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dc.contributor.authorKang, HJ-
dc.contributor.authorKim, SH-
dc.contributor.authorPae, AN-
dc.contributor.authorKoh, HY-
dc.contributor.authorChang, MH-
dc.contributor.authorChoi, KI-
dc.contributor.authorHan, SY-
dc.contributor.authorCho, YS-
dc.date.accessioned2024-01-21T06:05:58Z-
dc.date.available2024-01-21T06:05:58Z-
dc.date.created2021-09-04-
dc.date.issued2004-11-22-
dc.identifier.issn0936-5214-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/137050-
dc.description.abstractA novel methodology for the diastereoselective synthesis of seven- and eight-membered oxabicycles bearing dimethylidene via Prins-type cyclization was developed. The reaction takes place in the presence of TMSOTf in diethyl ether at -78 degreesC.-
dc.languageEnglish-
dc.publisherGEORG THIEME VERLAG KG-
dc.subjectTETRAHYDROPYRANS-
dc.subjectCYCLOADDITIONS-
dc.subjectCARBOCYCLES-
dc.titleDiastereoselective synthesis of seven- and eight-membered oxabicycles via prins-type cyclization-
dc.typeArticle-
dc.identifier.doi10.1055/s-2004-834841-
dc.description.journalClass1-
dc.identifier.bibliographicCitationSYNLETT, no.14, pp.2545 - 2548-
dc.citation.titleSYNLETT-
dc.citation.number14-
dc.citation.startPage2545-
dc.citation.endPage2548-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000225425700018-
dc.identifier.scopusid2-s2.0-9644276805-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.relation.journalResearchAreaChemistry-
dc.type.docTypeArticle-
dc.subject.keywordPlusTETRAHYDROPYRANS-
dc.subject.keywordPlusCYCLOADDITIONS-
dc.subject.keywordPlusCARBOCYCLES-
dc.subject.keywordAuthordiastereoselective synthesis-
dc.subject.keywordAuthorseven- and eight-membered oxabicycles-
dc.subject.keywordAuthorPrins reaction-
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