While C–H functionalizations at C2 and C4 positions of pyridines are enabled by their inherent reactivities, selective derivatization at the C3 position has long posed a significant challenge. Here, the authors report a mild and regioselective method for C3-amination that relies on the photochemical reaction of Zincke imines with amidyl radicals generated from N-aminopyridinium salts.
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