Evidence map›Paper›PMID 42837468›Full record

ArticleChemSusChem2026

Photobiocatalytic Linear Deracemization of β-Hydroxynitriles.

Sara Filgueira, Fernando López-Gallego, Vicente Gotor-Fernández

Abstract read
In one paragraph

Article in ChemSusChem, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Sara FilgueiraDepartment of Organic and Inorganic Chemistry, Instituto Universitario de Química Organometálica Enrique Moles, Universidad de Oviedo, Oviedo, Spain.ORCID https://orcid.org/0009-0009-6481-7750
Fernando López-GallegoHeterogeneous Biocatalysis Laboratory, CICbiomaGUNE, Basque Research and Technology Alliance (BRTA), Donostia-San Sebastián, Spain.ORCID https://orcid.org/0000-0003-0031-1880
Vicente Gotor-FernándezDepartment of Organic and Inorganic Chemistry, Instituto Universitario de Química Organometálica Enrique Moles, Universidad de Oviedo, Oviedo, Spain.ORCID https://orcid.org/0000-0002-9998-0656

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A photobiocatalytic strategy for the linear deracemization of β-hydroxynitriles is presented. This method consists of a two-step process, beginning with the oxidation of the corresponding alcohol racemate (250 mM) using tetrabutylammonium decatungstate (TBADT, 2.5-5.0 mol%) under 390 nm light irradiation in acetonitrile. The second step involves an asymmetric biocatalytic reduction, carried out sequentially by addition of the required reagents with or without solvent evaporation depending on the selected alcohol dehydrogenase (ADH) enzyme and its tolerance to the organic solvent. Under the resulting aqueous conditions (25-75 mM ketone intermediate), the enzymes exhibited high selectivity, enabling access to a series of optically active β-hydroxynitriles, predominantly with excellent optical purities, leading to nine pairs of enantiomers in 88 to >99% ee. The integration of two sustainable technologies, photo- and biocatalysis, provides a straightforward route to chiral β-hydroxynitriles. In addition, sunlight-driven applicability and scalability are demonstrated.

Indexed as

alcohol oxidationcarbonyl bioreductionlinear deracemizationphotocatalysisβ‐hydroxynitriles

Identifiers

PMID42837468
PMCPMC13641688

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.