首页> 外文期刊>Research on Chemical Intermediates >Practical one-pot synthesis of semicarbazone derivatives via semicarbazide, and evaluation of their antibacterial activity
【24h】

Practical one-pot synthesis of semicarbazone derivatives via semicarbazide, and evaluation of their antibacterial activity

机译:通过氨基脲实际一锅法合成氨基脲衍生物并评估其抗菌活性

获取原文
获取原文并翻译 | 示例
           

摘要

New series of 2-(aryl or alkyl)-N-phenylhydrazine-1-carboxamides 1a-j were synthesized through one-pot reactions of aldehyde or ketones, hydrazine hydrate, and phenylisocyanate in MeOH. The structure of products was confirmed by Fourier transform infrared (FT-IR), proton nuclear magnetic resonance (H-1 NMR), and C-13 NMR spectra. Minimum inhibitory concentration (MIC) of antibacterial activity of 1a-j was screened against five bacterial strains. Compound 1f showed antibacterial activity against Pseudomonas aeruginosa and Staphylococcus aureus.
机译:通过醛或酮,水合肼和苯基异氰酸酯在MeOH中的一锅反应,合成了一系列新的2-(芳基或烷基)-N-苯基肼-1-羧酰胺1a-j。产物的结构通过傅里叶变换红外(FT-IR),质子核磁共振(H-1 NMR)和C-13 NMR光谱确认。针对五种细菌菌株筛选了1a-j抗菌活性的最小抑制浓度(MIC)。化合物1f对铜绿假单胞菌和金黄色葡萄球菌具有抗菌活性。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号