已合成了咪唑/苯并三唑类似物取代的哌啶-4-一衍生物(17-26)。通过IR,1 H NMR,13 C NMR和质谱分析对它们的化学结构进行表征。另外,还已经记录了化合物21和23的单晶X射线衍射。合成的化合物具有针对病原性微生物菌株的体外抗菌和抗真菌活性。结果指出,针对枯草芽孢杆菌的化合物19和24和针对大肠杆菌的化合物20和24 探索了优异的抑制活性。
Imidazole/benzotriazole analogues substituted piperidin-4-one derivatives (17–26) have been synthesized. Their chemical structures were characterized by IR, 1H NMR, 13C NMR and mass spectral analysis. In addition, single crystal X-ray diffraction has also been recorded for compounds 21 and 23. The synthesized compounds were subjected to their in vitro antibacterial and antifungal activities against
已合成了咪唑/苯并三唑类似物取代的哌啶-4-一衍生物(17-26)。通过IR,1 H NMR,13 C NMR和质谱分析对它们的化学结构进行表征。另外,还已经记录了化合物21和23的单晶X射线衍射。合成的化合物具有针对病原性微生物菌株的体外抗菌和抗真菌活性。结果指出,针对枯草芽孢杆菌的化合物19和24和针对大肠杆菌的化合物20和24 探索了优异的抑制活性。