Jingrui He , Xinrui Zhou , Haibo Mei , Ata Makarem , Ramin Javahershenas , Vadim A. Soloshonok , Jianlin Han
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Electrochemical reaction of indole-tethered alkynes enabling stereoselective synthesis of iodovinyl spiroindolenine-cyclopentanes†
A novel electrochemical iodination/spirocyclization reaction of 3-alkynyl indoles with n-Bu4NI as coupling partner and electrolyte is developed, which affords iodovinyl spiroindolenine-cyclopentanes as products in excellent yields and high E-stereoselectivities. This reaction tolerates a wide range of 3-alkynyl indoles and iodide sources, which represents the first example of the electrosynthesis of spiroindolenine-cycloalkanes.
期刊介绍:
ChemComm (Chemical Communications) is renowned as the fastest publisher of articles providing information on new avenues of research, drawn from all the world''s major areas of chemical research.