DSpace at KISTKIST Article2003

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dc.contributor.authorKim, HY-
dc.contributor.authorChoi, KI-
dc.contributor.authorPae, AN-
dc.contributor.authorKoh, HY-
dc.contributor.authorChoi, JH-
dc.contributor.authorCho, YS-
dc.date.accessioned2024-01-21T08:37:59Z-
dc.date.available2024-01-21T08:37:59Z-
dc.date.created2021-09-01-
dc.date.issued2003-07-
dc.identifier.issn0039-7911-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/138447-
dc.description.abstractIn/InCl3-mediated addition of allyl iodide to alpha,beta-unsaturated carbonyl compounds gave moderate to high yields of 1,2-addition products. The reactions covered acylic and cyclic alpha,beta-unsaturated carbonyl compounds. Indium trichloride was effective for these Barbier-type allylation reactions.-
dc.languageEnglish-
dc.publisherTAYLOR & FRANCIS INC-
dc.subjectAQUEOUS-MEDIA-
dc.subjectINDIUM-
dc.subjectREAGENT-
dc.titleIn/InCl3-mediated 1,2-addition of allyl group to alpha,beta-unsaturated carbonyl compounds-
dc.typeArticle-
dc.identifier.doi10.1081/SCC-120020201-
dc.description.journalClass1-
dc.identifier.bibliographicCitationSYNTHETIC COMMUNICATIONS, v.33, no.11, pp.1899 - 1904-
dc.citation.titleSYNTHETIC COMMUNICATIONS-
dc.citation.volume33-
dc.citation.number11-
dc.citation.startPage1899-
dc.citation.endPage1904-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000183159000013-
dc.identifier.scopusid2-s2.0-0038244900-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.relation.journalResearchAreaChemistry-
dc.type.docTypeArticle-
dc.subject.keywordPlusAQUEOUS-MEDIA-
dc.subject.keywordPlusINDIUM-
dc.subject.keywordPlusREAGENT-
dc.subject.keywordAuthorindium-
dc.subject.keywordAuthorindium trichloride-
dc.subject.keywordAuthor1,2-addition-
dc.subject.keywordAuthorallylation-
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