Organocatalytic Asymmetric Michael Addition of 1,3-Cyclohexanedione to Benzylidenemalonitriles

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WEB OF SCIENCE

27
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SCOPUS

28

초록

The organocatalytic enantioselective Michael addition reaction promoted by chiral binaphthyl-modified squaramide catalyst have been developed, allowing facile synthesis of the corresponding chiral 2-amino-4H-chromenes derivatives with excellent enantioselectivity (up to 99% ee). The method reported represents a practical entry for the preparation of chiral 2-amino-4H-chromenes derivatives.

키워드

Asymmetric catalysis; Organocatalysis; Michael addition; 2-Amino-4H-chromenes; CATALYTIC ENANTIOSELECTIVE FLUORINATION; MANNICH-TYPE REACTIONS; BETA-KETO-ESTERS; CONJUGATE ADDITION; ALPHA,BETA-UNSATURATED KETONES; QUATERNARY STEREOCENTERS; ALPHA-HYDRAZINATION; KETOESTERS; ENONES; CONSTRUCTION
제목
Organocatalytic Asymmetric Michael Addition of 1,3-Cyclohexanedione to Benzylidenemalonitriles
저자
Suh, Chang Won; Kim, Dae Young
DOI
10.5012/bkcs.2014.35.1.98
발행일
2014-01-20
유형
Article
저널명
Bulletin of the Korean Chemical Society
권
35
호
1
페이지
98 ~ 102