SYNTHESIS OF 5-AZIDO-1,4-DI-O-BENZYL-5-DEOXY-2-O-PARA TOLYLSULFONYL-D-RIBITOL AND 2-AZIDO-2-DEOXY-3,4-O-ISOPROPYLIDENE-1-O-(TETRAHYDROPYRAN-2-YL)-5-O-PARA TOLYLSULFONYL-L-ARABINITOL FROM D-RIBONO-1,4-LACTONE

被引：5

作者：

SEPULCHRE, AM ^{[1
]}

GATEAU, A ^{[1
]}

GERO, SD ^{[1
]}

机构：

[1] CNRS, INST CHIM SUBST NAT, GIF YVETTE 91, FRANCE

来源：

CARBOHYDRATE RESEARCH | 1972年 / 24卷 / 02期

关键词：

D O I：

10.1016/S0008-6215(00)85064-8

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：311 / 318

页数：8

共 11 条

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[2]

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[3] THE PREPARATION OF SOME DERIVATIVES OF D-RIBONO-1-]4-LACTONE AND D-RIBITOL [J].

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[6]

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[7] D-MANNOFURANOSE 2,3-CARBONATE . PREFERRED SIZE OF SUGAR RING IN SOME FUSED-RING DERIVATIVES [J].

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[8]

SAEKI H, 1968, CHEM PHARM BULL, V16, P2477

[9] SYNTHESIS OF PYROLIDINE DERIVATIVES - INTRAMOLECULAR CYCLIZATION CONDUCTING TO 1,4-2,5-DIANHYDRO-2,3,4-TRIDEOXY-2,4-BIS-(PARA-TOLUENESULFONAMIDO)-D-THREO-PENITOL [J].

SEPULCHR.AM ;

CLEOPHAX, J ;

HILDESHE.J ;

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[10]

SEPULCHRE AM, 1969, CR ACAD SCI C CHIM, V269, P1312

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