364-76-1Relevant articles and documents
Unlocking Amides through Selective C–N Bond Cleavage: Allyl Bromide-Mediated Divergent Synthesis of Nitrogen-Containing Functional Groups
Govindan, Karthick,Chen, Nian-Qi,Chuang, Yu-Wei,Lin, Wei-Yu
supporting information, p. 9419 - 9424 (2021/11/30)
We report a new set of reactions based on the unlocking of amides through simple treatment with allyl bromide, creating a common platform for accessing a diverse range of nitrogen-containing functional groups such as primary amides, sulfonamides, primary amines, N-acyl compounds (esters, thioesters, amides), and N-sulfonyl esters. The method has potential industrial applicability, as demonstrated through gram-scale syntheses in batch and in a continuous flow system.
Selective partial hydrogenation of dinitrobenzenes to nitroanilines catalyzed by Ru/C
Hou, Jie,Ma, Yonghuan,Li, Yuhan,Guo, Fang,Lu, Lianhai
scheme or table, p. 974 - 975 (2009/04/06)
Ru/C was found to be a highly effective catalyst for the selective partial hydrogenation of a range of dinitrobenzenes to their corresponding nitroanilines with excellent selectivity under mild conditions. Furthermore, the effect from other substitute groups of dinitrobenzenes on partial hydrogenation was also explored in this study. Copyright
Heterogeneous catalytic transfer hydrogenation of aromatic nitro and carbonyl compounds over cobalt(II) substituted hexagonal mesoporous aluminophosphate molecular sieves
Mohapatra, Susanta K,Sonavane, Sachin U,Jayaram, Radha V,Selvam, Parasuraman
, p. 8527 - 8529 (2007/10/03)
Catalytic transfer hydrogenation of aromatic nitro and carbonyl compounds was carried out using novel cobalt(II) substituted hexagonal mesoporous aluminophosphate molecular sieves. The catalyst showed excellent yield with good recycling capability.
