{"title":"[18F]三氟化单氟烷基酯的放射性标记氟化合成[18]二氟甲基化烷烃","authors":"Yuan-Zhan Han, Peng-Fei Song, Hai-Yang Zhao, Junbin Han, Xingang Zhang","doi":"10.1039/d5cc00869g","DOIUrl":null,"url":null,"abstract":"An efficient method for the synthesis of [18F]-difluoromethylated alkanes has been developed by combining [18F]radiofluoride with monofluoroalkyl triflates. This method uses [18F]KF/K2.2.2. as the fluorine source. It features synthetic simplicity without tedious precursor preparation, high RCC and RCY, good functional group tolerance, and is silver salt-free, providing potential for developing new PET agents.","PeriodicalId":67,"journal":{"name":"Chemical Communications","volume":"139 1","pages":""},"PeriodicalIF":4.3000,"publicationDate":"2025-04-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"[18F]Radiolabeling Fluorination of Monofluoroalkyl Triflates for the Synthesis of [18]Difluoromethylated Alkanes\",\"authors\":\"Yuan-Zhan Han, Peng-Fei Song, Hai-Yang Zhao, Junbin Han, Xingang Zhang\",\"doi\":\"10.1039/d5cc00869g\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"An efficient method for the synthesis of [18F]-difluoromethylated alkanes has been developed by combining [18F]radiofluoride with monofluoroalkyl triflates. This method uses [18F]KF/K2.2.2. as the fluorine source. It features synthetic simplicity without tedious precursor preparation, high RCC and RCY, good functional group tolerance, and is silver salt-free, providing potential for developing new PET agents.\",\"PeriodicalId\":67,\"journal\":{\"name\":\"Chemical Communications\",\"volume\":\"139 1\",\"pages\":\"\"},\"PeriodicalIF\":4.3000,\"publicationDate\":\"2025-04-11\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Chemical Communications\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1039/d5cc00869g\",\"RegionNum\":2,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chemical Communications","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1039/d5cc00869g","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
[18F]Radiolabeling Fluorination of Monofluoroalkyl Triflates for the Synthesis of [18]Difluoromethylated Alkanes
An efficient method for the synthesis of [18F]-difluoromethylated alkanes has been developed by combining [18F]radiofluoride with monofluoroalkyl triflates. This method uses [18F]KF/K2.2.2. as the fluorine source. It features synthetic simplicity without tedious precursor preparation, high RCC and RCY, good functional group tolerance, and is silver salt-free, providing potential for developing new PET agents.
期刊介绍:
ChemComm (Chemical Communications) is renowned as the fastest publisher of articles providing information on new avenues of research, drawn from all the world''s major areas of chemical research.