S. Debnath, Malla Reddy V, Manjunath S Y, Francis Saleshier M
{"title":"传统和微波辅助合成新型吡喃、氰吡喃希夫斯碱及其抑菌活性","authors":"S. Debnath, Malla Reddy V, Manjunath S Y, Francis Saleshier M","doi":"10.37285/ijpsn.2010.3.3.15","DOIUrl":null,"url":null,"abstract":"Ethyl2-amino-4-(4-chlorophenyl)-6-(4-methylphenyl)-4H-pyran-3-carboxylate and 2-amino-4-(4-chlorophenyl)-6-(4-methylphenyl)-4H-pyran-3-carbonitrile and their respective Schiffs bases were prepared by conventional and microwave methods. The required α, β - unsaturated ketone (chalcone) were prepared by the Claisen-Schmidt reaction using appropriate aromatic aldehyde and me","PeriodicalId":14382,"journal":{"name":"International Journal of Pharmaceutical Sciences and Nanotechnology","volume":"54 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2020-06-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"3","resultStr":"{\"title\":\"Conventional and Microwave Assisted Synthesis of New Pyran, Cyanopyran Schiffs Bases and their Anti-microbial Activities\",\"authors\":\"S. Debnath, Malla Reddy V, Manjunath S Y, Francis Saleshier M\",\"doi\":\"10.37285/ijpsn.2010.3.3.15\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Ethyl2-amino-4-(4-chlorophenyl)-6-(4-methylphenyl)-4H-pyran-3-carboxylate and 2-amino-4-(4-chlorophenyl)-6-(4-methylphenyl)-4H-pyran-3-carbonitrile and their respective Schiffs bases were prepared by conventional and microwave methods. The required α, β - unsaturated ketone (chalcone) were prepared by the Claisen-Schmidt reaction using appropriate aromatic aldehyde and me\",\"PeriodicalId\":14382,\"journal\":{\"name\":\"International Journal of Pharmaceutical Sciences and Nanotechnology\",\"volume\":\"54 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2020-06-10\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"3\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"International Journal of Pharmaceutical Sciences and Nanotechnology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.37285/ijpsn.2010.3.3.15\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Journal of Pharmaceutical Sciences and Nanotechnology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.37285/ijpsn.2010.3.3.15","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Conventional and Microwave Assisted Synthesis of New Pyran, Cyanopyran Schiffs Bases and their Anti-microbial Activities
Ethyl2-amino-4-(4-chlorophenyl)-6-(4-methylphenyl)-4H-pyran-3-carboxylate and 2-amino-4-(4-chlorophenyl)-6-(4-methylphenyl)-4H-pyran-3-carbonitrile and their respective Schiffs bases were prepared by conventional and microwave methods. The required α, β - unsaturated ketone (chalcone) were prepared by the Claisen-Schmidt reaction using appropriate aromatic aldehyde and me