Catalytic Enantioselective Functionalization of Maleimides: An Update

Comprehensive Summary Maleimide derivatives are well‐established reactive intermediates also found in natural products, synthetic pharmaceuticals and functional polymers. Their specific reactivity found widespread applications in the field of bioconjugation and allowed for the development of highly selective functionalizations based on simple additions and cycloadditions with the possible control of central and C–N axial chirality. These multisite‐reactive scaffolds have aroused a long‐standing interest throughout the scientific community more particularly as powerful electrophilic partners and more recently as nucleophilic partners in some specific transformations. The persistent interest in these easily accessible synthetic platforms over the last decade has enabled the development of new enantioselective transformations and the major advancements in this field are presented in this review. Key Scientists

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Publication Details

Journal
Chinese Journal of Chemistry
Published
2024-11-13
DOI
https://doi.org/10.1002/cjoc.202400787
Citations
8
Primary Topic
Asymmetric Synthesis and Catalysis
Type
article
Field-Weighted Citation Impact
2.00

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article

Catalytic Enantioselective Functionalization of Maleimides: An Update

Damien Bonne, Muriel Amatore, Thierry Constantieux, Jean Rodríguez
8 citations
Chinese Journal of Chemistry
Asymmetric Synthesis and Catalysis
2.00
article

Catalytic Enantioselective Functionalization of Maleimides: An Update

Damien Bonne, Muriel Amatore, Thierry Constantieux, Jean Rodríguez
article en
8 citations

Abstract

Comprehensive Summary Maleimide derivatives are well‐established reactive intermediates also found in natural products, synthetic pharmaceuticals and functional polymers. Their specific reactivity found widespread applications in the field of bioconjugation and allowed for the development of highly selective functionalizations based on simple additions and cycloadditions with the possible control of central and C–N axial chirality. These multisite‐reactive scaffolds have aroused a long‐standing interest throughout the scientific community more particularly as powerful electrophilic partners and more recently as nucleophilic partners in some specific transformations. The persistent interest in these easily accessible synthetic platforms over the last decade has enabled the development of new enantioselective transformations and the major advancements in this field are presented in this review. Key Scientists

Chinese Journal of ChemistryVol. 42(24)
Centre National de la Recherche Scientifique (FR), Aix-Marseille Université (FR), Centrale Méditerranée (FR)
Aix-Marseille Université, Centre National de la Recherche Scientifique
Openalex Percentile: Top 14%
Asymmetric Synthesis and Catalysis
2.00
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Catalytic Enantioselective Functionalization of Maleimides: An Update — Damien Bonne, Muriel Amatore, et al. · Chinese Journal of Chemistry (2024) | TGRS Research Map | TGRS