Some of Schiff base derivatives were separated by condensing 3-formyl-2-quinolinone with various primary amine derivatives in ethanol, in which water is expelled. Moreover, substituted acryloylphenyliminomethylquinolinone chalcone derivatives were prepared by the process of condensation reaction of aldehyde derivatives with 3-acetylphenylquinolinone in dilute solution of ethanolic sodium hydroxide via Claisen-Schmidt condensation method. Cyclization reaction of the quinolinone chalcones with malononitrile, phenylhydrazine, urea and thiourea were also investigated. The structures of these compounds have been elucidated on the bases of spectral data. The novel products were also evaluated for their antimicrobial activity.
CITATION STYLE
Maigali, S. S., Tawfik, H. A., Abd-El-Maksoud, M. A., Soliman, F. M., Moharam, M. E., & Dondeti, M. F. (2020). Synthesis, molecular docking and antimicrobial activities of 3-formyl-2-(1h)quinolinone schiff base derivatives and 3-(((3-acetylphenyl)imino)- methyl)quinolin-2-(1h)-one chalcone derivatives. Egyptian Journal of Chemistry, 63(10), 3903–3914. https://doi.org/10.21608/EJCHEM.2020.27574.2580
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