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dc.contributor.author정낙신-
dc.date.accessioned2017-02-15T08:02:37Z-
dc.date.available2017-02-15T08:02:37Z-
dc.date.issued2006-
dc.identifier.issn1523-7060-
dc.identifier.otherOAK-3602-
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/234135-
dc.description.abstract(Chemical Equation Presented) Stereoselective synthesis of 2′-C-methyl-cyclopropyl-fused carbanucleosides was accomplished via stereoselective cyclopropanation, regioselective cleavage of the isopropylidene group, stereoselective Grignard reaction, and cyclic sulfate chemistry. © 2006 American Chemical Society.-
dc.languageEnglish-
dc.titleStereoselective synthesis of 2′-C-methyl-cyclopropyl-fused carbanucleosides as potential anti-HCV agents-
dc.typeArticle-
dc.relation.issue22-
dc.relation.volume8-
dc.relation.indexSCI-
dc.relation.indexSCIE-
dc.relation.indexSCOPUS-
dc.relation.startpage5081-
dc.relation.lastpage5083-
dc.relation.journaltitleOrganic Letters-
dc.identifier.doi10.1021/ol061959f-
dc.identifier.wosidWOS:000241381800025-
dc.identifier.scopusid2-s2.0-33750907520-
dc.author.googleLee J.A.-
dc.author.googleHea O.K.-
dc.author.googleTosh D.K.-
dc.author.googleHyung R.M.-
dc.author.googleKim S.-
dc.author.googleLak S.J.-
dc.contributor.scopusid정낙신(16028528200)-
dc.date.modifydate20211210153610-
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약학대학 > 약학과 > Journal papers
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