Experimental study demonstrates photoinduced pyridine N-oxide-catalyzed C–H alkylation of heterocycles, indicating a sustainable transition-metal-free route for radical-mediated synthesis.
A photoinduced pyridine N-oxide-catalyzed C–H alkylation of azauracils and quinoxalinones with alkyl boronic acids has been developed. The transformation proceeds under transition-metal-free aerobic conditions without requiring a separate photoredox catalyst or photosensitizer and exhibits broad substrate scope, including late-stage functionalization of biorelevant molecules and gram-scale synthesis. Mechanistic studies support alkyl radical generation from alkyl boronic acids by photoexcited pyridine N-oxide. This study highlights the potential of pyridine N-oxide organophotocatalysis for radical-mediated synthetic transformations.
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Sudharsan et al. (2026) studied this question.
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