Electrochemical Oxidative Halogenation of <i>N</i>-Aryl Alkynamides for the Synthesis of Spiro[4.5]trienones
Ke Yu, Xianqiang Kong, Jiajun Yang, Guodong Li, Bo Xu, Qianjin Chen
Abstract
We developed a green method for the synthesis of spiro[4.5]trienones through an electrochemical oxidative halocyclization with N-aryl alkynamides. This reaction was conducted under metal-catalyst- and exogenous-oxidant-free conditions at room temperature. Using readily available LiCl, LiBr, and LiI as the halogen source, a variety of dearomative halo-spirocyclization products were obtained in good to excellent yields with a broad scope and functional group tolerance.
Topics & Concepts
HalogenationArylElectrochemistryHalogenCatalysisOxidative phosphorylationChemistryCombinatorial chemistryNuclear chemistryOrganic chemistryElectrodeBiochemistryPhysical chemistryAlkylOxidative Organic Chemistry ReactionsCatalytic C–H Functionalization MethodsRadical Photochemical Reactions