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dc.contributor.authorSong, CE-
dc.contributor.authorKim, YH-
dc.contributor.authorLee, KC-
dc.contributor.authorLee, S-
dc.contributor.authorJin, BW-
dc.date.accessioned2024-01-21T18:04:36Z-
dc.date.available2024-01-21T18:04:36Z-
dc.date.created2021-09-04-
dc.date.issued1997-09-11-
dc.identifier.issn0957-4166-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/143593-
dc.description.abstractUsing new C-2-symmetric chiral ketones 4 and 6 as precursors for chiral dioxiranes generated in situ, the asymmetric epoxidation of olefins has been achieved in moderate ee. (C) 1997 Elsevier Science Ltd.-
dc.languageEnglish-
dc.publisherPERGAMON-ELSEVIER SCIENCE LTD-
dc.subjectGENERATED IN-SITU-
dc.subjectDIOXIRANE-
dc.subjectALKENES-
dc.subjectOXAZIRIDINES-
dc.subjectOXIDATIONS-
dc.subjectREACTIVITY-
dc.subjectCHEMISTRY-
dc.titleNew C-2-symmetric chiral ketones for catalytic asymmetric epoxidation of unfunctionalized olefins-
dc.typeArticle-
dc.identifier.doi10.1016/S0957-4166(97)00352-2-
dc.description.journalClass1-
dc.identifier.bibliographicCitationTETRAHEDRON-ASYMMETRY, v.8, no.17, pp.2921 - 2926-
dc.citation.titleTETRAHEDRON-ASYMMETRY-
dc.citation.volume8-
dc.citation.number17-
dc.citation.startPage2921-
dc.citation.endPage2926-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosidA1997XY65700009-
dc.identifier.scopusid2-s2.0-0030865630-
dc.relation.journalWebOfScienceCategoryChemistry, Inorganic & Nuclear-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.relation.journalWebOfScienceCategoryChemistry, Physical-
dc.relation.journalResearchAreaChemistry-
dc.type.docTypeArticle-
dc.subject.keywordPlusGENERATED IN-SITU-
dc.subject.keywordPlusDIOXIRANE-
dc.subject.keywordPlusALKENES-
dc.subject.keywordPlusOXAZIRIDINES-
dc.subject.keywordPlusOXIDATIONS-
dc.subject.keywordPlusREACTIVITY-
dc.subject.keywordPlusCHEMISTRY-
dc.subject.keywordAuthorC//2-symmetric chiral ketones-
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