Radical transfer strategy constructs bioactive oxime ethers in alkyl boronates, suggesting agrochemical potential.
A visible-light-induced radical transfer strategy has been developed for the efficient construction of oxime ethers using alkyl boronic esters under mild, oxidant-free conditions. The protocol exhibits a broad substrate scope and excellent functional group tolerance. Crucially, several synthesized compounds displayed potent in vitro antifungal activities against Rhizoctonia solani, matching the efficacy of commercial fungicides and highlighting their potential as promising agrochemical leads.
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Zhang et al. (2026) studied this question.
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