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Efficient Palladium-Catalyzed Coupling of Baylis-Hillman Acetates with an Allylstannane

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dc.contributor.authorPark, Jinhyung-
dc.contributor.authorKwon, Young Bum-
dc.contributor.authorYang, Kyungmo-
dc.contributor.authorRhee, Hakjune-
dc.contributor.authorYoon, Cheol Min-
dc.date.accessioned2021-09-08T05:39:50Z-
dc.date.available2021-09-08T05:39:50Z-
dc.date.created2021-06-11-
dc.date.issued2010-02-
dc.identifier.issn0039-7881-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/117130-
dc.description.abstractAcetates of Baylis-Hillman adducts derived from ethyl acrylate, methyl vinyl ketone, and acrylonitrile were coupled with allyltributylstannane using Pd(PPh3)(4) or Pd(dba)(2) as the catalyst at room temperature to afford the corresponding trisubstituted alka-1,5-dienes in good to high yields.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherGEORG THIEME VERLAG KG-
dc.subjectACTIVATED DOUBLE-BONDS-
dc.subjectNECIC ACID SYNTHONS-
dc.subjectSTEREOSELECTIVE-SYNTHESIS-
dc.subject(Z)-TRISUBSTITUTED ALKENES-
dc.subjectCHEMOSELECTIVE ALLYLATION-
dc.subjectADDUCTS-
dc.subjectALDEHYDES-
dc.subjectELECTROPHILES-
dc.subjectISOMERIZATION-
dc.subjectREACTIVITY-
dc.titleEfficient Palladium-Catalyzed Coupling of Baylis-Hillman Acetates with an Allylstannane-
dc.typeArticle-
dc.contributor.affiliatedAuthorYoon, Cheol Min-
dc.identifier.doi10.1055/s-0029-1218612-
dc.identifier.scopusid2-s2.0-76249115691-
dc.identifier.wosid000274246100014-
dc.identifier.bibliographicCitationSYNTHESIS-STUTTGART, no.4, pp.661 - 665-
dc.relation.isPartOfSYNTHESIS-STUTTGART-
dc.citation.titleSYNTHESIS-STUTTGART-
dc.citation.number4-
dc.citation.startPage661-
dc.citation.endPage665-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.subject.keywordPlusACTIVATED DOUBLE-BONDS-
dc.subject.keywordPlusNECIC ACID SYNTHONS-
dc.subject.keywordPlusSTEREOSELECTIVE-SYNTHESIS-
dc.subject.keywordPlus(Z)-TRISUBSTITUTED ALKENES-
dc.subject.keywordPlusCHEMOSELECTIVE ALLYLATION-
dc.subject.keywordPlusADDUCTS-
dc.subject.keywordPlusALDEHYDES-
dc.subject.keywordPlusELECTROPHILES-
dc.subject.keywordPlusISOMERIZATION-
dc.subject.keywordPlusREACTIVITY-
dc.subject.keywordAuthorBaylis-Hillman acetates-
dc.subject.keywordAuthorallyltributylstannane-
dc.subject.keywordAuthorbis-pi-allylpalladium-
dc.subject.keywordAuthor1,5-diene-
dc.subject.keywordAuthorallylation-
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