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dc.contributor.authorLee, JG-
dc.contributor.authorChoi, KI-
dc.contributor.authorKoh, HY-
dc.contributor.authorKim, Y-
dc.contributor.authorKang, Y-
dc.contributor.authorCho, YS-
dc.date.accessioned2024-01-21T13:01:37Z-
dc.date.available2024-01-21T13:01:37Z-
dc.date.created2022-01-11-
dc.date.issued2001-01-
dc.identifier.issn0039-7881-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/140776-
dc.description.abstractIndium mediated reduction of azide and nitro groups in the presence of HCl (1.5 equiv based on indium) at room temperature in aqueous THF successfully provided the corresponding amine in high to quantitative yields. Under the same reaction conditions, selective reduction of azide and nitro group in the presence of vinyl group could be accomplished.-
dc.languageEnglish-
dc.publisherGEORG THIEME VERLAG KG-
dc.subjectALPHA,BETA-UNSATURATED NITROCOMPOUNDS-
dc.subjectNITROALKANES-
dc.titleIndium mediated reduction of nitro and azide groups in the presence of HCl in aqueous media-
dc.typeArticle-
dc.description.journalClass1-
dc.identifier.bibliographicCitationSYNTHESIS-STUTTGART, no.1, pp.81 - 84-
dc.citation.titleSYNTHESIS-STUTTGART-
dc.citation.number1-
dc.citation.startPage81-
dc.citation.endPage84-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000166236500012-
dc.identifier.scopusid2-s2.0-0035151428-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.relation.journalResearchAreaChemistry-
dc.type.docTypeArticle-
dc.subject.keywordPlusALPHA,BETA-UNSATURATED NITROCOMPOUNDS-
dc.subject.keywordPlusNITROALKANES-
dc.subject.keywordAuthornitro compounds-
dc.subject.keywordAuthorazides-
dc.subject.keywordAuthorreductions-
dc.subject.keywordAuthorindium-
dc.subject.keywordAuthoramines-
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KIST Article > 2001
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