The presence of 2-deoxy-2-['sF]fluoro-D-mannose (['sF]FDM) in 2-deoxy-2-['\*F]fluoro-o-glucose (['aF]FDG) prepared by the reaction of 3,4,6-tri-0-acetyi-D-glucal (TAG) with ['\*F]acetyl hypofluorite ([r\*F]CHsCOOF) or ['sF]Fr was quantified by radio HPLC analysis of reacetylated ['\*F]FDG. The solve
Synthesis and purification of 2-deoxy-2-[18F]fluoro-d-glucose and 2-deoxy-2-[18F]fluoro-d-mannose: characterization of products by 1H- and 19F-NMR spectroscopy
โ Scribed by Franz Oberdorfer; William E. Hull; Birgitt C. Traving; Wolfgang Maier-Borst
- Publisher
- Elsevier Science
- Year
- 1986
- Weight
- 430 KB
- Volume
- 37
- Category
- Article
- ISSN
- 0883-2889
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โฆ Synopsis
A procedure has been developed that allows the separation of 2-deoxy-2-[18F]fluoro-D-glucose from 2-deoxy-2-[18F]fluoro-D-mannose employing selectively optimized ion-moderated partition chromatography. Both compounds can be obtained with a greater than 98% chemical and radiochemical purity in about one half-life of 18F. Both the alpha- and beta-anomers of both sugars were completely characterized by high-resolution 1H- and 19F-NMR spectroscopy. Various convenient preparation methods for 2-deoxy-2-[18F]fluoro-D-glucose were compared.
๐ SIMILAR VOLUMES
## Abstract A convenient method for the synthesis of ^18^Fโ2โdeoxyโ2โfluoroโDโglucose (4) and ^18^Fโ2โdeoxyโ2โfluoroโDโmannose (8) by the direct fluorination of 3,4,6โtriโ0โacetylโDโglucal with ^18^FโF~2~ is described. ^14^Cโ2โdeoxyโ2โfluoroโDโglucose has been synthesized from ^14^Cโ3,4,6โtriโ0โace
A combined study of the labelling methods of two important glucose-derivatives i.e. [18F]2-deoxy-2-fluoro-D-glucose ([laF]2-FDG) and [lSF]3-deoxy-3-fluoro-D-glucose ([18F]3-FDG) is described. Using [ISF]fluoride as reacting agent produced in a water target via the 180(p, n)'SF and ~60(3He, p)~SF rea