Csp3-Csp2 Coupling of Isonitriles and (Hetero)arenes through a Photoredox-Catalyzed Double Decyanation Process

04 April 2024, Version 1
This content is a preprint and has not undergone peer review at the time of posting.

Abstract

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 Csp3-Csp2 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 terciary substrates, including amino acid derivatives and druglike molecules.

Keywords

Isonitriles
Pyridines
C-N cleavage
photoredox catalysis

Supplementary materials

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Supplementary Information
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Materials and methods, experimental procedures, complete computational details, 1H and 13C NMR spectra, and HRMS data are available in the Supplementary Information.
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