An efficient method synthesizes β-hydroxysulfones in high yields, indicating strong catalyst interaction.
An efficient method is developed for the synthesis of β ‐hydroxysulfones from difunctionalized olefins and substituted sodium sulfinates with Mn(OAc) 3 /Lewis acid catalyst through aerobic oxidation, which provides β ‐hydroxysulfones in middle to high yields with broad compatibility of functional groups. The high efficiency is attributed to the interaction between the Mn(III) species and Lewis acid such as Ce(OTf) 3 that enhances its redox potential, thus accelerating Mn(III)‐catalyzed sulfonyl radical formation from sulfonates through single‐electron transfer mechanism.
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Li et al. (2026) studied this question.
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