Asymmetric Synthesis of Highly Substituted Spiro[<i>2H‐</i>pyrrole‐2,3‐Succinimide] Derivatives by Copper‐Catalyzed Post‐Ugi Reactions

Abstract Herein we present a novel one‐pot methodology for the synthesis of enantioenriched 2 H ‐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.

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Publication Details

Journal
Advanced Synthesis & Catalysis
Published
2025-04-22
DOI
https://doi.org/10.1002/adsc.202500166
Citations
3
Primary Topic
Multicomponent Synthesis of Heterocycles
Type
article
Field-Weighted Citation Impact
2.81
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article

Asymmetric Synthesis of Highly Substituted Spiro[2H‐pyrrole‐2,3‐Succinimide] Derivatives by Copper‐Catalyzed Post‐Ugi Reactions

Roberto Quesada
3 citations
Advanced Synthesis & Catalysis
Multicomponent Synthesis of Heterocycles
2.81
article

Asymmetric Synthesis of Highly Substituted Spiro[2H‐pyrrole‐2,3‐Succinimide] Derivatives by Copper‐Catalyzed Post‐Ugi Reactions

Roberto Quesada
article en
3 citations

Abstract

Abstract Herein we present a novel one‐pot methodology for the synthesis of enantioenriched 2 H ‐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.

Advanced Synthesis & CatalysisVol. 367(13)
Universidad de Burgos (ES)
Openalex Percentile: Top 11%
Multicomponent Synthesis of Heterocycles
2.81
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