DSpace at KISTKIST Article2004

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dc.contributor.authorKim, SH-
dc.contributor.authorShin, C-
dc.contributor.authorPae, AN-
dc.contributor.authorKoh, HY-
dc.contributor.authorChang, MH-
dc.contributor.authorChung, BY-
dc.contributor.authorCho, YS-
dc.date.accessioned2024-01-21T06:41:23Z-
dc.date.available2024-01-21T06:41:23Z-
dc.date.created2021-09-04-
dc.date.issued2004-07-05-
dc.identifier.issn0039-7881-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/137418-
dc.description.abstractDeoxygenative allylations of benzylic and allylic alcohols and acetates with allyltrimethylsilane in the presence of a catalytic amount of InBr3 (5 mol%) were successfully achieved in high yields.-
dc.languageEnglish-
dc.publisherGEORG THIEME VERLAG KG-
dc.subjectELECTROPHILIC ATTACK-
dc.subjectALLYLSILANES-
dc.subjectSOLVENT-
dc.titleInBr3-catalyzed deoxygenative allylation of benzylic and allylic alcohols and acetates with allyltrimethylsilane-
dc.typeArticle-
dc.identifier.doi10.1055/s-2004-829109-
dc.description.journalClass1-
dc.identifier.bibliographicCitationSYNTHESIS-STUTTGART, no.10, pp.1581 - 1584-
dc.citation.titleSYNTHESIS-STUTTGART-
dc.citation.number10-
dc.citation.startPage1581-
dc.citation.endPage1584-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000222752800009-
dc.identifier.scopusid2-s2.0-3142727810-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.relation.journalResearchAreaChemistry-
dc.type.docTypeArticle-
dc.subject.keywordPlusELECTROPHILIC ATTACK-
dc.subject.keywordPlusALLYLSILANES-
dc.subject.keywordPlusSOLVENT-
dc.subject.keywordAuthorbenzyl alcohol-
dc.subject.keywordAuthorallyl acetate-
dc.subject.keywordAuthorbenzyl acetate-
dc.subject.keywordAuthordeoxygenative-
dc.subject.keywordAuthorallylation-
dc.subject.keywordAuthorindium halide-
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