Benas Balandis, K. Anusevičius, V. Mickevičius, M. Stasevych, V. Novikov
{"title":"Synthesis and antibacterial activity of novel 3-substituted 1-(2-methyl-5-nitrophenyl)-5-oxopyrrolidine derivatives","authors":"Benas Balandis, K. Anusevičius, V. Mickevičius, M. Stasevych, V. Novikov","doi":"10.23939/cte2019.01.247","DOIUrl":null,"url":null,"abstract":"– The synthesis of novel azole derivatives has been accomplished during chemical transformations of the 1-(2-methyl-5-nitrophenyl)-5-oxopyrrolidine-3-carbohydrazide. The structure of the synthesized compounds was determined by NMR and IR spectroscopies. Most of the synthesized compounds were screened for their antibacterial activity against S. aureus, L. monocytogenes, E. coli, and P. aeruginosa bacteria strains. was used as a control for S. aureus, E. coli , P. aeruginosa , and L. monocytogenes .","PeriodicalId":9818,"journal":{"name":"Chemical technology and engineering. Proceedings.2019.№1","volume":"44 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2019-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chemical technology and engineering. Proceedings.2019.№1","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.23939/cte2019.01.247","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
– The synthesis of novel azole derivatives has been accomplished during chemical transformations of the 1-(2-methyl-5-nitrophenyl)-5-oxopyrrolidine-3-carbohydrazide. The structure of the synthesized compounds was determined by NMR and IR spectroscopies. Most of the synthesized compounds were screened for their antibacterial activity against S. aureus, L. monocytogenes, E. coli, and P. aeruginosa bacteria strains. was used as a control for S. aureus, E. coli , P. aeruginosa , and L. monocytogenes .