铑(III)通过转金属化引发的C-H活化催化芳基硼试剂和7-叠氮杂氮二烯的氧化[3+2]环化。

IF 4.2 2区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
Xuejing Yao, Shunle Hu, Lijuan Jv, Ruijie Mi and Xingwei Li
{"title":"铑(III)通过转金属化引发的C-H活化催化芳基硼试剂和7-叠氮杂氮二烯的氧化[3+2]环化。","authors":"Xuejing Yao, Shunle Hu, Lijuan Jv, Ruijie Mi and Xingwei Li","doi":"10.1039/D5CC02745D","DOIUrl":null,"url":null,"abstract":"<p >Rh(<small>III</small>)-catalyzed oxidative [3+2] annulation between arylboron reagents and azabicyclic olefins is presented. This system offers an effective example of transmetalation-promoted C–H activation using easily available arylboron reagents, which provides a series of <em>cis</em>-fused dihydrocarbazoles <em>via</em> both <em>ipso</em> and <em>ortho</em> functionalization of the arylboron reagents. Importantly, this annulation reaction circumvents the reliance on a directing group in the arene ring.</p>","PeriodicalId":67,"journal":{"name":"Chemical Communications","volume":" 60","pages":" 11231-11234"},"PeriodicalIF":4.2000,"publicationDate":"2025-06-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Rhodium(iii)-catalyzed oxidative [3+2] annulation of arylboron reagents and 7-azabenzonorbornadienes via transmetalation-initiated C–H activation†\",\"authors\":\"Xuejing Yao, Shunle Hu, Lijuan Jv, Ruijie Mi and Xingwei Li\",\"doi\":\"10.1039/D5CC02745D\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >Rh(<small>III</small>)-catalyzed oxidative [3+2] annulation between arylboron reagents and azabicyclic olefins is presented. This system offers an effective example of transmetalation-promoted C–H activation using easily available arylboron reagents, which provides a series of <em>cis</em>-fused dihydrocarbazoles <em>via</em> both <em>ipso</em> and <em>ortho</em> functionalization of the arylboron reagents. Importantly, this annulation reaction circumvents the reliance on a directing group in the arene ring.</p>\",\"PeriodicalId\":67,\"journal\":{\"name\":\"Chemical Communications\",\"volume\":\" 60\",\"pages\":\" 11231-11234\"},\"PeriodicalIF\":4.2000,\"publicationDate\":\"2025-06-19\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Chemical Communications\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://pubs.rsc.org/en/content/articlelanding/2025/cc/d5cc02745d\",\"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://pubs.rsc.org/en/content/articlelanding/2025/cc/d5cc02745d","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

介绍了Rh(III)催化芳基硼试剂与氮杂环烯烃之间的氧化[3+2]环反应。该体系提供了一个使用容易获得的芳基硼试剂进行转金属化促进C-H活化的有效例子,该体系通过芳基硼试剂的邻位官能团和邻位官能团提供了一系列顺式融合的二氢咔唑。重要的是,这种环化反应避免了对芳烃环中导向基团的依赖。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Rhodium(iii)-catalyzed oxidative [3+2] annulation of arylboron reagents and 7-azabenzonorbornadienes via transmetalation-initiated C–H activation†

Rhodium(iii)-catalyzed oxidative [3+2] annulation of arylboron reagents and 7-azabenzonorbornadienes via transmetalation-initiated C–H activation†

Rh(III)-catalyzed oxidative [3+2] annulation between arylboron reagents and azabicyclic olefins is presented. This system offers an effective example of transmetalation-promoted C–H activation using easily available arylboron reagents, which provides a series of cis-fused dihydrocarbazoles via both ipso and ortho functionalization of the arylboron reagents. Importantly, this annulation reaction circumvents the reliance on a directing group in the arene ring.

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:604180095
Book学术官方微信