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분자활성촉매반응연구단
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Gold(I)-Catalyzed Hydroxy Group Assisted C(sp2)-H Alkylation of Enaminones with Diazo Compounds to Access 3-Alkyl Chromones

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dc.contributor.authorPradip N. Bagle-
dc.contributor.authorManoj V. Mane-
dc.contributor.authorShashank P. Sancheti-
dc.contributor.authorAmol B. Gade-
dc.contributor.authorSamir R. Shaikh-
dc.contributor.authorMu-Hyun Baik-
dc.contributor.authorNitin T. Patil-
dc.date.available2019-02-20T08:15:51Z-
dc.date.created2019-01-28-
dc.date.issued2019-01-
dc.identifier.issn1523-7060-
dc.identifier.urihttps://pr.ibs.re.kr/handle/8788114/5597-
dc.description.abstractA strategy for expedient synthesis of 3-substituted chromones from easily available o-hydroxyarylenaminones and diazo compounds has been developed. Carefully conducted experimental and computational studies led us to propose an uncommon mechanistic pathway involving the hydroxyl group assisted alkylation of enaminones with in situ generated gold carbenes. © 2018 American Chemical Society-
dc.description.uri1-
dc.language영어-
dc.publisherAMER CHEMICAL SOC-
dc.titleGold(I)-Catalyzed Hydroxy Group Assisted C(sp2)-H Alkylation of Enaminones with Diazo Compounds to Access 3-Alkyl Chromones-
dc.typeArticle-
dc.type.rimsART-
dc.identifier.wosid000455285800072-
dc.identifier.scopusid2-s2.0-85059585694-
dc.identifier.rimsid66784-
dc.contributor.affiliatedAuthorManoj V. Mane-
dc.contributor.affiliatedAuthorMu-Hyun Baik-
dc.identifier.doi10.1021/acs.orglett.8b03989-
dc.identifier.bibliographicCitationORGANIC LETTERS, v.21, no.1, pp.335 - 339-
dc.citation.titleORGANIC LETTERS-
dc.citation.volume21-
dc.citation.number1-
dc.citation.startPage335-
dc.citation.endPage339-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
Appears in Collections:
Center for Catalytic Hydrocarbon Functionalizations(분자활성 촉매반응 연구단) > 1. Journal Papers (저널논문)
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