Evidence map›Paper›PMID 39660434›Full record

ArticleOrganic & biomolecular chemistry2025

Simple and versatile electrochemical synthesis of highly substituted 2,1-benzisoxazoles.

Marola S Lenhard, Johannes Winter, Alexander Sandvoß, María de Jesús Gálvez-Vázquez, Dieter Schollmeyer, Siegfried R Waldvogel

Abstract read
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Article in Organic & biomolecular chemistry, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
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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

6 authors.

Marola S LenhardDepartment of Chemistry, Johannes Gutenberg University, Duesbergweg 10-14, 55128 Mainz, Germany. siegfried.waldvogel@cec.mpg.de.ORCID http://orcid.org/0009-0006-4597-6236
Johannes WinterDepartment of Chemistry, Johannes Gutenberg University, Duesbergweg 10-14, 55128 Mainz, Germany. siegfried.waldvogel@cec.mpg.de.ORCID http://orcid.org/0000-0001-9307-1497
Alexander SandvoßDepartment of Chemistry, Johannes Gutenberg University, Duesbergweg 10-14, 55128 Mainz, Germany. siegfried.waldvogel@cec.mpg.de.ORCID http://orcid.org/0000-0002-2456-5597
María de Jesús Gálvez-VázquezDepartment of Chemistry, Johannes Gutenberg University, Duesbergweg 10-14, 55128 Mainz, Germany. siegfried.waldvogel@cec.mpg.de.ORCID http://orcid.org/0000-0002-0416-6556
Dieter SchollmeyerDepartment of Chemistry, Johannes Gutenberg University, Duesbergweg 10-14, 55128 Mainz, Germany. siegfried.waldvogel@cec.mpg.de.
Siegfried R WaldvogelDepartment of Chemistry, Johannes Gutenberg University, Duesbergweg 10-14, 55128 Mainz, Germany. siegfried.waldvogel@cec.mpg.de.ORCID http://orcid.org/0000-0002-7949-9638

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A sustainable, general and scalable electrochemical protocol for direct access to 3-(acylamidoalkyl)-2,1-benzisoxazoles by cathodic reduction of widely accessible nitro arenes is established. The method is characterised by a simple undivided set-up under constant current conditions, inexpensive and reusable carbon-based electrodes, and environmentally benign reaction conditions. The versatility of the developed protocol is demonstrated on 39 highly diverse examples with up to 81% yield. A 50-fold scale-up electrolysis highlights its relevance for preparative applications.

Identifiers

PMID39660434
PMCPMC11632592

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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.