"Naked Nickel"-Catalyzed Amination of Heteroaryl Bromides.

Org Lett

Max-Planck-Institut für Kohlenforschung, Department of Organometallic Chemistry, Kaiser-Wilhelm-Platz 1, 45470 Mülheim an der Ruhr, North Rhine-Westphalia, Germany.

Published: July 2024

In this Letter, we report that the air-stable "naked nickel" [Ni(stb)] is a competent catalyst in thermal C-N bond formation between (hetero)aryl bromides and -based nucleophiles. The catalytic system is characterized by a "naked nickel" complex and Zn and by the absence of external light sources, photocatalysts, exogenous ligands, and electrical setups. Upon application of this method, various heteroaryls bearing Lewis-basic heteroatoms can be accommodated and directly aminated with a set of primary and secondary amines.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11267598PMC
http://dx.doi.org/10.1021/acs.orglett.4c01738DOI Listing

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