Incorporating a sulfonyl group into parent molecules
has been shown
to effectively improve their synthetic applications and bioactivities.
In this study, we present a straightforward and practical approach
for the ring-opening reaction of alkenyl–aryl sulfonium salts
with sodium sulfinates to produce a range of sulfur-containing alkyl
sulfones. This method offers the benefits of mild reaction conditions,
easily accessible raw materials, wide substrate applicability, good
functional group compatibility, and operational simplicity. Importantly,
the resulting products can be readily converted into sulfoxides, sulfones,
sulfoximines, and some heterocyclic compounds.