Convenient synthesis, antimicrobial evaluation and molecular modeling of some novel quinoline derivatives
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https://tandf.figshare.com/articles/dataset/A_Convenient_Synthesis_Antimicrobial_Evaluation_and_Molecular_Modeling_of_Some_Novel_Quinoline_Derivatives/4239602/2
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资源简介：
<i>α, β</i>-Unsaturated carbonyl compounds <b>2a, 2b, 3,</b> and <b>4</b> were synthesized by the Knoevenagel condensation between 2-substituted quionoline-3-carboxaldehyde <b>1a</b> and/or <b>1b</b> with active methylene compounds. In addition, the synthesis of azlactone is achieved starting from <b>1a</b> and <i>N</i>-acetylglycine. Synthesis of pyridine, pyrene, and pyrimidine derivatives <b>6</b>–<b>8</b> were accomplished via one-pot multicomponent reaction of <b>1b</b> with acetyl acetone, malononitrile, and ammonium acetate; acetophenone, malononitrile, and NaOH; or acetyl acetone and urea in acidic medium. The new synthesized compounds showed good antimicrobial activities. The DFT calculations have been used to predict the electronic properties of the studied compounds.
提供机构：
Taylor & Francis
创建时间：
2017-01-12
