Tao Ye , Na Lin , Jia-Huan Shen , Lichun Kong , Yang-Zi Liu , Quannan Wang , Wei-Ping Deng
{"title":"硝酸铁催化取代呋喃的有氧氧化开环立体选择性合成(Z)-1,4-烯二酮","authors":"Tao Ye , Na Lin , Jia-Huan Shen , Lichun Kong , Yang-Zi Liu , Quannan Wang , Wei-Ping Deng","doi":"10.1016/j.gresc.2023.11.007","DOIUrl":null,"url":null,"abstract":"<div><div>A simple and highly efficient catalytic system for the selective aerobic oxidative ring-opening of substituted furans has been achieved using Fe(NO<sub>3</sub>)<sub>3</sub><strong>·</strong>9H<sub>2</sub>O as a catalyst and air as an oxidant under mild conditions. A series of (<em>Z</em>)-1,4-enediones were obtained in good yields (up to 97 %) with excellent stereoselectivity (up to > 20:1 <em>Z</em>/<em>E</em> ratio). The present synthetic method exhibits perfect atom economy, wide substrate scope, and highly functionalized products allowing diverse transformations.</div></div>","PeriodicalId":12794,"journal":{"name":"Green Synthesis and Catalysis","volume":"6 2","pages":"Pages 179-182"},"PeriodicalIF":0.0000,"publicationDate":"2025-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Ferric nitrate-catalyzed aerobic oxidative ring-opening of substituted furans for the stereoselective synthesis of (Z)-1,4-enediones\",\"authors\":\"Tao Ye , Na Lin , Jia-Huan Shen , Lichun Kong , Yang-Zi Liu , Quannan Wang , Wei-Ping Deng\",\"doi\":\"10.1016/j.gresc.2023.11.007\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>A simple and highly efficient catalytic system for the selective aerobic oxidative ring-opening of substituted furans has been achieved using Fe(NO<sub>3</sub>)<sub>3</sub><strong>·</strong>9H<sub>2</sub>O as a catalyst and air as an oxidant under mild conditions. A series of (<em>Z</em>)-1,4-enediones were obtained in good yields (up to 97 %) with excellent stereoselectivity (up to > 20:1 <em>Z</em>/<em>E</em> ratio). The present synthetic method exhibits perfect atom economy, wide substrate scope, and highly functionalized products allowing diverse transformations.</div></div>\",\"PeriodicalId\":12794,\"journal\":{\"name\":\"Green Synthesis and Catalysis\",\"volume\":\"6 2\",\"pages\":\"Pages 179-182\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2025-05-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Green Synthesis and Catalysis\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2666554923001011\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Green Synthesis and Catalysis","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2666554923001011","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Ferric nitrate-catalyzed aerobic oxidative ring-opening of substituted furans for the stereoselective synthesis of (Z)-1,4-enediones
A simple and highly efficient catalytic system for the selective aerobic oxidative ring-opening of substituted furans has been achieved using Fe(NO3)3·9H2O as a catalyst and air as an oxidant under mild conditions. A series of (Z)-1,4-enediones were obtained in good yields (up to 97 %) with excellent stereoselectivity (up to > 20:1 Z/E ratio). The present synthetic method exhibits perfect atom economy, wide substrate scope, and highly functionalized products allowing diverse transformations.