{"title":"用分子内电荷转移配合物对C(sp2)-H的二氟烷基化进行可见光诱导的碘化磷盐直接光解。","authors":"Jie Sun,Jintong Xie,Wen Lin,Jianjun Li","doi":"10.1021/acs.orglett.5c03255","DOIUrl":null,"url":null,"abstract":"Green, safe, simple, and efficient strategies for generating fluoroalkyls are an ongoing challenge for the synthetic community. Generally, the main form of synthesizing difluoroalkylated heteroaromatic compounds is to use catalysts, oxidants, and a high temperature to generate difluoroalkyl radicals and react with heteroaromatic hydrocarbons. In contrast, the strategy of using intramolecular charge-transfer complexes (ICTCs) to generate difluoroalkylated heteroaromatic compounds remains an unexplored challenge. Here, for the first time, we carried out a difluoromethylation reaction between various difluoroalkyl radicals generated in the form of photoactivated ICTCs and heteroaromatic C(sp2)-H compounds (with high stability and multiple active sites) to obtain various fluorine-containing compounds. This method only depends on the substrate in the reaction, avoiding the need for a metal, exogenous photocatalyst, and oxidant. In addition, this metal-free approach provides controlled synthetic conditions, employs a scalable flow technique with high temporal and spatial efficiency, and demonstrates successful gram-scale applications, thus proving the usefulness and versatility of this new scheme.","PeriodicalId":54,"journal":{"name":"Organic Letters","volume":"148 1","pages":""},"PeriodicalIF":5.0000,"publicationDate":"2025-09-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Visible-Light-Induced Direct Photolysis of Phosphorus Iodide Salts for Difluoroalkylation of C(sp2)-H by an Intramolecular Charge-Transfer Complex.\",\"authors\":\"Jie Sun,Jintong Xie,Wen Lin,Jianjun Li\",\"doi\":\"10.1021/acs.orglett.5c03255\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Green, safe, simple, and efficient strategies for generating fluoroalkyls are an ongoing challenge for the synthetic community. Generally, the main form of synthesizing difluoroalkylated heteroaromatic compounds is to use catalysts, oxidants, and a high temperature to generate difluoroalkyl radicals and react with heteroaromatic hydrocarbons. In contrast, the strategy of using intramolecular charge-transfer complexes (ICTCs) to generate difluoroalkylated heteroaromatic compounds remains an unexplored challenge. Here, for the first time, we carried out a difluoromethylation reaction between various difluoroalkyl radicals generated in the form of photoactivated ICTCs and heteroaromatic C(sp2)-H compounds (with high stability and multiple active sites) to obtain various fluorine-containing compounds. This method only depends on the substrate in the reaction, avoiding the need for a metal, exogenous photocatalyst, and oxidant. In addition, this metal-free approach provides controlled synthetic conditions, employs a scalable flow technique with high temporal and spatial efficiency, and demonstrates successful gram-scale applications, thus proving the usefulness and versatility of this new scheme.\",\"PeriodicalId\":54,\"journal\":{\"name\":\"Organic Letters\",\"volume\":\"148 1\",\"pages\":\"\"},\"PeriodicalIF\":5.0000,\"publicationDate\":\"2025-09-30\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Organic Letters\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1021/acs.orglett.5c03255\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, ORGANIC\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Organic Letters","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1021/acs.orglett.5c03255","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
Visible-Light-Induced Direct Photolysis of Phosphorus Iodide Salts for Difluoroalkylation of C(sp2)-H by an Intramolecular Charge-Transfer Complex.
Green, safe, simple, and efficient strategies for generating fluoroalkyls are an ongoing challenge for the synthetic community. Generally, the main form of synthesizing difluoroalkylated heteroaromatic compounds is to use catalysts, oxidants, and a high temperature to generate difluoroalkyl radicals and react with heteroaromatic hydrocarbons. In contrast, the strategy of using intramolecular charge-transfer complexes (ICTCs) to generate difluoroalkylated heteroaromatic compounds remains an unexplored challenge. Here, for the first time, we carried out a difluoromethylation reaction between various difluoroalkyl radicals generated in the form of photoactivated ICTCs and heteroaromatic C(sp2)-H compounds (with high stability and multiple active sites) to obtain various fluorine-containing compounds. This method only depends on the substrate in the reaction, avoiding the need for a metal, exogenous photocatalyst, and oxidant. In addition, this metal-free approach provides controlled synthetic conditions, employs a scalable flow technique with high temporal and spatial efficiency, and demonstrates successful gram-scale applications, thus proving the usefulness and versatility of this new scheme.
期刊介绍:
Organic Letters invites original reports of fundamental research in all branches of the theory and practice of organic, physical organic, organometallic,medicinal, and bioorganic chemistry. Organic Letters provides rapid disclosure of the key elements of significant studies that are of interest to a large portion of the organic community. In selecting manuscripts for publication, the Editors place emphasis on the originality, quality and wide interest of the work. Authors should provide enough background information to place the new disclosure in context and to justify the rapid publication format. Back-to-back Letters will be considered. Full details should be reserved for an Article, which should appear in due course.