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Cited 28 time in webofscience Cited 33 time in scopus
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dc.contributor.authorKim, SG-
dc.contributor.authorCho, CW-
dc.contributor.authorAhn, KH-
dc.date.accessioned2016-03-31T13:40:08Z-
dc.date.available2016-03-31T13:40:08Z-
dc.date.created2009-08-07-
dc.date.issued1999-08-13-
dc.identifier.issn0040-4020-
dc.identifier.other1999-OAK-0000000844-
dc.identifier.urihttps://oasis.postech.ac.kr/handle/2014.oak/20339-
dc.description.abstractChiral biferrocene-based bis(oxazoline) compounds, which have both planar and central chirality, are synthesized. The Cu(I)-complexes of the bis(oxazolinyl)biferrocenes were found to be conformationally flexible and have a wide bile angle (136 degrees) by NMR and molecular modeling studies. The complexes catalyzed the intramolecular cyclopropanation reaction of ene-diazoacetates, and low to moderate enantioselectivities and decreased reactivity were observed, compared to known malonate-derived bis(oxazoline) systems. (C) 1999 Elsevier Science Ltd. All rights reserved.-
dc.description.statementofresponsibilityX-
dc.languageEnglish-
dc.publisherPERGAMON-ELSEVIER SCIENCE LTD-
dc.relation.isPartOfTETRAHEDRON-
dc.subjectENANTIOSELECTIVE INTRAMOLECULAR CYCLOPROPANATION-
dc.subjectCATALYSTS-
dc.subjectOLEFINS-
dc.subjectLITHIATION-
dc.subjectCOMPLEXES-
dc.subjectLACTONES-
dc.titleChiral biferrocene-based bis(oxazolines): Ligands for Cu(I)-catalyzed asymmetric cyclopropanations of ene-diazoacetates-
dc.typeArticle-
dc.contributor.college분자소재융합계의 전자-광 거동연구센터-
dc.identifier.doi10.1016/S0040-4020(99)00542-6-
dc.author.googleKim, SG-
dc.author.googleCho, CW-
dc.author.googleAhn, KH-
dc.relation.volume55-
dc.relation.issue33-
dc.relation.startpage10079-
dc.relation.lastpage10086-
dc.contributor.id10087916-
dc.relation.journalTETRAHEDRON-
dc.relation.indexSCI급, SCOPUS 등재논문-
dc.relation.sciSCI-
dc.collections.nameJournal Papers-
dc.type.rimsART-
dc.identifier.bibliographicCitationTETRAHEDRON, v.55, no.33, pp.10079 - 10086-
dc.identifier.wosid000081824200011-
dc.date.tcdate2019-01-01-
dc.citation.endPage10086-
dc.citation.number33-
dc.citation.startPage10079-
dc.citation.titleTETRAHEDRON-
dc.citation.volume55-
dc.contributor.affiliatedAuthorAhn, KH-
dc.identifier.scopusid2-s2.0-0033551816-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.wostc27-
dc.type.docTypeArticle-
dc.subject.keywordPlusENANTIOSELECTIVE INTRAMOLECULAR CYCLOPROPANATION-
dc.subject.keywordPlusCATALYSTS-
dc.subject.keywordPlusOLEFINS-
dc.subject.keywordPlusLITHIATION-
dc.subject.keywordPlusCOMPLEXES-
dc.subject.keywordPlusLACTONES-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-

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안교한AHN, KYO HAN
Dept of Chemistry
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