4.8 Article

Copper-Catalyzed Intermolecular Trifluoromethylarylation of Alkenes: Mutual Activation of Arylboronic Acid and CF3+ Reagent

Journal

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 136, Issue 29, Pages 10202-10205

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ja504458j

Keywords

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Funding

  1. 973 program [2011CB808700]
  2. NSFC [21225210, 21202185, 21121062]
  3. STCSM [11JC1415000]
  4. CAS/SAFEA International Partnership Program for Creative Research Teams

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A novel copper-catalyzed intermolecular trifluoromethylarylation of alkenes is developed using less active ether-type Togni's reagent under mild reaction conditions. Various alkenes and diverse arylboronic acids are compatible with these conditions. Preliminary mechanistic studies reveal that a mutual activation process between arylboronic acid and CF3+ reagent is essential. In addition, the reaction might involve a rate-determining transmetalation, and the final aryl C-C bond is derived from reductive elimination of the aryl(alkyl)Cu(III) intermediate.

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