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Solvent Free Microwave Accelerated Synthesis of Heterocyclic Thiazolidin-4-ones as Antimicrobial and Antifungal Agents

机译:无溶剂微波加速杂环噻唑烷-4-酮作为抗菌剂和抗真菌剂的合成

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摘要

A simple and efficient method has been developed for conversion of arenecarbaldehyde-3-methylquinoxalin-2-yl-hydrazones to 3-(2-methylquinoxalin-3-yl)-2-(substitutedphenyl)thiazolidin-4-ones in good yields using microwave irradiation technique on silica as solid support under solvent free conditions. The synthesized compounds were characterized by elemental microanalysis, infrared spectroscopy, H NMR, and mass spectroscopy. All the synthesized thiazolidinones were investigated for their antimicrobial and antifungal activities. The results of the biological activities revealed that the compounds 3b, 3d, 3f and 3h exhibited excellent antibacterial activities while 3d and 3h exhibited good antifungal activity.
机译:已经开发了一种简单有效的方法,使用微波将芳烃甲醛-3-甲基喹喔啉-2-基-转化为3-(2-甲基喹喔啉-3-基)-2-(取代苯基)噻唑烷酮-4-酮无溶剂条件下以二氧化硅为固体载体的紫外辐射技术。通过元素微分析,红外光谱,1 H NMR和质谱对合成的化合物进行表征。研究了所有合成的噻唑烷酮的抗微生物和抗真菌活性。生物学活性的结果表明,化合物3b,3d,3f和3h表现出优异的抗菌活性,而3d和3h表现出良好的抗真菌活性。

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