Photoinduced defluorinative alkylation of trifluoromethyl alkenes with carbonyl derivatives by C–C bond scission
Literature Information
Lu-Yu Yan, Tian-Zhen Zhang, Ze-Zhong Lv, Ming-Chen Fu
The development of novel radical precursors for the preparation of structurally diverse gem-difluoroalkenes is still in great demand, especially those enabled by metal-free catalysis. In this context, a metal-free photoinduced method for the synthesis of gem-difluoroalkenes was established, in which various carbonyl derivatives were successfully used as alkyl radical precursors via C–C bond cleavage to react with available α-trifluoromethylstyrenes. In particular, the successful gram-scale synthesis and late-stage modification for biologically active molecules highlights their potential value in drug discovery.
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Source Journal
Organic Chemistry Frontiers

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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