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Synthesis of chromene-2-thiones and in vitro evaluation of their antifungal and antibacterial activities

机译:色烯-2-硫酮的合成及其抗真菌和抗菌活性的体外评价

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摘要

Cyclocondensation of β-oxodilhioeslers with substituted 2-hydroxy benzaldehydes in presence of copper(II)chloride as the catalyst yields 3-alkanoyl/aroy)/heteroaroyl-2H-chromene-2-thiones (87-95% yields). These reactions are carried out under solvent-free conditions. All the synthesized compounds have been evaluated for their antifungal and antibacterial activities using tube dilution technique. Only five compounds are found exhibiting good antifungal and antibacterial activities.
机译:在氯化铜(II)作为催化剂的存在下,β-氧杂环丁烯与取代的2-羟基苯甲醛进行环缩合反应生成3-烷酰基/芳基/杂芳酰基-2H-亚甲基-2-硫酮(87-95%的产率)。这些反应在无溶剂条件下进行。使用试管稀释技术评估了所有合成的化合物的抗真菌和抗菌活性。发现仅五种化合物表现出良好的抗真菌和抗菌活性。

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