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dc.contributor.author정낙신-
dc.date.accessioned2016-08-28T12:08:06Z-
dc.date.available2016-08-28T12:08:06Z-
dc.date.issued2008-
dc.identifier.issn0253-2964-
dc.identifier.otherOAK-5200-
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/220094-
dc.description.abstractNovel bicyclo[3.1.0]hexanyl purine nucleoside analogues were synthesized as potential antiherpetic agents via a bicyclo[3.1.0]hexanol (±)-8, which was prepared using a highly efficient carbenoid cycloaddition reaction. A highly diastereoselective reduction of ketone and a Mitsunobu reaction for the condensation of glycosyl donor (±)-12 with 6-chloropurine were employed.-
dc.languageEnglish-
dc.titleSynthesis of methyl-substituted bicyclic carbanucleoside analogs as potential antiherpetic agents-
dc.typeArticle-
dc.relation.issue10-
dc.relation.volume29-
dc.relation.indexSCI-
dc.relation.indexSCIE-
dc.relation.indexSCOPUS-
dc.relation.indexKCI-
dc.relation.startpage1977-
dc.relation.lastpage1982-
dc.relation.journaltitleBulletin of the Korean Chemical Society-
dc.identifier.wosidWOS:000260810500022-
dc.identifier.scopusid2-s2.0-55249123154-
dc.author.googleKim K.R.-
dc.author.googlePark A.-Y.-
dc.author.googleLee H.-R.-
dc.author.googleKang J.-A.-
dc.author.googleWon H.K.-
dc.author.googleChun P.-
dc.author.googleJang H.B.-
dc.author.googleLak S.J.-
dc.author.googleHyung R.M.-
dc.contributor.scopusid정낙신(16028528200)-
dc.date.modifydate20211210153610-
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약학대학 > 약학과 > Journal papers
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