An Amberlyst-15® Mediated Synthesis of New Functionalized Dioxoloquinolinone Derivatives

R. Abonía, Paola Cuervo, B. Insuasty, J. Quiroga, M. Nogueras, J. Cobo, H. Meier, E. Lotero
{"title":"An Amberlyst-15® Mediated Synthesis of New Functionalized Dioxoloquinolinone Derivatives","authors":"R. Abonía, Paola Cuervo, B. Insuasty, J. Quiroga, M. Nogueras, J. Cobo, H. Meier, E. Lotero","doi":"10.2174/1874095200801020026","DOIUrl":null,"url":null,"abstract":"The commercially available Amberlyst ® -15 in the presence of AcOH was conveniently used to catalyze the in- tramolecular cyclization of a series of 2´-amino(1,3)dioxolochalcones to the corresponding dihydroquinolin-8-ones. This procedure is compatible with different functional groups and may be used as an alternative strategy for the synthesis of this important family of heterocyclic compounds.","PeriodicalId":23020,"journal":{"name":"The Open Organic Chemistry Journal","volume":"89 1","pages":"26-34"},"PeriodicalIF":0.0000,"publicationDate":"2008-04-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"13","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Open Organic Chemistry Journal","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2174/1874095200801020026","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 13

Abstract

The commercially available Amberlyst ® -15 in the presence of AcOH was conveniently used to catalyze the in- tramolecular cyclization of a series of 2´-amino(1,3)dioxolochalcones to the corresponding dihydroquinolin-8-ones. This procedure is compatible with different functional groups and may be used as an alternative strategy for the synthesis of this important family of heterocyclic compounds.
Amberlyst-15介导的新型功能化二氧喹啉酮衍生物的合成
在AcOH存在下,市售Amberlyst®-15被方便地用于催化一系列2´-氨基(1,3)二氧氯查尔酮的分子内环化成相应的二氢喹啉-8-酮。该方法与不同的官能团兼容,可作为合成这一重要杂环化合物家族的替代策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信