Organocatalytic Enantioselective Michael Addition of alpha-Nitroacetate to alpha,beta-Unsaturated Enones: A Route to Chiral gamma-Nitro Ketones and delta-Keto Esters

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WEB OF SCIENCE

26
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SCOPUS

28

초록

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
DOI
10.5012/bkcs.2011.32.1.291
발행일
2011-01-20
유형
Article
저널명
Bulletin of the Korean Chemical Society
권
32
호
1
페이지
291 ~ 295