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dc.contributor.author정낙신-
dc.date.accessioned2018-05-02T08:15:56Z-
dc.date.available2018-05-02T08:15:56Z-
dc.date.issued2004-
dc.identifier.issn0022-3263-
dc.identifier.otherOAK-2100-
dc.identifier.urihttp://dspace.ewha.ac.kr/handle/2015.oak/242838-
dc.description.abstractThe preparative and stereoselective synthesis (45-50% overall yields) of the target compound 17 has been accomplished from D-ribose. The bulky protecting groups such as TBDPS and Trityl enforced the facial selectivity during Grignard reaction to give the tertiary β-allylic alcohol 16 as the sole product, which was oxidatively rearranged to the key molecule 17 in excellent yield.-
dc.languageEnglish-
dc.titlePreparative and Stereoselective Synthesis of the Versatile Intermediate for Carbocyclic Nucleosides: Effects of the Bulky Protecting Groups to Enforce Facial Selectivity-
dc.typeArticle-
dc.relation.issue7-
dc.relation.volume69-
dc.relation.indexSCI-
dc.relation.indexSCIE-
dc.relation.indexSCOPUS-
dc.relation.startpage2634-
dc.relation.lastpage2636-
dc.relation.journaltitleJournal of Organic Chemistry-
dc.identifier.doi10.1021/jo0356762-
dc.identifier.wosidWOS:000220506200066-
dc.identifier.scopusid2-s2.0-1842607464-
dc.author.googleChoi W.J.-
dc.author.googleMoon H.R.-
dc.author.googleKim H.O.-
dc.author.googleYoo B.N.-
dc.author.googleLee J.A.-
dc.author.googleShin D.H.-
dc.author.googleJeong L.S.-
dc.date.modifydate20180501154214-
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약학대학 > 약학과 > Journal papers
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