首页> 外文期刊>Asian Journal of Chemistry: An International Quarterly Research Journal of Chemistry >Synthesis of N'-(Substituted benzylidene)-1-benzofuran-2-earbohydrazide and 5-(5-Substituted-1-benzofuran-2-yl)-1,3,4-oxadiazole-2-thiol as Potent Antioxidants
【24h】

Synthesis of N'-(Substituted benzylidene)-1-benzofuran-2-earbohydrazide and 5-(5-Substituted-1-benzofuran-2-yl)-1,3,4-oxadiazole-2-thiol as Potent Antioxidants

机译:N'-(取代的亚苄基)-1-苯并呋喃-2-乙酰肼和5-(5-取代的-1-苯并呋喃-2-基)-1,3,4-恶二唑-2-硫醇的合成作为有效的抗氧化剂

获取原文
获取原文并翻译 | 示例
           

摘要

The reactions of substituted benzofuran-2-carbohydrazide(1)with various aromatic substituted aldehydes and carbon disulphide yielded corresponding N'-(substituted benzyl-idene)-1-benzofuran-2-carbohydrazide(2a-f)and with carbon disulphide yielded 5-(5-substituted-1-benzofuran-2-yl)-1,3,4-oxadiazole-2-thiols(3a-c),respectively.These compounds were characterized by IR,~1H NMR and mass spectra.All the compounds were screened for their in vitro antioxidant activity using DPPH method and antimicrobial activity by cup-plate diffusion method.The compounds 2c,3a and 3b shown potent radical scavenging activity and 2a,2d,3b and 3c have shown moderate antimicrobial activity.
机译:取代的苯并呋喃-2-碳酰肼(1)与各种芳族取代醛和二硫化碳的反应生成相应的N'-(取代的苄叉基)-1-苯并呋喃-2-碳酰肼(2a-f)和二硫化碳-(5-取代的1-苯并呋喃-2-基)-1,3,4-恶二唑-2-硫醇(3a-c),分别经IR,〜1H NMR和质谱表征。用DPPH法筛选化合物的体外抗氧化活性,并通过杯板扩散法筛选其抗菌活性。化合物2c,3a和3b显示出有效的自由基清除活性,而2a,2d,3b和3c显示出中等的抗菌活性。

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