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    • Dpto. Química Orgánica
    • DEP67 - Artículos de revista
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    Por favor, use este identificador para citar o enlazar este ítem:https://uvadoc.uva.es/handle/10324/80120

    Título
    Synthesis of chiral α-alkynyl-α-hydroxyamides by enantioselective alkynylation of α-keto amides
    Autor
    Prieto, Elena
    Andrés, Celia
    Nieto, Javier
    Año del Documento
    2025
    Editorial
    The Royal Society of Chemistry
    Documento Fuente
    Organic & Biomolecular Chemistry, 2025, vol. 23, p 10596-10605.
    Abstract
    The 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.
    ISSN
    1477-0520
    Revisión por pares
    SI
    DOI
    10.1039/d5ob01546d
    Patrocinador
    Junta de Castilla y León (projects FEDER-VA115P17 and VA149G18)
    Idioma
    spa
    URI
    https://uvadoc.uva.es/handle/10324/80120
    Tipo de versión
    info:eu-repo/semantics/publishedVersion
    Derechos
    openAccess
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    • DEP67 - Artículos de revista [58]
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    Org. Biomol. Chem., 2025, 23, 10596–10605 .pdf
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