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dc.contributor.authorShin, C-
dc.contributor.authorChavre, SN-
dc.contributor.authorPae, AN-
dc.contributor.authorCha, JH-
dc.contributor.authorKoh, HY-
dc.contributor.authorChang, MH-
dc.contributor.authorChoi, JH-
dc.contributor.authorCho, YS-
dc.date.accessioned2024-01-21T04:38:12Z-
dc.date.available2024-01-21T04:38:12Z-
dc.date.created2021-09-03-
dc.date.issued2005-07-21-
dc.identifier.issn1523-7060-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/136283-
dc.description.abstractA novel synthetic methodology for 2,5-disubstituted tetrahydrofurans having an allenyl group at the 3-position via Prins-type cyclization was developed. The reaction led to excellent selectivity and moderate to high yields.-
dc.languageEnglish-
dc.publisherAMER CHEMICAL SOC-
dc.subjectDIASTEREOSELECTIVE SYNTHESIS-
dc.subjectTRANS-2,5-DISUBSTITUTED TETRAHYDROFURANS-
dc.subjectSTEREOSELECTIVE-SYNTHESIS-
dc.subjectMEDIATED CYCLIZATIONS-
dc.subjectCONVENIENT SYNTHESIS-
dc.subjectTETRAHYDROPYRANS-
dc.subjectETHERS-
dc.subjectCARBINOLS-
dc.subjectEPOXIDES-
dc.subjectALCOHOLS-
dc.titleHighly stereloselective synthesis of 2,5-disubstituted 3-vinylidene tetetrahydrofurans via Prins-type cyclization-
dc.typeArticle-
dc.identifier.doi10.1021/ol051058r-
dc.description.journalClass1-
dc.identifier.bibliographicCitationORGANIC LETTERS, v.7, no.15, pp.3283 - 3285-
dc.citation.titleORGANIC LETTERS-
dc.citation.volume7-
dc.citation.number15-
dc.citation.startPage3283-
dc.citation.endPage3285-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000230567200038-
dc.identifier.scopusid2-s2.0-23044510870-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.relation.journalResearchAreaChemistry-
dc.type.docTypeArticle-
dc.subject.keywordPlusDIASTEREOSELECTIVE SYNTHESIS-
dc.subject.keywordPlusTRANS-2,5-DISUBSTITUTED TETRAHYDROFURANS-
dc.subject.keywordPlusSTEREOSELECTIVE-SYNTHESIS-
dc.subject.keywordPlusMEDIATED CYCLIZATIONS-
dc.subject.keywordPlusCONVENIENT SYNTHESIS-
dc.subject.keywordPlusTETRAHYDROPYRANS-
dc.subject.keywordPlusETHERS-
dc.subject.keywordPlusCARBINOLS-
dc.subject.keywordPlusEPOXIDES-
dc.subject.keywordPlusALCOHOLS-
dc.subject.keywordAuthorstereoselective-
dc.subject.keywordAuthortetrahydrofuran-
dc.subject.keywordAuthorprins type cyclization-
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