Issue 13, 2021

Direct C–H aminocarbonylation of N-heteroarenes with isocyanides under transition metal-free conditions

Abstract

A C–C bond forming amide synthesis through direct C–H aminocarbonylation of N-heteroarenes with isocyanides was developed. The reaction was mediated by an inorganic persulfate salt under transition metal-free conditions. Mechanistic studies suggested a radical pathway for this reaction without the participation of H2O and O2. This method also showed merits of substrate availability, easy operation and atom economy. It provided an efficient route for straightforward synthesis of N-heteroaryl amides.

Graphical abstract: Direct C–H aminocarbonylation of N-heteroarenes with isocyanides under transition metal-free conditions

Supplementary files

Article information

Article type
Communication
Submitted
08 Feb 2021
Accepted
15 Mar 2021
First published
16 Mar 2021

Org. Biomol. Chem., 2021,19, 2917-2922

Direct C–H aminocarbonylation of N-heteroarenes with isocyanides under transition metal-free conditions

Z. Zhou, H. Ji, Q. Li, Q. Zhang and D. Li, Org. Biomol. Chem., 2021, 19, 2917 DOI: 10.1039/D1OB00245G

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