140140-09-6Relevant articles and documents
Room Temperature Acid-Free Greener Synthesis of Imine Using Cobalt-Doped Manganese Tungstate
Mal, Diptangshu Datta,Pradhan, Debabrata
supporting information, p. 2211 - 2218 (2022/01/31)
Facile synthesis of an imine compound through a greener route is still a challenging task. Industrial processes rely on the age-old Schiff reaction for the synthesis of imine, which are reversible and nongreen from an environmental viewpoint. Herein, coba
Synthesis of novel Schiff Bases containing acryloyl moiety and the investigation of spectroscopic and electrochemical properties
Silku, Pakize,?zkinali, Sevil,?ztürk, Zeynel,Asan, Abdurrahman,K?se, D. Ali
, p. 72 - 83 (2016/03/30)
A novel Schiff bases and their acryloyl derivatives were synthesized through the reaction of p-hydroxybenzaldehyde in order of with aniline, p-chloroaniline, p-nitroaniline, p-methylaniline and p-aminobenzoic acid. The structures of these compounds were characterised spectroscopic techniques such of IR, 1H NMR, 13C NMR and Mass spectroscopy. π→π?and n→π?transitions were determined via UV-vis spectroscopy studies performed in EtOH, CHCl3, and DMF. Furthermore, the inhibition efficiencies of these new compounds were investigated on the surface of steel within the solution of 0.1 M NaCl, 0.1 M NaOH and 0.10 M H2SO4 solution via cyclic voltammetry and Tafel extrapolation methods.
Microwave irradiated synthesis of some substituted imidazole derivatives as potential antibacterial and anticancer agents
Sharma, Gyanendra Kumar,Sharma, Naveen Kumar,Pathak, Devender
, p. 266 - 272 (2013/05/22)
The microwave assisted and solvent free synthesis of title compounds is described in this protocol. Ten new aryl imidazoles, which are incorporated with the chemotherapeutic pharmacophores, have been synthesized by adopting one pot multicomponent reaction. First, primary aromatic or heteryl amine has been condensed with aryl or heteryl aldehydes to afford corresponding Schiff base. The Schiff base on treatment with NH4OAc and benzil using silica gel as the solid support yields the corresponding aryl imidazoles. In this paper, a comparative study between the microwave method and conventional method is described. The synthesized compounds have been characterized by spectral and elemental analysis. The synthesized compounds have been evaluated for their antibacterial and short-term anticancer activity. All the synthesized substituted imidazoles have shown good antibacterial activity against gram negative bacterial strains Klebsiella pneumoniae and Escherichia coli. The synthesized imidazole derivatives possess significant cytotoxic activity against Ehrlich's Ascites Carcinoma (EAC) cell lines and Dalton's Lymphoma Ascites (DLA) cell lines.