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Metal‐Free C−H Functionalization via Diaryliodonium Salts with a Chemically Robust Dummy Ligand

Yixuan Chen, Yuefei Gu, Huan Meng, Qianzhen Shao, Zhenchuang Xu, Wenjing Bao, Yu‐Cheng Gu, Xiao‐Song Xue, Yanchuan Zhao

2022Angewandte Chemie International Edition47 citationsDOI

Abstract

A two-step strategy for the transition-metal-free C-H functionalization of arenes using unsymmetrical iodonium salts as versatile synthetic linchpins is presented. The key to the success of this strategy is the identification of the 3,5-dimethyl-4-isoxazolyl (DMIX) group as a superior dummy ligand, which enables not only site-selective C-H functionalization to afford unsymmetrical iodonium salts, but also highly selective aryl transfer during the subsequent metal-free coupling reaction. Both electron-rich and moderately electron-deficient arenes can be converted into the iodonium salts through C-H functionalization, allowing for diverse structural elaboration by metal-free C-N, C-C, C-S, and C-O coupling.

Topics & Concepts

Surface modificationChemistryLigand (biochemistry)ArylCombinatorial chemistryMetalTransition metalElectron transferChemical modificationPolymer chemistryPhotochemistryOrganic chemistryCatalysisAlkylReceptorPhysical chemistryBiochemistryCatalytic C–H Functionalization MethodsOxidative Organic Chemistry ReactionsSynthesis and Catalytic Reactions
Metal‐Free C−H Functionalization via Diaryliodonium Salts with a Chemically Robust Dummy Ligand | Litcius