Multicomponent alkene azidoarylation by anion-mediated dual catalysis was written by Bunescu, Ala;Abdelhamid, Yusra;Gaunt, Matthew J.. And the article was included in Nature (London, United Kingdom).HPLC of Formula: 1204518-02-4 The following contents are mentioned in the article:
The development of a dual catalysis platform that enabled a multicomponent coupling of alkenes, aryl electrophiles and a simple nitrogen nucleophile, providing single-step access to synthetically versatile and functionally diverse β-arylethylamines was reported. Driven by visible light, two discrete copper catalysts orchestrated aryl-radical formation and azido-group transfer, which underpin an alkene azidoarylation process. The process showed broad scope in alkene and aryl components and an azide anion performs a multifaceted role both as a nitrogen source and in mediating the redox-neutral dual catalysis via inner-sphere electron transfer. The synthetic capabilities of this anion-mediated alkene functionalization process are likely to be of use in a variety of pharmaceutically relevant and wider synthetic applications. This study involved multiple reactions and reactants, such as Mesityl(p-tolyl)iodonium trifluoromethanesulfonate (cas: 1204518-02-4HPLC of Formula: 1204518-02-4).
Mesityl(p-tolyl)iodonium trifluoromethanesulfonate (cas: 1204518-02-4) belongs to iodide derivatives. Indole exists overwhelmingly in the 1H-indole form as do other simple indoles. It is used in perfumery and in making tryptophan, an essential amino acid, and indoleacetic acid (heteroauxin), a hormone that promotes the development of roots in plant cuttings.HPLC of Formula: 1204518-02-4
Referemce:
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com