2022
DOI: 10.21608/ejchem.2022.134661.5925
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Synthesis and biological activity of 2-chloro-3-formyl-1,8-naphthyridine chalcone derivative

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Cited by 3 publications
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“…Spectra data is shown in Table (3) infrared spectrum and Table ( 4) nuclear magnetic resonance Also, Synthesis compound (6) [bis(O-methoxy benzylidine imine)] contains two Imine groups, which are similar in composition to the dienes structure. Hydrazine hydrate (80%) was used to prepare this compound with a ratio of 1 mol from hydrazine to 2 moles of benzaldehyde substitutes, and acetic acid was used as a catalyst to complete the reaction (25)(26)(27) . This compound was characterized by the following main absorption bands of IR (7)(8)(9)(10)(11) the di-imine compounds were reacted with Schiff bases in a reaction similar to the reactions of Diels-Aldur, where the substitutes for the Schiff bases (1-5) as dinofyl and the diamine compound (6) as diene (23) by reflux was used benzene as a solvent, the mechanism suggestion shown in figure (2) .…”
Section: Resultsmentioning
confidence: 99%
“…Spectra data is shown in Table (3) infrared spectrum and Table ( 4) nuclear magnetic resonance Also, Synthesis compound (6) [bis(O-methoxy benzylidine imine)] contains two Imine groups, which are similar in composition to the dienes structure. Hydrazine hydrate (80%) was used to prepare this compound with a ratio of 1 mol from hydrazine to 2 moles of benzaldehyde substitutes, and acetic acid was used as a catalyst to complete the reaction (25)(26)(27) . This compound was characterized by the following main absorption bands of IR (7)(8)(9)(10)(11) the di-imine compounds were reacted with Schiff bases in a reaction similar to the reactions of Diels-Aldur, where the substitutes for the Schiff bases (1-5) as dinofyl and the diamine compound (6) as diene (23) by reflux was used benzene as a solvent, the mechanism suggestion shown in figure (2) .…”
Section: Resultsmentioning
confidence: 99%
“…Antibacterial activity of new complexes is subjected on Escherichia coli, Pseudomonas aeruginosa via using disc diffusion method in DMSO. [27][28][29]The results are listed in table 7. Role of negative results are effective so, all new complexes exhibited no activity against Escherichia coli, Pseudomonas aeruginosa except complex 2a,d .…”
Section: Antibacterial Activitymentioning
confidence: 99%