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Lemaire, C.; Guillaume, M.; Plenevaux, A.; Cantineau, R.; Damhaut, P.; Christiaens, L.
Eighth international symposium on radiopharmaceutical chemistry. Abstracts: Final report1990
Eighth international symposium on radiopharmaceutical chemistry. Abstracts: Final report1990
AbstractAbstract
[en] This paper discusses the development of a fluorination pathway starting from the no carrier added fluorides and generating a family of secondary fluorinating precursors: the substituted 18F-fluoro aromatic aldehydes. Sever reactions with these precursors have been completed and possibilities for other reactions of interest for generation of radiopharmaceuticals are outlined
Source
Eckelman, W.C.; Squibb (E.R.) and Sons, Inc., New Brunswick, NJ (United States). Squibb Inst. for Medical Research; 458 p; 1990; p. 131-133; 8. international symposium on radiopharmaceutical chemistry; Princeton, NJ (United States); 24-29 Jun 1990; CONF-9006363--ABSTS; John Wiley and Sons Ltd., 605 Third Avenue, New York, NY 10158
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Report
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Conference
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Country of publication
AMINES, ANALEPTICS, BETA DECAY RADIOISOTOPES, BETA-PLUS DECAY RADIOISOTOPES, CARBOXYLIC ACIDS, CENTRAL NERVOUS SYSTEM AGENTS, DRUGS, FLUORINE ISOTOPES, HOURS LIVING RADIOISOTOPES, HYDROXY ACIDS, ISOMERIC TRANSITION ISOTOPES, ISOTOPES, KINETICS, LABELLED COMPOUNDS, LIGHT NUCLEI, MATERIALS, NUCLEI, ODD-ODD NUCLEI, ORGANIC ACIDS, ORGANIC COMPOUNDS, RADIOACTIVE MATERIALS, RADIOISOTOPES, REACTION KINETICS, SYMPATHOMIMETICS, SYNTHESIS
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