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Photoinduced inverse Sonogashira coupling reaction

Alkynes are widely used in chemistry, medicine and materials science. Here we demonstrate a transition-metal and photocatalyst-free inverse Sonogashira coupling reaction between iodoalkynes and (hetero)arenes or alkenes under visible-light irradiation. Mechanistic and computational studies suggest t...

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Detalles Bibliográficos
Autores principales: Zhang, Lizhu, Wei, Cunbo, Wu, Jiawen, Liu, Dan, Yao, Yinchao, Chen, Zhuo, Liu, Jianxun, Yao, Chang-Jiang, Li, Dinghua, Yang, Rongjie, Xia, Zhonghua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9241966/
https://www.ncbi.nlm.nih.gov/pubmed/35872819
http://dx.doi.org/10.1039/d2sc01933g
Descripción
Sumario:Alkynes are widely used in chemistry, medicine and materials science. Here we demonstrate a transition-metal and photocatalyst-free inverse Sonogashira coupling reaction between iodoalkynes and (hetero)arenes or alkenes under visible-light irradiation. Mechanistic and computational studies suggest that iodoalkynes can be directly activated by visible light irradiation, and an excited state iodoalkyne acted as an “alkynyl radical synthetic equivalent”, reacting with a series of C(sp(2))–H bonds for coupling products. This work should open new windows in radical chemistry and alkynylation method.