“Naked Nickel”-Catalyzed Amination of Heteroaryl Bromides

04 April 2024, Version 1
This content is a preprint and has not undergone peer review at the time of posting.

Abstract

In this article we report that the air-stable “naked nickel” [Ni(4-tBustb)3] is a competent catalyst in thermal C–N bond formation between (hetero)aryl bromides and N-based nucleophiles. The catalytic system is characterized by a “naked nickel” complex and Zn, the absence of external light sources, photocatalysts, exogeneous ligands, as well as electrical setups. By applying this method, various heteroaryls bearing Lewis-basic heteroatoms can be accommodated and directly aminated with a set of primary and secondary amines.

Keywords

amination
nickel
Buchwald-Hartwig
catalysis
cross-coupling

Supplementary materials

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Title
“Naked Nickel”-Catalyzed Amination of Heteroaryl Bromides
Description
Additional materials
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