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.
Authors
- Kathryn Yeow (ORCID: https://orcid.org/0000-0002-2532-7179)
- Uwe T. Bornscheuer (ORCID: https://orcid.org/0000-0003-0685-2696)
- Adam Cruise (ORCID: https://orcid.org/0000-0003-4471-7057)
- Thomas Bayer (ORCID: https://orcid.org/0000-0002-0656-3280)
- Benjamin Baumert
- Marcus Baumann (ORCID: https://orcid.org/0000-0002-6996-5893)
- Roi Boris Tchuemmogne Tchuente
- Christopher Thomas
Institutions
- University College Dublin (IE)
- Universitätsmedizin Greifswald (DE)
- Universität Greifswald (DE)
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
Funders
- Science Foundation Ireland