{"title":"α,β-不饱和羰基化合物的光催化α-亲核氟化反应","authors":"Fang Wang, Jie Gong, Jian-Ping Qu, Yan-Biao Kang","doi":"10.1039/d5qo00877h","DOIUrl":null,"url":null,"abstract":"We report redox-neutral photocatalytic α-nucleophilic fluorination of α,β-unsaturated carbonyl compounds, in which an α-carbonyl cation is involved, under mild conditions. The protocol offers practical and efficient access to α-fluorinated carbonyl compounds and has demonstrated potential applications in the late-stage fluorination of bioactive molecules.","PeriodicalId":97,"journal":{"name":"Organic Chemistry Frontiers","volume":"8 1","pages":""},"PeriodicalIF":4.7000,"publicationDate":"2025-08-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Photocatalytic α-Nucleophilic Fluorination of α,β-Unsaturated Carbonyl Compounds\",\"authors\":\"Fang Wang, Jie Gong, Jian-Ping Qu, Yan-Biao Kang\",\"doi\":\"10.1039/d5qo00877h\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"We report redox-neutral photocatalytic α-nucleophilic fluorination of α,β-unsaturated carbonyl compounds, in which an α-carbonyl cation is involved, under mild conditions. The protocol offers practical and efficient access to α-fluorinated carbonyl compounds and has demonstrated potential applications in the late-stage fluorination of bioactive molecules.\",\"PeriodicalId\":97,\"journal\":{\"name\":\"Organic Chemistry Frontiers\",\"volume\":\"8 1\",\"pages\":\"\"},\"PeriodicalIF\":4.7000,\"publicationDate\":\"2025-08-02\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Organic Chemistry Frontiers\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1039/d5qo00877h\",\"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 Chemistry Frontiers","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1039/d5qo00877h","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
Photocatalytic α-Nucleophilic Fluorination of α,β-Unsaturated Carbonyl Compounds
We report redox-neutral photocatalytic α-nucleophilic fluorination of α,β-unsaturated carbonyl compounds, in which an α-carbonyl cation is involved, under mild conditions. The protocol offers practical and efficient access to α-fluorinated carbonyl compounds and has demonstrated potential applications in the late-stage fluorination of bioactive molecules.
期刊介绍:
Organic Chemistry Frontiers is an esteemed journal that publishes high-quality research across the field of organic chemistry. It places a significant emphasis on studies that contribute substantially to the field by introducing new or significantly improved protocols and methodologies. The journal covers a wide array of topics which include, but are not limited to, organic synthesis, the development of synthetic methodologies, catalysis, natural products, functional organic materials, supramolecular and macromolecular chemistry, as well as physical and computational organic chemistry.