4.8 Article

Organocatalytic Asymmetric Decarboxylative Amination of β-Keto Acids: Access to Optically Active α-Amino Ketones and 1,2-Amino Alcohols

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ORGANIC LETTERS
卷 19, 期 8, 页码 2162-2165

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AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.7b00797

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资金

  1. National Natural Science Foundation of China [21225208, 21472137, 21532008]
  2. National Basic Research Program of China (973 Program) [2014CB745100]
  3. Tianjin Municipal Science & Technology Commission [14JCZDJC33400]

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An organocatalytic asymmetric decarboxylative amination reaction of ss-keto acids is described. Under mild reaction conditions, a series of chiral alpha-amino ketones were obtained in good to high yields (up to 99%) and enantioselectivities (up to 95% ee). A chiral 1,2-amino alcohol was synthesized from the corresponding decarboxylative amination product in several steps without loss of enantioselectivity.

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