Synthesis
DOI: 10.1055/a-2643-6539
Paper
Published as part of the Special Topic Dedicated to Prof. Paul Knochel

Nickel-Catalyzed Enantioconvergent C(sp3)–C(sp3) Cross-Coupling between α-Iodogermanes and Alkylzinc Reagents

Institut für Chemie, Technische Universität Berlin, Berlin, Germany
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Institut für Chemie, Technische Universität Berlin, Berlin, Germany
› Institutsangaben

Gefördert durch: Einstein Stiftung Berlin None
Gefördert durch: Deutsche Forschungsgemeinschaft Oe 249/25-1
Funding Information This research was supported by the Deutsche Forschungsgemeinschaft (Oe 249/25-1).


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Dedication

Dedicated to Professor Paul Knochel on the occasion of his 70th birthday.

Abstract

We report a nickel-catalyzed enantioconvergent C(sp3)–C(sp3) cross-coupling between α-iodogermanes and alkylzinc reagents to access α-chiral alkylgermanes. This transformation, a strategy previously established for silicon-based electrophiles, extends to germanium, enabling the enantioselective formation of α-chiral germanes from simple, unactivated alkyl chains. While yields and enantioselectivities remain moderate, the reaction outcome was finely tuned through the design and evaluation of a library of over 30 ligands, including more than a dozen novel scaffolds. Notably, two distinct NiBr₂∙PyBox complexes allowed for access to products of opposite absolute configuration, and preformed nickel complexes were required to reach synthetically useful conversions. These findings highlight the challenges of asymmetric catalysis with heavier main-group elements and provide a platform for the future design of ligands tailored to organogermanium chemistry.

Supplementary Material



Publikationsverlauf

Eingereicht: 15. Juni 2025

Angenommen nach Revision: 25. Juni 2025

Accepted Manuscript online:
25. Juni 2025

Artikel online veröffentlicht:
18. August 2025

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