Mechanistically orthogonal radical strategies converging on programmable site-selective halogenation of quinoxalinones
Abstract
We report reagent-programmed C3-, C6-, and C7-halogenation of quinoxalinones via two orthogonal radical pathways converging on identical products. A sunlight-driven PDI photoredox system activates inorganic halides, while a moisture assisted N-halosuccinimide radical chain yields 7-halodihydroquinoxalin-2,3-diones with high selectivity and 6,7-dihalo products at higher halide loadings.

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