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Click Chemistry Approach: Regioselective One-pot Synthesis of Some New 8-Trifluoromethylquinoline Based 1,2,3-Triazoles as Potent Antimicrobial Agents

机译:单击化学方法:区域选择性一锅合成一些新的基于8,三氟甲基喹啉的1,2,3-三唑类作为有效的抗菌剂

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摘要

Three series of 8-trifluoromethylquinoline based 1,2,3-triazoles derivatives (5a–c, 6a–d and 7a–c) were synthesized by multi-step reactions by click chemistry approach. Synthesized compounds were characterized by spectral studies and X-ray analysis. The final compounds were screened for their in-vitro antimicrobial activity by well plate method (zone of inhibition). Compounds 5c, 6b, 8b, 11 and 12 were found to be active against tested microbial strains. The results are summarized in Tables 5 and 6.
机译:通过点击化学方法通过多步反应合成了三组基于8-三氟甲基喹啉的1,2,3-三唑衍生物(5a–c,6a–d和7a–c)。通过光谱研究和X射线分析对合成的化合物进行表征。通过孔板法(抑制区)筛选最终化合物的体外抗菌活性。发现化合物5c,6b,8b,11和12对测试的微生物菌株具有活性。结果总结在表5和6中。

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