Copper-catalyzed synthesis of phenol and diaryl ether derivatives via hydroxylation of diaryliodoniums was written by Ye, Lianbao;Han, Chao;Shi, Peiqi;Gao, Wei;Mei, Wenjie. And the article was included in RSC Advances in 2019.Formula: C17H18F3IO3S The following contents are mentioned in the article:
A copper-catalyzed hydroxylation of diaryliodoniums to generate phenols and diaryl ethers was reported. This method allowed the synthesis of diversely functionalized phenols under mild reaction conditions without the need for a strong inorganic base or an expensive noble-metal catalyst. Significantly, convenient application of diaryliodoniums was demonstrated in the preparation of diaryl ethers in a one-pot operation. This study involved multiple reactions and reactants, such as Mesityl(p-tolyl)iodonium trifluoromethanesulfonate (cas: 1204518-02-4Formula: C17H18F3IO3S).
Mesityl(p-tolyl)iodonium trifluoromethanesulfonate (cas: 1204518-02-4) belongs to iodide derivatives. Indole could be stereoselectively alkylated with chiral cyclopentyl sulfone reagent. Due to this activity, the indole ring system has become an important component or intermediate in the synthesis of heterocycles.Formula: C17H18F3IO3S
Referemce:
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com