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Domino Process in Silver-Catalyzed Reactions of N-Arylformimidates and Active Methylene Compounds Involving Cycloisomerization and 1,3-Alkenyl Shift

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dc.contributor.authorOh, Chang Ho-
dc.contributor.authorKarmakar, Swastik-
dc.contributor.authorPark, HyoSeung-
dc.contributor.authorAhn, YoungCheon-
dc.contributor.authorKim, Jung Wook-
dc.date.accessioned2022-12-20T19:11:45Z-
dc.date.available2022-12-20T19:11:45Z-
dc.date.issued2010-02-
dc.identifier.issn0002-7863-
dc.identifier.issn1520-5126-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/175519-
dc.description.abstractWe have developed an efficient method for the synthesis of 2,3-disubstituted indoles from alkyne iminoethers I that employs a domino process involving Ag-catalyzed condensation followed by a tandem Ag-induced cycloisomerization and 1,3-alkenyl shift to Ag-activated carbon. This methodology can be useful in regioselectively constructing 3-alkylated indoles. which are part of the structures of biologically active compounds and important alkaloids.-
dc.format.extent2-
dc.language영어-
dc.language.isoENG-
dc.publisherAmerican Chemical Society-
dc.titleDomino Process in Silver-Catalyzed Reactions of N-Arylformimidates and Active Methylene Compounds Involving Cycloisomerization and 1,3-Alkenyl Shift-
dc.typeArticle-
dc.publisher.location미국-
dc.identifier.doi10.1021/ja9106226-
dc.identifier.scopusid2-s2.0-77249085671-
dc.identifier.wosid000275085000030-
dc.identifier.bibliographicCitationJournal of the American Chemical Society, v.132, no.6, pp 1792 - 1793-
dc.citation.titleJournal of the American Chemical Society-
dc.citation.volume132-
dc.citation.number6-
dc.citation.startPage1792-
dc.citation.endPage1793-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.subject.keywordPlusCONTAINING AZOMETHINE YLIDES-
dc.subject.keywordPlusO-ALKYNYLTRIFLUOROACETANILIDES-
dc.subject.keywordPlusBIMETALLIC CATALYST-
dc.subject.keywordPlusAMINATION REACTIONS-
dc.subject.keywordPlusEFFICIENT SYNTHESIS-
dc.subject.keywordPlusINDOLES-
dc.subject.keywordPlusCYCLIZATION-
dc.subject.keywordPlusGOLD-
dc.subject.keywordPlusINHIBITORS-
dc.subject.keywordPlusALKALOIDS-
dc.identifier.urlhttps://pubs.acs.org/doi/10.1021/ja9106226-
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서울 자연과학대학 > 서울 화학과 > 1. Journal Articles
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