A HIGHLY STEREOSELECTIVE SYNTHESIS OF ARYL 2-DEOXY-BETA-GLYCOSIDES VIA THE MITSUNOBU REACTION

被引：68
|
作者：
ROUSH, WR
LIN, XF
机构：
[1] Department of Chemistry, Indiana University, Bloomington
来源：
JOURNAL OF ORGANIC CHEMISTRY | 1991年 / 56卷 / 20期
关键词：
D O I：
10.1021/jo00020a003
中图分类号：
O62 [有机化学];
学科分类号：
070303 ; 081704 ;
摘要：
A highly stereoselective (6.5- > 20:1) synthesis of aryl 2-deoxy-beta-D-glycosides is described. This method involves the Mitsunobu coupling of phenols and 2-alpha-(thiophenyl)- or 2-alpha-(selenophenyl)-alpha-D-pyranoses 3-6, 18, and 19 followed by Bu3SnH reduction of the PhS- and PhSe-groups.
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页码：5740 / 5742
页数：3
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