Affiliation:
1. Chemical Synthesis and Pollution Control Key Laboratory of Sichuan Province China West Normal University Nanchong 637002 P. R. China
2. National Engineering Technology Research Center of Chiral Pharmaceutical Lunan Pharmaceutical Group Co., Ltd Linyi City, Shandong 276005 P. R. China
Abstract
AbstractHerein, we report the first electricity‐driven and metal‐free C(3)−H fluoroalkoxylation of quinoxalin‐2(1H)‐ones with both α‐monosubstituted and α,α‐disubstituted fluoroalkyl alcohols. This strategy features the advantages of convenience, mildness, effEctiveness and broad substrate practicality for synthesizing a new type of 3‐fluoroalkoxylated quinoxalin‐2(1H)‐ones.