共 119 条
Catalytic Enantioselective Functionalization of Maleimides: An Update
被引:6
作者:

Amatore, Muriel
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Aix Marseille Univ, CNRS, Cent Med, iSm2, F-13013 Marseille, France Aix Marseille Univ, CNRS, Cent Med, iSm2, F-13013 Marseille, France

Bonne, Damien
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Aix Marseille Univ, CNRS, Cent Med, iSm2, F-13013 Marseille, France Aix Marseille Univ, CNRS, Cent Med, iSm2, F-13013 Marseille, France

Constantieux, Thierry
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机构:
Aix Marseille Univ, CNRS, Cent Med, iSm2, F-13013 Marseille, France Aix Marseille Univ, CNRS, Cent Med, iSm2, F-13013 Marseille, France

Rodriguez, Jean
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Aix Marseille Univ, CNRS, Cent Med, iSm2, F-13013 Marseille, France Aix Marseille Univ, CNRS, Cent Med, iSm2, F-13013 Marseille, France
机构:
[1] Aix Marseille Univ, CNRS, Cent Med, iSm2, F-13013 Marseille, France
关键词:
Maleimides;
Enantioselective catalysis;
Additions;
Cycloadditions;
Heterocycles;
Domino reactions;
ASYMMETRIC MICHAEL ADDITION;
FRIEDEL-CRAFTS REACTIONS;
BAYLIS-HILLMAN REACTION;
ARYLBORONIC ACIDS;
AZOMETHINE YLIDES;
3+2 ANNULATION;
CONJUGATE ADDITION;
1,3-DIPOLAR CYCLOADDITION;
N-ARYLMALEIMIDES;
CHIRAL LIGANDS;
D O I:
10.1002/cjoc.202400787
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
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.
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页码:3605 / 3622
页数:18
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