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dc.contributor.authorSong, CE-
dc.contributor.authorYang, JW-
dc.contributor.authorHa, HJ-
dc.contributor.authorLee, SG-
dc.date.accessioned2024-01-21T19:40:17Z-
dc.date.available2024-01-21T19:40:17Z-
dc.date.created2021-09-05-
dc.date.issued1996-03-
dc.identifier.issn0957-4166-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/144523-
dc.description.abstractHigh enantioselectivity (>99% ee) and reactivity in heterogeneous catalytic asymmetric dihydroxylation (AD) of olefins have been achieved using new polymeric cinchona alkaloids containing 1,4-bis(9-O-quininyl)phthalazine ((QN)(2)-PHAL), which can be synthesized more economically than their homogeneous analogue, 1,4-bis(9-O-dihydroquininyl)phthalazine ((DHQ)(2)-PHAL). (C) 1996 Elsevier Science Ltd-
dc.languageEnglish-
dc.publisherPERGAMON-ELSEVIER SCIENCE LTD-
dc.subjectALKENES-
dc.subjectIMPROVEMENT-
dc.subjectSCOPE-
dc.titleEfficient and practical polymeric catalysts for heterogeneous asymmetric dihydroxylation of olefins-
dc.typeArticle-
dc.identifier.doi10.1016/0957-4166(96)00054-7-
dc.description.journalClass1-
dc.identifier.bibliographicCitationTETRAHEDRON-ASYMMETRY, v.7, no.3, pp.645 - 648-
dc.citation.titleTETRAHEDRON-ASYMMETRY-
dc.citation.volume7-
dc.citation.number3-
dc.citation.startPage645-
dc.citation.endPage648-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosidA1996UD02000010-
dc.identifier.scopusid2-s2.0-0029883631-
dc.relation.journalWebOfScienceCategoryChemistry, Inorganic & Nuclear-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.relation.journalWebOfScienceCategoryChemistry, Physical-
dc.relation.journalResearchAreaChemistry-
dc.type.docTypeArticle-
dc.subject.keywordPlusALKENES-
dc.subject.keywordPlusIMPROVEMENT-
dc.subject.keywordPlusSCOPE-
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