Demonstrates efficient bromo-alkyloxylation in conjugated alkenes, suggesting a novel synthetic approach.
A highly efficient bromo-alkyloxylation of conjugated alkenes through direct electrolysis under mild reaction conditions has been developed. This protocol provides an efficient approach to a series of bromo-alkyloxy-alkenes/alkynes bearing various functional groups, achieving moderate to high yields. Mechanistic studies revealed that the charge and ionization effects induce the high selectivity observed in the reaction of 1,3-dienes and 1,3-enynes.
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Xue et al. (2026) studied this question.
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