4.8 Article

Organocatalytic Asymmetric Biomimetic Transamination: From α-Keto Esters to Optically Active α-Amino Acid Derivatives

Journal

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 133, Issue 33, Pages 12914-12917

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ja203138q

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Funding

  1. National Basic Research Program of China (973 program) [2010CB833300]
  2. Chinese Academy of Sciences

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This paper describes an effective chiral base-catalyzed biomimetic transamination of a-keto esters using simple benzyl amines. A wide variety of a.-amino esters containing various functional groups can be synthesized in high enantioselectivity and reasonable yield.

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