Exploiting Biocatalysis for the Scalable Synthesis of Enantiopure γ‐Hydroxynitrile Building Blocks

We report the scalable biocatalyzed synthesis of γ‐hydroxynitriles from their corresponding prochiral ketone precursors. Screening of a panel of alcohol dehydrogenases (ADHs) identified RRADH as an ( S )‐selective ADH yielding the desired products in e.e. values of 99%, whereas LSADH gave ( R )‐configured γ‐hydroxynitriles (e.e. up to 95%). Optimization of this transformation allowed for reaction scale‐up to 5 mmol, affording the targets in gram quantities. Moreover, the absolute configuration of the ( S )‐configured products was unambiguously established by single‐crystal diffraction. This study showcases how chiral γ‐hydroxynitriles can be generated from readily available γ‐ketonitriles in an efficient and scalable manner, providing a robust and sustainable access to these valuable entities.

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Publication Details

Journal
European Journal of Organic Chemistry
Published
2026-08-25
DOI
https://doi.org/10.1002/ejoc.70782
Primary Topic
Enzyme Catalysis and Immobilization
Type
article
Field-Weighted Citation Impact
0.00

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article

Exploiting Biocatalysis for the Scalable Synthesis of Enantiopure γ‐Hydroxynitrile Building Blocks

Kathryn Yeow, Uwe T. Bornscheuer, Adam Cruise, Thomas Bayer et al.
European Journal of Organic Chemistry
Enzyme Catalysis and Immobilization
article

Exploiting Biocatalysis for the Scalable Synthesis of Enantiopure γ‐Hydroxynitrile Building Blocks

Kathryn Yeow, Uwe T. Bornscheuer, Adam Cruise, Thomas Bayer, Benjamin Baumert, Marcus Baumann, Roi Boris Tchuemmogne Tchuente, Christopher Thomas
article en

Abstract

We report the scalable biocatalyzed synthesis of γ‐hydroxynitriles from their corresponding prochiral ketone precursors. Screening of a panel of alcohol dehydrogenases (ADHs) identified RRADH as an ( S )‐selective ADH yielding the desired products in e.e. values of 99%, whereas LSADH gave ( R )‐configured γ‐hydroxynitriles (e.e. up to 95%). Optimization of this transformation allowed for reaction scale‐up to 5 mmol, affording the targets in gram quantities. Moreover, the absolute configuration of the ( S )‐configured products was unambiguously established by single‐crystal diffraction. This study showcases how chiral γ‐hydroxynitriles can be generated from readily available γ‐ketonitriles in an efficient and scalable manner, providing a robust and sustainable access to these valuable entities.

European Journal of Organic Chemistry
University College Dublin (IE), Universitätsmedizin Greifswald (DE), Universität Greifswald (DE)
Science Foundation Ireland
Responsible consumption and production
Openalex Percentile: Top 17%
Enzyme Catalysis and Immobilization
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