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Nickel-Catalyzed Amidation of Aryl Alkynyl Acids with Tetraalkylthiuram Disulfides: A Facile Synthesis of Aryl Alkynyl Amides

[Image: see text] Nickel-catalyzed amidation of aryl alkynyl acids using tetraalkylthiuram disulfides as the amine source is described, affording a series of aryl alkynyl amides in good to excellent yields under mild conditions. This general methodology provides an alternative pathway for the synthe...

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Detalles Bibliográficos
Autores principales: Wang, Longfei, Qiu, Jianhua, Zhang, Bohai, Chen, Mengqi, Wang, Hongxia, Miao, Xiaohui, Wu, Zhiyong, Zhao, Mingqin, Shen, Hongtao, Lai, Miao, Shi, Xiangdong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2023
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9979367/
https://www.ncbi.nlm.nih.gov/pubmed/36872968
http://dx.doi.org/10.1021/acsomega.2c07353
Descripción
Sumario:[Image: see text] Nickel-catalyzed amidation of aryl alkynyl acids using tetraalkylthiuram disulfides as the amine source is described, affording a series of aryl alkynyl amides in good to excellent yields under mild conditions. This general methodology provides an alternative pathway for the synthesis of useful aryl alkynyl amides in an operationally simple manner, which shows its practical synthetic value in organic synthesis. The mechanism of this transformation was explored through control experiments and DFT calculations.