Generation of aminyl radicals using sulfenamides as synthetic precursors was written by Bowman, W. Russell;Clark, David N.;Marmon, Robert J.. And the article was included in Tetrahedron in 1994.Recommanded Product: 14204-27-4 This article mentions the following:
Sulfenamides R1R2NSPh (R1, R2 = alkyl, cycloalkyl, bicycloalkyl, aryl et al.)are synthesized from reactions of R1R2NH and N-(benzenesulfenyl)phthalimide or PhSCl. The sulfenamides undergo reaction with Bu3SnH to yield aminyl radicals which can be cyclized onto suitable alkenes. In the experiment, the researchers used many compounds, for example, 2-(Phenylthio)isoindoline-1,3-dione (cas: 14204-27-4Recommanded Product: 14204-27-4).
2-(Phenylthio)isoindoline-1,3-dione (cas: 14204-27-4) belongs to indole derivatives. In addition to tryptophan, indigo, and indoleacetic acid, numerous compounds obtainable from plant or animal sources contain the indole molecular structure. They are capable of binding to a variety of receptors with high affinity and thus have applications in a wide range of therapeutic areas.Recommanded Product: 14204-27-4
Referemce:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles