NHC 催化的远程位点选择性炔烃 C-H 丙烯酸化反应

IF 11.5 Q1 CHEMISTRY, PHYSICAL
Jiamiao Jin, Shi-Chao Ren
{"title":"NHC 催化的远程位点选择性炔烃 C-H 丙烯酸化反应","authors":"Jiamiao Jin, Shi-Chao Ren","doi":"10.1016/j.checat.2024.101125","DOIUrl":null,"url":null,"abstract":"Recently, Li’s group designed a conceptually novel radical strategy for site-selective functionalization of ultra-remote arene C–H bond. The arenes were activated by intramolecular nitrogen-centered radical instead of generally used C–H metalation. The NHC-catalyzed radical cross-coupling acts as the key step to forging C–C bond at the para position of the arenes.","PeriodicalId":53121,"journal":{"name":"Chem Catalysis","volume":null,"pages":null},"PeriodicalIF":11.5000,"publicationDate":"2024-10-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"NHC-catalyzed remote site-selective arene C–H acylations\",\"authors\":\"Jiamiao Jin, Shi-Chao Ren\",\"doi\":\"10.1016/j.checat.2024.101125\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Recently, Li’s group designed a conceptually novel radical strategy for site-selective functionalization of ultra-remote arene C–H bond. The arenes were activated by intramolecular nitrogen-centered radical instead of generally used C–H metalation. The NHC-catalyzed radical cross-coupling acts as the key step to forging C–C bond at the para position of the arenes.\",\"PeriodicalId\":53121,\"journal\":{\"name\":\"Chem Catalysis\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":11.5000,\"publicationDate\":\"2024-10-17\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Chem Catalysis\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1016/j.checat.2024.101125\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, PHYSICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chem Catalysis","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1016/j.checat.2024.101125","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0

摘要

最近,李的研究小组设计了一种概念新颖的自由基策略,用于超偏远炔烃 C-H 键的位点选择性官能化。通过分子内以氮为中心的自由基激活炔,而不是通常使用的 C-H 金属化。NHC 催化的自由基交叉偶联是在炔烃对位形成 C-C 键的关键步骤。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
NHC-catalyzed remote site-selective arene C–H acylations
Recently, Li’s group designed a conceptually novel radical strategy for site-selective functionalization of ultra-remote arene C–H bond. The arenes were activated by intramolecular nitrogen-centered radical instead of generally used C–H metalation. The NHC-catalyzed radical cross-coupling acts as the key step to forging C–C bond at the para position of the arenes.
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
CiteScore
10.50
自引率
6.40%
发文量
0
期刊介绍: Chem Catalysis is a monthly journal that publishes innovative research on fundamental and applied catalysis, providing a platform for researchers across chemistry, chemical engineering, and related fields. It serves as a premier resource for scientists and engineers in academia and industry, covering heterogeneous, homogeneous, and biocatalysis. Emphasizing transformative methods and technologies, the journal aims to advance understanding, introduce novel catalysts, and connect fundamental insights to real-world applications for societal benefit.
×
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