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dc.contributor.authorYoo, BW-
dc.contributor.authorChoi, JW-
dc.contributor.authorHwang, SK-
dc.contributor.authorKim, DY-
dc.contributor.authorBaek, HS-
dc.contributor.authorChoi, KI-
dc.contributor.authorKim, JH-
dc.date.accessioned2024-01-21T08:15:07Z-
dc.date.available2024-01-21T08:15:07Z-
dc.date.created2021-09-01-
dc.date.issued2003-09-
dc.identifier.issn0039-7911-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/138305-
dc.description.abstractReduction of a variety of nitroaromatic compounds to the corresponding anilines occurs chemoselectively in high yields upon treatment with a new reduction system consisting of FeCl3.6H(2)O/indium in aqueous methanol.-
dc.languageEnglish-
dc.publisherTAYLOR & FRANCIS INC-
dc.subjectAROMATIC NITRO-COMPOUNDS-
dc.subjectINDIUM-
dc.subjectAMINES-
dc.subjectMILD-
dc.titleA facile reduction of nitroarenes to anilines using FeCl3 center dot 6H(2)O/indium-
dc.typeArticle-
dc.identifier.doi10.1081/SCC-120022471-
dc.description.journalClass1-
dc.identifier.bibliographicCitationSYNTHETIC COMMUNICATIONS, v.33, no.17, pp.2985 - 2988-
dc.citation.titleSYNTHETIC COMMUNICATIONS-
dc.citation.volume33-
dc.citation.number17-
dc.citation.startPage2985-
dc.citation.endPage2988-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000184971000007-
dc.identifier.scopusid2-s2.0-0041930581-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.relation.journalResearchAreaChemistry-
dc.type.docTypeArticle-
dc.subject.keywordPlusAROMATIC NITRO-COMPOUNDS-
dc.subject.keywordPlusINDIUM-
dc.subject.keywordPlusAMINES-
dc.subject.keywordPlusMILD-
dc.subject.keywordAuthornitroarene-
dc.subject.keywordAuthoraniline-
dc.subject.keywordAuthorferric chloride-
dc.subject.keywordAuthorindium-
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