Evidence map›Paper›PMID 42003382›Full record

ArticleOrganic letters2026

Nickel-Photocatalytic Deoxygenative Arylation toward β-Methyl-Branched α-Amino Acids.

Berjan Stouwie, Anna R Emmerich, Thomas Weyhermüller, Sebastian B Beil

Abstract read
In one paragraph

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

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

4 authors.

Berjan StouwieMax-Planck-Institute for Chemical Energy Conversion, Department for Electrosynthesis, Stiftstr. 34-36, 45470 Mülheim an der Ruhr, Germany.ORCID 0009-0006-1382-4326
Anna R EmmerichMax-Planck-Institute for Chemical Energy Conversion, Department for Electrosynthesis, Stiftstr. 34-36, 45470 Mülheim an der Ruhr, Germany.
Thomas WeyhermüllerMax-Planck-Institute for Chemical Energy Conversion, Department of Inorganic Spectroscopy, Stiftstr. 34-36, 45470 Mülheim an der Ruhr, Germany.ORCID 0000-0002-0399-7999
Sebastian B BeilMax-Planck-Institute for Chemical Energy Conversion, Department for Electrosynthesis, Stiftstr. 34-36, 45470 Mülheim an der Ruhr, Germany.ORCID 0000-0003-0373-3843

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

β-Methyl-branched α-amino acids are important motifs in peptide therapeutics. However, only few methods on their synthesis have been reported to date. Herein we report an efficient, one-step synthesis of these β-Me-branched α-amino acids through the deoxygenative arylation of threonine, yielding a diverse scope of noncanonical α-amino acids with good functional group tolerance. Our method could also be extended to the deoxygenative arylation of 3-hydroxyproline, giving access to various therapeutically relevant arylated amino acids.

Identifiers

PMID42003382
PMCPMC13140145

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Registered trials

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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.