DSpace at KISTKIST Article2002

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dc.contributor.authorYoo, BW-
dc.contributor.authorChoi, KH-
dc.contributor.authorLee, SJ-
dc.contributor.authorNam, GS-
dc.contributor.authorChang, KY-
dc.contributor.authorKim, SH-
dc.contributor.authorKim, JH-
dc.date.accessioned2024-01-21T11:09:09Z-
dc.date.available2024-01-21T11:09:09Z-
dc.date.created2021-09-05-
dc.date.issued2002-02-
dc.identifier.issn0039-7911-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/139820-
dc.description.abstractThe indium-mediated allylation reaction of acyl cyanides with allyl halides in aqueous media afforded a variety Of beta,gamma-unsaturated ketones in moderate to good yields under mild and neutral conditions.-
dc.languageEnglish-
dc.publisherTAYLOR & FRANCIS INC-
dc.subjectACID-CHLORIDES-
dc.subjectACYLATION-
dc.subjectFIELD-
dc.titleIndium-mediated allylation of acyl cyanides in aqueous media: A convenient synthesis of beta,gamma-unsaturated ketones-
dc.typeArticle-
dc.identifier.doi10.1081/SCC-120002691-
dc.description.journalClass1-
dc.identifier.bibliographicCitationSYNTHETIC COMMUNICATIONS, v.32, no.6, pp.839 - 846-
dc.citation.titleSYNTHETIC COMMUNICATIONS-
dc.citation.volume32-
dc.citation.number6-
dc.citation.startPage839-
dc.citation.endPage846-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000174948700003-
dc.identifier.scopusid2-s2.0-0036217434-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.relation.journalResearchAreaChemistry-
dc.type.docTypeArticle-
dc.subject.keywordPlusACID-CHLORIDES-
dc.subject.keywordPlusACYLATION-
dc.subject.keywordPlusFIELD-
dc.subject.keywordAuthorindium-
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