DSpace at KISTKIST Article2003

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dc.contributor.authorOh, BK-
dc.contributor.authorCha, JH-
dc.contributor.authorCho, YS-
dc.contributor.authorChoi, KI-
dc.contributor.authorKoh, HY-
dc.contributor.authorChang, MH-
dc.contributor.authorPae, AN-
dc.date.accessioned2024-01-21T09:09:23Z-
dc.date.available2024-01-21T09:09:23Z-
dc.date.created2021-09-03-
dc.date.issued2003-03-31-
dc.identifier.issn0040-4039-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/138733-
dc.description.abstractAllyl indium, prepared from allyl bromide and indium metal in aprotic solvent, reacts with terminal vinyl epoxides at room temperature to afford various bishomoallyl alcohols in moderate to high yields via consecutive 1,2-shift reaction and regioselective allylation. (C) 2003 Elsevier Science Ltd. All rights reserved.-
dc.languageEnglish-
dc.publisherPERGAMON-ELSEVIER SCIENCE LTD-
dc.subjectTERMINAL EPOXIDES-
dc.titleIndium-mediated consecutive 1,2-shift reaction and regioselective allylation of vinyl epoxides-
dc.typeArticle-
dc.identifier.doi10.1016/S0040-4039(03)00418-0-
dc.description.journalClass1-
dc.identifier.bibliographicCitationTETRAHEDRON LETTERS, v.44, no.14, pp.2911 - 2913-
dc.citation.titleTETRAHEDRON LETTERS-
dc.citation.volume44-
dc.citation.number14-
dc.citation.startPage2911-
dc.citation.endPage2913-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000181893800034-
dc.identifier.scopusid2-s2.0-0037474617-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.relation.journalResearchAreaChemistry-
dc.type.docTypeArticle-
dc.subject.keywordPlusTERMINAL EPOXIDES-
dc.subject.keywordAuthorindum-
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KIST Article > 2003
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