4.8 Article

Copper-Catalyzed Photoinduced Enantioselective Dual Carbofunctionalization of Alkenes

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ORGANIC LETTERS
卷 22, 期 4, 页码 1490-1494

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AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.0c00071

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资金

  1. NSFC [21772218, 21821002]
  2. State Key Laboratory of Organometallic Chemistry
  3. Shanghai Institute of Organic Chemistry
  4. Chinese Academy of Sciences
  5. [XDB20000000]

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A photoinduced, copper-catalyzed, highly enantioselective dual alkylation/arylation and alkynylation of alkene is reported. A single chiral copper(1) complex serves to enable photoredox catalysis and induce enantioselectivity during the reaction. This reaction couples three different components under mild reaction conditions, exhibits a broad substrate scope, and provides facile access to chiral propargylic systems, including those featuring valuable fluorinated substituents.

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