SPECIFIC ISOTOPIC LABELING OF SUGARS - SPECIFIC C-DEUTERATION OF 1,6-ANHYDRO-2,3-0-ISOPROPYLIDENE BETA-D-TALOPYRANOSE THROUGH ENOLIZATION OF AN ALDOSULOSE DERIVATIVE - NMR SPECTRAL STUDIES

被引：31

作者：

HORTON, D

JEWELL, JS

JUST, EK

WANDER, JD

机构：

来源：

CARBOHYDRATE RESEARCH | 1971年 / 18卷 / 01期

关键词：

D O I：

10.1016/S0008-6215(00)80258-X

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：49 / &

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共 20 条

[1] SYNTHESIS OF 1,6-ANHYDRO DERIVATIVES OF 2-AMINO-2-DEOXY-BETA-D-TALOPYRANOSE AND 4-AMINO-4-DEOXY-BETA-D-TALOPYRANOSE
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[8] ENOLIZATION OF ALDOSULOSE DERIVATIVES . 4-0-ACETYL-1,6-ANHYDRO-2,3-0-ISOPROPYLIDENE-BETA-D-THREO-HEX-3-ENOPYRANOSE 3,4-ENEDIOL ACETATE OF A FUSED-RING KETO SUGAR AND FORMATION OF A BRANCHED-CHAIN SUGAR DERIVATIVE
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[9] CALCULATION OF MOLECULAR ROTATION BY SUMMATION OF PARTIAL CONFORMATIONAL CONTRIBUTIONS .2. ROTATIONS OF 1,6-ANHYDRO-DEOXY-BETA-D-HEXOPYRANOSES, 2,7-ANHYDRO-BETA-D-HEPTULOPYRANOSES, AND THEIR ACETATES
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[J]. CARBOHYDRATE RESEARCH, 1970, 14 (01) : 83 - &
[10] CALCULATION OF MOLECULAR ROTATION BY SUMMATION OF PARTIAL CONFORMATIONAL CONTRIBUTIONS . ROTATIONS OF 8 1,6-ANHYDRO-BETA-D-HEXOPYRANOSES AND THEIR TRIACETATES
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