STUDIES ON CARBOHYDRATES .4. A NOVEL HIGHLY STEREOSELECTIVE SYNTHESIS OF 1-O-ACYL-BETA-D-GLUCOPYRANOSE TETRAACETATES VIA THE GLUCOSYL TRIFLUOROACETATE

被引：7

作者：

YU, CF ^{[1
]}

LI, ZJ ^{[1
]}

CAI, MS ^{[1
]}

机构：

[1] BEIJING MED UNIV,SCH PHARMACEUT SCI,DEPT ORGAN CHEM,BEIJING 100083,PEOPLES R CHINA

来源：

SYNTHETIC COMMUNICATIONS | 1990年 / 20卷 / 07期

关键词：

D O I：

10.1080/00397919008052796

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

2,3,4,6-Tetra-acetyl-glucose (1) reacted with trifluoroacetic anhydride to give good yield of 2,3,4, 6-tetra-0-acetyl-1-α-O-trifluoroacetyl-α-D-glucopyranose (2) which was converted into corresponding 1-0-acyl-β-glucopyranose tetraacetates. β-Anomers of glycosyl esters were obtained by this method. © 1990, Taylor & Francis Group, LLC. All rights reserved.

引用

页码：943 / 948

页数：6

共 8 条

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