Universidad de Burgos RIUBU Principal Default Universidad de Burgos RIUBU Principal Default
  • español
  • English
  • français
  • Deutsch
  • português (Brasil)
  • italiano
Universidad de Burgos RIUBU Principal Default
  • Ayuda
  • Contact Us
  • Send Feedback
  • Acceso abierto
    • Archivar en RIUBU
    • Acuerdos editoriales para la publicación en acceso abierto
    • Controla tus derechos, facilita el acceso abierto
    • Sobre el acceso abierto y la UBU
    • español
    • English
    • français
    • Deutsch
    • português (Brasil)
    • italiano
    • español
    • English
    • français
    • Deutsch
    • português (Brasil)
    • italiano
    JavaScript is disabled for your browser. Some features of this site may not work without it.

    Browse

    All of RIUBUCommunities and CollectionsBy Issue DateAuthorsTitlesSubjectsThis CollectionBy Issue DateAuthorsTitlesSubjects

    My Account

    LoginRegister

    Statistics

    View Usage Statistics

    Compartir

    View Item 
    •   RIUBU Home
    • E-Prints
    • Untitled
    • Untitled
    • Artículos SINTORG
    • View Item
    •   RIUBU Home
    • E-Prints
    • Untitled
    • Untitled
    • Artículos SINTORG
    • View Item

    Por favor, use este identificador para citar o enlazar este ítem: http://hdl.handle.net/10259/3799

    Título
    Solvent- and ligand-induced switch of selectivity in gold(I)-catalyzed tandem reactions of 3-propargylindoles
    Autor
    Álvarez Manuel, EstelaUBU authority
    Miguel, DeliaUBU authority Orcid
    García García, Patricia
    Fernández Rodríguez, Manuel A.UBU authority Orcid
    Rodríguez, Félix
    Sanz Díez, RobertoUBU authority Orcid
    Serie/N.º
    Gold catalysis for organic synthesis
    Publicado en
    Beilstein Journal of Organic Chemistry. 2011, v. 7, p. 786–793
    Editorial
    Beilstein-Institut
    Fecha de publicación
    2011-06
    ISSN
    1860-5397
    DOI
    10.3762/bjoc.7.89
    Abstract
    The selectivity of our previously described gold-catalyzed tandem reaction, 1,2-indole migration followed by aura-iso-Nazarov cyclization, of 3-propargylindoles bearing (hetero)aromatic substituents at both the propargylic and terminal positions, was reversed by the proper choice of the catalyst and the reaction conditions. Thus, 3-(inden-2-yl)indoles, derived from an aura-Nazarov cyclization (instead of an aura-iso-Nazarov cyclization), were obtained in moderate to good yields from a variety of 3-propargylindoles
    Palabras clave
    catalysis
    gold
    indoles
    Nazarov cyclizations
    selectivity
    Materia
    Química orgánica
    Chemistry, Organic
    URI
    http://hdl.handle.net/10259/3799
    Versión del editor
    http://dx.doi.org/10.3762/bjoc.7.89
    Collections
    • Artículos SINTORG
    Attribution 4.0 International
    Documento(s) sujeto(s) a una licencia Creative Commons Attribution 4.0 International
    Files in this item
    Nombre:
    Beilstein_J._Org._Chem._2011.pdf
    Tamaño:
    467.5Kb
    Formato:
    Adobe PDF
    Thumbnail
    FilesOpen

    Métricas

    Citas

    Academic Search
    Ver estadísticas de uso

    Export

    RISMendeleyRefworksZotero
    • edm
    • marc
    • xoai
    • qdc
    • ore
    • ese
    • dim
    • uketd_dc
    • oai_dc
    • etdms
    • rdf
    • mods
    • mets
    • didl
    • premis
    Show full item record