Direct Access to Isoindolin-1-one Scaffolds by Copper-Catalyzed Divergent Cyclizations of 2-Formylbenzonitrile and Diaryliodonium Salts was written by Liu, Li;Qiang, Jian;Bai, Shu-Hua;Sung, Hui-Ling;Miao, Chun-Bao;Li, Jian. And the article was included in Advanced Synthesis & Catalysis in 2017.Quality Control of Mesityl(p-tolyl)iodonium trifluoromethanesulfonate The following contents are mentioned in the article:
Copper-catalyzed cascade transformations of 2-formylbenzonitrile and diaryliodonium salts were carried out to efficiently afford isoindolin-1-one scaffolds. The process proceeded through a copper-catalyzed tandem C-H/N-H arylation, producing two different isoindolin-1-one derivatives under different reaction conditions. This study involved multiple reactions and reactants, such as Mesityl(p-tolyl)iodonium trifluoromethanesulfonate (cas: 1204518-02-4Quality Control of Mesityl(p-tolyl)iodonium trifluoromethanesulfonate).
Mesityl(p-tolyl)iodonium trifluoromethanesulfonate (cas: 1204518-02-4) belongs to iodide derivatives. Indole is an important structural motif of various drugs, therapeutic leads besides its prevalence in numerous natural products, agrochemicals, perfumery, and dyes.Indole was synthesized in moderate yield via an o-naphthoquinone catalyzed tandem cross-coupling of substituted aniline and benzylamine under aerobic oxidation conditions.Quality Control of Mesityl(p-tolyl)iodonium trifluoromethanesulfonate
Referemce:
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com