Abstract
AbstractA visible‐light‐induced direct C(sp2)−H amination of quinoxalin‐2(1H)‐ones toward the synthesis of substituted 3‐aminoquinoxalin‐2(1H)‐ones with TMSN3 has been firstly developed. This transformation achieved C(sp2)−H/N−H coupling in the absence of external ligand and oxidant. Notably, this methodology features mild reaction conditions, broad substrate scope and operational simplicity.magnified image
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