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dc.contributor.authorKIM, DJ-
dc.contributor.authorSHIN, KJ-
dc.contributor.authorKIM, IY-
dc.contributor.authorPARK, SW-
dc.date.accessioned2024-01-21T21:31:27Z-
dc.date.available2024-01-21T21:31:27Z-
dc.date.created2022-01-11-
dc.date.issued1994-10-24-
dc.identifier.issn0040-4039-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/145480-
dc.description.abstract(-)-Reiswigin A (1), a novel anti-viral diterpene, has been synthesized in a highly stereoselective manner utilizing a sequential Claisen rearrangement - intramolecular ester enolate alkylation strategy.-
dc.languageEnglish-
dc.publisherPERGAMON-ELSEVIER SCIENCE LTD-
dc.subjectRELATIVE CONFIGURATION-
dc.subjectWITTIG REACTION-
dc.subjectASSIGNMENT-
dc.subjectABSOLUTE-
dc.titleA TOTAL SYNTHESIS OF (-)-REISWIGIN A VIA SEQUENTIAL CLAISEN REARRANGEMENT INTRAMOLECULAR ESTER ENOLATE ALKYLATION-
dc.typeArticle-
dc.identifier.doi10.1016/S0040-4039(00)78395-X-
dc.description.journalClass1-
dc.identifier.bibliographicCitationTETRAHEDRON LETTERS, v.35, no.43, pp.7957 - 7960-
dc.citation.titleTETRAHEDRON LETTERS-
dc.citation.volume35-
dc.citation.number43-
dc.citation.startPage7957-
dc.citation.endPage7960-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosidA1994PP33800019-
dc.identifier.scopusid2-s2.0-0028091969-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.relation.journalResearchAreaChemistry-
dc.type.docTypeArticle-
dc.subject.keywordPlusRELATIVE CONFIGURATION-
dc.subject.keywordPlusWITTIG REACTION-
dc.subject.keywordPlusASSIGNMENT-
dc.subject.keywordPlusABSOLUTE-
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