Issue 46, 2021, Issue in Progress

Palladium-catalyzed bisthiolation of terminal alkynes for the assembly of diverse (Z)-1,2-bis(arylthio)alkene derivatives

Abstract

An efficient and straightforward palladium-catalyzed three-component cascade bisthiolation of terminal alkynes and arylhydrazines with sodium thiosulfate (Na2S2O3) 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–Cl2 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.

Graphical abstract: Palladium-catalyzed bisthiolation of terminal alkynes for the assembly of diverse (Z)-1,2-bis(arylthio)alkene derivatives

Supplementary files

Article information

Article type
Paper
Submitted
29 Jul 2021
Accepted
18 Aug 2021
First published
23 Aug 2021
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2021,11, 28447-28451

Palladium-catalyzed bisthiolation of terminal alkynes for the assembly of diverse (Z)-1,2-bis(arylthio)alkene derivatives

Y. Lai, S. Yan, D. He, L. Zhou, Z. Chen, Y. Du and J. Li, RSC Adv., 2021, 11, 28447 DOI: 10.1039/D1RA05773A

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