Recent developments for the photoinduced Ar–X bond dissociation reaction

Literature Information

Publication Date 2016-06-13
DOI 10.1039/C6QO00103C
Impact Factor 5.281
Authors

Guanyinsheng Qiu, Yuewen Li


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Abstract

Recent developments in the photochemical carbon–carbon and carbon–heteroatom bond formation via photoinduced Ar–X bond dissociation are summarized. The transformations through the Ar–X bond dissociation enabled by photoenergy include nucleophilic substitution, arylation, alkylation, aminocarbonylation, aminosulfonylation and decarboxylative coupling reactions. Usually, the reactions undergo one-electron-transfer couplings and aryl radicals or cations are involved as the key intermediates. Under ultraviolet irradiation or visible light, the reactions of aryl halides with reactive partners proceed smoothly under mild conditions. In some cases, the transformations can proceed without any metals or photo-redox catalysts. Moreover, the broad reaction scope is demonstrated with good functional group tolerance.

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Organic Chemistry Frontiers

Organic Chemistry Frontiers
CiteScore: 7.8
Self-citation Rate: 8.7%
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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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