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":2.7000,"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.