4.2 Article

ENANTIOSELECTIVE SYNTHESIS OF 2-ARYL-2,3-DIHYDRO-4-QUINOLONES BY CHIRAL BRONSTED ACID CATALYZED INTRAMOLECULAR AZA-MICHAEL ADDITION REACTION

期刊

HETEROCYCLES
卷 80, 期 2, 页码 765-771

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.3987/COM-09-S(S)66

关键词

Asymmetric Catalysis; N-Triflylphosphoramide; Enantioselectivity; Michael Addition; Organocatalysis

资金

  1. National Natural Science Foundation of China [20732006, 20821002]
  2. National Basic Research Program of China [2010CB833300]
  3. Chinese Academy of Sciences

向作者/读者索取更多资源

Asymmetric intramolecular aza-Michael addition of activated alpha,beta-unsaturated ketones catalyzed by chiral N-triflyl phosphoramide was realized. Enantioenriched 2-aryl-2,3-dihydroquinolin-4-ones can be obtained in excellent yields (77-98%) with up to 82% ee.

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