상세 보기
Organocatalytic Enantioselective Michael Addition of alpha-Nitroacetate to alpha,beta-Unsaturated Enones: A Route to Chiral gamma-Nitro Ketones and delta-Keto Esters
- Moon, Hyoung Wook;
- Kim, Dae Young
Citations
WEB OF SCIENCE
26Citations
SCOPUS
28초록
The catalytic enantioselective conjugate addition reaction of alpha-nitroacetate to alpha,beta-unsaturated enones promoted by chiral bifunctional organocatalysts is described. The treatment of a-nitroacetate to alpha,beta-unsaturated enones afforded the corresponding Michael adducts with high enantioselectivity. The conjugate addition adducts are easily converted to chiral gamma-nitro ketones and delta-keto esters.
키워드
Bifunctional organocatalysts; Asymmetric catalysis; Michael reaction; alpha-Nitroacetate; gamma-Nitro ketones; delta-Keto esters; ASYMMETRIC CONJUGATE ADDITION; FLUORO-BETA-KETOESTERS; MANNICH-TYPE REACTIONS; ORGANIC-REACTIONS; ALDOL REACTIONS; CYANO ACETATES; NITROALKANES; FLUORINATION; CATALYSIS; AMINATION
- 제목
- Organocatalytic Enantioselective Michael Addition of alpha-Nitroacetate to alpha,beta-Unsaturated Enones: A Route to Chiral gamma-Nitro Ketones and delta-Keto Esters
- 저자
- Moon, Hyoung Wook; Kim, Dae Young
- 발행일
- 2011-01-20
- 유형
- Article
- 권
- 32
- 호
- 1
- 페이지
- 291 ~ 295
- 언어
- ENG
- 출판사
- 대한화학회
- 발행국가
- 대한민국
- 분량
- 5 페이지
- ISSN
- E 1229-5949
P 0253-2964