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Organocatalytic Oxidative Functionalizations of Alkynes

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dc.contributor.authorPatil, Dilip V.-
dc.contributor.authorShin, Seunghoon-
dc.date.accessioned2022-07-10T14:54:58Z-
dc.date.available2022-07-10T14:54:58Z-
dc.date.created2021-05-12-
dc.date.issued2019-01-
dc.identifier.issn2193-5807-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/148497-
dc.description.abstractThe catalytic oxidation of alkynes has traditionally belonged to the domain of transition metal catalysis. Recently, several promising organocatalytic methods have been developed, leading to selective oxidative transformations of alkynes. For example, ynamides, because of their electron-rich alkynes, are ideal candidates for Bronsted acid-catalysis. A closely related keteniminium intermediate could also be accessed via amide activation. A particularly interesting aspect in this regard is a facile access to umpolung enolates, which would enable novel disconnections with complementary selectivity to traditional methods.-
dc.language영어-
dc.language.isoen-
dc.publisherWILEY-V C H VERLAG GMBH-
dc.titleOrganocatalytic Oxidative Functionalizations of Alkynes-
dc.typeArticle-
dc.contributor.affiliatedAuthorShin, Seunghoon-
dc.identifier.doi10.1002/ajoc.201800632-
dc.identifier.scopusid2-s2.0-85058847474-
dc.identifier.wosid000456244000006-
dc.identifier.bibliographicCitationASIAN JOURNAL OF ORGANIC CHEMISTRY, v.8, no.1, pp.63 - 73-
dc.relation.isPartOfASIAN JOURNAL OF ORGANIC CHEMISTRY-
dc.citation.titleASIAN JOURNAL OF ORGANIC CHEMISTRY-
dc.citation.volume8-
dc.citation.number1-
dc.citation.startPage63-
dc.citation.endPage73-
dc.type.rimsART-
dc.type.docTypeReview-
dc.description.journalClass1-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.subject.keywordPlusSTEREOSELECTIVE CIS-HYDROARYLATION-
dc.subject.keywordPlusHIGHLY EFFICIENT SYNTHESIS-
dc.subject.keywordPlusSITE-SELECTIVE SYNTHESIS-
dc.subject.keywordPlusGOLD-CATALYZED SYNTHESIS-
dc.subject.keywordPlusFORMAL 3+2 CYCLOADDITION-
dc.subject.keywordPlusMETAL-FREE-
dc.subject.keywordPlusELECTROPHILIC ACTIVATION-
dc.subject.keywordPlusREGIOSELECTIVE SYNTHESIS-
dc.subject.keywordPlusKETENIMINIUM SALTS-
dc.subject.keywordPlusCOUPLING REACTIONS-
dc.subject.keywordAuthoralkyne oxidation-
dc.subject.keywordAuthororganocatalysis-
dc.subject.keywordAuthorketeniminium ions-
dc.subject.keywordAuthorumpolung-
dc.subject.keywordAuthoralkynes-
dc.identifier.urlhttps://onlinelibrary.wiley.com/doi/10.1002/ajoc.201800632-
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