4.8 Article

Iron- or Copper-Catalyzed Trifluoromethylation of Acrylamide-Tethered Alkylidenecyclopropanes: Facile Synthesis of CF3-Containing Polycyclic Benzazepine Derivatives

Journal

ACS CATALYSIS
Volume 6, Issue 2, Pages 526-531

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acscatal.5b02400

Keywords

iron or copper catalysis; alkylidenecyclopropanes; tetracyclic benzazepine derivatives; radical addition; activated alkenes; ring opening

Funding

  1. National Basic Research Program of China [(973)-2015CB856603]
  2. National Natural Science Foundation of China [20472096, 21372241, 21361140350, 20672127, 21421091, 21372250, 21121062, 21302203, 20732008, 21572052]

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A novel iron- or copper-catalyzed trifluoromethylation of acrylamide-tethered alkylidenecyclopropanes with Togni reagent II to construct CF3-containing tetracyclic benzazepine derivatives under mild and convenient conditions has been disclosed. The chemoselective addition of in situ generated trifluoromethyl radical onto the activated alkenes triggers the reaction followed by a ring-opening process of alkylidenecyclopropanes, leading to the formation of two types of CF3-containing tetracyclic benzazepine derivatives in moderate to good yields, respectively, with excellent functional group tolerance.

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