Formal base-free homolytic aromatic substitutions via photoredox catalysis

Literature Information

Publication Date 2015-03-26
DOI 10.1039/C5QO00031A
Impact Factor 5.281
Authors

Filipe Gomes, Vanessa Narbonne, Florent Blanchard


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Abstract

We developed a simple and convenient method to assemble biaryls exploiting a photoredox catalyst and visible light. Diazonium salts generate aryl radicals that could then add on unactivated (hetero)arenes and the sequence eventually delivers products via formal homolytic aromatic substitutions. The direct C–H arylation of these usually unreactive substrates is achieved at room temperature using low catalyst loadings and shows broad functional group tolerance.

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Organic Chemistry Frontiers

Organic Chemistry Frontiers
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Organic Chemistry Frontiers publishes high-quality research from across organic chemistry. Emphases are placed on studies that make significant contributions to the field of organic chemistry by reporting either new or significantly improved protocols or methodologies. Topics include, but are not limited to the following: Organic synthesis Development of synthetic methodologies Catalysis Natural products Functional organic materials Supramolecular and macromolecular chemistry Physical and computational organic chemistry

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