20772-73-0Relevant academic research and scientific papers
Vanadyl binary schiff base complexes containing N2O2 coordination sphere: Synthesis, ab initio calculations and thermodynamic properties
Asadi, Mozaffar,Ghatee, Mohammad Hadi,Torabi, Susan,Mohammadi, Khosro,Moosavi, Fatemeh
, p. 63 - 72 (2013/07/25)
Some vanadyl complexes were synthesized by treating a methanolic solution of the appropriate Schiff base ligand and one equivalent of VO(SO 4)2 to yield [(VOL2 1-14)](L= Salicylaldehyde's derivatives, Schemes 1,
Design, synthesis and biological evaluation of urea derivatives from o-hydroxybenzylamines and phenylisocyanate as potential FabH inhibitors
Li, Zi-Lin,Li, Qing-Shan,Zhang, Hong-Jia,Hu, Yang,Zhu, Di-Di,Zhu, Hai-Liang
experimental part, p. 4413 - 4420 (2011/09/19)
FabH, β-ketoacyl-acyl carrier protein (ACP) synthase III, is a particularly attractive target, since it is central to the initiation of fatty acid biosynthesis and is highly conserved among Gram-positive and Gram-negative bacteria. A series of o-hydroxybe
Antihyperglycemic, α-glucosidase inhibitory and DPPH free radical scavenging activity of 5-bromosalicylaldehyde and schiff bases
Misra, Sristicheta,Pandeya, Krishna Bihari,Tiwari, Ashok Kumar,Ali, Amtul Zehra,Saradamani, Thimmapatruni,Agawane, Sachin Bharat,Madhusudana, Kuncha
experimental part, p. 1431 - 1437 (2012/05/20)
α-Glucosidase inhibition and DPPH free radical scavenging by 5-bromosalicylaldehyde and some Schiff bases have been measured. 5-Bromosalicylaldehyde shows lowest IC50 value (8.80 μM) for α-glucosidase inhibition and also shows good results in in vivo experiments for antihyperglycemic potential. Springer Science+Business Media, LLC 2010.
Catalytic asymmetric mannich-ketalization reaction: Highly enantioselective synthesis of aminobenzopyrans
Rueping, Magnus,Lin, Ming-Yuan
supporting information; experimental part, p. 4169 - 4172 (2010/07/05)
"Chemical Equation Present" Domino catalysis: We have developed the first enantioselective domino Mannich-ketalization reaction of o-hydroxy benzaldimines with electron-rich alkenes (see scheme). The new reaction sequence provides an easy and direct acces
