Electroreductive Remote Benzylic C(sp<sup>3</sup>)–H Arylation of Aliphatic Ethers Using Cyanoarenes for the Synthesis of α-(Hetero)aryl Ethers
Liang Zeng, Hua-Zhan Ren, Gui‐Fen Lv, Xuan‐Hui Ouyang, Deliang He, Jin‐Heng Li
Abstract
An iodoarene-driven electroreductive remote C(sp 3 )–H arylation of unsymmetrical 1-( o -iodoaryl)alkyl ethers with cyanoarenes for the site selective synthesis of α-(hetero)aryl ethers is developed. With the introduction of cyanoarenes as both aryl sources and electron transfer mediators, this method includes an iodoarene-driven strategy to enable the regiocontrollable formation of two new bonds, one C(sp 2 )–H bond, and one C(sp 2 )–C(sp 3 ) bond, in a single reaction step through the sequence of halogen atom transfer (XAT), hydrogen atom transfer (HAT), radical–radical coupling, and decyanation.
Topics & Concepts
ChemistryArylAlkylHalogenHydrogen atomMedicinal chemistryStereochemistryHydrogen bondCombinatorial chemistryElectron transferMoleculeOrganic chemistryCatalytic C–H Functionalization MethodsRadical Photochemical ReactionsSulfur-Based Synthesis Techniques