Csp <sup>3</sup> –Csp <sup>2</sup> Coupling of Isonitriles and (Hetero)arenes through a Photoredox-Catalyzed Double Decyanation Process
María Martín, R. Martín Romero, Chiara Portolani, Mariola Tortosa
Abstract
High Resolution Image Download MS PowerPoint Slide Herein, we demonstrate the ability of isonitriles to be used as alkyl radical precursors in a photoredox-catalyzed transformation involving selective C–N cleavage and Csp 3 –Csp 2 bond formation. This protocol allows for the preparation of functionalized heteroarenes from readily available isonitriles through a decyanation process. The reaction is general for primary, secondary, and tertiary substrates, including amino acid derivatives and druglike molecules.
Topics & Concepts
CatalysisChemistryPhotoredox catalysisCoupling (piping)Combinatorial chemistryOrganic chemistryMaterials sciencePhotocatalysisMetallurgyRadical Photochemical ReactionsCatalytic C–H Functionalization MethodsSulfur-Based Synthesis Techniques