光诱导三酰基亚硝基铁的亲电芳香取代

IF 2.2 4区 化学 Q2 CHEMISTRY, ORGANIC
Ming Hou, Zhide Zhang, Xiaojing Lai, Qianzhou Zong, Miaofeng Ren, Tianwen Bai, Guanyinsheng Qiu
{"title":"光诱导三酰基亚硝基铁的亲电芳香取代","authors":"Ming Hou, Zhide Zhang, Xiaojing Lai, Qianzhou Zong, Miaofeng Ren, Tianwen Bai, Guanyinsheng Qiu","doi":"10.1055/a-2183-0262","DOIUrl":null,"url":null,"abstract":"A photo-induced intramolecular electron-aromatic-substitution (SEAr) of N-acyloxybenzozmide under 20 mol% FeCl3 at 1, 4-dioxane is reported for the synthesis of biologically interesting benzoxazin-3(4H)-ones. In the reaction, it is believed that blue LED facilitates the reaction, like reaction temperature serving as source of energy. The reaction SEAr pathway was ascribed to the electron effect in aryl ring of substrates. The reaction was also applicable for the synthesis of useful scaffolds possessing a quinolin-2-one core, such as anticancer reagent 4, brexipiprazole and cilostamide analogues.","PeriodicalId":49451,"journal":{"name":"Synthesis-Stuttgart","volume":"78 1","pages":"0"},"PeriodicalIF":2.2000,"publicationDate":"2023-09-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Photo-Induced Electrophilic Aromatic Substitution of Ferric Acyl Nitrene\",\"authors\":\"Ming Hou, Zhide Zhang, Xiaojing Lai, Qianzhou Zong, Miaofeng Ren, Tianwen Bai, Guanyinsheng Qiu\",\"doi\":\"10.1055/a-2183-0262\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"A photo-induced intramolecular electron-aromatic-substitution (SEAr) of N-acyloxybenzozmide under 20 mol% FeCl3 at 1, 4-dioxane is reported for the synthesis of biologically interesting benzoxazin-3(4H)-ones. In the reaction, it is believed that blue LED facilitates the reaction, like reaction temperature serving as source of energy. The reaction SEAr pathway was ascribed to the electron effect in aryl ring of substrates. The reaction was also applicable for the synthesis of useful scaffolds possessing a quinolin-2-one core, such as anticancer reagent 4, brexipiprazole and cilostamide analogues.\",\"PeriodicalId\":49451,\"journal\":{\"name\":\"Synthesis-Stuttgart\",\"volume\":\"78 1\",\"pages\":\"0\"},\"PeriodicalIF\":2.2000,\"publicationDate\":\"2023-09-27\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Synthesis-Stuttgart\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1055/a-2183-0262\",\"RegionNum\":4,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, ORGANIC\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Synthesis-Stuttgart","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1055/a-2183-0262","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
引用次数: 0

摘要

报道了在1,4 -二恶烷下,在20 mol% FeCl3下光诱导n-酰基氧基苯并胺的分子内电子-芳香取代(SEAr),合成了具有生物学意义的苯并恶嗪-3(4H)-ones。在反应中,蓝色LED被认为促进了反应,如反应温度作为能量来源。SEAr反应途径归因于底物芳基环上的电子效应。该反应也适用于合成具有喹啉-2- 1核心的有用支架,如抗癌试剂4、布雷西哌唑和西洛胺类似物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Photo-Induced Electrophilic Aromatic Substitution of Ferric Acyl Nitrene
A photo-induced intramolecular electron-aromatic-substitution (SEAr) of N-acyloxybenzozmide under 20 mol% FeCl3 at 1, 4-dioxane is reported for the synthesis of biologically interesting benzoxazin-3(4H)-ones. In the reaction, it is believed that blue LED facilitates the reaction, like reaction temperature serving as source of energy. The reaction SEAr pathway was ascribed to the electron effect in aryl ring of substrates. The reaction was also applicable for the synthesis of useful scaffolds possessing a quinolin-2-one core, such as anticancer reagent 4, brexipiprazole and cilostamide analogues.
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
Synthesis-Stuttgart
Synthesis-Stuttgart 化学-有机化学
CiteScore
4.50
自引率
7.70%
发文量
435
审稿时长
1 months
期刊介绍: SYNTHESIS is an international full-paper journal devoted to the advancement of the science of chemical synthesis. It covers all fields of organic chemistry involving synthesis, including catalysis, organometallic, medicinal, biological, and photochemistry, but also related disciplines. SYNTHESIS provides dependable research results with detailed and reliable experimental procedures and full characterization of all important new products as well as scientific primary data.
×
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