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
Publicado en
Advanced Synthesis & Catalysis. 2025, e202500166
Editorial
Wiley
Fecha de publicación
2025-05
ISSN
1615-4150
DOI
10.1002/adsc.202500166
Resumen
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
Versión del editor
Aparece en las colecciones
Documento(s) sujeto(s) a una licencia Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 Internacional
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