Evidence map›Paper›PMID 39317660›Full record

ArticleAngewandte Chemie (International ed. in English)2024

An Automated Electrochemical Flow Platform to Accelerate Library Synthesis and Reaction Optimization.

Eduardo Rial-Rodríguez, Jason D Williams, David Cantillo, Thomas Fuchß, Alena Sommer, Hans-Michael Eggenweiler, C Oliver Kappe, Gabriele Laudadio

Abstract read
In one paragraph

Article in Angewandte Chemie (International ed. in English), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Accelerated Porosity Screening Using a Multichannel Colorimetric Array.Angewandte Chemie (International ed. in English) · 2025
    Article
  7. Advancing Organic Chemistry Using High-Throughput Experimentation.Angewandte Chemie (International ed. in English) · 2025
    Review
  8. Article
  9. Article
  10. Review
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

8 authors.

Eduardo Rial-RodríguezInstitute of Chemistry, NAWI Graz,. Department, University of Graz, Heinrichstrasse 28, 8010, Graz, Austria.
Jason D WilliamsInstitute of Chemistry, NAWI Graz,. Department, University of Graz, Heinrichstrasse 28, 8010, Graz, Austria.
David CantilloInstitute of Chemistry, NAWI Graz,. Department, University of Graz, Heinrichstrasse 28, 8010, Graz, Austria.ORCID 0000-0001-7604-8711
Thomas FuchßMedicinal Chemistry and Drug Design, Merck Healthcare KGaA, Frankfurter Strasse 250, 64293, Darmstadt, Germany.
Alena SommerMedicinal Chemistry and Drug Design, Merck Healthcare KGaA, Frankfurter Strasse 250, 64293, Darmstadt, Germany.
Hans-Michael EggenweilerMedicinal Chemistry and Drug Design, Merck Healthcare KGaA, Frankfurter Strasse 250, 64293, Darmstadt, Germany.ORCID 0000-0003-2202-5826
C Oliver KappeInstitute of Chemistry, NAWI Graz,. Department, University of Graz, Heinrichstrasse 28, 8010, Graz, Austria.ORCID 0000-0003-2983-6007
Gabriele LaudadioInstitute of Chemistry, NAWI Graz,. Department, University of Graz, Heinrichstrasse 28, 8010, Graz, Austria.ORCID 0000-0002-2749-8393

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Automated batch and flow setups are well-established for high throughput experimentation in both thermal chemistry and photochemistry. However, the development of automated electrochemical platforms is hindered by cell miniaturization challenges in batch and difficulties in designing effective single-pass flow systems. In order to address these issues, we have designed and implemented a new, slug-based automated electrochemical flow platform. This platform was successfully demonstrated for electrochemical C-N cross-couplings of E3 ligase binders with diverse amines (44 examples), which were subsequently transferred to a continuous-flow mode for confirmation and isolation, showing its applicability for medicinal chemistry purposes. To further validate the versatility of the platform, Design of Experiments (DoE) optimization was performed for an unsuccessful library target. This optimization process, fully automated by the platform, resulted in a remarkable 6-fold increase in reaction yield.

Indexed as

Electrochemical TechniquesAminesAutomationMolecular StructureSmall Molecule LibrariesAminesSmall Molecule LibrariesAutomationElectrocatalysisElectrochemistryLibrary SynthesisMedicinal Chemistry

Identifiers

PMID39317660
PMCPMC11627123

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

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.