Evidence map›Paper›PMID 33760338›Full record

ArticleAngewandte Chemie (International ed. in English)2021

Redox-Neutral Selenium-Catalysed Isomerisation of para-Hydroxamic Acids into para-Aminophenols.

Hsiang-Yu Chuang, Manuel Schupp, Ricardo Meyrelles, Boris Maryasin, Nuno Maulide

Abstract read
In one paragraph

Article in Angewandte Chemie (International ed. in English), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. 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

5 authors.

Hsiang-Yu ChuangUniversity of Vienna, Institute of Organic Chemistry, Währinger Strasse 38, 1090, Vienna, Austria.
Manuel SchuppUniversity of Vienna, Institute of Organic Chemistry, Währinger Strasse 38, 1090, Vienna, Austria.
Ricardo MeyrellesUniversity of Vienna, Institute of Organic Chemistry, Währinger Strasse 38, 1090, Vienna, Austria.
Boris MaryasinUniversity of Vienna, Institute of Organic Chemistry, Währinger Strasse 38, 1090, Vienna, Austria.
Nuno MaulideUniversity of Vienna, Institute of Organic Chemistry, Währinger Strasse 38, 1090, Vienna, Austria.ORCID 0000-0003-3643-0718

Funding

Austrian Science Fund FWF P 30226
6 · The paper itself

Abstract

A selenium-catalysed para-hydroxylation of N-aryl-hydroxamic acids is reported. Mechanistically, the reaction comprises an N-O bond cleavage and consecutive selenium-induced [2,3]-rearrangement to deliver para-hydroxyaniline derivatives. The mechanism is studied through both

Indexed as

[2,3]-rearrangementaminophenolhydroxamic acidN−O bond cleavageselenium

Identifiers

PMID33760338
PMCPMC8252732

What OpenQuestion holds

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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.