| Literature DB >> 31406389 |
Quentin D Tercenio1, Erik J Alexanian1.
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.Entities:
Keywords: C−H alkylation; Nickel catalysis; Unactivated halides; carbocyclization
Year: 2019 PMID: 31406389 PMCID: PMC6690380 DOI: 10.1016/j.tet.2019.05.047
Source DB: PubMed Journal: Tetrahedron ISSN: 0040-4020 Impact factor: 2.457