1374639-67-4Relevant academic research and scientific papers
Expedient synthesis of tetrafluorophenoxthiines and derivatives by copper(I)-catalyzed cross-coupling reaction
Yu, Chuanming,Hu, Gaobo,Zhang, Cuiling,Wu, Ran,Ye, Haiwei,Yang, Guanghui,Shi, Xiangjun
, p. 33 - 38 (2013)
In this research, tetrafluorophenoxthiines were successfully synthesized from pentafluorobenzene and aryl thiols or diaryl disulfides in the presence of copper catalyst and ligand by using O2 as the oxidant, t-BuOLi as the base at 100 8C. The ligand (E)-3-(dimethylamino)-1-(2-hydroxyphenyl)prop-2-en-1-one (L) played an indispensable role in the reaction. This work contains a notable mode of C-F bond activation, which is in the ortho position to the C-H bond of pentafluorobenzene.
The thiolation of pentafluorobenzene with disulfides by C-H, C-F bond activation and C-S bond formation
Liu, Zijian,Ouyang, Kunbing,Yang, Nianfa
supporting information, p. 988 - 992 (2018/02/19)
A metal-free thiolation reaction between pentafluorobenzene and disulfides by C-H, C-F bond activation and C-S bond formation is reported. Bisthiolated tetrafluorobenzene derivatives would be prepared in moderate to good yields from pentafluorobenzene and disulfides under mild conditions. A possible mechanism for the reaction was given.
Copper-catalyzed direct thiolation of pentafluorobenzene with diaryl disulfides or aryl thiols by C-H and C-F bond activation
Yu, Chuanming,Zhang, Cuiling,Shi, Xiangjun
experimental part, p. 1953 - 1959 (2012/05/05)
A Cu-catalyzed cross-coupling reaction of diaryl disulfides or aryl thiols with pentafluorobenzene using CuBr as the catalyst, tBuOLi or tBuOK as the base in DMSO at 60 °C under an O2 atmosphere was investigated. The corresponding bisarylthiola
