Catalytic and non-catalytic selective aryl transfer from (mesityl)iodonium(III) salts to diarylsulfide compounds was written by Takenaga, Naoko;Yoto, Yusuke;Hayashi, Takumi;Miyamoto, Naoki;Nojiri, Haruna;Kumar, Ravi;Dohi, Toshifumi. And the article was included in ARKIVOC (Gainesville, FL, United States) in 2022.Recommanded Product: Mesityl(p-tolyl)iodonium trifluoromethanesulfonate The following contents are mentioned in the article:
A facile synthesis of triarylsulfonium triflates I [Ar = Ph, 4-MeC6H4, 2-naphthyl, etc.; Ar1 = Ph, 4-BrC6H4, 2,4,6-tri-OMeC6H2, etc.; Ar2 = Ph, 4-CF3C6H4, 4-OMeC6H4, etc.] by selective aryl transfer from readily available mesityl iodonium(III) salts to diarylsulfides in the presence of a copper catalyst was described. The advantage of this protocol was the iodonium(III) salts bearing a mesitylene (Mes) auxiliary efficiently promote selective S-arylation of diarylsulfides to produce the desired triarylsulfonium triflates I without the formation of Mes-derived byproduct salts. This study involved multiple reactions and reactants, such as Mesityl(p-tolyl)iodonium trifluoromethanesulfonate (cas: 1204518-02-4Recommanded Product: Mesityl(p-tolyl)iodonium trifluoromethanesulfonate).
Mesityl(p-tolyl)iodonium trifluoromethanesulfonate (cas: 1204518-02-4) belongs to iodide derivatives. Indole, also called Benzopyrrole, a heterocyclic organic compound occurring in some flower oils, such as jasmine and orange blossom, in coal tar, and in fecal matter. Moreover, it is known that it controls biofilm formation. However, the role of indole in the cell has not been fully elucidated.Recommanded Product: Mesityl(p-tolyl)iodonium trifluoromethanesulfonate
Referemce:
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com