{"title":"通过 CN 偶联和多组分自由基/极性交叉光氧催化烯烃的双官能化","authors":"","doi":"10.1016/j.tetlet.2024.155223","DOIUrl":null,"url":null,"abstract":"<div><p>We reported an alkyl-thianthrenium salts (TTs) involved three-component radical alkene difunctionalization reaction. Alkylation of anilines has been realized <em>via</em> this mild method. An oxidative radical/polar crossover may be involved in the strategy, which realizing the combination of polar chemistry and radical chemistry. A variety of anilines, primary alkyl-substituted TTs, secondary alkyl-substituted TTs and olefins could be accessed in medium to good yield. Our work provides a valuable approach to producing diverse functionalized aniline derivatives.</p></div>","PeriodicalId":438,"journal":{"name":"Tetrahedron Letters","volume":null,"pages":null},"PeriodicalIF":1.5000,"publicationDate":"2024-08-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Photoredox-catalyzed difunctionalization of alkenes through CN coupling and multicomponent radical/polar crossover\",\"authors\":\"\",\"doi\":\"10.1016/j.tetlet.2024.155223\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>We reported an alkyl-thianthrenium salts (TTs) involved three-component radical alkene difunctionalization reaction. Alkylation of anilines has been realized <em>via</em> this mild method. An oxidative radical/polar crossover may be involved in the strategy, which realizing the combination of polar chemistry and radical chemistry. A variety of anilines, primary alkyl-substituted TTs, secondary alkyl-substituted TTs and olefins could be accessed in medium to good yield. Our work provides a valuable approach to producing diverse functionalized aniline derivatives.</p></div>\",\"PeriodicalId\":438,\"journal\":{\"name\":\"Tetrahedron Letters\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":1.5000,\"publicationDate\":\"2024-08-14\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Tetrahedron Letters\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0040403924003186\",\"RegionNum\":4,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"CHEMISTRY, ORGANIC\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Tetrahedron Letters","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0040403924003186","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
Photoredox-catalyzed difunctionalization of alkenes through CN coupling and multicomponent radical/polar crossover
We reported an alkyl-thianthrenium salts (TTs) involved three-component radical alkene difunctionalization reaction. Alkylation of anilines has been realized via this mild method. An oxidative radical/polar crossover may be involved in the strategy, which realizing the combination of polar chemistry and radical chemistry. A variety of anilines, primary alkyl-substituted TTs, secondary alkyl-substituted TTs and olefins could be accessed in medium to good yield. Our work provides a valuable approach to producing diverse functionalized aniline derivatives.
期刊介绍:
Tetrahedron Letters provides maximum dissemination of outstanding developments in organic chemistry. The journal is published weekly and covers developments in techniques, structures, methods and conclusions in experimental and theoretical organic chemistry. Rapid publication of timely and significant research results enables researchers from all over the world to transmit quickly their new contributions to large, international audiences.