M. Natarajan, Elanchezhian Balachandravinayagam, S. Ganesan, M. Selvaraju
{"title":"Triaza和Dioxa Aza类螺旋衍生物的合成、光谱表征及体外抗菌评价研究","authors":"M. Natarajan, Elanchezhian Balachandravinayagam, S. Ganesan, M. Selvaraju","doi":"10.9734/bpi/nicb/v2/4167f","DOIUrl":null,"url":null,"abstract":"Six compounds 7,9-diphenyl-1,4-dioxa-8-azaspiro[4.5]decane 1-6 have been synthesized by Mannich reaction and cyclo condensation. The structures and stereochemistry established by Elemental analysis, Mass, IR, 1H,13C, NMR studies. The purities were checked by elemental analysis. The synthesized compounds 1-6 adopt chair conformation with equatorial orientation of the aryl groups by coupling constant values of 1H NMR. All the compounds were screened for their antibacterial activity against Proteus mirabilis, Klebsiella oxytoca, Staphylococcus aureus and Salmonella paratyphi. The compound 5 exhibited excellent in vitro antibacterial activity in all species.","PeriodicalId":19155,"journal":{"name":"New Innovations in Chemistry and Biochemistry Vol. 2","volume":"10 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2021-08-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Study on Synthesis, Spectral Characterization and in vitro Antibacterial Evaluation of Triaza and Dioxa Aza Spiro Derivatives\",\"authors\":\"M. Natarajan, Elanchezhian Balachandravinayagam, S. Ganesan, M. Selvaraju\",\"doi\":\"10.9734/bpi/nicb/v2/4167f\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Six compounds 7,9-diphenyl-1,4-dioxa-8-azaspiro[4.5]decane 1-6 have been synthesized by Mannich reaction and cyclo condensation. The structures and stereochemistry established by Elemental analysis, Mass, IR, 1H,13C, NMR studies. The purities were checked by elemental analysis. The synthesized compounds 1-6 adopt chair conformation with equatorial orientation of the aryl groups by coupling constant values of 1H NMR. All the compounds were screened for their antibacterial activity against Proteus mirabilis, Klebsiella oxytoca, Staphylococcus aureus and Salmonella paratyphi. The compound 5 exhibited excellent in vitro antibacterial activity in all species.\",\"PeriodicalId\":19155,\"journal\":{\"name\":\"New Innovations in Chemistry and Biochemistry Vol. 2\",\"volume\":\"10 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2021-08-26\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"New Innovations in Chemistry and Biochemistry Vol. 2\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.9734/bpi/nicb/v2/4167f\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"New Innovations in Chemistry and Biochemistry Vol. 2","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.9734/bpi/nicb/v2/4167f","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Study on Synthesis, Spectral Characterization and in vitro Antibacterial Evaluation of Triaza and Dioxa Aza Spiro Derivatives
Six compounds 7,9-diphenyl-1,4-dioxa-8-azaspiro[4.5]decane 1-6 have been synthesized by Mannich reaction and cyclo condensation. The structures and stereochemistry established by Elemental analysis, Mass, IR, 1H,13C, NMR studies. The purities were checked by elemental analysis. The synthesized compounds 1-6 adopt chair conformation with equatorial orientation of the aryl groups by coupling constant values of 1H NMR. All the compounds were screened for their antibacterial activity against Proteus mirabilis, Klebsiella oxytoca, Staphylococcus aureus and Salmonella paratyphi. The compound 5 exhibited excellent in vitro antibacterial activity in all species.