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Organocatalytic Asymmetric Michael Addition of 1,3-Cyclohexanedione to Benzylidenemalonitriles
- Suh, Chang Won;
- Kim, Dae Young
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28초록
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
- 발행일
- 2014-01-20
- 유형
- Article
- 권
- 35
- 호
- 1
- 페이지
- 98 ~ 102
- 언어
- ENG
- 출판사
- 대한화학회
- 발행국가
- 대한민국
- 분량
- 5 페이지
- ISSN
- E 1229-5949
P 0253-2964