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Novel strategy transforms alpha-beta-unsaturated ketones into furan skeletons using visible light catalysis.
A novel visible light-catalyzed strategy for single-carbon-atom skeletal editing of acyclic electron-deficient alkenes has been developed. This method offers an efficient approach for the high-value transformation of α,β-unsaturated ketones into multifunctionalized furan skeletons by employing α-iodonium diazo compounds as carbyne precursors under photoredox conditions.
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Peng et al. (2026) studied this question.
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