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Quinolines are privileged scaffolds in various bioactive natural products and pharmaceuticals.1 Therefore,many methods for the synthesis of quinolines have been developed including Combes quinoline synthesis,Friedlander synthesis,Skraup synthesis and so on.Based on our previous studies on the diaryliodonium salts,we herein reported a novel copper-catalyze tandem arylation-cyclization process for the preparation of quinolines from readily available isothiocyanates with diaryliodonium salts.