Ji, Xiaoyun published the artcileHighly regioselective aminobromination of α,β-unsaturated nitro compounds with benzyl carbamate/N-bromosuccinimide as nitrogen/bromine source, Category: nitriles-buliding-blocks, the publication is RSC Advances (2012), 2(13), 5565-5570, database is CAplus.
Aminobromination of α,β-unsaturated nitro compounds with benzyl carbamate and N-bromosuccinimide as nitrogen/bromine sources was reported. This new catalytic system tolerates a wide range of aromatic substrates, as well as heterocyclic and aliphatic substrates, resulting in good chem. yields. The reaction also proceeds smoothly with water as a medium in high efficiency. This practical aminobromination method was also suitable for large-scale preparation Furthermore, the N-carbobenzoxy protecting group could be easily cleaved to afford the free vicinal haloamines.
RSC Advances published new progress about 5153-73-1. 5153-73-1 belongs to nitriles-buliding-blocks, auxiliary class Nitrile,Alkenyl,Nitro Compound,Benzene, name is (E)-4-(2-Nitrovinyl)benzonitrile, and the molecular formula is C9H6N2O2, Category: nitriles-buliding-blocks.
Referemce:
https://en.wikipedia.org/wiki/Nitrile,
Nitriles – Chemistry LibreTexts