THE DOUBLE MICHAEL REACTION OF ALPHA,BETA-UNSATURATED KETONES WITH SILOXYDIENES CATALYZED BY TRITYL PERCHLORATE FORMING 6-MEMBERED RING-SYSTEMS

被引：45

作者：

MUKAIYAMA, T

SAGAWA, Y

KOBAYASHI, S

机构：

来源：

CHEMISTRY LETTERS | 1986年 / 11期

关键词：

D O I：

10.1246/cl.1986.1821

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

引用

页码：1821 / 1824

页数：4

共 14 条

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[10] THE HIGHLY STEREOSELECTIVE MICHAEL REACTION OF ALPHA,BETA-UNSATURATED KETONES WITH SILYL ENOL ETHERS OF THIOESTERS CATALYZED BY TRITYL SALTS - A FACILE STEREOSELECTIVE SYNTHESIS OF 5-OXOCARBOXYLIC ACID ESTER DERIVATIVES [J].

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KOBAYASHI, S .

CHEMISTRY LETTERS, 1986, (11) :1817-1820

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