![]() Enantioselective syntheses of n.c.a. L-(a-methyl)-[b-11C]-4-chlorophenylalanine and L-(a-[11C]methyl-tryptophan.Plenevaux, Alain ; ; Lemaire, Christian et alin Journal of Labelled Compounds & Radiopharmaceuticals (1994), 35 ![]() Non-activated 18F-fluorinated aromatic compounds through nucleophilic substitution and decarbonylation reactions using RhCl[P(C6H5)3]3.Plenevaux, Alain ; Lemaire, Christian ; et alin Journal of Labelled Compounds & Radiopharmaceuticals (1993), 32 Detailed reference viewed: 8 (0 ULg)![]() Asymmetric synthesis of n.c.a. L-[2-11C]-4-chlorophenylalanine.Plenevaux, Alain ; ; Lemaire, Christian et alin Journal of Labelled Compounds & Radiopharmaceuticals (1993), 32 Detailed reference viewed: 5 (0 ULg)![]() NCA asymmetric synthesis of 2-[18F]fluoro-L-tyrosine.Lemaire, Christian ; Plenevaux, Alain ; et alin Journal of Labelled Compounds & Radiopharmaceuticals (1993), 32 Detailed reference viewed: 4 (2 ULg) Synthesis and preliminary animal studies of [131I]iodotropapride: a cerebral dopamine D2 receptor ligand.; ; Plenevaux, Alain et alin Journal of Labelled Compounds & Radiopharmaceuticals (1991), 30 Detailed reference viewed: 6 (1 ULg) 18F-substituted aromatic aldehydes, key intermediates for nca radiosyntheses.Lemaire, Christian ; ; Plenevaux, Alain et alin Journal of Labelled Compounds & Radiopharmaceuticals (1991), 30 Detailed reference viewed: 14 (0 ULg) NCA asymmetric synthesis of 6-[18F]fluoro-L-dopa.Lemaire, Christian ; ; et alin Journal of Labelled Compounds & Radiopharmaceuticals (1991), 30 Detailed reference viewed: 8 (1 ULg) Routine production and improvement in the purification of 3-N-(2'-[18F]fluoroethyl)spiperone for clinical use.Plenevaux, Alain ; ; et alin Journal of Labelled Compounds & Radiopharmaceuticals (1991), 30 Detailed reference viewed: 6 (0 ULg) NCA synthesis of an N-w-[18F]fluoroethyl analog of altanserine, a serotonine S2 receptor ligand.Lemaire, Christian ; ; et alin Journal of Labelled Compounds & Radiopharmaceuticals (1991), 30 Detailed reference viewed: 14 (0 ULg)![]() Chemical processing for the production of carrier free selenium-73 from germanium and arsenic targets and synthesis of L-[73Se]selenomethionine.Plenevaux, Alain ; ; et alin Journal of Labelled Compounds & Radiopharmaceuticals (1991), 30 Detailed reference viewed: 3 (1 ULg) Synthesis of 75Se-2-phenyl-1,2-benzisoselenazol-3-(2H)-one (PZ 51; EBSELEN*). A novel biologically active organo-selenium compound; ; Plenevaux, Alain et alin Journal of Labelled Compounds & Radiopharmaceuticals (1986), 23(1), 59-65 The preparation of 75Se-ebselen (75Se-PZ 51) in a high radiochemica] yield (~40 %) and with a specific act'ivity of 240 mCi/mM (8.9 GBq/mM) is described. Detailed reference viewed: 33 (1 ULg) New trends in selenium-labeled compounds synthesis.; ; Luxen, André et alin Journal of Labelled Compounds & Radiopharmaceuticals (1982), 19 Detailed reference viewed: 10 (8 ULg) |
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