Micellar photocatalysis has {recently|lately|not too long ago} opened new avenues to activate {strong|powerful|robust|sturdy} carbon halide bonds. So far, {however|nevertheless|nonetheless|even so|on the other hand|having said that}, it has {mainly|primarily|mostly} explored strongly {reducing|decreasing|lowering|minimizing} {conditions|circumstances|situations} restricting the {available|accessible|obtainable|offered|readily available|out there} chemical space to radical or anionic reactivity. {Here|Right here}, we demonstrate a radical-polar crossover {process|procedure|method|approach|course of action} involving cationic intermediates, which enables chemodivergent modification of chlorinated benzamide derivatives {via|by way of|through|by means of} either C H arylation or N dealkylation. The catalytic {system|method|program|technique} operates {under|below|beneath} mild {conditions|circumstances|situations} employing methylene blue as a photocatalyst and blue LEDs {as the|because the} light {source|supply}. {Factors|Elements|Aspects|Variables|Components|Things} {determining|figuring out} the reactivity of substrates and preliminary mechanistic {studies|research} are presented. 1041026-70-3 custom synthesis 3-Amino-4-pyridinecarboxaldehyde structure PMID:23074147

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