Chiral Biaryl N-Heterocyclic Carbene–Palladium Catalysts with Anagostic C–H···Pd Interaction for Enantioselective Desymmetric C–N Cross-Coupling

Novel chiral biaryl imidazo[1,5-<i>a</i>]pyridine carbene-palladium complexes (ImPy-Pd) featuring an anagostic C-H···Pd interaction and a C5-aryl substituent have been developed and successfully applied to the Pd-catalyzed enantioselective desymmetric C-N cross-coupling of malonamide derivatives, providing chiral 3,4-dihydroquinoline-2-ones with quaternary stereocenters in high yields (≤99%) and enantioselectivities (≤97:3 er). The chiral catalyst exerts stereocontrol by restricting the rotation of substituents around the metal center through anagostic interactions with sterically bulky substituents.

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Publication Details

Journal
Organic Letters
Published
2024-11-11
DOI
https://doi.org/10.1021/acs.orglett.4c03709
Citations
3
Primary Topic
Catalytic Cross-Coupling Reactions
Type
article
Field-Weighted Citation Impact
0.75

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article

Chiral Biaryl N-Heterocyclic Carbene–Palladium Catalysts with Anagostic C–H···Pd Interaction for Enantioselective Desymmetric C–N Cross-Coupling

Huijeong Ryu, Woosong Han, Sukwon Hong, Changmuk Kang
3 citations
Organic Letters
Catalytic Cross-Coupling Reactions
0.75
article

Chiral Biaryl N-Heterocyclic Carbene–Palladium Catalysts with Anagostic C–H···Pd Interaction for Enantioselective Desymmetric C–N Cross-Coupling

Huijeong Ryu, Woosong Han, Sukwon Hong, Changmuk Kang
article en
3 citations

Abstract

Novel chiral biaryl imidazo[1,5-<i>a</i>]pyridine carbene-palladium complexes (ImPy-Pd) featuring an anagostic C-H···Pd interaction and a C5-aryl substituent have been developed and successfully applied to the Pd-catalyzed enantioselective desymmetric C-N cross-coupling of malonamide derivatives, providing chiral 3,4-dihydroquinoline-2-ones with quaternary stereocenters in high yields (≤99%) and enantioselectivities (≤97:3 er). The chiral catalyst exerts stereocontrol by restricting the rotation of substituents around the metal center through anagostic interactions with sterically bulky substituents.

Organic LettersVol. 26(46)
Gwangju Institute of Science and Technology (KR)
National Research Foundation of Korea
Openalex Percentile: Top 31%
Catalytic Cross-Coupling Reactions
0.75
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