4.8 Article

Catalytic Asymmetric Mukaiyama-Mannich Reaction of Cyclic C-Acylimines with Difluoroenoxysilanes: Access to Difluoroalkylated Indolin-3-ones

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ORGANIC LETTERS
卷 19, 期 23, 页码 6364-6367

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AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.7b03213

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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 AMP
  4. Technology Commission [14JCZDJC33400]

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A catalytic enantioselective Mukaiyama-Mannich reaction of cyclic C-acylimines with difluoroenoxysilanes is reported.(S)-TRIP enables the enantioselective synthesis of a series of novel difluoroalkylated indolin-3-ones bearing a quaternary stereocenter in up to 97% yield and 98% ee. The synthetic utility of this protocol is highlighted by efficient conversion of the products to the corresponding indolin-3-one derivatives without any erosion of the enantiopurity.

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