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dc.contributor.author정낙신-
dc.contributor.author최원준-
dc.date.accessioned2016-11-25T02:11:30Z-
dc.date.available2016-11-25T02:11:30Z-
dc.date.issued2008-
dc.identifier.issn1746-8272-
dc.identifier.otherOAK-18109-
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/232819-
dc.description.abstractThe structure of 2',3'-didehydro-2',3'-dideoxynucleosides (d4Ns) was applied to design the novel bioisosteric 4'-seleno-d4Ns as potential inhibitors of human immunodeficiency virus reverse transcriptase (HIV RT). Conversion of 2',3'-dihydroxyl groups of 4'-selenoribofuranosyl pyrimidines into the olefin was accomplished by treatment of cyclic 2',3'-thiocarbonate with 1,3-dimethyl-2-phenyl-1,3,2-diazaphospholidine.-
dc.languageEnglish-
dc.titleSynthesis and conformational analysis of novel 2',3'-didehydo-2',3'-dideoxy-4'-selenonucleosides.-
dc.typeArticle-
dc.relation.issue52-
dc.relation.indexSCOPUS-
dc.relation.startpage555-
dc.relation.lastpage556-
dc.relation.journaltitleNucleic acids symposium series (2004)-
dc.identifier.scopusid2-s2.0-78649393546-
dc.author.googleKo Y.J.-
dc.author.googleChoi W.J.-
dc.author.googleJun J.H.-
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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