Mechanochemical Decarbonylative Cross-Coupling of Amides via Cooperative Catalysis and Triple C–N/C–C/C–H Activation

Mechanochemical solvent-less cross-couplings have emerged as a powerful frontier in the formation of carbon–carbon and carbon–heteroatom bonds under sustainable conditions. However, despite considerable progress, mechanochemical decarbonylative cross-couplings have been unexplored. Herein, we report the first decarbonylative mechanochemical cross-coupling for the heteroarylation of amides by a triple C–N/C–C/C–H activation. The catalytic system exploits cooperative Ni/Cu catalysis to simultaneously activate the amide N–C(O) and the heterocycle C–H bonds, resulting in a highly chemoselective coupling. The reaction is characterized by a broad scope of the amide and the heterocyclic component to furnish heterobiaryls, which are among the most privileged scaffolds in organic synthesis. We demonstrate that decarbonylative mechanochemical cross-couplings will provide novel access to a range of valuable products that are among the most common structures in organic chemistry.

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Publication Details

Journal
ACS Sustainable Chemistry & Engineering
Published
2024-11-13
DOI
https://doi.org/10.1021/acssuschemeng.4c05179
Citations
10
Primary Topic
Advanced Synthetic Organic Chemistry
Type
article
Field-Weighted Citation Impact
2.50

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article

Mechanochemical Decarbonylative Cross-Coupling of Amides via Cooperative Catalysis and Triple C–N/C–C/C–H Activation

Wenxuan Yan, Sijie Zhou, Jin Zhang, Michal Szostak et al.
10 citations
ACS Sustainable Chemistry & Engineering
Advanced Synthetic Organic Chemistry
2.50
article

Mechanochemical Decarbonylative Cross-Coupling of Amides via Cooperative Catalysis and Triple C–N/C–C/C–H Activation

Wenxuan Yan, Sijie Zhou, Jin Zhang, Michal Szostak, Yangmin Ma
article en
10 citations

Abstract

Mechanochemical solvent-less cross-couplings have emerged as a powerful frontier in the formation of carbon–carbon and carbon–heteroatom bonds under sustainable conditions. However, despite considerable progress, mechanochemical decarbonylative cross-couplings have been unexplored. Herein, we report the first decarbonylative mechanochemical cross-coupling for the heteroarylation of amides by a triple C–N/C–C/C–H activation. The catalytic system exploits cooperative Ni/Cu catalysis to simultaneously activate the amide N–C(O) and the heterocycle C–H bonds, resulting in a highly chemoselective coupling. The reaction is characterized by a broad scope of the amide and the heterocyclic component to furnish heterobiaryls, which are among the most privileged scaffolds in organic synthesis. We demonstrate that decarbonylative mechanochemical cross-couplings will provide novel access to a range of valuable products that are among the most common structures in organic chemistry.

ACS Sustainable Chemistry & EngineeringVol. 12(47)
Rutgers, The State University of New Jersey (US), Shaanxi University of Science and Technology (CN)
Rutgers, The State University of New Jersey, National Natural Science Foundation of China, Scientific Research Plan Projects of Shaanxi Education Department, Division of Chemistry
Zero hunger
Openalex Percentile: Top 11%
Advanced Synthetic Organic Chemistry
2.50
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