946-65-6Relevant articles and documents
Electrochemical Trifluoromethylation of Thiophenols with Sodium Trifluoromethanesulfinate
Zhu, Xing-Xing,Wang, Huai-Qin,Li, Chen-Guang,Xu, Xiao-Lan,Xu, Jun,Dai, Jian-Jun,Xu, Hua-Jian
, p. 16114 - 16120 (2021/02/03)
We developed an electrochemical trifluoromethylation of thiophenols without the use of metal catalysts and oxidants. This reaction features mild reaction conditions, readily available substrate, as well as moderate to good yields. In addition, this protocol can be easily scaled up with moderate efficiency.
Sandmeyer trifluoromethylthiolation of arenediazonium salts with sodium thiocyanate and Ruppert-Prakash reagent
Danoun, Gregory,Bayarmagnai, Bilguun,Gruenberg, Matthias F.,Goossen, Lukas J.
, p. 1312 - 1316 (2014/03/21)
In the presence of copper thiocyanate, sodium thiocyanate and the inexpensive, easy-to-use trifluoromethylating reagent Me3Si-CF 3, diazonium salts are smoothly converted into the corresponding aryl trifluoromethyl thioethers. Combin
ACID-BASE PROPERTIES OF (PERFLUOROALKYLTHIO)- AND (PERFLUOROALKYLSULFONYL)-SUBSTITUTED BENZOIC ACIDS AND ANILINES
Kondratenko, N. V.,Kolomeitsev, A. A.,Popov, V. I.,Il'chenko, A. Ya.,Korzhenevskaya, N. G.,et al.
, p. 2254 - 2258 (2007/10/02)
-