THE MICHAEL REACTION OF VARIOUS QUINONES WITH SILYL ENOL ETHERS - A FACILE METHOD FOR THE PREPARATION OF BENZOFURAN AND INDOLE-DERIVATIVES

被引：29

作者：

MUKAIYAMA, T

SAGAWA, Y

KOBAYASHI, S

机构：

来源：

CHEMISTRY LETTERS | 1987年 / 11期

关键词：

D O I：

10.1246/cl.1987.2169

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

引用

收藏

页码：2169 / 2172

页数：4

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[7] TRITYL PERCHLORATE CATALYZED TANDEM MICHAEL-ALDOL REACTION - A FACILE METHOD FOR THE STEREOSELECTIVE SYNTHESES OF GAMMA-ACYL SUBSTITUTED SIGMA-HYDROXY KETONE DERIVATIVES [J].

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[9] THE STEREOSELECTIVE MICHAEL REACTION BETWEEN SILYL ENOL ETHERS AND ALPHA,BETA-UNSATURATED KETONES BY THE USE OF TRITYL PERCHLORATE AS A CATALYST [J].

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