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Bronsted acid-catalyzed alpha-halogenation of ynamides from halogenated solvents and pyridine-N-oxides

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dc.contributor.authorKim, Seung Woo-
dc.contributor.authorUm, Tae-Woong-
dc.contributor.authorShin, Seunghoon-
dc.date.accessioned2022-07-14T12:36:24Z-
dc.date.available2022-07-14T12:36:24Z-
dc.date.created2021-05-12-
dc.date.issued2017-03-
dc.identifier.issn1359-7345-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/152784-
dc.description.abstractThe keteniminium ions generated from the protonation of ynamides formed reversible adducts with counter anions and pyridine-N-oxides as well as halogenated solvents. Above 80 degrees C, the halonium ions selectively undergo a rate-limiting attack by pyridine-N-oxides, leading to (E)-haloenamides in good yields.-
dc.language영어-
dc.language.isoen-
dc.publisherROYAL SOC CHEMISTRY-
dc.titleBronsted acid-catalyzed alpha-halogenation of ynamides from halogenated solvents and pyridine-N-oxides-
dc.typeArticle-
dc.contributor.affiliatedAuthorShin, Seunghoon-
dc.identifier.doi10.1039/c6cc10286g-
dc.identifier.scopusid2-s2.0-85014253958-
dc.identifier.wosid000395883600020-
dc.identifier.bibliographicCitationCHEMICAL COMMUNICATIONS, v.53, no.18, pp.2733 - 2736-
dc.relation.isPartOfCHEMICAL COMMUNICATIONS-
dc.citation.titleCHEMICAL COMMUNICATIONS-
dc.citation.volume53-
dc.citation.number18-
dc.citation.startPage2733-
dc.citation.endPage2736-
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.keywordPlusSTEREOSELECTIVE CIS-HYDROARYLATION-
dc.subject.keywordPlusSITE-SELECTIVE SYNTHESIS-
dc.subject.keywordPlusOXO GOLD CARBENES-
dc.subject.keywordPlusTRANS-HYDROFLUORINATION-
dc.subject.keywordPlusAMIDES-
dc.subject.keywordPlusCYCLIZATION-
dc.subject.keywordPlusGENERATION-
dc.subject.keywordPlusREAGENTS-
dc.subject.keywordPlusALKYNES-
dc.subject.keywordPlusFUNCTIONALIZATION-
dc.identifier.urlhttps://pubs.rsc.org/en/content/articlelanding/2017/CC/C6CC10286G-
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