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Iminyl-Radical-Promoted C–C Bond Cleavage/Heck-Like Coupling via Dual Cobaloxime and Photoredox Catalysis

Jia‐Lin Tu, Wan Tang, Wei Xü, Feng Liu

2021The Journal of Organic Chemistry27 citationsDOI

Abstract

We report herein an unprecedented protocol for radical–olefin coupling of α-imino-oxy acids and alkenes for the synthesis of alkene-containing nitriles via synergistic photoredox and cobaloxime catalysis. With visible-light irradiation, the transformation provides a variety of corresponding alkene-containing nitriles under mild reaction conditions. The C–C bond cleavage/Heck-like coupling reaction could generate E-selective coupling products with excellent chemo- and stereo-selectivity. This iminyl-radical-mediated reaction is external-oxidant-free, exhibits wide functional-group compatibility, and occurs with the extrusion of acetone, H2, and CO2.

Topics & Concepts

AlkeneChemistryPhotoredox catalysisPhotochemistryCatalysisBond cleavageOlefin fiberCoupling reactionCombinatorial chemistryOrganic chemistryPhotocatalysisRadical Photochemical ReactionsCatalytic C–H Functionalization MethodsSulfur-Based Synthesis Techniques
Iminyl-Radical-Promoted C–C Bond Cleavage/Heck-Like Coupling via Dual Cobaloxime and Photoredox Catalysis | Litcius