Palladium-catalyzed bisthiolation of terminal alkynes for the assembly of diverse ( Z )-1,2-bis(arylthio)alkene derivatives.
Yin-Long LaiShaoxi YanDan HeLi-Zhen ZhouZi-Shen ChenYu-Long DuJianxiao LiPublished in: RSC advances (2021)
An efficient and straightforward palladium-catalyzed three-component cascade bisthiolation of terminal alkynes and arylhydrazines with sodium thiosulfate (Na 2 S 2 O 3 ) as the sulfur source for the assembly of functionalized ( Z )-1,2-bis(arylthio)alkene derivatives is described. Using 0.5 mol% IPr-Pd-Im-Cl 2 as the catalyst, a wide range of terminal alkynes and arylhydrazines are well tolerated, thus producing the desired products in good yields with good functional group tolerance and excellent regioselectivity. Moreover, this protocol could be readily scaled up, showing potential applications in organic synthesis and material science.