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A Versatile Rhodium(I) Catalyst System for the Addition of Heteroarenes to both Alkenes and Alkynes by a CH Bond Activation : A Versatile Rhodium(I) Catalyst System for the Addition of Heteroarenes to both Alkenes and Alkynes by a C-H Bond Activation

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dc.contributor.authorRyu, Jaeyune-
dc.contributor.authorCho, Seung Hwan-
dc.contributor.authorChang, Sukbok-
dc.date.accessioned2023-05-03T05:47:16Z-
dc.date.available2023-05-03T05:47:16Z-
dc.date.created2023-05-01-
dc.date.created2023-05-01-
dc.date.created2023-05-01-
dc.date.created2023-05-01-
dc.date.issued2012-04-
dc.identifier.citationAngewandte Chemie International Edition, Vol.51 No.15, pp.3677-3681-
dc.identifier.issn1433-7851-
dc.identifier.urihttps://hdl.handle.net/10371/191827-
dc.description.abstractRhod to Addition: A highly efficient and convenient rhodium catalyst system was developed for the title transformation. A base co-catalyst was found to facilitate the key arene CH bond-activation step and substrate scope was very broad, including both electron-deficient pyridine N-oxides, and electron-rich azoles. The catalytic system was effective for the hydroheteroarylation of both alkenes and alkynes and gave excellent regio- and stereoselectivity.-
dc.language영어-
dc.publisherJohn Wiley & Sons Ltd.-
dc.titleA Versatile Rhodium(I) Catalyst System for the Addition of Heteroarenes to both Alkenes and Alkynes by a CH Bond Activation-
dc.title.alternativeA Versatile Rhodium(I) Catalyst System for the Addition of Heteroarenes to both Alkenes and Alkynes by a C-H Bond Activation-
dc.typeArticle-
dc.identifier.doi10.1002/anie.201200120-
dc.citation.journaltitleAngewandte Chemie International Edition-
dc.identifier.wosid000302348200031-
dc.identifier.scopusid2-s2.0-84859526044-
dc.citation.endpage3681-
dc.citation.number15-
dc.citation.startpage3677-
dc.citation.volume51-
dc.description.isOpenAccessN-
dc.contributor.affiliatedAuthorRyu, Jaeyune-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.subject.keywordPlusPYRIDINE-N-OXIDES-
dc.subject.keywordPlusNICKEL/LEWIS ACID CATALYSIS-
dc.subject.keywordPlusH BOND-
dc.subject.keywordPlusARYLBORONIC ACIDS-
dc.subject.keywordPlusCONJUGATE ADDITION-
dc.subject.keywordPlusDIRECT ARYLATION-
dc.subject.keywordPlusASYMMETRIC 1,4-ADDITION-
dc.subject.keywordPlusSELECTIVE ALKENYLATION-
dc.subject.keywordPlusCOUPLING REACTIONS-
dc.subject.keywordPlusAROMATIC IMINES-
dc.subject.keywordAuthoralkenes-
dc.subject.keywordAuthoralkynes-
dc.subject.keywordAuthorhomogeneous catalysis-
dc.subject.keywordAuthorhydroheteroarylation-
dc.subject.keywordAuthorpyridine N-oxides-
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  • College of Engineering
  • School of Chemical and Biological Engineering
Research Area Catalysis, Nano Materials, Physical E-Chem, 무기화학, 물리전기화학

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