DSpace at KISTKIST Article2001

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dc.contributor.authorKang, KH-
dc.contributor.authorChoi, KI-
dc.contributor.authorKoh, HY-
dc.contributor.authorKim, Y-
dc.contributor.authorChung, BY-
dc.contributor.authorCho, YS-
dc.date.accessioned2024-01-21T12:04:37Z-
dc.date.available2024-01-21T12:04:37Z-
dc.date.created2021-09-05-
dc.date.issued2001-08-
dc.identifier.issn0039-7911-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/140285-
dc.description.abstractIndium mediated allylation of nitro group was first achieved with four allyl bromides in aqueous media. Nitro- benzenes bearing 3- and/or 4-substituent(s) gave mainly N,N-diallylated (I or I') and/or N,O-diallylated (II) products by Method A. Allylation of nitrobenzenes having 2- (and 5-) substituent(s) could be achieved only with crotyl bromide by Method B.-
dc.languageEnglish-
dc.publisherMARCEL DEKKER INC-
dc.subjectN-ARYLHYDROXYLAMINES-
dc.subjectCHLORIDE-
dc.subjectNITROARENES-
dc.subjectREDUCTION-
dc.titleIndium mediated allylation of nitro group on nitrobenzene derivatives in aqueous media-
dc.typeArticle-
dc.identifier.doi10.1081/SCC-100104827-
dc.description.journalClass1-
dc.identifier.bibliographicCitationSYNTHETIC COMMUNICATIONS, v.31, no.15, pp.2277 - 2286-
dc.citation.titleSYNTHETIC COMMUNICATIONS-
dc.citation.volume31-
dc.citation.number15-
dc.citation.startPage2277-
dc.citation.endPage2286-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000170244600009-
dc.identifier.scopusid2-s2.0-0034903609-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.relation.journalResearchAreaChemistry-
dc.type.docTypeArticle-
dc.subject.keywordPlusN-ARYLHYDROXYLAMINES-
dc.subject.keywordPlusCHLORIDE-
dc.subject.keywordPlusNITROARENES-
dc.subject.keywordPlusREDUCTION-
dc.subject.keywordAuthorindium-
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