Atom- and step-economic 1,3-thiosulfonylation of activated allenes with thiosulfonates to access vinyl sulfones/sulfides.
Xiao XiaoHong-Yu TianYin-Qiu HuangYin-Jie LuJing-Jie FangGao-Jie ZhouXiangtao ChenPublished in: Chemical communications (Cambridge, England) (2022)
A new type of organocatalyzed 1,3-thiosulfonylation has been developed to straightforwardly access highly functionalized vinyl sulfones, which features mild conditions, atom- and step-economy, practicability, conciseness, and environmental friendliness. Moreover, these valuable products can be transformed to vinyl sulfides via a base-promoted isomerization. The versatile route can efficiently and rapidly introduce SCD 3 groups with excellent levels of deuterium content (>99% D) by utilizing our newly developed SCD 3 reagents. Gram-scale operations and further transformations are smoothly carried out, providing promising applications for drug discovery.