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Gold-catalyzed waste-free generation and reaction of azomethine ylides: Internal redox/dipolar cycloaddition cascade

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dc.contributor.authorYeom, Hyttn-Suk-
dc.contributor.authorLee, Ji-Eun-
dc.contributor.authorShin, Setinghoon-
dc.date.accessioned2022-10-07T10:03:07Z-
dc.date.available2022-10-07T10:03:07Z-
dc.date.created2022-08-26-
dc.date.issued2008-09-
dc.identifier.issn1433-7851-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/171863-
dc.description.abstract(Chemical Equation Presented) High-octane synthesis: Azomethine ylides can be generated from an internal redox reaction of a nitrone-tethered alkyne under electrophilic metal catalysis (see scheme; M=metal). This novel and atom-economical generation of an azomethine ylide does not involve potentially explosive diazo derivatives. The azomethine ylide can participate in a dipolar cycloaddition cascade to provide an azabicyclo[3.2.1]octane.-
dc.language영어-
dc.language.isoen-
dc.publisherWILEY-V C H VERLAG GMBH-
dc.titleGold-catalyzed waste-free generation and reaction of azomethine ylides: Internal redox/dipolar cycloaddition cascade-
dc.typeArticle-
dc.contributor.affiliatedAuthorShin, Setinghoon-
dc.identifier.doi10.1002/anie.200802802-
dc.identifier.scopusid2-s2.0-54749085339-
dc.identifier.wosid000259041000017-
dc.identifier.bibliographicCitationANGEWANDTE CHEMIE-INTERNATIONAL EDITION, v.47, no.37, pp.7040 - 7043-
dc.relation.isPartOfANGEWANDTE CHEMIE-INTERNATIONAL EDITION-
dc.citation.titleANGEWANDTE CHEMIE-INTERNATIONAL EDITION-
dc.citation.volume47-
dc.citation.number37-
dc.citation.startPage7040-
dc.citation.endPage7043-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.subject.keywordPlus1,3-DIPOLAR CYCLOADDITION-
dc.subject.keywordPlusSYNTHETIC ACCESS-
dc.subject.keywordPlusDERIVATIVES-
dc.subject.keywordPlusCYCLIZATION-
dc.subject.keywordPlusINSERTION-
dc.subject.keywordPlusACTIVATION-
dc.subject.keywordPlusCOMPLEXES-
dc.subject.keywordPlusALKALOIDS-
dc.subject.keywordPlusTANDEM-
dc.subject.keywordAuthorazomethine ylides-
dc.subject.keywordAuthorcarbenes-
dc.subject.keywordAuthorcyclization-
dc.subject.keywordAuthorhomogeneous catalysis-
dc.subject.keywordAuthorredox chemistry-
dc.identifier.urlhttps://onlinelibrary.wiley.com/doi/10.1002/anie.200802802-
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