Issue 27, 2019

Nickel-catalyzed decarbonylation of N-acylated N-heteroarenes

Abstract

Nickel-catalyzed decarbonylation of N-acylated N-heteroarenes is developed. This method can be used to produce a variety of N-aryl heteroarenes, including pyrroles, indoles, carbazoles and phenoxazines, using benzoic acid derivatives as arylating reagents. Arylnickelamide intermediates that are relevant to the catalytic reaction were characterized by X-ray crystallography. When N-acylated benzimidazoles are used as substrates, decarbonylation accompanied 1,2-migration to form 2-arylated benzimidazoles.

Graphical abstract: Nickel-catalyzed decarbonylation of N-acylated N-heteroarenes

Supplementary files

Article information

Article type
Edge Article
Submitted
25 Apr 2019
Accepted
27 May 2019
First published
29 May 2019
This article is Open Access

All publication charges for this article have been paid for by the Royal Society of Chemistry
Creative Commons BY-NC license

Chem. Sci., 2019,10, 6666-6671

Nickel-catalyzed decarbonylation of N-acylated N-heteroarenes

T. Morioka, S. Nakatani, Y. Sakamoto, T. Kodama, S. Ogoshi, N. Chatani and M. Tobisu, Chem. Sci., 2019, 10, 6666 DOI: 10.1039/C9SC02035G

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