Sustainable, precious-metal-free C–N cross coupling through photocatalysis†

IF 2.5 3区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
Mohammad Hassam, Samuelu Mamidipalli, Akhila Ailaveni, Pankajkumar Singh and Shambabu Joseph Maddirala
{"title":"Sustainable, precious-metal-free C–N cross coupling through photocatalysis†","authors":"Mohammad Hassam, Samuelu Mamidipalli, Akhila Ailaveni, Pankajkumar Singh and Shambabu Joseph Maddirala","doi":"10.1039/D4NJ04300F","DOIUrl":null,"url":null,"abstract":"<p >Photoredox catalysis has evolved as a sustainable method of constructing C–N bonds. Herein, we have reported a visible-light organic-photoredox-catalyzed method that enables C–N cross-coupling under mild and sustainable reaction conditions. This catalytic system is suitable for both aromatic and aliphatic amines, as well as electron-rich and -deficient aryl bromides, exhibits broad functional group tolerance, and provides good-to-excellent yields. The noteworthy aspects of milder reaction conditions at room temperature without the addition of any additional ligands make this procedure attractive.</p>","PeriodicalId":95,"journal":{"name":"New Journal of Chemistry","volume":" 9","pages":" 3436-3441"},"PeriodicalIF":2.5000,"publicationDate":"2025-02-04","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/d4nj04300f","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

Photoredox catalysis has evolved as a sustainable method of constructing C–N bonds. Herein, we have reported a visible-light organic-photoredox-catalyzed method that enables C–N cross-coupling under mild and sustainable reaction conditions. This catalytic system is suitable for both aromatic and aliphatic amines, as well as electron-rich and -deficient aryl bromides, exhibits broad functional group tolerance, and provides good-to-excellent yields. The noteworthy aspects of milder reaction conditions at room temperature without the addition of any additional ligands make this procedure attractive.

Abstract Image

可持续的,通过光催化的无贵金属C-N交叉偶联†
光氧化还原催化已经发展成为一种可持续的构建碳氮键的方法。在此,我们报道了一种可见光有机光氧化催化方法,在温和和可持续的反应条件下实现了C-N交叉偶联。该催化体系适用于芳香胺和脂肪胺,以及富电子和缺电子芳基溴,具有广泛的官能团耐受性,并提供良好到优异的产率。值得注意的是,在室温下没有添加任何额外配体的温和反应条件使该过程具有吸引力。
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:604180095
Book学术官方微信