106877-42-3Relevant articles and documents
Copper-catalyzed trifluoromethylation of aryl- and vinylboronic acids with generation of CF3-radicals
Li, Yang,Wu, Lipeng,Neumann, Helfried,Beller, Matthias
, p. 2628 - 2630 (2013)
The selective trifluoromethylation of aryl- and vinylboronic acids proceeds smoothly with CF3SO2Na (Langlois reagent) in the presence of copper catalysts and t-BuOOH. Therefore, the method relies both on transition metal catalysis an
The 2,4-dimethyl-7-pentafluorosulfanyl-5-(trifluoromethyl)dibenzo[b,d] thiophenium trifluoromethanesulfonate: The SF5-analog of Umemoto salt
Okazaki, Takao,Laali, Kenneth K.,Reddy, A. Srinivas
, p. 91 - 95 (2014)
The SF5-analog of the Umemoto salt was synthesized in just two steps by combining our recently reported SF5-biaryl synthesis, via Suzuki coupling with 4-(pentafluorosulfanyl)benzenediazonium tetrafluoroborate, with Magnier's one-pot synthesis of dibenzothiophenium salts employing CF 3SO2Na and triflic anhydride. The trifluoromethylating power of this novel onium salt toward reactive arenes was tested in a survey study on small scale.
COMPOUNDS
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Page/Page column 111, (2020/01/11)
A compound of formula (I), or a pharmaceutical salt thereof.
VINYLFLUOROALKANE SULFONATE COMPOUND AND METHOD OF PRODUCING THE SAME
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Paragraph 0036; 0037; 0038, (2019/05/09)
PROBLEM TO BE SOLVED: To provide a technique of regioselectively introducing a fluoroalkyl group such as a trifluoromethyl group to an outer carbon of 1,3-diketone. SOLUTION: The present invention provides a method for producing a vinylfluoroalkane sulfon