Darvin Jesús Torres Ribón , Luis Fernando Roa de la Fuente , Nancy Romero Ceronio , Oswaldo Hernández Abreu , Madeleyne Ramos Rivera , Jorge R. Juárez , Rosalía Torralba , Manuel Velasco Ximello , Quirino Torres Sauret , Cuauhtémoc Alvarado Sánchez
{"title":"Iodine promoted one-pot synthesis of flavones","authors":"Darvin Jesús Torres Ribón , Luis Fernando Roa de la Fuente , Nancy Romero Ceronio , Oswaldo Hernández Abreu , Madeleyne Ramos Rivera , Jorge R. Juárez , Rosalía Torralba , Manuel Velasco Ximello , Quirino Torres Sauret , Cuauhtémoc Alvarado Sánchez","doi":"10.1016/j.rechem.2024.101968","DOIUrl":null,"url":null,"abstract":"<div><div>A novel <em>one-pot</em> methodology for the synthesis of flavones starting from simple precursors such as 2′-hydroxyacetophenone and benzaldehyde derivatives in pentan-1-ol (a green solvent), without additives, mediated by iodine and with short reaction times (1 h) is described. A scope of 21 products in yields ranging from 28 % to 90 % is presented. Results demonstrated that the yield was enhanced by the use of benzaldehyde derivatives with activating substituents on the <em>para</em>-position.</div></div>","PeriodicalId":420,"journal":{"name":"Results in Chemistry","volume":"13 ","pages":"Article 101968"},"PeriodicalIF":2.5000,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Results in Chemistry","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2211715624006647","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
A novel one-pot methodology for the synthesis of flavones starting from simple precursors such as 2′-hydroxyacetophenone and benzaldehyde derivatives in pentan-1-ol (a green solvent), without additives, mediated by iodine and with short reaction times (1 h) is described. A scope of 21 products in yields ranging from 28 % to 90 % is presented. Results demonstrated that the yield was enhanced by the use of benzaldehyde derivatives with activating substituents on the para-position.