4.8 Article

A Method for the Catalytic Enantioselective Synthesis of Chiral α-Azido and α-Amino Ketones from Racemic α-Bromo Ketones, and Its Generalization to the Formation of Bonds to C, O, and S

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JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 141, 期 51, 页码 20058-20061

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AMER CHEMICAL SOC
DOI: 10.1021/jacs.9b12315

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  1. Pfizer Inc.
  2. Bristol-Myers Squibb

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A new and practical method has been developed for the transformation of racemic alpha-bromo ketones to chiral alpha-azido and alpha-amino ketones with high enantioselectivity using phase transfer, ion-pair mediated reactions with a recoverable chiral quaternary salt (10 mol %) as catalyst in fluorobenzene-water. The process has been generalized to a variety of other attachments including of C, O, S, and NHR.

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