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- W2950888916 abstract "Abstract d - and l -Carbocyclic 4′-fluoro-2′,3′-dideoxynucleosides have been synthesized from 2 , which can be conveniently prepared from 1,2:5,6-di- O -isopropylidene- d -mannitol 1 in eight steps. Ruthenium-catalyzed ring-closing metathesis has been employed in the synthesis of d -nucleosides, whereas the l -series have been obtained through an intramolecular nucleophilic substitution reaction. The Mitsunobu condensation was used as a general tool for the synthesis of both purine and pyrimidine nucleosides." @default.
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- W2950888916 date "2010-05-25" @default.
- W2950888916 modified "2023-09-24" @default.
- W2950888916 title "ChemInform Abstract: A Divergent Synthesis of D- and L-Carbocyclic 4′-Fluoro-2′,3′-dideoxynucleosides as Potential Antiviral Agents." @default.
- W2950888916 cites W1966630733 @default.
- W2950888916 doi "https://doi.org/10.1002/chin.200125190" @default.
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