{"title":"1,3-偶极环加成硝基与4-氨基安替芘的制备与表征","authors":"D. Mutlaq, Raad J. Ali","doi":"10.32792/utq/utj/vol11/4/5","DOIUrl":null,"url":null,"abstract":"Some nitrones (1-5), derived from N–phenyl hydroxylamine with substituted benzaldehyde such as (3-chlorobenzaldehyde, 4-chlorobenzaldehyde, 3-nitrobenzaldehyde, 4-florobenzaldehyde, 2-nitrobenzaldehyde). In subsequent 1,3-dipolar cycloaddition reactions of nitrones with 4-amino antipyrene give isoxazolidines (6-10), They have been identified by 1HNMR, 13CNMR, IR and Mass spectra","PeriodicalId":23465,"journal":{"name":"University of Thi-Qar Journal","volume":"81 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2019-04-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Preparation and Charactrisation of 1,3-dipolar cycloaddition of nitrones with 4-amino antipyrene\",\"authors\":\"D. Mutlaq, Raad J. Ali\",\"doi\":\"10.32792/utq/utj/vol11/4/5\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Some nitrones (1-5), derived from N–phenyl hydroxylamine with substituted benzaldehyde such as (3-chlorobenzaldehyde, 4-chlorobenzaldehyde, 3-nitrobenzaldehyde, 4-florobenzaldehyde, 2-nitrobenzaldehyde). In subsequent 1,3-dipolar cycloaddition reactions of nitrones with 4-amino antipyrene give isoxazolidines (6-10), They have been identified by 1HNMR, 13CNMR, IR and Mass spectra\",\"PeriodicalId\":23465,\"journal\":{\"name\":\"University of Thi-Qar Journal\",\"volume\":\"81 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2019-04-22\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"University of Thi-Qar Journal\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.32792/utq/utj/vol11/4/5\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"University of Thi-Qar Journal","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.32792/utq/utj/vol11/4/5","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Preparation and Charactrisation of 1,3-dipolar cycloaddition of nitrones with 4-amino antipyrene
Some nitrones (1-5), derived from N–phenyl hydroxylamine with substituted benzaldehyde such as (3-chlorobenzaldehyde, 4-chlorobenzaldehyde, 3-nitrobenzaldehyde, 4-florobenzaldehyde, 2-nitrobenzaldehyde). In subsequent 1,3-dipolar cycloaddition reactions of nitrones with 4-amino antipyrene give isoxazolidines (6-10), They have been identified by 1HNMR, 13CNMR, IR and Mass spectra
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