% IMPORTANT: The following is UTF-8 encoded. This means that in the presence % of non-ASCII characters, it will not work with BibTeX 0.99 or older. % Instead, you should use an up-to-date BibTeX implementation like “bibtex8” or % “biber”. @ARTICLE{Zischler:825303, author = {Zischler, Johannes and Krapf, Philipp and Richarz, Raphael and Zlatopolskiy, Boris D. and Neumaier, Bernd}, title = {{A}utomated synthesis of 4-[$^{18}${F}]fluoroanisole, [$^{18}${F}]{DAA}1106 and 4-[$^{18}${F}]{FP}he using {C}u-mediated radiofluorination under “minimalist” conditions}, journal = {Applied radiation and isotopes}, volume = {115}, issn = {0969-8043}, address = {Amsterdam [u.a.]}, publisher = {Elsevier Science}, reportid = {FZJ-2016-07767}, pages = {133 - 137}, year = {2016}, abstract = {The application of the “minimalist” approach to Cu-mediated radiofluorination allows the efficient preparation of 18F-labeled arenes regardless of their electronic properties. The implementation of this methodology on a commercially available synthesis module (hotboxthree, Scintomics, Germany) enabled the automated production of 4-[18F]fluoroanisole as well as the clinically relevant PET-tracers, 4-[18F]FPhe and [18F]DAA1106, in radiochemical yields of $41–61\%$ and radiochemical purities of $>95\%$ within 30–60 min. These results demonstrated the high efficacy and versatility of the developed method that will open up opportunities for a broad application of Cu-mediated radiofluorination in PET-chemistry.}, cin = {INM-5}, ddc = {530}, cid = {I:(DE-Juel1)INM-5-20090406}, pnm = {573 - Neuroimaging (POF3-573)}, pid = {G:(DE-HGF)POF3-573}, typ = {PUB:(DE-HGF)16}, UT = {WOS:000382594900022}, doi = {10.1016/j.apradiso.2016.04.030}, url = {https://juser.fz-juelich.de/record/825303}, }