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@PHDTHESIS{Kronenberg:15864,
author = {Kronenberg, U.},
title = {{S}ynthesis and radiofluorination of putative {NMDA}
receptor ligands},
volume = {4338},
school = {Univ. Köln},
type = {Dr. (Univ.)},
address = {Jülich},
publisher = {Forschungszentrum Jülich GmbH Zentralbibliothek, Verlag},
reportid = {PreJuSER-15864, Juel-4338},
series = {Berichts des Forschungszentrums Jülich},
pages = {III, 95 p.},
year = {2010},
note = {Record converted from JUWEL: 18.07.2013; Köln, Univ.,
Diss., 2010},
abstract = {In the course of this work on the synthesis of radioligands
for the NMDA receptor the authentic standards and labeling
precursors of four compounds with an amidine structure was
performed. Synthesis of the precursors followed reaction
conditions given in the literature and was successful. The
imidoesters used for the synthesis were obtained from their
nitriles in a Pinner synthesis, while 2-hydroxybenzylamine
was synthesized in a reduction of 2-hydroxybenzonitrile
using borane as a reducing agent. After a coupling reaction
of the amine and the imidoester in DMF using triethylamine
as base the precursors were obtained in good yields and
purified by crystallization from methanol. The cyclic
standard compound was synthesized directly from
2-(bromomethyl)- benzonitrile and 2-hydroxybenzylamine in a
ring closing reaction. Similar to the other precursors,
crystallization from methanol produced a pure compound....},
cin = {INM-5},
ddc = {500},
cid = {I:(DE-Juel1)INM-5-20090406},
pnm = {Funktion und Dysfunktion des Nervensystems},
pid = {G:(DE-Juel1)FUEK409},
typ = {PUB:(DE-HGF)11 / PUB:(DE-HGF)3},
url = {https://juser.fz-juelich.de/record/15864},
}