1606128-29-3Relevant academic research and scientific papers
UV-Light-Irradiated Trifluoromethylation of Diheteroaryl Disulfides with CF3SO2Na
Cao, Bao-Qian,Qiu, Yi-Feng,Zhang, Xi,Zhu, Zheng-He,Quan, Zheng-Jun,Wang, Xi-Cun
, p. 1208 - 1214 (2019)
A simple protocol for the UV light irradiated preparation of heteroaryl trifluoromethyl thioethers from disulfides and inexpensive, environmentally sodium triflinate (CF3SO2Na) has been developed. The features of simple and clean rea
Metal- And Oxidant-Free Electrochemical Oxidative Desulfurization C-O Coupling of Thiourea-Type Compounds with Alcohols
Cao, Bao-Qian,Quan, Zheng-Jun,Ren, Ming-Zhe,Wang, Xi-Cun,Zhu, Zheng-He
, p. 1634 - 1642 (2020/05/25)
An efficient desulfurization C-O coupling reaction of 3,4-dihydropyrimidine-2(1 H)-thiones (including thioureas) with alcohols was developed under electrochemical oxidation conditions. Herein, transition--metal catalysts and additives are not required and
Chemoselective carbon-carbon cross-coupling via palladium-catalyzed copper-mediated C-S cleavage of disulfides
Quan, Zheng-Jun,Lv, Ying,Jing, Fu-Qiang,Jia, Xiao-Dong,Huo, Cong-De,Wang, Xi-Cun
supporting information, p. 325 - 332 (2014/05/20)
An efficient method for carbon-carbon bond formation is described. The process employs the palladium-catalyzed copper-mediated cross-coupling of diheteroaryl disulfides with arylboronic acids or alkynes to deliver C-C coupling products through unreactive C-S bond cleavage. The scope of the coupling reactions, including both the disulfides and arylboronic acids or alkynes, are documented.
