NOVEL GLYCOSYLATION REAGENTS - SYNTHESIS OF DISACCHARIDES CONTAINING 2-DEOXY-2-IODO-ALPHA-D-TALOPYRANOSYL GROUPS

被引：8

作者：

GAREGG, PJ ^{[1
]}

SAMUELSSON, B ^{[1
]}

KONRADSSON, P ^{[1
]}

KVARNSTROM, I ^{[1
]}

SVENSSON, SCT ^{[1
]}

机构：

[1] LINKOPING UNIV,DEPT CHEM,S-58183 LINKOPING,SWEDEN

来源：

CARBOHYDRATE RESEARCH | 1981年 / 92卷 / 01期

关键词：

D O I：

10.1016/S0008-6215(00)85992-3

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：157 / 159

页数：3

共 9 条

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[3] SYNTHESIS OF 1D-2-0 AND 1D-5-0-(ALPHA-D-GALACTOPYRANOSYL)-4-0-METHYLCHIRO-INOSITOL - PREFERENCE FOR EQUATORIAL HYDROXYL-GROUPS IN THE IMIDATE GALACTOSYLATION PROCEDURE [J].

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[5]

GAREGG PJ, UNPUBLISHED

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[7] NOVEL SYNTHESIS OF 2-DEOXY-ALPHA-GLYCOSIDES [J].

TATSUTA, K ;

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UMEZAWA, S .

CARBOHYDRATE RESEARCH, 1977, 54 (01) :85-104

[8] SYNTHETIC APPLICATION OF 2,6-DIDEOXYGLYCOSYL HALIDES - CONSTRUCTION OF THE B-A DISACCHARIDE GLYCOSIDE IN CHROMOMYCIN-A-3 [J].

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CHEMISCHE BERICHTE-RECUEIL, 1980, 113 (09) :3058-3066

[9]

WYSS G, 1877, BER DTSCH CHEM GES, V10, P1365

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