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    Por favor, use este identificador para citar o enlazar este ítem: https://hdl.handle.net/10259/10644

    Título
    Asymmetric Synthesis of Highly Substituted Spiro[2H‐pyrrole‐2,3‐Succinimide] Derivatives by Copper‐Catalyzed Post‐Ugi Reactions
    Autor
    Gómez Ayuso, JavierUBU authority Orcid
    Carreira Barral, IsraelUBU authority Orcid
    Quesada Pato, RobertoUBU authority Orcid
    García Valverde, MaríaUBU authority Orcid
    Publicado en
    Advanced Synthesis & Catalysis. 2025, e202500166
    Editorial
    Wiley
    Fecha de publicación
    2025-05
    ISSN
    1615-4150
    DOI
    10.1002/adsc.202500166
    Abstract
    Herein we present a novel one-pot methodology for the synthesis of enantioenriched 2H-pyrrolespirosuccinimides by copper-catalyzed reactions on Ugi adducts derived from enantiopure α-alkylbenzyl amines through a chirality transfer process. We have proposed a mechanism, supported by density functional theory (DFT) calculations, where a hydrogen radical-shuttle (HRS) process explains the chemical and stereochemical results. This work demonstrates the efficient stereoselective synthesis of structurally unique, highly functionalized nitrogen heterocyclic systems using simple protocols and affordable starting materials.
    Palabras clave
    Multicomponent reactions
    Radical reactions
    Copper catalys
    Succinimide
    Spirosuccinimide
    Spiro-2H-pyrrole
    Materia
    Química orgánica
    Chemistry, Organic
    URI
    https://hdl.handle.net/10259/10644
    Versión del editor
    https://doi.org/10.1002/adsc.202500166
    Collections
    • Artículos BIOORG
    Attribution-NonCommercial-NoDerivatives 4.0 Internacional
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