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@ARTICLE{Cavani:824538,
author = {Cavani, Melanie and Bier, Dirk and Holschbach, Marcus and
Coenen, Heinrich Hubert},
title = {{E}fficient synthesis of [$^{18}$ {F}]{FP}y{ME}: {A} new
approach for the preparation of maleimide-containing
prosthetic groups for the conjugation with thiols},
journal = {Journal of labelled compounds and radiopharmaceuticals},
volume = {60},
number = {1},
issn = {0362-4803},
address = {New York, NY [u.a.]},
publisher = {Wiley},
reportid = {FZJ-2016-07110},
pages = {87-92},
year = {2017},
abstract = {An improved high yielding radiosynthesis of the known
thiol-reactive maleimide-containing prosthetic
group1-[3-(2-[18F]fluoropyridine-3-yloxy)propyl]pyrrole-2,5-dione
([18F]FPyME) is described. The target compound was obtained
by a two-step one-pot procedure starting from a
maleimide-containing nitro-precursor that was protected as a
Diels-Alder adduct with 2,5-dimethylfurane. Nucleophilic
radiofluorination followed by heat induced deprotection
through a Retro Diels Alder reaction yielded, after
chromatographic isolation, [18F]FPyME with a radiochemical
yield of $20\%$ in about 60 min overall synthesis time. A
variety of other [18F]fluoropyridine based
maleimide-containing prosthetic groups should be accessible
via the described synthetic strategy.},
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:000393835900011},
doi = {10.1002/jlcr.3469},
url = {https://juser.fz-juelich.de/record/824538},
}