERASES OF STREPTOCOCCUS-SOBRINUS

被引：25

|

作者：

SHIMAMURA, A

机构：

来源：

CARBOHYDRATE RESEARCH | 1989年 / 185卷 / 02期

关键词：

D O I：

10.1016/0008-6215(89)80039-4

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：

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页码：239 / 248

页数：10

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[1] C-13-NMR STUDY OF METHYL-ETHER AND BENZYL-ETHER OF L-ARABINOSE AND OLIGOSACCHARIDES HAVING L-ARABINOSE AT THE REDUCING END - SYNTHESIS OF 2-O-BETA-D-GLUCOPYRANOSYL-L-ARABINOSE 2-O-ALPHA-L-RHAMNOPYRANOSYL-, 3-O-BETA-D-GLUCOPYRANOSYL-2-O-ALPHA-L-RHAMNOPYRANOSYL-L-ARABINOSE AND 4-O-BETA-D-GLUCOPYRANOSYL-2-O-ALPHA-L-RHAMNOPYRANOSYL-L-ARABINOSEIN
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[2] UNUSUAL DEXTRANS .8. STRUCTURAL-ANALYSIS OF LEUCONOSTOC DEXTRANS CONTAINING 3-O-ALPHA-D-GLUCOSYLATED ALPHA-D-GLUCOSYL RESIDUES IN BOTH LINEAR-CHAIN AND BRANCH-POINT POSITIONS, OR ONLY IN BRANCH-POINT POSITIONS, BY METHYLATION AND BY C-13-NMR SPECTROSCOP
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