首页> 外文期刊>Journal of Heterocyclic Chemistry: The International Journal of Heterocyclic Chemistry >Synthesis and antimicrobial activity of some 7-aryl-5,6-dihydro-14-aza[1] benzopyrano[3,4-b]phenanthren-8H-ones
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Synthesis and antimicrobial activity of some 7-aryl-5,6-dihydro-14-aza[1] benzopyrano[3,4-b]phenanthren-8H-ones

机译:一些7-芳基-5,6-二氢-14-氮杂[1]苯并吡喃并[3,4-b]菲蒽-8H-ones的合成及抑菌活性

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摘要

Figure represented. The title compounds, 7-aryl-5,6-dihydro-14-aza[1] benzopyrano[3,4-b]phenanthren-8H-ones 3a-l have been synthesized by reacting various 4-hydroxy coumarins 1a-c with 2-arylidene-1-tetralones 2a-d in the presence of ammonium acetate and acetic acid under Krohnke's reaction condition. The structures of all the synthesized compounds were supported by analytical, IR, ~1H-NMR, and ~(13)C-NMR data. All the synthesized compounds 3a-l have been screened for their antibacterial activities against Escherichia coli (Gram -ve bacteria), Bacillus subtilis (Gram +ve bacteria), and antifungal activity against Candida albicans (Fungi).
机译:图代表。标题化合物7-芳基-5,6-二氢-14-氮杂[1]苯并吡喃并[3,4-b]菲蒽-8H-酮3a-1是通过使各种4-羟基香豆素1a-c与在克罗恩克反应条件下,在乙酸铵和乙酸的存在下,形成2-亚芳基-1-四酮2a-d。所有合成化合物的结构均由分析,IR,〜1H-NMR和〜(13)C-NMR数据支持。已经筛选了所有合成的化合物3a-1对大肠杆菌(Gram-ve细菌),枯草芽孢杆菌(Gram + ve细菌)的抗菌活性以及对白色念珠菌(Fungi)的抗菌活性。

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