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Updated: Jan 21, 2026

Palladium N-Heterocyclic Carbene Complexes: Synthesis from Benzimidazolium Salts and Catalytic Activity in Carbon-carbon Bond-forming Reactions
Published on: July 30, 2017
Nickel-catalyzed, ring-forming aromatic C-H alkylations with unactivated alkyl halides
Quentin D Tercenio1, Erik J Alexanian1
1Department of Chemistry, The University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, United States.
Abstract:
The development of a nickel-catalyzed C-H alkylation of aromatic substrates with unactivated alkyl halides is described. This carbocyclization facilitates the synthesis of diverse fused ring systems from simple aromatic substrates and is an attractive alternative to traditional polar or radical-mediated ring formations. The present system uses unactivated primary and secondary alkyl bromides and chlorides, while avoiding the use of precious palladium catalysts and more reactive alkyl halides commonly used in related C-H alkylations.
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