Clay Montmorillonite: An Efficient, Heterogeneous Catalyst for Michael Reactions of Silyl Ketene Acetals and Silyl Enol Ethers with α,β-Unsaturated Carbonyl Compounds-Reference-Cited by-同舟云学术

Clay Montmorillonite: An Efficient, Heterogeneous Catalyst for Michael Reactions of Silyl Ketene Acetals and Silyl Enol Ethers with α,β-Unsaturated Carbonyl Compounds

Published:1988-06 Issue:6 Volume:61 Page:2157-2164
ISSN:0009-2673
Container-title:Bulletin of the Chemical Society of Japan
language:en
Short-container-title:BCSJ

Author:

Kawai Motomitsu,Onaka Makoto,Izumi Yusuke

Publisher

The Chemical Society of Japan

Subject

General Chemistry

Link

https://www.jstage.jst.go.jp/article/bcsj1926/61/6/61_6_2157/_pdf

Reference30 articles.

1. Conjugate and direct addition of ester enolates to cyclohexenone. Selective control of reaction composition

2. Acyclic stereoselection. 30. Stereoselection in the Michael addition reaction. 2. Stereochemistry of the kinetic Michael reaction of amide enolates with enones

3. Acyclic stereoselection. 31. Stereoselection in the Michael addition reaction. 3. Relationship between ester enolate geometry and adduct stereochemistry in the kinetic Michael reaction of lithium enolates with enones

4. A highly stereoselective Michael reaction of simple ester enolates to α,β-unsaturated esters

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