{"title":"新型n -烯丙基-2,6-二芳基哌酮o -烯丙基肟的合成、光谱表征及抗菌评价","authors":"K. Narayanan, M. Shanmugam, S. Kabilan","doi":"10.1109/ICSCAN49426.2020.9262427","DOIUrl":null,"url":null,"abstract":"A new series of 1-allyl-2,6-diarylpiperidone $O$-allyl oximes 13–18 were synthesized from 2,6-diarylpiperidones through various steps. The structures of all the compounds are characterized by their IR, NMR, (1D & 2D NMR) and mass spectral studies. Based on the spectral values and coupling constants all the compounds exist in chair conformation except 18 in boat conformation. Also, all the synthesized compounds are screened for their antimicrobial activity against several bacterial and fungal strains. p-Chloro-2,6-diphenyl substituted compound 15, showed remarkable activity against A.niger and compound 17 against Pseudomonas and A.flavus strains.","PeriodicalId":6744,"journal":{"name":"2020 International Conference on System, Computation, Automation and Networking (ICSCAN)","volume":"171 1","pages":"1-6"},"PeriodicalIF":0.0000,"publicationDate":"2020-07-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Synthesis, spectral characterization and antimicrobial evaluation of some novel N-allyl-2,6-diarylpiperidone O-allyl oximes\",\"authors\":\"K. Narayanan, M. Shanmugam, S. Kabilan\",\"doi\":\"10.1109/ICSCAN49426.2020.9262427\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"A new series of 1-allyl-2,6-diarylpiperidone $O$-allyl oximes 13–18 were synthesized from 2,6-diarylpiperidones through various steps. The structures of all the compounds are characterized by their IR, NMR, (1D & 2D NMR) and mass spectral studies. Based on the spectral values and coupling constants all the compounds exist in chair conformation except 18 in boat conformation. Also, all the synthesized compounds are screened for their antimicrobial activity against several bacterial and fungal strains. p-Chloro-2,6-diphenyl substituted compound 15, showed remarkable activity against A.niger and compound 17 against Pseudomonas and A.flavus strains.\",\"PeriodicalId\":6744,\"journal\":{\"name\":\"2020 International Conference on System, Computation, Automation and Networking (ICSCAN)\",\"volume\":\"171 1\",\"pages\":\"1-6\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2020-07-03\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"2020 International Conference on System, Computation, Automation and Networking (ICSCAN)\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1109/ICSCAN49426.2020.9262427\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"2020 International Conference on System, Computation, Automation and Networking (ICSCAN)","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1109/ICSCAN49426.2020.9262427","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Synthesis, spectral characterization and antimicrobial evaluation of some novel N-allyl-2,6-diarylpiperidone O-allyl oximes
A new series of 1-allyl-2,6-diarylpiperidone $O$-allyl oximes 13–18 were synthesized from 2,6-diarylpiperidones through various steps. The structures of all the compounds are characterized by their IR, NMR, (1D & 2D NMR) and mass spectral studies. Based on the spectral values and coupling constants all the compounds exist in chair conformation except 18 in boat conformation. Also, all the synthesized compounds are screened for their antimicrobial activity against several bacterial and fungal strains. p-Chloro-2,6-diphenyl substituted compound 15, showed remarkable activity against A.niger and compound 17 against Pseudomonas and A.flavus strains.