CATALYTIC STEREOSELECTIVE SYNTHESIS OF BETA-RIBONUCLEOSIDES FROM METHYL RIBOFURANOSYL CARBONATE AND TRIMETHYLSILYLATED NUCLEOSIDE BASES BY COMBINED USE OF SILVER SALTS AND DIPHENYLTIN SULFIDE

被引：13

作者：

MUKAIYAMA, T

MATSUTANI, T

SHIMOMURA, N

机构：

来源：

CHEMISTRY LETTERS | 1993年 / 09期

关键词：

D O I：

10.1246/cl.1993.1627

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

Catalytic stereoselective synthesis of several ribonucleosides from 2,3,5-tri-O-benzoyl-beta-D-ribofuranosyl methyl carbonate and trimethylsilylated nucleoside bases is efficiently carried out by combined use of silver salts and diphenyltin sulfide (Ph2Sn=S) under mild conditions.

引用

页码：1627 / 1630

页数：4

共 13 条

[11] NEW GLYCOSIDATION REACTION .2. PREPARATION OF 1-FLUORO-D-DESOSAMINE DERIVATIVE AND ITS EFFICIENT GLYCOSIDATION BY THE USE OF CP2HFCL2-AGCLO4 AS THE ACTIVATOR [J].