DSpace at KISTKIST Article2002

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dc.contributor.authorCho, YS-
dc.contributor.authorKim, HY-
dc.contributor.authorCha, JH-
dc.contributor.authorPae, AN-
dc.contributor.authorKoh, HY-
dc.contributor.authorChoi, JH-
dc.contributor.authorChang, MH-
dc.date.accessioned2024-01-21T10:33:10Z-
dc.date.available2024-01-21T10:33:10Z-
dc.date.created2021-09-01-
dc.date.issued2002-06-13-
dc.identifier.issn1523-7060-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/139437-
dc.description.abstract[GRAPHIC] Intramolecular Prins-type reactions of compounds having both functionalities of homoallyl alcohol and acetal moiety are described. The intramolecular Prins cyclizations were performed using indium trichloride in chloroform or 25% aqueous THE Both 9-oxabicyclo[3.3.1]nonane and 3,9-dioxabicyclo[3.3.1]nonane compounds were successfully obtained in moderate yields.-
dc.languageEnglish-
dc.publisherAMER CHEMICAL SOC-
dc.subjectACETALS-
dc.titleIndium trichloride mediated intramolecular Prins-type cyclization-
dc.typeArticle-
dc.identifier.doi10.1021/ol025856i-
dc.description.journalClass1-
dc.identifier.bibliographicCitationORGANIC LETTERS, v.4, no.12, pp.2025 - 2028-
dc.citation.titleORGANIC LETTERS-
dc.citation.volume4-
dc.citation.number12-
dc.citation.startPage2025-
dc.citation.endPage2028-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000176185300012-
dc.identifier.scopusid2-s2.0-0013154464-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.relation.journalResearchAreaChemistry-
dc.type.docTypeArticle-
dc.subject.keywordPlusACETALS-
dc.subject.keywordAuthorintramolecular prins-type cyclization-
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