3-Acyl imidazo[1,5-a]pyridines, featured pharmaceutical moieties that were prepared by a three-step reaction conventionally, could be obtained in one step by an electrochemical tandem sp3 (C–H) double amination of acetophenones with… Click to show full abstract
3-Acyl imidazo[1,5-a]pyridines, featured pharmaceutical moieties that were prepared by a three-step reaction conventionally, could be obtained in one step by an electrochemical tandem sp3 (C–H) double amination of acetophenones with pyridine ethylamines using ammonium iodide as a redox mediator.
               
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