CLAY MONTMORILLONITE-CATALYZED MICHAEL REACTIONS OF SILYL KETENE ACETALS AND A SILYL ENOL ETHER WITH ALPHA,BETA-UNSATURATED CARBONYL-COMPOUNDS

被引：22

作者：

KAWAI, M ^{[1
]}

ONAKA, M ^{[1
]}

IZUMI, Y ^{[1
]}

机构：

[1] NAGOYA UNIV,FAC ENGN,DEPT SYNTHET CHEM,FURO CHO,CHIKUSA KU,NAGOYA,AICHI 464,JAPAN

来源：

JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS | 1987年 / 15期

关键词：

D O I：

10.1039/c39870001203

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

引用

页码：1203 / 1204

页数：2

共 16 条

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[8]

MATSUMOTO K, 1985, SYNTHESIS-STUTTGART, P1

[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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[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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