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분자활성촉매반응연구단
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Catalytic Alkyne Arylation Using Traceless Directing Groups

DC Field Value Language
dc.contributor.authorJung-Woo Park-
dc.contributor.authorBubwoong Kang-
dc.contributor.authorVy M. Dong-
dc.date.available2019-01-03T05:33:20Z-
dc.date.created2018-10-15-
dc.date.issued2018-08-
dc.identifier.issn1433-7851-
dc.identifier.urihttps://pr.ibs.re.kr/handle/8788114/5223-
dc.description.abstractBy using Pd0/Mandyphos, we achieved a three-component aminoarylation of alkynes to generate enamines, which are then hydrolyzed to either α-arylphenones or α,α-diarylketones. This Pd-catalyzed method overcomes established known pathways to enable the use of amines as traceless directing groups for C−C bond formation. © 2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinhei-
dc.description.uri1-
dc.language영어-
dc.publisherWILEY-V C H VERLAG GMBH-
dc.subjectalkynes-
dc.subjectaminoarylation-
dc.subjectmulticomponent coupling-
dc.subjectpalladium-
dc.subjectregiocontrol-
dc.titleCatalytic Alkyne Arylation Using Traceless Directing Groups-
dc.typeArticle-
dc.type.rimsART-
dc.identifier.wosid000446306600040-
dc.identifier.scopusid2-s2.0-85053554362-
dc.identifier.rimsid65782-
dc.contributor.affiliatedAuthorJung-Woo Park-
dc.identifier.doi10.1002/anie.201804955-
dc.identifier.bibliographicCitationANGEWANDTE CHEMIE-INTERNATIONAL EDITION, v.57, no.41, pp.13598 - 13602-
dc.citation.titleANGEWANDTE CHEMIE-INTERNATIONAL EDITION-
dc.citation.volume57-
dc.citation.number41-
dc.citation.startPage13598-
dc.citation.endPage13602-
dc.embargo.liftdate9999-12-31-
dc.embargo.terms9999-12-31-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.subject.keywordAuthoralkynes-
dc.subject.keywordAuthoraminoarylation-
dc.subject.keywordAuthormulticomponent coupling-
dc.subject.keywordAuthorpalladium-
dc.subject.keywordAuthorregiocontrol-
Appears in Collections:
Center for Catalytic Hydrocarbon Functionalizations(분자활성 촉매반응 연구단) > 1. Journal Papers (저널논문)
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