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Mechanochemical Decarbonylative Cross-Coupling of Amides via Cooperative Catalysis and Triple C-N/C-C/C-H Activation
被引:0
|作者:
Zhang, Jin
[1
]
Zhang, Jiaojiao
[1
]
Yan, Wenxuan
[1
]
Zhou, Sijie
[1
]
Ma, Yangmin
[1
]
Szostak, Michal
[2
]
机构:
[1] Shaanxi Univ Sci & Technol, Coll Chem & Chem Engn, Xian 710021, Shaanxi, Peoples R China
[2] Rutgers State Univ, Dept Chem, 73 Warren St, Newark, NJ 07102 USA
来源:
ACS SUSTAINABLE CHEMISTRY & ENGINEERING
|
2024年
/
12卷
/
47期
基金:
中国国家自然科学基金;
关键词:
mechanochemistry;
amide bonds;
N-C cleavage;
solvent-free;
decarbonylative cross-coupling;
ARYL BOND FORMATION;
CARBOXYLIC-ACIDS;
ARYLATION;
ESTERS;
AZOLES;
D O I:
10.1021/acssuschemeng.4c05179
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
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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页码:17127 / 17134
页数:8
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