Litcius/Paper detail

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

2024ACS Catalysis15 citationsDOIOpen Access PDF

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