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dc.contributor.authorKim, S-
dc.contributor.authorKo, H-
dc.contributor.authorSon, S-
dc.contributor.authorShin, Kye Jung-
dc.contributor.authorKim, Dong Jin-
dc.date.accessioned2024-01-21T11:40:38Z-
dc.date.available2024-01-21T11:40:38Z-
dc.date.created2022-04-05-
dc.date.issued2001-10-
dc.identifier.issn0040-4039-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/140116-
dc.description.abstractSelective and practical asymmetric syntheses of (+)-decursinol (1) and (+)-trans-decursidinol (2) have been achieved using naturally occurring umbelliferone, demethylsuberosin, and xanthyletin as the synthetic intermediates. The absolute stereochemistry was established in the late stage of synthesis by employing Jacobsen's enantioselective epoxidation conditions. (C) 2001 Elsevier Science Ltd. All rights reserved.-
dc.languageEnglish-
dc.publisherElsevier BV-
dc.titleEnantioselective syntheses of (+)-decursinol and (+)-trans-decursidinol-
dc.typeArticle-
dc.identifier.doi10.1016/S0040-4039(01)01652-5-
dc.description.journalClass1-
dc.identifier.bibliographicCitationTetrahedron Letters, v.42, no.43, pp.7641 - 7643-
dc.citation.titleTetrahedron Letters-
dc.citation.volume42-
dc.citation.number43-
dc.citation.startPage7641-
dc.citation.endPage7643-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000171556600027-
dc.identifier.scopusid2-s2.0-0035935099-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.relation.journalResearchAreaChemistry-
dc.type.docTypeArticle-
dc.subject.keywordPlusANGELICA-GIGAS-
dc.subject.keywordPlusACTIVATOR-
dc.subject.keywordPlusAGENT-
dc.subject.keywordPlusROOT-
dc.subject.keywordAuthordecursinol-
dc.subject.keywordAuthordecursidinol-
dc.subject.keywordAuthorJacobsen&apos-
dc.subject.keywordAuthors epoxidation-
dc.subject.keywordAuthorbiomimetic synthesis-
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KIST Article > 2001
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