DSpace at KISTKIST Article2001

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dc.contributor.authorKwon, JS-
dc.contributor.authorPae, AN-
dc.contributor.authorChoi, KI-
dc.contributor.authorKoh, HY-
dc.contributor.authorKim, Y-
dc.contributor.authorCho, YS-
dc.date.accessioned2024-01-21T12:38:13Z-
dc.date.available2024-01-21T12:38:13Z-
dc.date.created2021-09-05-
dc.date.issued2001-03-04-
dc.identifier.issn0040-4039-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/140620-
dc.description.abstractIndium mediated allylation and propargylation reactions of acetals and ketals with various allyl or propargyl bromides in aqueous media successfully provided the corresponding homoallylic or homopropargylic (and allenylic) alcohol, respectively, in moderate to good yields. Highly chemoselective allylation is also described. The ketal and aryl acetal could be selectively allylated over the aliphatic one in 80-84% yields. (C) 2001 Published by Elsevier Science Ltd.-
dc.languageEnglish-
dc.publisherPERGAMON-ELSEVIER SCIENCE LTD-
dc.subjectAQUEOUS-MEDIA-
dc.titleIndium mediated allylation and propargylation reactions of dimethyl acetals and ketals-
dc.typeArticle-
dc.identifier.doi10.1016/S0040-4039(01)00042-9-
dc.description.journalClass1-
dc.identifier.bibliographicCitationTETRAHEDRON LETTERS, v.42, no.10, pp.1957 - 1959-
dc.citation.titleTETRAHEDRON LETTERS-
dc.citation.volume42-
dc.citation.number10-
dc.citation.startPage1957-
dc.citation.endPage1959-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000167353100040-
dc.identifier.scopusid2-s2.0-0035804462-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.relation.journalResearchAreaChemistry-
dc.type.docTypeArticle-
dc.subject.keywordPlusAQUEOUS-MEDIA-
dc.subject.keywordAuthorindium-
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KIST Article > 2001
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