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@ARTICLE{Krapf:825304,
author = {Krapf, Philipp and Richarz, Raphael and Urusova, Elizaveta
A. and Neumaier, Bernd and Zlatopolskiy, Boris D.},
title = {{S}eyferth-{G}ilbert {H}omologation as a {R}oute to 18
{F}-{L}abeled {B}uilding {B}locks: {P}reparation of
{R}adiofluorinated {P}henylacetylenes and {T}heir
{A}pplication in {PET} {C}hemistry},
journal = {European journal of organic chemistry},
volume = {2016},
number = {3},
issn = {1434-193X},
address = {Weinheim},
publisher = {Wiley-VCH Verl.},
reportid = {FZJ-2016-07768},
pages = {430 - 433},
year = {2016},
abstract = {A convenient method for the preparation of hitherto unknown
([F-18]fluorophenyl)acetylenes ([F-18]FPAs) using the
Seyferth-Gilbert homologation is reported. The novel
building blocks were efficiently prepared from easily
accessible [F-18]fluorobenzaldehydes by using the
Bestmann-Ohira reagent. High radiochemical yields and
excellent radiochemical purities were achieved within only
20 min of reaction time; 2- and 4-[F-18]FPAs were applied to
prepare radiofluorinated heterocycles by using different
cycloaddition and cross-coupling reactions. Additionally,
these building blocks were used to prepare three novel PET
tracers. Thus, an artificial radiofluorinated protected
amino acid [F-18]10, a COX-2-specific ligand [F-18]14, and a
PSMA-selective inhibitor [F-18]16 were obtained in high
radiochemical yields.},
cin = {INM-5},
ddc = {540},
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:000368815700003},
doi = {10.1002/ejoc.201501377},
url = {https://juser.fz-juelich.de/record/825304},
}