Ni-Catalyzed Enantioconvergent Kumada–Corriu Cross-Coupling between β-Bromostyrenes and Secondary Grignard Reagents: Reaction Development, Scope and Mechanistic Investigations

A Ni-catalyzed enantioconvergent cross-coupling between β-bromostyrenes and secondary Grignard reagents is reported. This C(sp2)–C(sp3) cross-coupling is applicable to a broad range of electrophilic and nucleophilic partners and affords the products in good to high levels of enantio-induction. Experimental mechanistic investigations revealed an unexpected binding mode of the chiral (P,N) ligand and support a radical rebound mechanism involving in-cage radicals. Kinetic experiments provide evidence for an off-cycle resting state featuring dinuclear species. Computational analyses are in line with this hypothesis and coherent with a catalytic cycle proceeding via a Ni(I)/Ni(III) manifold. They further suggest an enantio-determining radical capture event and shed light on the origin of the Dynamic Kinetic Resolution process.

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Publication Details

Journal
ACS Catalysis
Published
2024-12-18
DOI
https://doi.org/10.1021/acscatal.4c06360
Citations
4
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
Field-Weighted Citation Impact
1.00

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article

Ni-Catalyzed Enantioconvergent Kumada–Corriu Cross-Coupling between β-Bromostyrenes and Secondary Grignard Reagents: Reaction Development, Scope and Mechanistic Investigations

Laure Guénée, Amalia I. Poblador‐Bahamonde, Baptiste Leforestier, Clément Mazet et al.
4 citations
ACS Catalysis
Catalytic C–H Functionalization Methods
1.00
article

Ni-Catalyzed Enantioconvergent Kumada–Corriu Cross-Coupling between β-Bromostyrenes and Secondary Grignard Reagents: Reaction Development, Scope and Mechanistic Investigations

Laure Guénée, Amalia I. Poblador‐Bahamonde, Baptiste Leforestier, Clément Mazet, Céline Besnard, Svetlana Kucher, Kaidi Li
article en
4 citations

Abstract

A Ni-catalyzed enantioconvergent cross-coupling between β-bromostyrenes and secondary Grignard reagents is reported. This C(sp2)–C(sp3) cross-coupling is applicable to a broad range of electrophilic and nucleophilic partners and affords the products in good to high levels of enantio-induction. Experimental mechanistic investigations revealed an unexpected binding mode of the chiral (P,N) ligand and support a radical rebound mechanism involving in-cage radicals. Kinetic experiments provide evidence for an off-cycle resting state featuring dinuclear species. Computational analyses are in line with this hypothesis and coherent with a catalytic cycle proceeding via a Ni(I)/Ni(III) manifold. They further suggest an enantio-determining radical capture event and shed light on the origin of the Dynamic Kinetic Resolution process.

ACS CatalysisVol. 15(1)
University of Geneva (CH)
Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung, Université de Genève
Openalex Percentile: Top 26%
Catalytic C–H Functionalization Methods
1.00
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Ni-Catalyzed Enantioconvergent Kumada–Corriu Cross-Coupling between β-Bromostyrenes and Secondary Grignard Reagents: Reaction Development, Scope and Mechanistic Investigations — Laure Guénée, Amalia I. Poblador‐Bahamonde, et al. · ACS Catalysis (2024) | TGRS Research Map | TGRS