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Stereoselective synthesis of (-)-centrolobine

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dc.contributor.authorYang, Zunhua-
dc.contributor.authorKim, Hee-Doo-
dc.date.available2021-02-22T12:01:02Z-
dc.date.issued2014-02-
dc.identifier.issn0957-4166-
dc.identifier.issn1362-511X-
dc.identifier.urihttps://scholarworks.sookmyung.ac.kr/handle/2020.sw.sookmyung/10970-
dc.description.abstractThe stereoselective synthesis of (-)-centrolobine has been accomplished starting from D-glyceraldehyde acetonide by a combination of chelation-controlled diastereoselective alkylation and ring-closing metathesis. A high degree of 1,3-asymmetric induction has been realized in an ether system. (C) 2014 Elsevier Ltd. All rights reserved.-
dc.format.extent5-
dc.language영어-
dc.language.isoENG-
dc.publisherElsevier Ltd-
dc.titleStereoselective synthesis of (-)-centrolobine-
dc.typeArticle-
dc.publisher.location영국-
dc.identifier.doi10.1016/j.tetasy.2013.12.019-
dc.identifier.scopusid2-s2.0-84896083202-
dc.identifier.wosid000333791800003-
dc.identifier.bibliographicCitationTETRAHEDRON-ASYMMETRY, v.25, no.4, pp 305 - 309-
dc.citation.titleTETRAHEDRON-ASYMMETRY-
dc.citation.volume25-
dc.citation.number4-
dc.citation.startPage305-
dc.citation.endPage309-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryChemistry, Inorganic & Nuclear-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.relation.journalWebOfScienceCategoryChemistry, Physical-
dc.subject.keywordPlusENANTIOSELECTIVE TOTAL-SYNTHESIS-
dc.subject.keywordPlusASYMMETRIC-SYNTHESIS-
dc.subject.keywordPlusPRINS CYCLIZATIONS-
dc.subject.keywordPlusEFFICIENT APPROACH-
dc.subject.keywordPlusMACROLIDE-
dc.subject.keywordPlusTETRAHYDROPYRANS-
dc.subject.keywordPlusEPIMERIZATION-
dc.subject.keywordPlusDIHYDROPYRANS-
dc.subject.keywordPlusCONSTRUCTION-
dc.subject.keywordPlusSUPPRESSION-
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