An Efficient Copper-Catalyzed C(sp2)–S Formation Starting from Aryl Iodides and Tetramethylthiuram Monosulfide (TMTM)

Yue-Xiao Wu; Kang Peng; Jing-Hang Li; Zhi-Bing Dong

doi:10.1055/s-0040-1707899

Synthesis, Inhaltsverzeichnis

Synthesis 2020; 52(20): 3001-3006
DOI: 10.1055/s-0040-1707899

paper

An Efficient Copper-Catalyzed C(sp²)–S Formation Starting from Aryl Iodides and Tetramethylthiuram Monosulfide (TMTM)

Yue-Xiao Wu

^aSchool of Chemistry and Environmental Engineering, Wuhan Institute of Technology, Wuhan 430205, P. R. of China

,

Kang Peng

^aSchool of Chemistry and Environmental Engineering, Wuhan Institute of Technology, Wuhan 430205, P. R. of China

,

Jing-Hang Li

^aSchool of Chemistry and Environmental Engineering, Wuhan Institute of Technology, Wuhan 430205, P. R. of China

,

Zhi-Bing Dong ∗

^aSchool of Chemistry and Environmental Engineering, Wuhan Institute of Technology, Wuhan 430205, P. R. of China

^bKey Laboratory of Green Chemical Process, Ministry of Education, Wuhan Institute of Technology, Wuhan 430205, P. R. of China

^cMinistry of Education Key Laboratory for the Synthesis and Application of Organic Functional Molecules, Hubei University, Wuhan 430062, P. R. of China

^dHubei Key Laboratory of Novel Reactor and Green Chemistry Technology, Wuhan Institute of Technology, Wuhan 430205, P. R. of China eMail: dzb04982@wit.edu.cn

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Abstract

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Abstract

A new, efficient copper-catalyzed C(sp²)–S formation of phenyl dithiocarbamates starting from aryl iodides and tetramethylthiuram monosulfide (TMTM) was developed. The target compounds, phenyl dithiocarbamates with active sites, were synthesized smoothly in good to excellent yields. The easy performance, high yields, decent functional group compatibility, and cost-effective substrates make the protocol practical and attractive in C–S bond formation.

Key words

aryl iodide - thiuram - sulfur - bond formation - dithiocarbamates

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References

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