scholarly journals SYNTHESIS OF BIARYLS FROM ARYL IODIDES AND ZINC POWDER BY MEANS OF NICKEL CATALYST

1979 ◽  
Vol 8 (8) ◽  
pp. 917-918 ◽  
Author(s):  
Kentaro Takagi ◽  
Naomi Hayama ◽  
Saburo Inokawa
1978 ◽  
Vol 7 (2) ◽  
pp. 191-192 ◽  
Author(s):  
Kentaro Takagi ◽  
Naomi Hayama ◽  
Tadashi Okamoto

Synthesis ◽  
2018 ◽  
Vol 50 (07) ◽  
pp. 1527-1534 ◽  
Author(s):  
Zhi-Bing Dong ◽  
Qiang Cao ◽  
Han-Ying Peng ◽  
Yu Cheng

A highly efficient copper(II)-catalyzed C–S cross-coupling reaction of aryl iodides with tetraalkylthiuram disulfides was developed. With only 1 mol% of CuCl2 as catalyst, zinc powder as reductant, and K2CO3 as base, aryl iodides reacted with tetraalkylthiuram disulfides in DMSO furnishing the corresponding aryl dithiocarbamates in good to excellent yields. This protocol is an improvement of previous work, it features convenient performance, low addition of catalyst, no requirement for any ligand, and provides good yields. The method has a broad substrate scope and uses cheap and readily available starting materials.


2020 ◽  
Vol 7 (19) ◽  
pp. 2938-2943
Author(s):  
Yeojin Kim ◽  
Kwang Ho Song ◽  
Sunwoo Lee

Aryl sulfonyl hydrazide reacted with aryl iodide in the presence of CO to give the corresponding S-aryl thioesters.


2020 ◽  
Vol 7 (6) ◽  
pp. 885-889 ◽  
Author(s):  
Xinxin Qi ◽  
Zhi-Peng Bao ◽  
Xiao-Feng Wu

A palladium-catalyzed carbonylative transformation of aryl iodides and sulfonyl chlorides to thioesters has been studied.


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