4.8 Article

Nickel-Catalyzed Cycloaddition of Vinylcyclopropanes to Imines

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ORGANIC LETTERS
卷 15, 期 8, 页码 1791-1793

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AMER CHEMICAL SOC
DOI: 10.1021/ol4005068

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资金

  1. JST
  2. ACT-C
  3. Ministry of Education, Culture, Sports, Science, and Technology, Japan
  4. Grants-in-Aid for Scientific Research [21106001, 23655035, 21106005, 23350017] Funding Source: KAKEN

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Nickel-catalyzed intermolecular [3 + 2] cycloaddition of vinylcyclopropanes to imines has been developed. This transformation generates substituted pyrrolidines in high yields, with good regio- and diastereo- selectivity under mild reaction conditions. A variety of imines can be used in this reaction. An asymmetric variant of the reaction has also been demonstrated.

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