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@ARTICLE{Coenen:848310,
author = {Coenen, Heinz H. and Ermert, Johannes},
title = {18{F}-labelling innovations and their potential for
clinical application},
journal = {Clinical and translational imaging},
volume = {6},
number = {3},
issn = {2281-7565},
address = {Berlin},
publisher = {Springer Milan},
reportid = {FZJ-2018-03555},
pages = {169 - 193},
year = {2018},
abstract = {An impressive variety of new methodologies for the
preparation of 18F-labelled tracers and ligands has appeared
over the last decade. Most strategies of the newly developed
radiofluorination methods predominantly aim at products of
high molar activity by ‘late-stage’ labelling of small
(hetero)aromatic molecules and the use of transition metals.
This is accompanied by the improvement of technical
procedures, like preparation of reactive [18F]fluoride and
automated syntheses. The newly introduced procedures reflect
a high innovative level and creativity in
radio(pharmaceutical) chemistry at present, which are based
on modern chemical methods and deep mechanistic insights.
Taking also automation and quality control into
consideration, major recently developed radiofluorination
methods, most of those still under development, are compiled
here in view of their potential for clinical PET imaging and
thus the ability to advance molecular imaging.},
cin = {INM-5},
ddc = {610},
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:000435539000002},
doi = {10.1007/s40336-018-0280-0},
url = {https://juser.fz-juelich.de/record/848310},
}