Regioselective bromination of pyrrolo[1,2-a]quinoxalines†

IF 3.9 3区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
RSC Advances Pub Date : 2024-11-15 DOI:10.1039/D4RA07358D
Yingqian Li, Yali Liu, Di Hao, Liang Xu and Ping Liu
{"title":"Regioselective bromination of pyrrolo[1,2-a]quinoxalines†","authors":"Yingqian Li, Yali Liu, Di Hao, Liang Xu and Ping Liu","doi":"10.1039/D4RA07358D","DOIUrl":null,"url":null,"abstract":"<p >In this study, we report a novel and efficient method for the regioselective bromination of pyrrolo[1,2-<em>a</em>]quinoxalines using tetrabutylammonium tribromide (TBATB). This method exploits the mild nature of TBATB to obtain highly selective C3-brominated or C1, C3-dibrominated products in good yields. Notably, the reaction has a broad substrate applicability, and the C3-brominated product can be synthesized on a gram scale and can be further converted into structurally diverse pyrrolo[1,2-<em>a</em>]quinoxaline derivatives.</p>","PeriodicalId":102,"journal":{"name":"RSC Advances","volume":null,"pages":null},"PeriodicalIF":3.9000,"publicationDate":"2024-11-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://pubs.rsc.org/en/content/articlepdf/2024/ra/d4ra07358d?page=search","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"RSC Advances","FirstCategoryId":"92","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2024/ra/d4ra07358d","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

In this study, we report a novel and efficient method for the regioselective bromination of pyrrolo[1,2-a]quinoxalines using tetrabutylammonium tribromide (TBATB). This method exploits the mild nature of TBATB to obtain highly selective C3-brominated or C1, C3-dibrominated products in good yields. Notably, the reaction has a broad substrate applicability, and the C3-brominated product can be synthesized on a gram scale and can be further converted into structurally diverse pyrrolo[1,2-a]quinoxaline derivatives.

吡咯并[1,2-a]喹喔啉的区域选择性溴化反应†
在本研究中,我们报告了一种利用四丁基三溴化铵(TBATB)对吡咯并[1,2-a]喹喔啉进行区域选择性溴化的新型高效方法。该方法利用 TBATB 的温和性质,以良好的收率获得高选择性的 C3 溴化或 C1、C3 二溴化产物。值得注意的是,该反应具有广泛的底物适用性,C3-溴化产物可在克级规模上合成,并可进一步转化为结构多样的吡咯并[1,2-a]喹喔啉衍生物。
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
RSC Advances
RSC Advances chemical sciences-
CiteScore
7.50
自引率
2.60%
发文量
3116
审稿时长
1.6 months
期刊介绍: An international, peer-reviewed journal covering all of the chemical sciences, including multidisciplinary and emerging areas. RSC Advances is a gold open access journal allowing researchers free access to research articles, and offering an affordable open access publishing option for authors around the world.
×
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