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Enantioselective Michael Addition of 3-Aryl-Substituted Oxindoles to Methyl Vinyl Ketone Catalyzed by a Binaphthyl-Modified Bifunctional Organocatalyst

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dc.contributor.authorLee, Hyun Joo-
dc.contributor.authorWoo, Saet Byeol-
dc.contributor.authorKim, Dae Young-
dc.date.accessioned2021-08-12T03:24:52Z-
dc.date.available2021-08-12T03:24:52Z-
dc.date.issued2012-06-
dc.identifier.issn1420-3049-
dc.identifier.urihttps://scholarworks.bwise.kr/sch/handle/2021.sw.sch/15120-
dc.description.abstractThe enantioselective conjugate addition reaction of 3-aryl-substituted oxindoles with methyl vinyl ketone promoted by binaphthyl-modified bifunctional organocatalysts was investigated. The corresponding Michael adducts, containing a quaternary center at the C3-position of the oxindoles, were generally obtained in high yields with excellent enantioselectivities (up to 91% ee).-
dc.format.extent10-
dc.language영어-
dc.language.isoENG-
dc.publisherMultidisciplinary Digital Publishing Institute (MDPI)-
dc.titleEnantioselective Michael Addition of 3-Aryl-Substituted Oxindoles to Methyl Vinyl Ketone Catalyzed by a Binaphthyl-Modified Bifunctional Organocatalyst-
dc.typeArticle-
dc.publisher.location스위스-
dc.identifier.doi10.3390/molecules17067523-
dc.identifier.scopusid2-s2.0-84862983942-
dc.identifier.wosid000305800400091-
dc.identifier.bibliographicCitationMolecules, v.17, no.6, pp 7523 - 7532-
dc.citation.titleMolecules-
dc.citation.volume17-
dc.citation.number6-
dc.citation.startPage7523-
dc.citation.endPage7532-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.subject.keywordPlusMANNICH-TYPE REACTIONS-
dc.subject.keywordPlusELECTROPHILIC ALPHA-AMINATION-
dc.subject.keywordPlusFLUORO-BETA-KETOESTERS-
dc.subject.keywordPlusCONJUGATE ADDITION-
dc.subject.keywordPlusASYMMETRIC-SYNTHESIS-
dc.subject.keywordPlusALPHA,BETA-UNSATURATED KETONES-
dc.subject.keywordPlusQUATERNARY STEREOCENTERS-
dc.subject.keywordPlus3-SUBSTITUTED OXINDOLES-
dc.subject.keywordPlusCARBENE LIGANDS-
dc.subject.keywordPlusALKYLATION-
dc.subject.keywordAuthoroxindole-
dc.subject.keywordAuthormethyl vinyl ketone-
dc.subject.keywordAuthorconjugate addition-
dc.subject.keywordAuthorbifunctional organocatalysis-
dc.subject.keywordAuthorasymmetric catalysis-
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