Tandem indole C-H alkenylation/arylation for tetra-substituted alkene synthesis was written by Suarez, Laura Lopez;Greaney, Michael F.. And the article was included in Chemical Communications (Cambridge, United Kingdom) in 2011.Application of 1204518-02-4 The following contents are mentioned in the article:
Alkynylbenzylindoles undergo a novel sequence of Pd-catalyzed indole C-H activation/alkyne carbopalladation/arylation, with diaryliodonium salts providing the aryl components. An array of functionalized indole alkenes have been prepared in good to excellent yield, with the reaction being selective for the Z-alkene. This study involved multiple reactions and reactants, such as Mesityl(p-tolyl)iodonium trifluoromethanesulfonate (cas: 1204518-02-4Application of 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. In addition to indole, the strain-release chemistry worked for numerous substrates including amines, alcohols, thiols, carboxylic acids, imidazoles, and pyrazoles.Application of 1204518-02-4
Referemce:
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com