可见光诱导EDA配合物促进五氟苯乙烯脱胺烷基化反应

IF 2 3区 化学 Q3 CHEMISTRY, ORGANIC Synthetic Communications Pub Date : 2025-03-19 Epub Date: 2025-02-12 DOI:10.1080/00397911.2025.2462668
Bei-Lei Wang , Lin-Yuan Zeng , Pei-Zhen Qu , De-Zhi Yang
{"title":"可见光诱导EDA配合物促进五氟苯乙烯脱胺烷基化反应","authors":"Bei-Lei Wang ,&nbsp;Lin-Yuan Zeng ,&nbsp;Pei-Zhen Qu ,&nbsp;De-Zhi Yang","doi":"10.1080/00397911.2025.2462668","DOIUrl":null,"url":null,"abstract":"<div><div>Polyfluoroaromatic compounds are important components in medicinal and material science, however, methodologies for the synthesis of alkylated pentafluoroarenes remains limited. Here we developed a deaminative coupling reaction of Katritzky salts with pentafluorostyrene to construct C<sub>6</sub>F<sub>5</sub>-C(sp<sup>3</sup>) bonds promoted by the photochemical activity of electron donor-acceptor (EDA) complexes. This method features simple reaction conditions, a broad substrate scope, and good functional group tolerance.</div></div>","PeriodicalId":22119,"journal":{"name":"Synthetic Communications","volume":"55 6","pages":"Pages 476-484"},"PeriodicalIF":2.0000,"publicationDate":"2025-03-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Visible light induced deaminative alkylation of pentafluorostyrene promoted by EDA complex\",\"authors\":\"Bei-Lei Wang ,&nbsp;Lin-Yuan Zeng ,&nbsp;Pei-Zhen Qu ,&nbsp;De-Zhi Yang\",\"doi\":\"10.1080/00397911.2025.2462668\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Polyfluoroaromatic compounds are important components in medicinal and material science, however, methodologies for the synthesis of alkylated pentafluoroarenes remains limited. Here we developed a deaminative coupling reaction of Katritzky salts with pentafluorostyrene to construct C<sub>6</sub>F<sub>5</sub>-C(sp<sup>3</sup>) bonds promoted by the photochemical activity of electron donor-acceptor (EDA) complexes. This method features simple reaction conditions, a broad substrate scope, and good functional group tolerance.</div></div>\",\"PeriodicalId\":22119,\"journal\":{\"name\":\"Synthetic Communications\",\"volume\":\"55 6\",\"pages\":\"Pages 476-484\"},\"PeriodicalIF\":2.0000,\"publicationDate\":\"2025-03-19\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Synthetic Communications\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/org/science/article/pii/S0039791125000190\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/2/12 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q3\",\"JCRName\":\"CHEMISTRY, ORGANIC\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Synthetic Communications","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/org/science/article/pii/S0039791125000190","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/2/12 0:00:00","PubModel":"Epub","JCR":"Q3","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
引用次数: 0

摘要

多氟芳香族化合物是医药和材料科学中的重要成分,然而合成烷基化五氟苯乙烯的方法仍然有限。在此,我们开发了一种卡氏盐与五氟苯乙烯的脱氨基偶联反应,在电子供体-受体(EDA)复合物的光化学活性的促进下构建 C6F5-C(sp3)键。该方法具有反应条件简单、底物范围广、官能团耐受性好等特点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Visible light induced deaminative alkylation of pentafluorostyrene promoted by EDA complex
Polyfluoroaromatic compounds are important components in medicinal and material science, however, methodologies for the synthesis of alkylated pentafluoroarenes remains limited. Here we developed a deaminative coupling reaction of Katritzky salts with pentafluorostyrene to construct C6F5-C(sp3) bonds promoted by the photochemical activity of electron donor-acceptor (EDA) complexes. This method features simple reaction conditions, a broad substrate scope, and good functional group tolerance.
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
Synthetic Communications
Synthetic Communications 化学-有机化学
CiteScore
4.40
自引率
4.80%
发文量
156
审稿时长
4.3 months
期刊介绍: Synthetic Communications presents communications describing new methods, reagents, and other synthetic work pertaining to organic chemistry with sufficient experimental detail to permit reported reactions to be repeated by a chemist reasonably skilled in the art. In addition, the Journal features short, focused review articles discussing topics within its remit of synthetic organic chemistry.
期刊最新文献
Ugi reaction-based synthesis of piperazine-2,5-diones and related heterocycles A new, efficient, and improved process for the synthesis of key dihydrospiro cyclopenta pyridine intermediate for the preparation of CGRP antagonist drugs New chromene-based 1-aryl-1H-pyrazole-3-carboxylate hybrids linked to 1,3,4-oxadiazole and/or arene units with potential bacterial and DNA gyrase inhibitory potency Synthesis of pyrimidines from flavokavains and their 2′-hydroxychalcone analogues Ultrasonic-induced synthesis of novel diverse N-aryl-2-[2-cyanoimino-5-oxo-4,4-diphenylimidazolidin-1-yl]acetamides
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1