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dc.contributor.authorSong, CE-
dc.contributor.authorRoh, EJ-
dc.contributor.authorYu, BM-
dc.contributor.authorChi, DY-
dc.contributor.authorKim, SC-
dc.contributor.authorLee, KJ-
dc.date.accessioned2024-01-21T14:10:58Z-
dc.date.available2024-01-21T14:10:58Z-
dc.date.created2021-09-05-
dc.date.issued2000-04-
dc.identifier.issn1359-7345-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/141487-
dc.description.abstractExcellent enantioselectivity (e.g. 92% ee for 2,2-dimethylchromene) has been achieved in heterogeneous asymmetric epoxidation using a polymer-bound (pyrrolidine salen)-manganese(III) complex; however, this polymeric catalyst underwent partial decomposition under epoxidation conditions.-
dc.languageEnglish-
dc.publisherROYAL SOC CHEMISTRY-
dc.subjectENANTIOSELECTIVE EPOXIDATION-
dc.subjectOLEFINS-
dc.titleHeterogeneous asymmetric epoxidation of alkenes catalysed by a polymer-bound (pyrrolidine salen)manganese(III) complex-
dc.typeArticle-
dc.identifier.doi10.1039/b000876l-
dc.description.journalClass1-
dc.identifier.bibliographicCitationCHEMICAL COMMUNICATIONS, no.7, pp.615 - 616-
dc.citation.titleCHEMICAL COMMUNICATIONS-
dc.citation.number7-
dc.citation.startPage615-
dc.citation.endPage616-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000086373000044-
dc.identifier.scopusid2-s2.0-0002958115-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.relation.journalResearchAreaChemistry-
dc.type.docTypeArticle-
dc.subject.keywordPlusENANTIOSELECTIVE EPOXIDATION-
dc.subject.keywordPlusOLEFINS-
dc.subject.keywordAuthorheterogeneous asymmetric epoxidation-
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