% 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{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}, }