Copper-Catalyzed S-Arylation of Tetraalkylthiuram Disulfides by Using Diaryliodonium Salts was written by Zeng, Meng-Tian;Xu, Wan;Liu, Xing;Chang, Cai-Zhu;Zhu, Hui;Dong, Zhi-Bing. And the article was included in European Journal of Organic Chemistry in 2017.Related Products of 139139-80-3 The following contents are mentioned in the article:
An efficient and convenient procedure for the S-arylation of tetraalkylthiuram disulfides by using diaryliodonium salts was explored. In the presence of CuI/KOtBu, two kinds of S-aryl dithiocarbamates I (R1 = H, 4-Me, 4-OMe, etc.; R2 = Me, Et, n-Bu) could be obtained in good to excellent yields at one time with no clear selectivity. This method has the advantages of efficiency, good atom economy, and broad substrate scope. This protocol allows the facile and convenient preparation of some potentially biol. active compounds This study involved multiple reactions and reactants, such as Bis(2,4,6-trimethylphenyl)iodonium triflate (cas: 139139-80-3Related Products of 139139-80-3).
Bis(2,4,6-trimethylphenyl)iodonium triflate (cas: 139139-80-3) belongs to iodide derivatives. Indole, first isolated in 1866, and it is commonly synthesized from phenylhydrazine and pyruvic acid, although several other procedures have been discovered. They are capable of binding to a variety of receptors with high affinity and thus have applications in a wide range of therapeutic areas.Related Products of 139139-80-3
Referemce:
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com