Asymmetric 1,4-Michael Addition Reactions Catalyzed by a Cinchona Alkaloid Derived Primary Amine: A Theoretical Investigation of the Reaction Mechanism and Enantioselectivity-Reference-Cited by-同舟云学术

Asymmetric 1,4-Michael Addition Reactions Catalyzed by a Cinchona Alkaloid Derived Primary Amine: A Theoretical Investigation of the Reaction Mechanism and Enantioselectivity

Published:2013-02-06 Issue:9 Volume:2013 Page:1706-1715
ISSN:1434-193X
Container-title:European Journal of Organic Chemistry
language:en
Short-container-title:Eur. J. Org. Chem.

Author:

Su Zhishan,Lee Hai Whang,Kim Chan Kyung

Publisher

Wiley

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Reference89 articles.

1. Enantioselective Michael Addition to α,β-Unsaturated Imides Catalyzed by a Bifunctional Organocatalyst

2. Michael Additions of Aldehydes and Ketones toβ-Nitrostyrenes in an Ionic Liquid

3. Double Catalytic Activation with Chiral Lewis Acid and Amine Catalysts

4. Enantio- and Diastereoselective Michael Reaction of 1,3-Dicarbonyl Compounds to Nitroolefins Catalyzed by a Bifunctional Thiourea

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