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dc.contributor.authorKang, Jihun-
dc.contributor.authorRhee, Young Ho-
dc.date.accessioned2024-03-05T00:40:08Z-
dc.date.available2024-03-05T00:40:08Z-
dc.date.created2023-03-30-
dc.date.issued2023-02-
dc.identifier.issn0022-3263-
dc.identifier.urihttps://oasis.postech.ac.kr/handle/2014.oak/120799-
dc.description.abstractA de novo synthesis of the tetrasaccharide fragment of tetrocarcin A is described. The key feature of this approach is highlighted by the regio- and diastereoselective Pd-catalyzed hydroalkoxylation of ene-alkoxyallenes with an unprotected l-digitoxose glycoside. The subsequent reaction with digitoxal in combination with chemoselective hydrogenation generated the target molecule.-
dc.languageEnglish-
dc.publisherAmerican Chemical Society-
dc.relation.isPartOfJournal of Organic Chemistry-
dc.titleSynthesis of the Tetrasaccharide Glycone Part of Tetrocarcin A-
dc.typeArticle-
dc.identifier.doi10.1021/acs.joc.2c02832-
dc.type.rimsART-
dc.identifier.bibliographicCitationJournal of Organic Chemistry, v.88, no.5, pp.3326 - 3329-
dc.identifier.wosid000935891500001-
dc.citation.endPage3329-
dc.citation.number5-
dc.citation.startPage3326-
dc.citation.titleJournal of Organic Chemistry-
dc.citation.volume88-
dc.contributor.affiliatedAuthorKang, Jihun-
dc.contributor.affiliatedAuthorRhee, Young Ho-
dc.identifier.scopusid2-s2.0-85148852753-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.isOpenAccessN-
dc.type.docTypeArticle; Early Access-
dc.subject.keywordPlusSTEREOSELECTIVE O-GLYCOSYLATION-
dc.subject.keywordPlusDE-NOVO SYNTHESIS-
dc.subject.keywordPlusCONVERGENT SYNTHESIS-
dc.subject.keywordPlusOLIGOSACCHARIDES-
dc.subject.keywordPlusANTIBIOTICS-
dc.subject.keywordPlusFRAGMENT-
dc.subject.keywordPlusACETALS-
dc.subject.keywordPlusAGLYCON-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-

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