ArticleChemical science2026
Electrochemically cooperative halogen-cation delivery enables modular electrophilic haloesterification of both activated and unactivated alkenes.
Article in Chemical science, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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Abstract
Intermolecular haloesterification of alkenes is a practical platform for modular ester synthesis. However, current methods are restricted to aryl-activated and directing-group-containing alkenes, leaving low-reactivity, electron-deficient alkenes with alkyl substituents largely underexplored. Notably, electrophilic reactions involving chloroesterification of electron-deficient alkenes are also challenging due to the difficulty in controlling selectivity. In this work, we present an electrochemically cooperative halogen-cation delivery strategy that achieves modular electrophilic haloesterification of both activated and unactivated alkenes with good chemo-, regio-, and diastereoselectivity levels. It exhibits enhanced reactivity (with yields of up to 90%) and selectivity (regioselectivities and diastereoselectivities exceeding 20 : 1), as the amide mediates the transfer of Cl
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