THE TRITYL CATION CATALYZED MICHAEL TYPE REACTION OF STANNYLATED NUCLEOPHILES WITH ETHYLTHIOKETENE DITHIOACETALS

被引：16

|

作者：

HASHIMOTO, Y

SUGUMI, H

OKAUCHI, T

MUKAIYAMA, T

机构：

来源：

CHEMISTRY LETTERS | 1987年 / 09期

关键词：

D O I：

10.1246/cl.1987.1695

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

引用

收藏

页码：1695 / 1698

页数：4

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[1] THE TRITYL CATION MEDIATED MICHAEL REACTION OF ETHYLTHIOKETENE DITHIOACETALS WITH SILYL ENOL ETHERS
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[8] Trityl Cation-Catalyzed Hosomi-Sakurai Reaction of Allylsilane with β,γ-Unsaturated α-Ketoester to Form γ,γ-Disubstituted α-Ketoesters
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[9] A HIGHLY STEREOSELECTIVE SYNTHESIS OF GAMMA-ACYL-DELTA-LACTONES BY THE TRITYL PERCHLORATE CATALYZED TANDEM MICHAEL-ALDOL REACTION
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[10] Iron-Catalyzed Coupling of Alkenes and Enones: Sakurai-Michael-type Conjugate Addition of Catalytic Allyliron Nucleophiles
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