IMPROVEMENT IN O-]C-GLYCOSIDE REARRANGEMENT APPROACH TO C-ARYL GLYCOSIDES - USE OF 1-O-ACETYL SUGAR AS STABLE BUT EFFICIENT GLYCOSYL DONOR

被引：97

作者：

MATSUMOTO, T ^{[1
]}

HOSOYA, T ^{[1
]}

SUZUKI, K ^{[1
]}

机构：

[1] KEIO UNIV,DEPT CHEM,YOKOHAMA,KANAGAWA 223,JAPAN

来源：

TETRAHEDRON LETTERS | 1990年 / 31卷 / 32期

关键词：

D O I：

10.1016/S0040-4039(00)97693-7

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

1-O-Acetyl sugars serve as efficient glycosyl donor in the O→C-glycoside rearrangement approach to Caryl glycosides. Model study was carried out on three types of 2-deoxy-glycosyl acetates including amino sugar derivative. Comparison of the promoters, Cp2HfCl2-AgClO4, SnCl4, BF3·OEt2 is described. © 1990.

引用

页码：4629 / 4632

页数：4

共 18 条

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