Zobrazeno 1 - 10
of 104
pro vyhledávání: '"F. Füchtner"'
Autor:
Harald Mau, Wolfgang Mohnike, Oliver Blankenstein, Susann Empting, Martin Koch, Winfried Barthlen, F. Füchtner, Traugott Eberhard, Klaus Mohnike, L. von Rohden
Publikováno v:
Ultraschall in der Medizin 32(2011), 74-80
Zusammenfassung Der kongenitale Hyperinsulinismus (CHI), Synonym Nesidioblastose, ist die häufigste Ursache persistierender, rezidivierender Hypoglykämien im Säuglingsalter. Ein Drittel der Patienten weist einen umschriebenen Fokus auf. Die Enukle
Autor:
Timo Otonkoski, Wolfgang Mohnike, F. Füchtner, Oliver Blankenstein, Klaus Mohnike, Heikki Minn
Publikováno v:
Hormone Research in Paediatrics. 70:65-72
In recent years, considerable progress has been made in the biochemical, morphological and molecular genetic differentiation of congenital hyperinsulinism (CHI). Fluorine-18 L-3,4-dihydroxyphenylalanine positron emission tomography (18F-DOPA-PET) has
Publikováno v:
Journal of Labelled Compounds and Radiopharmaceuticals. 49:357-365
The 11C-labelling of the taxane derivative BAY 59-8862 (1), a potent anticancer drug, was carried out as a module-assisted automated multi-step synthesis procedure. The radiotracer [11C]1 was synthesized by reacting [1-11C]acetyl chloride (6) with th
Autor:
Volker Derdau, Jens Atzrodt, István E. Markó, Simon J. Harwood, Th. Moenius, R. Salter, B. Wietfeld, P. Burtscher, C. Zueger, Jonathan Clayden, K. Bordeaux, Y. Metz, I. Rodriguez, R. Ruetsch, R. Voges, John M. Gardiner, William Stimpson, Nitesh Panchal, John Herbert, George J. Ellames, Matthias Beller, Ján Kozempel, Jan Kadeřávek, Ladislav Lešetický, Ondřej Lebeda, Kristiina Wähälä, Paula Kiuru, Eija Leppälä, Monika Pohjoispää, Kirsti Parikka, Barbara Raffaelli, John M. Herbert, Cor G. M. Janssen, Willy L. M. Verluyten, Maarten Vliegen, P. Mäding, F. Füchtner, R. Bergmann, J. Pietzsch, C. Hultsch, F. Wüst, M. Scheunemann, J. Vercouillie, St. Fischer, D. Sorger, U. Großmann, R. Schliebs, O. Sabri, J. Steinbach
Publikováno v:
Journal of Labelled Compounds and Radiopharmaceuticals. 49:197-227
I. E. Marko [Universite catholique de Louvain, Belgium]—Novel Orthoesters in Organic Synthesis. S. J. Harwood [GlaxoSmithKline, UK]—The Synthesis of Stable Labelled Ketamine. Th. Moenius, R. Salter, B. Wietfeld, P. Burtscher, C. Zueger [Novartis,
Autor:
M. Halks-Miller, P. Mäding, Joerg Steinbach, R. Horuk, F. Füchtner, R. Mohan, M. Friebe, Christoph Stephan Hilger, B. Johannsen
Publikováno v:
Journal of Labelled Compounds and Radiopharmaceuticals. 49:253-262
The synthesis of 1-(5-chloro-2-{2-[(2R)-4-(4-[18F]fluorobenzyl)-2-methylpiperazin-1-yl]-2-oxoethoxy}phenyl)urea ([18F]4), a potent nonpeptide CCR1 antagonist, is described as a module-assisted two-step one-pot procedure. The final product was obtaine
Publikováno v:
Applied Radiation and Isotopes. 63:329-332
The three-step radiosynthesis of N-succinimidyl 4-[(18)F]fluorobenzoate ([(18)F]SFB) was adapted to a remotely controlled synthesis module. After optimization of the reaction conditions, the final [(18)F]SFB was obtained in decay-corrected radiochemi
Autor:
V. Snieckus, N. J. Geach, G. P. Randall, C. J. Winfield, A. Studer, A. C. Spivey, T. Jones, C. Noban, G. J. Ellames, A. Kohler, H. Wadsworth, J. Rieke-Zapp, S. Stone-Elander, J. Goehl, B. Perry, J. Windels, M. H. Marx, J. Krüger, B. Manmontri, G. Fels, F. Wüst, T. Kniess, R. Bergmann, P. Mäding, F. Füchtner, C. S. Hilger, M. Halks-Miller, R. Horuk, L. Matei, C. Postolache, V. Fugaru, E. Condac, A. Dinischiotu, M. Costache, J. Atzrodt, V. Derdau
Publikováno v:
Journal of Labelled Compounds and Radiopharmaceuticals. 47:1035-1060
V Snieckus [Queen's University, Canada]—The Directed Ortho Metalation—Cross Coupling Symbiosis in Aromatic Synthesis. N Geach, GP Randall, CJ Winfield [Scynexis, UK]—Isotopically Labelled 4-Formylimidazole. A Studer [Marburg University, Germany
Autor:
J Steinbach, F Füchtner
Publikováno v:
Applied Radiation and Isotopes. 58:575-578
The 18F-labelled amino acid derivative 3-O-methyl-6-[18F]fluoro- l -DOPA ([18F]OMFD) is a potential radiotracer for imaging tumour tissue using positron emission tomography. The precursor N-formyl-3-O-methyl-4-O-boc-6-trimethyl-stannyl- l -DOPA-ethyl
Publikováno v:
Journal of Labelled Compounds and Radiopharmaceuticals. 44:689-700
After successfully synthesizing 16α-[18F]fluoroestradiol-3,17β-disulphamate in an automatic procedure, we studied the conditions for obtaining 16α-[18F]fluoroestradiol-monosulphamates in a similar manner. The described procedure can simultaneously
Publikováno v:
Journal of Labelled Compounds and Radiopharmaceuticals. 43:425-436
The synthesis of 16α-[18F]Fluoroestradiol-3,17β-disulphamate ([18F]FESDS) is described. 16α-[18F]Fluoroestradiol ([18F]FES) is converted using excess sulphamoyl chloride in absolute acetonitrile in the presence of Kryptofix 2.2.2 and potassium car