苯胺与乙烯基氮丙啶在六氟异丙醇中的正烯丙基化反应

Jing-Jing Nie , Zhong-Xia Wang
{"title":"苯胺与乙烯基氮丙啶在六氟异丙醇中的正烯丙基化反应","authors":"Jing-Jing Nie ,&nbsp;Zhong-Xia Wang","doi":"10.1039/d4qo01719f","DOIUrl":null,"url":null,"abstract":"<div><div>Transition-metal-free reaction of <em>N</em>,<em>N</em>-dialkylanilines with 1-sulfonyl-2-vinylaziridines in hexafluoroisopropanol under air gave <em>ortho</em>-allylated anilines in moderate to excellent yields. The reaction also features mild reaction conditions, <em>ortho</em>-monoallylation selectivity, <em>E</em>-configured C–C double bonds, wide substrate scope and good compatibility of functional groups.</div></div>","PeriodicalId":94379,"journal":{"name":"Organic chemistry frontiers : an international journal of organic chemistry","volume":"12 2","pages":"Pages 629-635"},"PeriodicalIF":0.0000,"publicationDate":"2024-11-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"ortho-Allylation of anilines with vinylaziridines in hexafluoroisopropanol†\",\"authors\":\"Jing-Jing Nie ,&nbsp;Zhong-Xia Wang\",\"doi\":\"10.1039/d4qo01719f\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Transition-metal-free reaction of <em>N</em>,<em>N</em>-dialkylanilines with 1-sulfonyl-2-vinylaziridines in hexafluoroisopropanol under air gave <em>ortho</em>-allylated anilines in moderate to excellent yields. The reaction also features mild reaction conditions, <em>ortho</em>-monoallylation selectivity, <em>E</em>-configured C–C double bonds, wide substrate scope and good compatibility of functional groups.</div></div>\",\"PeriodicalId\":94379,\"journal\":{\"name\":\"Organic chemistry frontiers : an international journal of organic chemistry\",\"volume\":\"12 2\",\"pages\":\"Pages 629-635\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-11-19\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Organic chemistry frontiers : an international journal of organic chemistry\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/org/science/article/pii/S2052412924008088\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2024/11/14 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Organic chemistry frontiers : an international journal of organic chemistry","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/org/science/article/pii/S2052412924008088","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/11/14 0:00:00","PubModel":"Epub","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

在六氟异丙醇中,N,N-二烷基苯胺与 1-磺酰基-2-乙烯基氮丙啶在空气中进行无过渡金属反应,可获得中等至极好收率的正烯丙基苯胺。该反应还具有反应条件温和、正单烯丙基化选择性高、C-C 双键为 E 构型、底物范围广以及官能团兼容性好等特点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

摘要图片

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
ortho-Allylation of anilines with vinylaziridines in hexafluoroisopropanol†
Transition-metal-free reaction of N,N-dialkylanilines with 1-sulfonyl-2-vinylaziridines in hexafluoroisopropanol under air gave ortho-allylated anilines in moderate to excellent yields. The reaction also features mild reaction conditions, ortho-monoallylation selectivity, E-configured C–C double bonds, wide substrate scope and good compatibility of functional groups.
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
7.80
自引率
0.00%
发文量
0
期刊最新文献
Capturing CO: palladium-catalyzed, BrCF2COOK-mediated one-pot carbonylative coupling for the synthesis of oxindoles A 4-nitro-3-arylpyrrole platform for the divergent synthesis of marine natural products: Ningalins and Lamellarins Visible-light-induced acylation of active olefins by a C–C bond cleavage/Smiles rearrangement radical relay strategy via EDA complexes α-Borylcarbene precursors: design, generation, and synthetic opportunities Sacrifice of diorganyl diselenide enables cyclization of aryl propargyl ethers in the synthesis of 3-organoselenyl chromenones
×
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