低负荷[3 + 3]苯并环法制备多功能化三氟甲基芳烃的无金属催化新结构

Qing He , Yu-Qi Xiang , Rui Zhou , Bin Liu , Rong-Hua Wang , Xiang-Kai Kong , Song Bai , Miao Li , Guang-Jun Yang , Gao-Feng Zhu
{"title":"低负荷[3 + 3]苯并环法制备多功能化三氟甲基芳烃的无金属催化新结构","authors":"Qing He ,&nbsp;Yu-Qi Xiang ,&nbsp;Rui Zhou ,&nbsp;Bin Liu ,&nbsp;Rong-Hua Wang ,&nbsp;Xiang-Kai Kong ,&nbsp;Song Bai ,&nbsp;Miao Li ,&nbsp;Guang-Jun Yang ,&nbsp;Gao-Feng Zhu","doi":"10.1039/d5qo00013k","DOIUrl":null,"url":null,"abstract":"<div><div>A low catalyst loading and transition metal-free benzannulation of β,γ-alkynyl-α-keto esters and CF<sub>3</sub>-alkenes has been developed through Michael-triggered [3 + 3] annulation. The newly developed methodology provides highly efficient and rapid access to a variety of multi-functionalised trifluoromethylarene derivatives in generally good to excellent yields. The late-stage functionalisation of some natural products and bioactive molecules and the gram-scale reaction as well as transformation of the products indicate that the present protocol has significant practical value and reliability.</div></div>","PeriodicalId":94379,"journal":{"name":"Organic chemistry frontiers : an international journal of organic chemistry","volume":"12 8","pages":"Pages 2670-2675"},"PeriodicalIF":0.0000,"publicationDate":"2025-02-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Metal-free catalytic de novo construction of multi-functionalized trifluoromethylarenes through [3 + 3] benzannulation at low catalyst loadings†\",\"authors\":\"Qing He ,&nbsp;Yu-Qi Xiang ,&nbsp;Rui Zhou ,&nbsp;Bin Liu ,&nbsp;Rong-Hua Wang ,&nbsp;Xiang-Kai Kong ,&nbsp;Song Bai ,&nbsp;Miao Li ,&nbsp;Guang-Jun Yang ,&nbsp;Gao-Feng Zhu\",\"doi\":\"10.1039/d5qo00013k\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>A low catalyst loading and transition metal-free benzannulation of β,γ-alkynyl-α-keto esters and CF<sub>3</sub>-alkenes has been developed through Michael-triggered [3 + 3] annulation. The newly developed methodology provides highly efficient and rapid access to a variety of multi-functionalised trifluoromethylarene derivatives in generally good to excellent yields. The late-stage functionalisation of some natural products and bioactive molecules and the gram-scale reaction as well as transformation of the products indicate that the present protocol has significant practical value and reliability.</div></div>\",\"PeriodicalId\":94379,\"journal\":{\"name\":\"Organic chemistry frontiers : an international journal of organic chemistry\",\"volume\":\"12 8\",\"pages\":\"Pages 2670-2675\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2025-02-12\",\"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/S2052412925001081\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/2/25 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/S2052412925001081","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/2/25 0:00:00","PubModel":"Epub","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

采用michael -触发[3 + 3]环法制备了β,γ-炔基-α-酮酯和cf3 -烯烃的低催化剂负载和无过渡金属环。新开发的方法提供了高效和快速获取各种多功能三氟甲基芳烃衍生物的途径,收率通常很高。一些天然产物和生物活性分子的后期功能化以及产物的克级反应和转化表明,本方案具有重要的实用价值和可靠性。
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

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
Metal-free catalytic de novo construction of multi-functionalized trifluoromethylarenes through [3 + 3] benzannulation at low catalyst loadings†
A low catalyst loading and transition metal-free benzannulation of β,γ-alkynyl-α-keto esters and CF3-alkenes has been developed through Michael-triggered [3 + 3] annulation. The newly developed methodology provides highly efficient and rapid access to a variety of multi-functionalised trifluoromethylarene derivatives in generally good to excellent yields. The late-stage functionalisation of some natural products and bioactive molecules and the gram-scale reaction as well as transformation of the products indicate that the present protocol has significant practical value and reliability.
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