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Stereoselective synthesis of (+)-lauthisan

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dc.contributor.authorRhee, HJ-
dc.contributor.authorBeom, HY-
dc.contributor.authorKim, HD-
dc.date.available2021-02-22T16:01:47Z-
dc.date.issued2004-10-
dc.identifier.issn0040-4039-
dc.identifier.urihttps://scholarworks.sookmyung.ac.kr/handle/2020.sw.sookmyung/15818-
dc.description.abstractStereo selective synthesis of (+)-lauthisan has been accomplished starting from D-glyceraidehyde acetonide by combination of diastereoselective alkylation and ring-closing metathesis. High degree of 1,3-asymmetric induction has been realized in ether system. (C) 2004 Elsevier Ltd. All rights reserved.-
dc.format.extent4-
dc.language영어-
dc.language.isoENG-
dc.publisherPERGAMON-ELSEVIER SCIENCE LTD-
dc.titleStereoselective synthesis of (+)-lauthisan-
dc.typeArticle-
dc.publisher.location영국-
dc.identifier.doi10.1016/j.tetlet.2004.09.001-
dc.identifier.scopusid2-s2.0-4644308302-
dc.identifier.wosid000224447600010-
dc.identifier.bibliographicCitationTETRAHEDRON LETTERS, v.45, no.43, pp 8019 - 8022-
dc.citation.titleTETRAHEDRON LETTERS-
dc.citation.volume45-
dc.citation.number43-
dc.citation.startPage8019-
dc.citation.endPage8022-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.subject.keywordPlusRING-CLOSING METATHESIS-
dc.subject.keywordPlusENANTIOSELECTIVE SYNTHESIS-
dc.subject.keywordPlusCONSTRUCTION-
dc.subject.keywordPlusHETEROCYCLES-
dc.subject.keywordPlusDERIVATIVES-
dc.subject.keywordAuthor(+)-lauthisan-
dc.subject.keywordAuthordiastereoselective alkylation-
dc.subject.keywordAuthorring-closing metathesis-
dc.subject.keywordAuthorcyclic ether-
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