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Ruthenium-Na2CO3-catalyzed one-pot synthesis of ring-hydrogenated carbamates from aromatic amines and organic carbonates under H-2

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dc.contributor.authorMishra, Vivek-
dc.contributor.authorCho, Jin Ku-
dc.contributor.authorShin, Seung-Han-
dc.contributor.authorSuh, Young-Woong-
dc.contributor.authorKim, Hoon Sik-
dc.contributor.authorKim, Yong Jin-
dc.date.accessioned2022-07-16T02:43:42Z-
dc.date.available2022-07-16T02:43:42Z-
dc.date.created2021-05-12-
dc.date.issued2014-10-
dc.identifier.issn0926-860X-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/159005-
dc.description.abstractA facile and efficient one-pot procedure for the synthesis of ring hydrogenated carbamates from aromatic amine and alkylene carbonate under H-2 gas pressure has been developed using a heterogeneous catalyst system comprising ruthenium and alkali metal carbonates. The effects of temperature, H-2 pressure, catalyst (types of loaded metal and their supports), molar ratio of substrate/catalyst, and solvent were also investigated. Among the alkali metal carbonates, the sodium carbonate was found as best promoter for nucleophilic attack and ring-opening (NARO) reaction and thus increased the yield of ring hydrogenated carbamate up to 88% when using Ru/C as ring hydrogenation (RH) catalyst. This catalyst system could be reused at least five times without significant loss of activity, which makes this process cost-effective and eco-friendly.-
dc.language영어-
dc.language.isoen-
dc.publisherELSEVIER SCIENCE BV-
dc.titleRuthenium-Na2CO3-catalyzed one-pot synthesis of ring-hydrogenated carbamates from aromatic amines and organic carbonates under H-2-
dc.typeArticle-
dc.contributor.affiliatedAuthorSuh, Young-Woong-
dc.identifier.doi10.1016/j.apcata.2014.09.013-
dc.identifier.scopusid2-s2.0-85041788399-
dc.identifier.wosid000345479000009-
dc.identifier.bibliographicCitationAPPLIED CATALYSIS A-GENERAL, v.487, pp.82 - 90-
dc.relation.isPartOfAPPLIED CATALYSIS A-GENERAL-
dc.citation.titleAPPLIED CATALYSIS A-GENERAL-
dc.citation.volume487-
dc.citation.startPage82-
dc.citation.endPage90-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalResearchAreaEnvironmental Sciences & Ecology-
dc.relation.journalWebOfScienceCategoryChemistry, Physical-
dc.relation.journalWebOfScienceCategoryEnvironmental Sciences-
dc.subject.keywordPlusOXIDATIVE CARBONYLATION-
dc.subject.keywordPlusALKYLENE CARBONATES-
dc.subject.keywordPlusCATALYST-
dc.subject.keywordPlusCYCLOHEXYLAMINE-
dc.subject.keywordPlusISOCYANATES-
dc.subject.keywordPlusREDUCTION-
dc.subject.keywordPlusPHOSGENE-
dc.subject.keywordPlusANILINE-
dc.subject.keywordPlusSYSTEM-
dc.subject.keywordPlusUREAS-
dc.subject.keywordAuthorAromatic amine-
dc.subject.keywordAuthorAlkylene carbonate-
dc.subject.keywordAuthorCarbamate-
dc.subject.keywordAuthorRing hydrogenation-
dc.subject.keywordAuthorRuthenium catalyst-
dc.subject.keywordAuthorSodium carbonate-
dc.identifier.urlhttps://www.sciencedirect.com/science/article/pii/S0926860X14005638?via%3Dihub-
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