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Enantioselective Carbonyl Catalysis Enabled by Chiral Aldehydes

Journal

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
Volume 58, Issue 21, Pages 6818-6825

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.201808700

Keywords

asymmetric catalysis; carbonyl catalysis; chiral aldehydes; Mannich reaction; organocatalysis

Funding

  1. National Key Research and Development Program of China [2016YFA0202900]
  2. NSFC [21332009]
  3. Chinese Academy of Sciences [XDB20000000, QYZDY-SSW-SLH012]

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Organocatalytic methods have achieved spectacular advancements for the preparation of chiral molecules in highly enantioenriched forms. The fast development of this field can mainly be attributed to the evolution of general and reliable activation modes. The discovery and identification of new activation modes are therefore highly desirable to push the boundaries of asymmetric reactions. In this Minireview, recent advances in enantioselective carbonyl catalysis, one useful subbranch of organocatalysis for the efficient activation of simple amines, will be summarized. With elegantly designed chiral aldehyde catalysts, highly enantioselective and efficient asymmetric reactions can be developed. Continued development of enantioselective carbonyl catalysis is expected in the future.

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