Matsuo, Jun-ichi published the artcilePolymer-supported sulfinimidoyl chlorides: A convenient reagent for oxidation of alcohols, Safety of N-(tert-Butyl)-S-phenylthiohydroxylamine, the publication is Bulletin of the Chemical Society of Japan (2003), 76(7), 1433-1440, database is CAplus.
Two polymer-supported sulfinimidoyl chlorides, i.e., N-(1,1-dimethylethyl)-4-methoxybenzenesulfinimidoyl chloride and N-(1,1-dimethylethyl)benzenesulfinimidoyl chloride, were prepared from chloromethylpolystyrene and polystyrene, resp. Stoichiometric or catalytic oxidation of various primary and secondary alcs. using these polymer-supported sulfinimidoyl chlorides proceeded smoothly, and the corresponding aldehydes and ketones were conveniently prepared in good-to-high yields by simple work-up procedures. The polymer-supported N-(1,1-dimethylethyl)benzenesulfinimidoyl chloride (oxidant) was recycled repeatedly by chlorination of a used polymer-bound N-(1,1-dimethylethyl)benzenesulfinimidoyl chloride with N-chlorosuccinimide after stoichiometric oxidation
Bulletin of the Chemical Society of Japan published new progress about 19117-31-8. 19117-31-8 belongs to catalysis-chemistry, auxiliary class Oxidant, name is N-(tert-Butyl)-S-phenylthiohydroxylamine, and the molecular formula is C10H15NS, Safety of N-(tert-Butyl)-S-phenylthiohydroxylamine.
Referemce:
https://courses.lumenlearning.com/boundless-chemistry/chapter/catalysis/,
Catalysis – Wikipedia