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Exploiting Transient Radical Cations as Brønsted Acids for Allylic C–H Heteroarylation of Enol Silyl Ethers
Authors:Dr Tsubasa Nakashima  Haruka Fujimori  Dr Kohsuke Ohmatsu  Prof Takashi Ooi
Institution:Institute of Transformative Bio-Molecules (WPI-ITbM), and Department of Molecular and Macromolecular Chemistry, Graduate School of Engineering, Nagoya University, Nagoya, 464-8601 Japan
Abstract:Intermediary radical cations, generated through single-electron oxidation of enol silyl ethers by excited Ir-based photocatalysts, can be exploited as Brønsted acids for the activation of heteroarylcyanides. This strategy enables the direct allylic C?H heteroarylation of enol silyl ethers under visible-light irradiation.
Keywords:C?H functionalization  enol silyl ethers  heteroarylation  photoredox catalysis  radical cations
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