Issue 24, 2021

Nickel-catalyzed direct cross-coupling of heterocyclic phosphonium salts with aryl bromides

Abstract

The direct cross-coupling of heterocyclic phosphonium salts with aryl bromides was successfully realized by performing the reactions in THF at ambient temperature with the aid of a nickel(II) catalyst, the 1,10-phenanthroline-5,6-dione ligand, magnesium turnings, and lithium chloride, providing an easy access to 4-arylated pyridine, quinoline, quinoxaline, and pyrazine.

Graphical abstract: Nickel-catalyzed direct cross-coupling of heterocyclic phosphonium salts with aryl bromides

Supplementary files

Article information

Article type
Research Article
Submitted
30 Sep 2021
Accepted
25 Oct 2021
First published
26 Oct 2021

Org. Chem. Front., 2021,8, 6931-6936

Nickel-catalyzed direct cross-coupling of heterocyclic phosphonium salts with aryl bromides

Y. Cui, W. Li, N. Ma, C. Shen, X. Zhou, X. Chu, W. Rao and Z. Shen, Org. Chem. Front., 2021, 8, 6931 DOI: 10.1039/D1QO01474A

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