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Bronsted Acid Catalyzed Oxygenative Bimolecular Friedel-Crafts-type Coupling of Ynamides

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dc.contributor.authorPatil, Dilip V.-
dc.contributor.authorKim, Seung Woo-
dc.contributor.authorNguyen, Quynh H.-
dc.contributor.authorKim, Hanbyul-
dc.contributor.authorWang, Shan-
dc.contributor.authorHoang, Tuan-
dc.contributor.authorShin, Seunghoon-
dc.date.accessioned2022-07-14T15:07:37Z-
dc.date.available2022-07-14T15:07:37Z-
dc.date.created2021-05-12-
dc.date.issued2017-03-
dc.identifier.issn1433-7851-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/152835-
dc.description.abstractA non-metal approach for accessing alpha-oxo carbene surrogates for a C-C bond-forming bimolecular coupling between ynamides and nucleophilic arenes was developed. This acid-catalyzed coupling features mild temperature, which is critical for the required temporal chemoselectivity among nucleophiles. The scope of nucleophiles includes indoles, pyrroles, anilines, phenols and silyl enolethers. Furthermore, a direct test of S(N)2' mechanism has been provided by employing chiral N,N'-dioxides which also enlightens the nature of the intermediates in related metal-catalyzed processes.-
dc.language영어-
dc.language.isoen-
dc.publisherWILEY-V C H VERLAG GMBH-
dc.titleBronsted Acid Catalyzed Oxygenative Bimolecular Friedel-Crafts-type Coupling of Ynamides-
dc.typeArticle-
dc.contributor.affiliatedAuthorShin, Seunghoon-
dc.identifier.doi10.1002/anie.201612471-
dc.identifier.scopusid2-s2.0-85013635533-
dc.identifier.wosid000397339400042-
dc.identifier.bibliographicCitationANGEWANDTE CHEMIE-INTERNATIONAL EDITION, v.56, no.13, pp.3670 - 3674-
dc.relation.isPartOfANGEWANDTE CHEMIE-INTERNATIONAL EDITION-
dc.citation.titleANGEWANDTE CHEMIE-INTERNATIONAL EDITION-
dc.citation.volume56-
dc.citation.number13-
dc.citation.startPage3670-
dc.citation.endPage3674-
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.keywordPlusOXO GOLD CARBENES-
dc.subject.keywordPlusSTEREOSELECTIVE CIS-HYDROARYLATION-
dc.subject.keywordPlusOXIDATIVE CYCLIZATION-
dc.subject.keywordPlusALKYNES-
dc.subject.keywordPlusCASCADE-
dc.subject.keywordPlusCYCLOADDITION-
dc.subject.keywordPlusCOMPLEXES-
dc.subject.keywordPlusEFFICIENT-
dc.subject.keywordPlusFUNCTIONALIZATION-
dc.subject.keywordPlusCYCLOPROPANATION-
dc.subject.keywordAuthorBronsted acid catalysis-
dc.subject.keywordAuthorintermolecular trapping-
dc.subject.keywordAuthorpyridine-N-oxides-
dc.subject.keywordAuthorynamides-
dc.subject.keywordAuthoralpha-oxo carbene surrogate-
dc.identifier.urlhttps://onlinelibrary.wiley.com/doi/10.1002/anie.201612471-
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