4.8 Article

Nickel-Catalyzed Reductive Coupling of Aryl Halides with Secondary Alkyl Bromides and Allylic Acetate

Journal

ORGANIC LETTERS
Volume 14, Issue 13, Pages 3352-3355

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ol3013342

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Funding

  1. Chinese NSF [2097209, 21172140]
  2. Program for Professor of Special Appointment (Eastern Scholar) at Shanghai Institutions of Higher Learning, Shanghai Education Committee [10YZ04]
  3. Shanghai Leading Academic Discipline Project [S30107]

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A room-temperature Ni-catalyzed reductive method for the coupling of aryl bromides with secondary alkyl bromides has been developed, providing C(sp(2))-C(sp(3)) products in good to excellent yields. Slight modification of this protocol allows efficient coupling of activated aryl chlorides with cyclohexyl bromide and aryl bromides with allylic acetate.

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