## 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
Design and Synthesis of 2-Deoxy-2-[18F]fluoro-D-glucose
โ Scribed by Joanna S. Fowler; Tatsuo Ido
- Publisher
- John Wiley and Sons
- Year
- 2005
- Weight
- 15 KB
- Volume
- 36
- Category
- Article
- ISSN
- 0931-7597
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๐ SIMILAR VOLUMES
18F labelled compounds. Thus, a synthetic route to ("F)2-Deoxy-2-fluoro-~glucose was studied which should run as simple and hot-cell-friendly as possible and shc~uld deliver the sugar with high yield and free of diastereomers, even by use of high I8F acitivities
Two alternative routes to no-carrier-added synthesis of 2-deoxy-2-[ "F] f luoro-D-glucose (2-18FDG) involving nucleophilic displacements of methyl 3-0-benzyl-4,6-0-benzylidene-2-O-(trifluoromethanesulfonyl~-~-D-mannopyranoside (1) and l,6-anhydro-3,4-di-0-benzyl-2-O-(trifluoromethanesulfonyl)-~-D-ma
455 2 -( 1 8 F ) f l u o r o -2 -d e o x y -d -g l u c o s e p r o d u c e d w i t h a n e l e c t r o n a c c e l e r a t o r .
A nucleophilic radiofluorination of methyl 3,4-0-isopropylidene-2-0-(trif luoromethanesulfonyl) -6-O-trityl-/3-D-talopyranoside (1) with aninopolyether Hydrolysis of 2 with 6N HCl followed by passage through an ion retardation resin column and a neutral alumina column gave 2-deoxy-2-[18F1 f luoro-