Sweetening Pharmaceutical Radiochemistry by18F-Fluoroglycosylation: A Short Review
نویسندگان
چکیده
منابع مشابه
Sweetening Pharmaceutical Radiochemistry by 18F-Fluoroglycosylation: A Short Review
At the time when the highly efficient [(18)F]FDG synthesis was discovered by the use of the effective precursor 1,3,4,6-tetra-O-acetyl-2-O-trifluoromethanesulfonyl- β -D-mannopyranose (mannose triflate) for nucleophilic (18)F-substitution, the field of PET in nuclear medicine experienced a long-term boom. Thirty years later, various strategies for chemoselective (18)F-labeling of biomolecules h...
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1 Molecular Imaging andRadiochemistry, Department ofNuclearMedicine, Friedrich-AlexanderUniversity Erlangen-Nürnberg (FAU), Erlangen, Germany 2Department of Nuclear Medicine, Medical University Innsbruck, Innsbruck, Austria 3 Department of Chemistry, University Oslo, Oslo, Norway 4 Institute of Radiochemistry and Experimental Molecular Imaging, University Clinic Cologne and Max Planck Institute...
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ژورنال
عنوان ژورنال: BioMed Research International
سال: 2014
ISSN: 2314-6133,2314-6141
DOI: 10.1155/2014/214748