STEREOCHEMISTRY OF NUCLEOPHILIC-ADDITION REACTIONS .7. PREPARATION OF METHYL 4,6-O-BENZYLIDENE-2,3-DIDEOXY-2,3-DINITRO-ALPHA-D-GLUCOPYRANOSIDE AND ITS SELECTIVE CONVERSION INTO THE CORRESPONDING 2-NITRO-2-ENOPYRANOSIDE

被引：9

作者：

TACHIMORI, Y

SAKAKIBARA, T

SUDOH, R

机构：

来源：

CARBOHYDRATE RESEARCH | 1980年 / 82卷 / 01期

关键词：

D O I：

10.1016/S0008-6215(00)85519-6

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：

引用

页码：51 / 58

页数：8

共 10 条

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[6] CONVENIENT SYNTHESIS OF D-GLUCOSE-2-C-D DERIVATIVES, AND OF METHYL 4,6-O-BENZYLIDENE-2-C-METHYL-ALPHA-D-GLUCOPYRANOSIDE [J].

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[7] PARTIAL ESTERIFICATION OF METHYL 4,6-O-BENZYLIDENE-ALPHA-D-GLUCOPYRANOSIDE IN PYRIDINE SOLUTION [J].

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[9] STEREOCHEMISTRY OF NUCLEOPHILIC-ADDITION REACTIONS .6. SYNTHESIS OF ISOXAZOLINE N-OXIDE DERIVATIVES FROM METHYL 4,6-O-BENZYLIDENE-2,3-DIDEOXY-3-NITRO-ALPHA-D-ERYTHRO-HEX-2-ENOPYRANOSIDE WITH SOME S-YLIDES [J].

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