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.
Authors
- Wenxuan Yan
- Sijie Zhou
- Jin Zhang (ORCID: https://orcid.org/0000-0002-6616-7087)
- Michal Szostak (ORCID: https://orcid.org/0000-0002-9650-9690)
- Yangmin Ma (ORCID: https://orcid.org/0000-0002-6980-9532)
Institutions
- Rutgers, The State University of New Jersey (US)
- Shaanxi University of Science and Technology (CN)
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
Funders
- Rutgers, The State University of New Jersey
- National Natural Science Foundation of China
- Scientific Research Plan Projects of Shaanxi Education Department
- Division of Chemistry