Rapid microwave-assisted fluorination yielding novel 5′-deoxy-5′-fluorouridine derivatives
A rapid fluorination at the 5′-position of nucleosides derivatives is achieved within 45 min providing yields of 75–92% by application of microwave. The preparation of 18F-labeled ligands for positron emission tomography (PET) and the subsequent imaging have to be completed within a half-life of the...
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Veröffentlicht in: | Bioorganic & medicinal chemistry letters 2006-12, Vol.16 (23), p.6139-6142 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | A rapid fluorination at the 5′-position of nucleosides derivatives is achieved within 45
min providing yields of 75–92% by application of microwave.
The preparation of
18F-labeled ligands for positron emission tomography (PET) and the subsequent imaging have to be completed within a half-life of the neutron-deficient isotope (
18F
=
110
min). In this paper, we report a rapid fluorination approach to obtain 5′-deoxy-5′-fluoro-substituted uracil nucleoside analogues. Nucleophilic substitution at the 5′-position of the nucleosides was achieved within 45
min providing excellent yields of 75–92% by application of microwaves. |
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ISSN: | 0960-894X 1464-3405 |
DOI: | 10.1016/j.bmcl.2006.08.093 |