| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 10584105 | Bioorganic & Medicinal Chemistry | 2013 | 6 Pages |
Abstract
In connection with prospective 18F-PET imaging studies, the potential for enzymatic synthesis of fluorine-labelled glycosides of small molecules was investigated. Approaches to the enzymatic synthesis of anomeric phosphates of d-gluco-configured fluorosugars proved ineffective. In contrast, starting in the d-galacto series and relying on the consecutive action of Escherichia coli galactokinase (GalK), galactose-1-phosphate uridylyltransferase (GalPUT), uridine-5â²-diphosphogalactose 4-epimerase (GalE) and oat root glucosyltransferase (SAD10), a quick and effective synthesis of 6-deoxy-6-fluoro-d-glucosyl N-methylanthranilate ester was achieved.
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Authors
Lorenzo Caputi, Martin Rejzek, Thomas Louveau, Ellis C. O'Neill, Lionel Hill, Anne Osbourn, Robert A. Field,
