Palladium-Catalyzed Denitrative C-N Coupling of Amides with Nitroarenes Enabled by Al(OTf) 3

Abstract

We report a Pd-catalyzed denitrative C-N coupling of amide nucleophiles with nitroarenes, providing direct and atomeconomical access to N-aryl amides from readily available nitroarene feedstocks. Al(OTf)3 is essential, both promoting the reaction and suppressing BrettPhos oxidation to maintain the active Pd-phosphine species. The method shows broad amide scope and delivers products in up to 95% yield.

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Article information

Article type
Communication
Submitted
02 Feb 2026
Accepted
18 Mar 2026
First published
19 Mar 2026
This article is Open Access
Creative Commons BY license

Chem. Commun., 2026, Accepted Manuscript

Palladium-Catalyzed Denitrative C-N Coupling of Amides with Nitroarenes Enabled by Al(OTf) 3

L. Yang, X. Wang and W. Chen, Chem. Commun., 2026, Accepted Manuscript , DOI: 10.1039/D6CC00697C

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