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@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},
}