Radical‐Promoted Distal C−H Functionalization of C(sp<sup>3</sup>) Centers with Fluorinated Moieties
Enzo Nobile, Thomas Castanheiro, Tatiana Besset
Abstract
Due to their unique properties, fluorinated scaffolds are pivotal compounds in pharmaceuticals, agrochemicals, and materials science. Over the last years, the development of versatile strategies for the selective synthesis of fluorinated molecules by direct C-H bond functionalization has attracted a lot of attention. In particular, the design of novel transformations based on a radical process was a bottleneck for distal C-H functionalization reactions, offering synthetic solutions for the selective introduction of fluorinated groups. This Minireview highlights the major contributions in this blossoming field. The development of new methodologies for the remote functionalization of aliphatic derivatives with various fluorinated groups based on a 1,5-hydrogen atom transfer process and a β-fragmentation reaction will be showcased and discussed.