Simple synthesis of 5-vinyl- and5-ethynyl-2′-deoxyuridine-5′-triphosphates
✍ Scribed by Teréz Kovács; Lázló Ötvös
- Publisher
- Elsevier Science
- Year
- 1988
- Tongue
- French
- Weight
- 225 KB
- Volume
- 29
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
Acid-sensitive nucleoside 5'-0-triphosphates can be obtained in good yield directly from the unprotected nucleosides in the presence of a proton sponge.
In the last decade, numerous pyrimidine nucleoside analogues have proven to be remarkably potent and selective in their activity against herpes simplex virus infections (for recent reviews see ref. 1). These nucleoside analogues all share the common feature that their biological function requires their intracellular conversion to the corresponding 5'-nucleotides.
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## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v
## Abstract The synthesis and preliminary biological evaluation of a lipophilic, fluorine‐18‐labeled 5‐ethynyl‐2′‐deoxyuridine derivative [^18^F]‐**3** is described. Initially, 5‐ethynyl‐2′‐deoxyuridine **5** was synthesized by coupling trimethylsilyl protected acetylene to 5‐iodo‐2′‐deoxyuridine *
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