{"title":"微波诱导，碘-氧化铝催化1-(2 ' -羟基)-3-(2-氯喹啉-3-基)-丙-2-烯-1- 1的转化","authors":"P. Venkatesan, K. Moorthi","doi":"10.1155/2012/354875","DOIUrl":null,"url":null,"abstract":"The chalcone derivatives, 1-(2′-hydroxyaryl)-3-(2-chloroquinolin-3-yl)-prop-2-en-1-one was transformed to corresponding flavone derivatives by iodine impregnated neutral alumina under microwave irradiation. The synthesized flavone derivatives were structurally confirmed by elemental analysis, UV, IR and 1H-NMR spectral data, and the notable yield obtained was compared with previously reported method.","PeriodicalId":11519,"journal":{"name":"E-journal of Chemistry","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2012-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1155/2012/354875","citationCount":"3","resultStr":"{\"title\":\"Microwave-Induced, Iodine-Alumina Catalyzed Transformations of 1-(2′-hydroxyaryl)-3-(2-chloroquinolin-3-yl)-prop-2-en-1-one\",\"authors\":\"P. Venkatesan, K. Moorthi\",\"doi\":\"10.1155/2012/354875\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"The chalcone derivatives, 1-(2′-hydroxyaryl)-3-(2-chloroquinolin-3-yl)-prop-2-en-1-one was transformed to corresponding flavone derivatives by iodine impregnated neutral alumina under microwave irradiation. The synthesized flavone derivatives were structurally confirmed by elemental analysis, UV, IR and 1H-NMR spectral data, and the notable yield obtained was compared with previously reported method.\",\"PeriodicalId\":11519,\"journal\":{\"name\":\"E-journal of Chemistry\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2012-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1155/2012/354875\",\"citationCount\":\"3\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"E-journal of Chemistry\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1155/2012/354875\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"E-journal of Chemistry","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1155/2012/354875","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Microwave-Induced, Iodine-Alumina Catalyzed Transformations of 1-(2′-hydroxyaryl)-3-(2-chloroquinolin-3-yl)-prop-2-en-1-one
The chalcone derivatives, 1-(2′-hydroxyaryl)-3-(2-chloroquinolin-3-yl)-prop-2-en-1-one was transformed to corresponding flavone derivatives by iodine impregnated neutral alumina under microwave irradiation. The synthesized flavone derivatives were structurally confirmed by elemental analysis, UV, IR and 1H-NMR spectral data, and the notable yield obtained was compared with previously reported method.
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