314283-98-2Relevant articles and documents
Bi-functional catalyst of porous N-doped carbon with bimetallic FeCu for solvent-free resultant imines and hydrogenation of nitroarenes
Wang, Kaizhi,Gao, Wenbing,Jiang, Pengbo,Lan, Kai,Yang, Ming,Huang, Xiaokang,Ma, Lei,Niu, Fang,Li, Rong
, p. 43 - 53 (2019/01/08)
The efficient and stable catalyst applied to the transformation of amines into the corresponding imines and hydrogenation of nitroarenes under mild reaction conditions is reported. The catalytic performance of porous N-doped carbon with FeCu (FeCu@NPC) catalyst are tested by aromatic alcohol-based N-alkylated of amines with solvent-free and hydrogenation of nitroarenes via N2H4·H2O. The results proved that the yield of these two reactions are all over 99.9% under optimum condition. Moreover, the synergistic effect of the catalyst for N-alkylated reaction was investigated through the kinetic study. The catalyst can be easily separated from reaction system by an external magnetism, and can be recycled and reutilized for at least 4 runs with conversions are all over 75%. The study of the catalyst indicated that it was suitable for the reactions in industry. Hence, the catalysis process by the inexpensive metals-based catalyst is green and sustainable.
Discovery of novel nonsteroidal glucocorticoid receptor modulators
Link,Sorensen, Bryan K.,Patel, Jyoti,Emery, Maurice,Grynfarb, Marlena,Goos-Nilsson, Annika
, p. 2209 - 2212 (2007/10/03)
A new class of selective nonsteroidal glucocorticoid receptor modulators typified by N-{3-[benzyl-(4-chloro-2-fluoro-benzyl)-amino]-2-methyl-phenyl}- methanesulfonamide 19 has been discovered.
Bile acid conjugates of a nonsteroidal glucocorticoid receptor modulator
Tu, Noah,Link,Sorensen, Bryan K.,Emery, Maurice,Grynfarb, Marlena,Goos-Nilsson, Annika,Nguyen, Bach
, p. 4179 - 4183 (2007/10/03)
Bile acid conjugates of a selective nonsteroidal glucocorticoid receptor modulator were prepared and evaluated. Potent GR binding conjugates that showed improved metabolic stability were discovered. However, cellular potency and pharmacokinetics were not substantially improved.