The [4+2] annulation of o-acylamino-aryl MBH carbonates with coumarins: facile access to tetrahydrochromeno[4,3-b]quinolin-6-ones†

IF 2.7 3区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
Min Xiang, Gang-Yong Liu, Hui-Mei Liu, Wen-Yi Zhou, Guang-Wei Wang, Fei Fei, Yun-Qing Jia and Li-Wen Shen
{"title":"The [4+2] annulation of o-acylamino-aryl MBH carbonates with coumarins: facile access to tetrahydrochromeno[4,3-b]quinolin-6-ones†","authors":"Min Xiang, Gang-Yong Liu, Hui-Mei Liu, Wen-Yi Zhou, Guang-Wei Wang, Fei Fei, Yun-Qing Jia and Li-Wen Shen","doi":"10.1039/D4NJ04654D","DOIUrl":null,"url":null,"abstract":"<p >A [4+2] annulation reaction of <em>o</em>-acylamino-aryl MBH carbonates with 3-substituted coumarins has been developed. This method exhibits excellent substrate tolerance and constructs a series of tetrahydrochromeno[4,3-<em>b</em>]quinolin-6-ones with yields up to 95%. The application value of this method has also been demonstrated through a 50-fold scale-up.</p>","PeriodicalId":95,"journal":{"name":"New Journal of Chemistry","volume":" 3","pages":" 683-686"},"PeriodicalIF":2.7000,"publicationDate":"2024-12-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"New Journal of Chemistry","FirstCategoryId":"92","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2025/nj/d4nj04654d","RegionNum":3,"RegionCategory":"化学","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 [4+2] annulation reaction of o-acylamino-aryl MBH carbonates with 3-substituted coumarins has been developed. This method exhibits excellent substrate tolerance and constructs a series of tetrahydrochromeno[4,3-b]quinolin-6-ones with yields up to 95%. The application value of this method has also been demonstrated through a 50-fold scale-up.

Abstract Image

邻酰基芳基MBH碳酸盐与香豆素的[4+2]环化:四氢染料[4,3-b]喹啉-6- 1†的易得性
研究了邻酰基芳基羰基碳酸氢盐与3-取代香豆素的[4+2]环化反应。该方法具有良好的底物耐受性,构建了一系列四氢色[4,3-b]喹啉-6- 1,产率高达95%。该方法的应用价值也通过50倍的放大实验得到了验证。
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
New Journal of Chemistry
New Journal of Chemistry 化学-化学综合
CiteScore
5.30
自引率
6.10%
发文量
1832
审稿时长
2 months
期刊介绍: A journal for new directions in chemistry
×
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