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Biaryl Formation via Base-Promoted Direct Coupling Reactions of Arenes with Aryl Halides.


ABSTRACT: In the absence of ligand, Cs2CO3-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.

SUBMITTER: Iqbal MA 

PROVIDER: S-EPMC8223439 | biostudies-literature | 2021 Jun

REPOSITORIES: biostudies-literature

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Biaryl Formation via Base-Promoted Direct Coupling Reactions of Arenes with Aryl Halides.

Iqbal Muhammad Asif MA   Lu Le L   Mehmood Hina H   Hua Ruimao R  

ACS omega 20210609 24


In the absence of ligand, Cs<sub>2</sub>CO<sub>3</sub>-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 b  ...[more]

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