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dc.contributor.authorPrieto, Elena
dc.contributor.authorAndrés, Celia
dc.contributor.authorNieto, Javier
dc.date.accessioned2025-11-27T11:31:56Z
dc.date.available2025-11-27T11:31:56Z
dc.date.issued2025
dc.identifier.citationOrganic & Biomolecular Chemistry, 2025, vol. 23, p 10596-10605.es
dc.identifier.issn1477-0520es
dc.identifier.urihttps://uvadoc.uva.es/handle/10324/80120
dc.description.abstractThe α-hydroxyamide moiety is an important structural component in a wide variety of biologically active compounds and natural products. Herein, we describe a highly efficient and practical approach towards chiral quaternary α-alkynyl-α-hydroxyamides by Me2Zn-mediated addition of terminal alkynes to α-keto amides. The desired products are obtained in good yields and enantioselectivities with broad substrate and reagent scopes.es
dc.format.mimetypeapplication/pdfes
dc.language.isospaes
dc.publisherThe Royal Society of Chemistryes
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses
dc.titleSynthesis of chiral α-alkynyl-α-hydroxyamides by enantioselective alkynylation of α-keto amideses
dc.typeinfo:eu-repo/semantics/articlees
dc.identifier.doi10.1039/d5ob01546des
dc.identifier.publicationfirstpage10596es
dc.identifier.publicationissue46es
dc.identifier.publicationlastpage10605es
dc.identifier.publicationtitleOrganic & Biomolecular Chemistryes
dc.identifier.publicationvolume23es
dc.peerreviewedSIes
dc.description.projectJunta de Castilla y León (projects FEDER-VA115P17 and VA149G18)es
dc.identifier.essn1477-0539es
dc.type.hasVersioninfo:eu-repo/semantics/publishedVersiones


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