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dc.contributor.author정낙신-
dc.date.accessioned2017-01-18T02:01:25Z-
dc.date.available2017-01-18T02:01:25Z-
dc.date.issued2007-
dc.identifier.issn1525-7770-
dc.identifier.otherOAK-4498-
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/233910-
dc.description.abstractPseudo-l-vinylcyclopropyl adenine and guanine nucleosides 11 and 12 were designed and enantiopurely synthesized starting from (S)-epichlorohydrin using tandem alkylation, regioselective oxirane-ring opening, and chemoselective reduction as key steps. Copyright © Taylor & Francis Group, LLC.-
dc.languageEnglish-
dc.titleSynthesis of enantiopure pseudo-L-vinylcyclopropyl nucleosides bearing quaternary carbon as potential anti-herpesvirus agent-
dc.typeArticle-
dc.relation.issue41495-
dc.relation.volume26-
dc.relation.indexSCIE-
dc.relation.indexSCOPUS-
dc.relation.startpage975-
dc.relation.lastpage978-
dc.relation.journaltitleNucleosides, Nucleotides and Nucleic Acids-
dc.identifier.doi10.1080/15257770701508372-
dc.identifier.wosidWOS:000251875400023-
dc.identifier.scopusid2-s2.0-36849061086-
dc.author.googleMoon H.R.-
dc.author.googlePark A.-Y.-
dc.author.googleKim K.R.-
dc.author.googleChun M.W.-
dc.author.googleJeong L.S.-
dc.contributor.scopusid정낙신(16028528200)-
dc.date.modifydate20211210153610-
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약학대학 > 약학과 > Journal papers
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