{"title":"Ru催化电氧化C-H / O-H键偶联:邻苯酞和萘[1,8-bc]呋喃†的制备","authors":"Nilam Patil , Ajay Dhapate , Twinkle Bharadwaj , Bhalchandra M. Bhanage","doi":"10.1039/d5cy00713e","DOIUrl":null,"url":null,"abstract":"<div><div>We hereby report ruthenium-catalyzed electrooxidative coupling of acrylates with benzoic acids and naphthol for the synthesis of phthalide and naphthofuran derivatives. The process is particularly effective for activating weakly coordinating O–H bonds using ruthenium catalysts. This method is workable and well-organized for the activation of carbon–hydrogen and oxygen–hydrogen bonds, demonstrating moderate to good yields across a diverse set of over 26 readily available substrates. The method proceeds under oxidant- and additive-free conditions, significantly reducing the reaction time while retaining a broad substrate scope. Our approach provides a green and user-friendly method for synthesizing phthalides and naphthofurans <em>via</em> weak coordination O–H and C–H bond activation, leveraging electricity as an oxidant.</div></div>","PeriodicalId":66,"journal":{"name":"Catalysis Science & Technology","volume":"15 17","pages":"Pages 4981-4987"},"PeriodicalIF":4.2000,"publicationDate":"2025-06-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Electrooxidative C–H/O–H bond coupling via Ru catalysis: access to phthalides and naphtho[1,8-bc]furans†\",\"authors\":\"Nilam Patil , Ajay Dhapate , Twinkle Bharadwaj , Bhalchandra M. Bhanage\",\"doi\":\"10.1039/d5cy00713e\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>We hereby report ruthenium-catalyzed electrooxidative coupling of acrylates with benzoic acids and naphthol for the synthesis of phthalide and naphthofuran derivatives. The process is particularly effective for activating weakly coordinating O–H bonds using ruthenium catalysts. This method is workable and well-organized for the activation of carbon–hydrogen and oxygen–hydrogen bonds, demonstrating moderate to good yields across a diverse set of over 26 readily available substrates. The method proceeds under oxidant- and additive-free conditions, significantly reducing the reaction time while retaining a broad substrate scope. Our approach provides a green and user-friendly method for synthesizing phthalides and naphthofurans <em>via</em> weak coordination O–H and C–H bond activation, leveraging electricity as an oxidant.</div></div>\",\"PeriodicalId\":66,\"journal\":{\"name\":\"Catalysis Science & Technology\",\"volume\":\"15 17\",\"pages\":\"Pages 4981-4987\"},\"PeriodicalIF\":4.2000,\"publicationDate\":\"2025-06-16\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Catalysis Science & Technology\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/org/science/article/pii/S2044475325003260\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, PHYSICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Catalysis Science & Technology","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/org/science/article/pii/S2044475325003260","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
Electrooxidative C–H/O–H bond coupling via Ru catalysis: access to phthalides and naphtho[1,8-bc]furans†
We hereby report ruthenium-catalyzed electrooxidative coupling of acrylates with benzoic acids and naphthol for the synthesis of phthalide and naphthofuran derivatives. The process is particularly effective for activating weakly coordinating O–H bonds using ruthenium catalysts. This method is workable and well-organized for the activation of carbon–hydrogen and oxygen–hydrogen bonds, demonstrating moderate to good yields across a diverse set of over 26 readily available substrates. The method proceeds under oxidant- and additive-free conditions, significantly reducing the reaction time while retaining a broad substrate scope. Our approach provides a green and user-friendly method for synthesizing phthalides and naphthofurans via weak coordination O–H and C–H bond activation, leveraging electricity as an oxidant.
期刊介绍:
A multidisciplinary journal focusing on cutting edge research across all fundamental science and technological aspects of catalysis.
Editor-in-chief: Bert Weckhuysen
Impact factor: 5.0
Time to first decision (peer reviewed only): 31 days