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dc.contributor.author이강만-
dc.contributor.author신윤용-
dc.contributor.author정낙신-
dc.date.accessioned2016-08-28T11:08:57Z-
dc.date.available2016-08-28T11:08:57Z-
dc.date.issued2005-
dc.identifier.issn1525-7770-
dc.identifier.otherOAK-2941-
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/219620-
dc.description.abstractThe preparative and stereoselective synthesis (45-50% overall yields, >50 g scale) of the key carbasugars 7a-d was achieved from D-ribose via stereoselective Grignard reaction and oxidative rearrangement as key reactions. Copyright © Taylor & Francis, Inc.-
dc.languageEnglish-
dc.titleStereoselective synthesis of 3-hydroxymethyl-D-cyclopentenone, the versatile intermediate for the synthesis of carbocyclic nucleosides-
dc.typeConference Paper-
dc.relation.issue41401-
dc.relation.volume24-
dc.relation.indexSCIE-
dc.relation.indexSCOPUS-
dc.relation.startpage611-
dc.relation.lastpage613-
dc.relation.journaltitleNucleosides, Nucleotides and Nucleic Acids-
dc.identifier.doi10.1081/NCN-200061832-
dc.identifier.wosidWOS:000232473500053-
dc.identifier.scopusid2-s2.0-26644475882-
dc.author.googleChoi W.J.-
dc.author.googleMoon H.R.-
dc.author.googleKim H.O.-
dc.author.googleKo Y.M.-
dc.author.googleKim H.J.-
dc.author.googleLee J.A.-
dc.author.googleLee K.M.-
dc.author.googleYun M.K.-
dc.author.googleShin D.H.-
dc.author.googleChun M.W.-
dc.author.googleSheen Y.Y.-
dc.author.googleKim K.-
dc.author.googleJeong L.S.-
dc.contributor.scopusid이강만(7501506362)-
dc.contributor.scopusid신윤용(6603872711)-
dc.contributor.scopusid정낙신(16028528200)-
dc.date.modifydate20230411104830-
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약학대학 > 약학과 > Journal papers
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