铑/硒双催化从n -磺酰基-1,2,3-三唑中获得2-氨基吡咯

IF 4.3 2区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
Chandra Volla, Kuntal Pal, Om Prakash Dash
{"title":"铑/硒双催化从n -磺酰基-1,2,3-三唑中获得2-氨基吡咯","authors":"Chandra Volla, Kuntal Pal, Om Prakash Dash","doi":"10.1039/d4cc06346e","DOIUrl":null,"url":null,"abstract":"Herein, we report a novel rhodium/selenium dual catalytic process for the synthesis of 2-aminopyrroles from N-sulfonyl-1,2,3-triazoles. The proposed cooperative catalytic mechanism involves Rh(II)-catalyzed formation of Rh-azavinyl carbene from triazole, followed by selenium-catalyzed generation of ylide, which subsequently undergoes annulation with another Rh-azavinyl carbene. The simple and mild dual catalytic strategy accommodates a variety of electron-withdrawing and electron-donating functional groups, affording various 2-aminopyrrole derivatives in moderate to good yields.","PeriodicalId":67,"journal":{"name":"Chemical Communications","volume":"12 1","pages":""},"PeriodicalIF":4.3000,"publicationDate":"2025-01-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Rhodium/Selenium Dual Catalysis for Accessing 2-Aminopyrroles from N-Sulfonyl-1,2,3-triazoles\",\"authors\":\"Chandra Volla, Kuntal Pal, Om Prakash Dash\",\"doi\":\"10.1039/d4cc06346e\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Herein, we report a novel rhodium/selenium dual catalytic process for the synthesis of 2-aminopyrroles from N-sulfonyl-1,2,3-triazoles. The proposed cooperative catalytic mechanism involves Rh(II)-catalyzed formation of Rh-azavinyl carbene from triazole, followed by selenium-catalyzed generation of ylide, which subsequently undergoes annulation with another Rh-azavinyl carbene. The simple and mild dual catalytic strategy accommodates a variety of electron-withdrawing and electron-donating functional groups, affording various 2-aminopyrrole derivatives in moderate to good yields.\",\"PeriodicalId\":67,\"journal\":{\"name\":\"Chemical Communications\",\"volume\":\"12 1\",\"pages\":\"\"},\"PeriodicalIF\":4.3000,\"publicationDate\":\"2025-01-23\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Chemical Communications\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1039/d4cc06346e\",\"RegionNum\":2,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chemical Communications","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1039/d4cc06346e","RegionNum":2,"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

摘要

本文报道了一种新的铑/硒双催化工艺,用于n -磺酰基-1,2,3-三唑合成2-氨基吡咯。所提出的协同催化机制包括:Rh(II)催化三唑生成Rh-azavinyl卡苯,然后硒催化生成ylide,随后与另一个Rh-azavinyl卡苯环合。简单温和的双催化策略可容纳多种吸电子和给电子官能团,以中高收率提供各种2-氨基吡咯衍生物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Rhodium/Selenium Dual Catalysis for Accessing 2-Aminopyrroles from N-Sulfonyl-1,2,3-triazoles
Herein, we report a novel rhodium/selenium dual catalytic process for the synthesis of 2-aminopyrroles from N-sulfonyl-1,2,3-triazoles. The proposed cooperative catalytic mechanism involves Rh(II)-catalyzed formation of Rh-azavinyl carbene from triazole, followed by selenium-catalyzed generation of ylide, which subsequently undergoes annulation with another Rh-azavinyl carbene. The simple and mild dual catalytic strategy accommodates a variety of electron-withdrawing and electron-donating functional groups, affording various 2-aminopyrrole derivatives in moderate to good yields.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Chemical Communications
Chemical Communications 化学-化学综合
CiteScore
8.60
自引率
4.10%
发文量
2705
审稿时长
1.4 months
期刊介绍: ChemComm (Chemical Communications) is renowned as the fastest publisher of articles providing information on new avenues of research, drawn from all the world''s major areas of chemical research.
×
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