Recent advances in radical-based C–F bond activation of polyfluoroarenes and gem-difluoroalkenes. Issue 92 (29th October 2021)

• Record Type: Journal Article
• Authors: Wang, Junlei; Gao, Han; Shi, Chengcheng; Chen, Guiling; Tan, Xia; Chen, Xuemei; Xu, Lei; Cai, Xiaodong; Huang, Binbin; Li, Hongqing
• Is Part Of: Chemical communications. Volume 57:Issue 92(2021)
• Page Start: 12203
• Page End: 12217
• Publication Date: 2021-10-29
• Subjects: Chemistry -- Periodicals; 540
• DOI: 10.1039/d1cc04189d
• Languages: English
• ISSNs: 1359-7345

Abstract

Abstract : The direct employment of polyfluoroarenes and gem -difluoroalkenes as building blocks is regarded as one of the most effective and straightforward strategies for the introduction of fluorine-containing moieties into organic skeletons. Abstract : The direct employment of polyfluoroarenes and gem -difluoroalkenes as building blocks is regarded as one of the most effective and straightforward strategies for the introduction of fluorine-containing moieties into organic skeletons. Accordingly, radical chemistry has gradually become a mild and powerful method for the activation of their C–F bonds. The radical-based transformations of polyfluoroarenes and gem -difluoroalkenes can be primarily categorized into three types based on the specific intermediates involved: (1) multifluoroaryl radical anions, (2) monofluoroalkenyl radicals and (3) other radicals. Compared with the more established multifluoroaryl radical anion pathway, the monofluoroalkenyl radical-involved cross-coupling reaction can proceed through C-radical cross-coupling, radical addition/elimination or the hydrogen atom transfer process. For the presented examples in this review, the typical reaction modes, substrate scope, radical-involved mechanisms, and late-stage applications in the modification of bioactive molecules are discussed, aiming to provide a comprehensive overview of the recent advances of the radical-based transformations of polyfluoroarenes and gem -difluoroalkenes.