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Synthesis and antiviral activity of L-2 '-deoxy-2 '-up-fluoro-4 '-thionucleosides

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dc.contributor.authorJeong, LS-
dc.contributor.authorMoon, HR-
dc.contributor.authorYoo, SJ-
dc.contributor.authorLee, SN-
dc.contributor.authorKim, HD-
dc.contributor.authorChun, MW-
dc.date.available2021-03-08T07:40:15Z-
dc.date.issued1999-04-
dc.identifier.issn0732-8311-
dc.identifier.issn1532-2335-
dc.identifier.urihttps://scholarworks.sookmyung.ac.kr/handle/2020.sw.sookmyung/17433-
dc.description.abstractL-2'-Deoxy-2'-up-fluoro-4'-thionucleoside were efficiently synthesized from D-xylose via L-4-thioarabitol derivative as a key intermediate and evaluated for antiviral activities against HIV-1, HSV-1,2 and HBV.-
dc.format.extent2-
dc.language영어-
dc.language.isoENG-
dc.publisherMARCEL DEKKER INC-
dc.titleSynthesis and antiviral activity of L-2 '-deoxy-2 '-up-fluoro-4 '-thionucleosides-
dc.typeArticle-
dc.publisher.location미국-
dc.identifier.doi10.1080/15257779908041497-
dc.identifier.scopusid2-s2.0-0001360511-
dc.identifier.wosid000081357300013-
dc.identifier.bibliographicCitationNUCLEOSIDES & NUCLEOTIDES, v.18, no.4-5, pp 571 - 572-
dc.citation.titleNUCLEOSIDES & NUCLEOTIDES-
dc.citation.volume18-
dc.citation.number4-5-
dc.citation.startPage571-
dc.citation.endPage572-
dc.type.docTypeArticle; Proceedings Paper-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.identifier.urlhttps://www.tandfonline.com/doi/abs/10.1080/15257779908041497-
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