New oxidative reactions of monovinylsilanes with sulfonamides was written by Astakhova, Vera V.;Moskalik, Mikhail Yu.;Sterkhova, Irina V.;Shainyan, Bagrat A.. And the article was included in Journal of Organometallic Chemistry in 2022.Recommanded Product: 1-Bromopyrrolidine-2,5-dione This article mentions the following:
The reactions of sulfonamidation of functionally substituted vinylsilanes having Si-Ph, Si-Cl or Si-O bonds (triphenylvinylsilane, trimethoxy(vinyl)silane, trichlorovinylsilane, dichloromethylvinylsilane, tris(2-methoxyethoxy)vinylsilane) with trifluoromethanesulfonamide, arenesulfonamides and methanesulfonamide in the presence of (t-BuOCl + NaI) or N-bromosuccinimide proceed in different manner depending on the substrate, reagent, and oxidant. The formation of the products of halosulfonamidation, heterocyclization, halogenation, solvent interception and desilylation is observed In the experiment, the researchers used many compounds, for example, 1-Bromopyrrolidine-2,5-dione (cas: 128-08-5Recommanded Product: 1-Bromopyrrolidine-2,5-dione).
1-Bromopyrrolidine-2,5-dione (cas: 128-08-5) belongs to organobromine compounds. Organo bromine compounds are versatile compounds and are widely used in diverse fields. Organo bromine derivatives are used in the dye sector, as an indicator in analytical chemistry (Bromothymol blue is a popular indicator). Many of the alkyl bromine derivatives are excellent alkylating agents since bromides are good leaving groups. Tribromides, like tetrabutylammonium tribromide, are used as a solid source of bromine. N-bromosuccimide (NBS) is used for the selective bromination of allylic bonds.Recommanded Product: 1-Bromopyrrolidine-2,5-dione
Referemce:
Bromide – Wikipedia,
bromide – Wiktionary