4.8 Article

Catalytic Enantioselective Allylic Amination of Unactivated Terminal Olefins via an Ene Reaction/[2,3]-Rearrangement

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JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 134, 期 45, 页码 18495-18498

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AMER CHEMICAL SOC
DOI: 10.1021/ja307851b

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资金

  1. W. W. Caruth, Jr. Endowed Scholarship
  2. Robert A. Welch Foundation [I-1748]
  3. American Cancer Society Petroleum Research Fund [51710-DN11]
  4. National Institutes of Health [1R01GM102604-01]

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The enantioselective allylic am nation. of unactivated terminal olefins represents a direct and attractive strategy for the synthesis of enantioenriched amines. We have developed the first use of a nitrogen. containing reagent and a chiral palladium catalyst to convert unfunctionalized olefins into enantioenriched allylic amines via an ene reaction/[2,3]-rearrangement.

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