Evidence map›Paper›PMID 36908965›Full record

ArticleChemical science2023

Simple and scalable electrosynthesis of 1

Olesja Koleda, Tobias Prenzel, Johannes Winter, Tomoki Hirohata, María de Jesús Gálvez-Vázquez, Dieter Schollmeyer, Shinsuke Inagi, Edgars Suna, Siegfried R Waldvogel

Abstract read
In one paragraph

Article in Chemical science, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Diamond Chemistry: Advances and Perspectives.Angewandte Chemie (International ed. in English) · 2025
    Review
  3. Article
  4. Highly Selective Electrosynthesis of 1Organic process research & development · 2024
    Article
  5. Article
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

9 authors.

Olesja KoledaDepartment of Chemistry, Johannes Gutenberg University Mainz Duesbergweg 10-14 55128 Mainz Germany waldvogel@uni-mainz.de https://www.aksw.uni-mainz.de/.ORCID https://orcid.org/0000-0002-5173-8561
Tobias PrenzelDepartment of Chemistry, Johannes Gutenberg University Mainz Duesbergweg 10-14 55128 Mainz Germany waldvogel@uni-mainz.de https://www.aksw.uni-mainz.de/.ORCID https://orcid.org/0000-0002-7489-2414
Johannes WinterDepartment of Chemistry, Johannes Gutenberg University Mainz Duesbergweg 10-14 55128 Mainz Germany waldvogel@uni-mainz.de https://www.aksw.uni-mainz.de/.ORCID https://orcid.org/0000-0001-9307-1497
Tomoki HirohataDepartment of Chemistry, Johannes Gutenberg University Mainz Duesbergweg 10-14 55128 Mainz Germany waldvogel@uni-mainz.de https://www.aksw.uni-mainz.de/.
María de Jesús Gálvez-VázquezDepartment of Chemistry, Johannes Gutenberg University Mainz Duesbergweg 10-14 55128 Mainz Germany waldvogel@uni-mainz.de https://www.aksw.uni-mainz.de/.
Dieter SchollmeyerDepartment of Chemistry, Johannes Gutenberg University Mainz Duesbergweg 10-14 55128 Mainz Germany waldvogel@uni-mainz.de https://www.aksw.uni-mainz.de/.
Shinsuke InagiDepartment of Chemical Science and Engineering, School of Materials and Chemical Technology, Tokyo Institute of Technology 4259 Nagatsuta-cho, Midori-ku Yokohama 226-8502 Japan.
Edgars SunaLatvian Institute of Organic Synthesis Aizkraukles 21 LV-1006 Riga Latvia.ORCID https://orcid.org/0000-0002-3078-0576
Siegfried R WaldvogelDepartment of Chemistry, Johannes Gutenberg University Mainz Duesbergweg 10-14 55128 Mainz Germany waldvogel@uni-mainz.de https://www.aksw.uni-mainz.de/.ORCID https://orcid.org/0000-0002-7949-9638

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cathodic synthesis provides sustainable access to 1-hydroxy- and 1-oxy-quinazolin-4-ones from easily accessible nitro starting materials. Mild reaction conditions, inexpensive and reusable carbon-based electrode materials, an undivided electrochemical setup, and constant current conditions characterise this method. Sulphuric acid is used as a simple supporting electrolyte as well as a catalyst for cyclisation. The broad applicability of this protocol is demonstrated in 27 differently substituted derivatives in high yields of up to 92%. Moreover, mechanistic studies based on cyclic voltammetry measurements highlight a selective reduction of the nitro substrate to hydroxylamine as a key step. The relevance for preparative applications is demonstrated by a 100-fold scale-up for gram-scale electrolysis.

Identifiers

PMID36908965
PMCPMC9993888

What OpenQuestion holds

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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.