{"title":"Photocatalytic defluoroalkylation of trifluoromethylaromatics with arylethylenes","authors":"Shiyong Guan, Yiteng Zheng, Zihan Cai, Yuegang Chen","doi":"10.1039/d6qo00541a","DOIUrl":null,"url":null,"abstract":"<div><div>We present a novel fluorine atom transfer technique for the selective functionalization of robust C–F bonds in trifluoromethylated aromatic compounds. This approach employs neutral boron radicals to generate aryl difluoromethyl radicals through a C–F cleavage process. These radicals engage in highly effective intermolecular coupling with aryl alkenes throughout the defluoroalkylation process. This mild, catalytic reaction system accommodates a diverse array of substrates, producing difluoroalkyl structures of medicinal importance with total regioselectivity.</div></div>","PeriodicalId":94379,"journal":{"name":"Organic chemistry frontiers : an international journal of organic chemistry","volume":"13 13","pages":"Pages 4064-4069"},"PeriodicalIF":0.0000,"publicationDate":"2026-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Organic chemistry frontiers : an international journal of organic chemistry","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/org/science/article/pii/S2052412926002317","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/5/14 0:00:00","PubModel":"Epub","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
We present a novel fluorine atom transfer technique for the selective functionalization of robust C–F bonds in trifluoromethylated aromatic compounds. This approach employs neutral boron radicals to generate aryl difluoromethyl radicals through a C–F cleavage process. These radicals engage in highly effective intermolecular coupling with aryl alkenes throughout the defluoroalkylation process. This mild, catalytic reaction system accommodates a diverse array of substrates, producing difluoroalkyl structures of medicinal importance with total regioselectivity.