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pubmed-article:14643345pubmed:dateCreated2003-12-3lld:pubmed
pubmed-article:14643345pubmed:abstractTextA series of optically pure 1,3-dioxolane nucleoside mimics was synthesized by a synthetic route that allowed incorporation of a 5R-methyl substituent from commercially available starting materials. The pyrrolo[2,3-d]pyrimidine heterocycle was chosen as a substitute for the purine derivative. Coupling of the pyrrolo[2,3-d]pyrimidine and the dioxolane was performed under solid-liquid phase transfer conditions. The ability to inhibit HCV RNA replication was assessed in a cell based subgenomic replicon assay. None of the described compounds displayed significant anti-HCV activity.lld:pubmed
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pubmed-article:14643345pubmed:articleTitleSynthesis and evaluation of optically pure dioxolanes as inhibitors of hepatitis C virus RNA replication.lld:pubmed
pubmed-article:14643345pubmed:affiliationDepartment of Medicinal Chemistry, Isis Pharmaceuticals, Carlsbad, CA 92008, USA.lld:pubmed
pubmed-article:14643345pubmed:publicationTypeJournal Articlelld:pubmed
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