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Biaryl Formation via Base-Promoted Direct Coupling Reactions of Arenes with Aryl Halides
[Image: see text] In the absence of ligand, Cs(2)CO(3)-promoted cross-coupling reaction of arenes with cyano-/nitro-substituted aryl halides in DMSO affording biaryls is reported. The cyano/nitro group in biaryls is useful and convenient for further transformation. The formation of dibenzofurans res...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8223439/ https://www.ncbi.nlm.nih.gov/pubmed/34179643 http://dx.doi.org/10.1021/acsomega.1c01736 |
Sumario: | [Image: see text] In the absence of ligand, Cs(2)CO(3)-promoted cross-coupling reaction of arenes with cyano-/nitro-substituted aryl halides in DMSO affording biaryls is reported. The cyano/nitro group in biaryls is useful and convenient for further transformation. The formation of dibenzofurans resulting from the reactions between arenes and 1-bromo-2-iodobenzene is also reported. On the basis of control experiments and theoretical studies, a radical mechanism is proposed for the formation of biaryls. |
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