Mawick, MatthiasJaworski, CarolinBittermann, JensIovkova, LjubaPu, YinglanWängler, CarmenWängler, BjörnJurkschat, KlausKrause, NorbertSchirrmacher, Ralf2024-08-292024-08-292023-10-18http://hdl.handle.net/2003/4266110.17877/DE290R-24497The ring-opening Si-fluorination of a variety of azasilole derivatives cyclo-1-(iPr2Si)−4-X−C6H3−2-CH2NR (4: R=2,6-iPr2C6H3, X=H; 4 a: R=2,4,6-Me3C6H2, X=H; 9: R=2,6-iPr2C6H3, X=tBuMe2SiO; 10: R=2,6-iPr2C6H3, X=OH; 13: R=2,6-iPr2C6H3, X=HCCCH2O; 22: R=2,6-iPr2C6H3, X=tBuMe2SiCH2O) with different 19F-fluoride sources was studied, optimized and the experience gained was used in a translational approach to create a straightforward 18F-labelling protocol for the azasilole derivatives [18F]6 and [18F]14. The latter constitutes a potential clickable CycloSiFA prosthetic group which might be used in PET tracer development using Cu-catalysed triazole formation. Based on our findings, CycloSiFA has the potential to become a new entry into non-canonical labelling methodologies for radioactive PET tracer development.enAngewandte Chemie / International edition;62(50)https://creativecommons.org/licenses/by-nc-nd/4.0/AzasiloleFluorinePositron emission tomographyRing openingSilicon540ResearchArticle