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dc.contributor.authorBeek, HS-
dc.contributor.authorLee, SJ-
dc.contributor.authorYoo, BW-
dc.contributor.authorKo, JJ-
dc.contributor.authorKim, SH-
dc.contributor.authorKim, JH-
dc.date.accessioned2024-01-21T13:32:15Z-
dc.date.available2024-01-21T13:32:15Z-
dc.date.created2021-09-05-
dc.date.issued2000-10-
dc.identifier.issn0040-4039-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/141065-
dc.description.abstractThe indium-mediated reductive coupling of acyl cyanides afforded the corresponding 1,2-diketones in moderate to good yields under neutral and mild conditions. (C) 2000 Elsevier Science Ltd. All rights reserved.-
dc.languageEnglish-
dc.publisherPERGAMON-ELSEVIER SCIENCE LTD-
dc.titleIndium-mediated reductive coupling of acyl cyanides: a convenient synthesis of 1,2-diketones-
dc.typeArticle-
dc.description.journalClass1-
dc.identifier.bibliographicCitationTETRAHEDRON LETTERS, v.41, no.42, pp.8097 - 8099-
dc.citation.titleTETRAHEDRON LETTERS-
dc.citation.volume41-
dc.citation.number42-
dc.citation.startPage8097-
dc.citation.endPage8099-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000089915800018-
dc.identifier.scopusid2-s2.0-0034649171-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.relation.journalResearchAreaChemistry-
dc.type.docTypeArticle-
dc.subject.keywordPlusALPHA-DIKETONES-
dc.subject.keywordPlusALLYLATION-
dc.subject.keywordPlusALDIMINES-
dc.subject.keywordPlusCHLORIDES-
dc.subject.keywordPlusESTERS-
dc.subject.keywordAuthorindium and compounds-
dc.subject.keywordAuthorcoupling reactions-
dc.subject.keywordAuthorcyanides-
dc.subject.keywordAuthorsonochemistry-
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