Panda, Biswajit published the artcileIron catalysis: rust-free future, Synthetic Route of 1293990-73-4, the publication is Chemistry & Biology Interface (2019), 9(6), 273-276, database is CAplus.
The addition of nitrogen to carbon compounds is generally a laborious process. To prevent undesired reactivity of nitrogen generally it needs protection, and sometimes removal of protecting group can be difficult, and also use of protection-deprotection strategy is contrary to the ideality of organic transformations from the point of step- and atom-economy. Legnani et al. reported a resourceful method to add simple NH2 to alkenes from a hydroxylamine derivative directly which is highlighted herein. A simple iron-catalyzed aminochlorination of alkenes using table salts as chloride source proceeds through a radical mechanism, where it is poised for a wide variety of further functionalization options.
Chemistry & Biology Interface published new progress about 1293990-73-4. 1293990-73-4 belongs to catalysis-chemistry, auxiliary class Aliphatic Chain, name is O-Pivaloylhydroxylamine trifluoromethanesulfonate, and the molecular formula is C6H12F3NO5S, Synthetic Route of 1293990-73-4.
Referemce:
https://courses.lumenlearning.com/boundless-chemistry/chapter/catalysis/,
Catalysis – Wikipedia