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.
Authors
- Laure Guénée (ORCID: https://orcid.org/0000-0002-2136-0510)
- Amalia I. Poblador‐Bahamonde (ORCID: https://orcid.org/0000-0002-5266-914X)
- Baptiste Leforestier (ORCID: https://orcid.org/0000-0001-8547-6021)
- Clément Mazet (ORCID: https://orcid.org/0000-0002-2385-280X)
- Céline Besnard (ORCID: https://orcid.org/0000-0001-5699-9675)
- Svetlana Kucher (ORCID: https://orcid.org/0000-0002-7522-9163)
- Kaidi Li (ORCID: https://orcid.org/0000-0003-1739-7051)
Institutions
- University of Geneva (CH)
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
Funders
- Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung
- Université de Genève