• Development of an α′-hydroxy enone for the aminocatalytic asymmetric formal conjugate addition of aldehydes to acrylates, vinyl ketones and acrolein 

      Odriozola Ibarguren, José Manuel Upna Orcid; Razkin Lizarraga, Jesús; Lorea Revilla, Beñat; Mielgo, Antonia; García Castillo, Jesús María Upna Orcid; Oiarbide, Mikel; Palomo, Claudio (Royal Society of Chemistry, 2023)   Artículo / Artikulua
      Aminocatalytic asymmetric conjugate addition of aldehydes to Michael acceptors is a well established C-C bond forming methodology. However, various acrylic-type acceptors, including acrylic acid derivatives and acrolein, ...
    • Enantioselective addition of alkynyl ketones to nitroolefins assisted by Brønsted base/H-bonding catalysis 

      Campano, Teresa E.; Iriarte, Igor; Olaizola, Olatz; Etxabe, Julen; Mielgo, Antonia; Ganboa, Iñaki; Odriozola Ibarguren, José Manuel Upna Orcid; García Castillo, Jesús María Upna Orcid; Oiarbide, Mikel; Palomo, Claudio (Wiley, 2019)   Artículo / Artikulua  OpenAccess
      Various sets of enolizable alkynyl ketones (including methyl ynones with α-aryl, α-alkenyl, and α-alkoxy groups) were able to react smoothly with nitroolefins with the assistance of bifunctional Brønsted base/H-bond catalysts ...
    • Organocatalytic Michael addition of unactivated a-branched nitroalkanes to afford optically active tertiary nitrocompounds 

      Lorea Revilla, Beñat; García-Urricelqui, Ane; Odriozola Ibarguren, José Manuel Upna Orcid; Razkin Lizarraga, Jesús; Espinal Viguri, Maialen Upna Orcid; Oiarbide, Mikel; Mielgo, Antonia; García Castillo, Jesús María Upna Orcid; Palomo, Claudio (ACS, 2023)   Artículo / Artikulua  OpenAccess
      The direct, asymmetric conjugate addition of unactivated ¿-branched nitroalkanes is developed based on the combined use of chiral amine/ureidoaminal bifunctional catalysts and a tunable acrylate template to provide tertiary ...
    • α-Hydroxy ketones as masked ester donors in Brønsted base catalyzed conjugate additions to nitroalkenes 

      Olaizola, Iurre; Campano, Teresa E.; Iriarte, Igor; Vera, Silvia; Mielgo, Antonia; García Castillo, Jesús María Upna Orcid; Odriozola Ibarguren, José Manuel Upna Orcid; Oiarbide, Mikel; Palomo, Claudio (Wiley, 2018)   Artículo / Artikulua  OpenAccess
      The catalyst-controlled enantioselective direct addition reaction of enolizable esters and related carboxylic acid derivatives to p electrophiles remains a difficult synthetic transformation. In this study, the suitability ...

      El Repositorio ha recibido la ayuda de la Fundación Española para la Ciencia y la Tecnología para la realización de actividades en el ámbito del fomento de la investigación científica de excelencia, en la Línea 2. Repositorios institucionales (convocatoria 2020-2021).
      Logo MinisterioLogo Fecyt