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dc.contributor.author정낙신-
dc.contributor.author최원준-
dc.date.accessioned2016-08-28T12:08:00Z-
dc.date.available2016-08-28T12:08:00Z-
dc.date.issued2008-
dc.identifier.issn0253-6269-
dc.identifier.otherOAK-4957-
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/220036-
dc.description.abstractOn the basis of potent anti-hepatitis C virus (HCV) activity of 2'-C-hydroxymethyladenosine, 3'-C-hydroxymethyl-substituted pyrimidine and purine nucleosides as potential anti-HCV agents were designed and synthesized from D-xylose via stereoselective Grignard reaction and conversion of the vinyl into hydroxymethyl group as key steps. © 2008 The Pharmaceutical Society of Korea.-
dc.languageEnglish-
dc.titleSynthesis of 3'-C-hydroxymethyl-substituted pyrimidine and purine nucleosides as potential anti-hepatitis C virus (HCV) agents-
dc.typeArticle-
dc.relation.issue7-
dc.relation.volume31-
dc.relation.indexSCIE-
dc.relation.indexSCOPUS-
dc.relation.indexKCI-
dc.relation.startpage843-
dc.relation.lastpage849-
dc.relation.journaltitleArchives of Pharmacal Research-
dc.identifier.doi10.1007/s12272-001-1236-z-
dc.identifier.wosidWOS:000257737100005-
dc.identifier.scopusid2-s2.0-49749093968-
dc.author.googlePei X.-
dc.author.googleChoi W.J.-
dc.author.googleKim Y.M.-
dc.author.googleZhao L.X.-
dc.author.googleJeong L.S.-
dc.contributor.scopusid정낙신(16028528200)-
dc.contributor.scopusid최원준(55732412300;57211762651)-
dc.date.modifydate20230627112239-
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약학대학 > 약학과 > Journal papers
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