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dc.contributor.authorSong, CE-
dc.contributor.authorShim, WH-
dc.contributor.authorRoh, EJ-
dc.contributor.authorChoi, JH-
dc.date.accessioned2024-01-21T14:37:40Z-
dc.date.available2024-01-21T14:37:40Z-
dc.date.created2021-09-05-
dc.date.issued2000-01-
dc.identifier.issn1359-7345-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/141705-
dc.description.abstractScandium(iii) triflate catalysed Friedel-Crafts alkylation of aromatic compounds with alkenes proceeded readily in the hydrophobic ionic liquid solvents based on 1,3-dialkylimidazolium salts with easy catalyst/solvent recycling, whereas these reactions did not occur in common organic solvents, water or hydrophilic ionic liquids at all.-
dc.languageEnglish-
dc.publisherROYAL SOC CHEMISTRY-
dc.subjectORGANIC-SYNTHESIS-
dc.titleScandium(III) triflate immobilised in ionic liquids: a novel and recyclable catalytic system for Friedel-Crafts alkylation of aromatic compounds with alkenes-
dc.typeArticle-
dc.identifier.doi10.1039/b005335j-
dc.description.journalClass1-
dc.identifier.bibliographicCitationCHEMICAL COMMUNICATIONS, no.17, pp.1695 - 1696-
dc.citation.titleCHEMICAL COMMUNICATIONS-
dc.citation.number17-
dc.citation.startPage1695-
dc.citation.endPage1696-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000088914800068-
dc.identifier.scopusid2-s2.0-0034618453-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.relation.journalResearchAreaChemistry-
dc.type.docTypeArticle-
dc.subject.keywordPlusORGANIC-SYNTHESIS-
dc.subject.keywordAuthorFriedel-Crafts alkylation-
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