Trifluoromethylthiolation of Unsymmetrical 位3-Iodane Derivatives: Additive-Free, Selective and Scalable Introduction of the SCF3 Group was written by Nikolaienko, Pavlo;Yildiz, Tuelay;Rueping, Magnus. And the article was included in European Journal of Organic Chemistry in 2016.Recommanded Product: 1-Iodo-4-(4-nitrophenoxy)benzene The following contents are mentioned in the article:
The reaction of copper trifluoromethyl sulfide with diaryliodonium salts provides a straightforward pathway for the synthesis of aryl trifluoromethyl thioethers under mild reaction conditions and within short reaction times. High chemoselectivity was achieved by using mesityl as a leaving group. A large range of novel [(het)aryl](mesityl)iodonium salts underwent this reaction under the optimized conditions to give the desired products in moderate to good yields. This study involved multiple reactions and reactants, such as 1-Iodo-4-(4-nitrophenoxy)benzene (cas: 21969-05-1Recommanded Product: 1-Iodo-4-(4-nitrophenoxy)benzene).
1-Iodo-4-(4-nitrophenoxy)benzene (cas: 21969-05-1) belongs to iodide derivatives. Indole could be stereoselectively alkylated with chiral cyclopentyl sulfone reagent. More than 200 indole derivatives have already been marketed as drugs or are under advanced stages of clinical trials.Recommanded Product: 1-Iodo-4-(4-nitrophenoxy)benzene
Referemce:
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com