Evidence map›Paper›PMID 32956584›Full record

ArticleThe Journal of organic chemistry2020

Dyedauxiliary Groups, an Emerging Approach in Organic Chemistry. The Case of Arylazo Sulfones.

Di Qiu, Chang Lian, Jinshan Mao, Maurizio Fagnoni, Stefano Protti

Abstract read
In one paragraph

Article in The Journal of organic chemistry, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Water Effect on the Photochemistry of Arylazo Sulfonates.The Journal of organic chemistry · 2025
    Article
  5. Article
  6. Article
  7. Article
  8. Recent Advances in Light-Induced Selenylation.ACS organic & inorganic Au · 2022
    Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Metal-Free Trifluoromethylthiolation of Arylazo Sulfones.The Journal of organic chemistry · 2021
    Article
  14. 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.

Di QiuTianjin Key Laboratory of Structure and Performance for Functional Molecules, College of Chemistry, Tianjin Normal University, Tianjin 300387, P.R. China.ORCID http://orcid.org/0000-0001-9706-6302
Chang LianTianjin Key Laboratory of Structure and Performance for Functional Molecules, College of Chemistry, Tianjin Normal University, Tianjin 300387, P.R. China.
Jinshan MaoTianjin Key Laboratory of Structure and Performance for Functional Molecules, College of Chemistry, Tianjin Normal University, Tianjin 300387, P.R. China.
Maurizio FagnoniPhotoGreen Lab, Department of Chemistry, University of Pavia, V. Le Taramelli 12, Pavia 27100, Italy.ORCID http://orcid.org/0000-0003-0247-7585
Stefano ProttiPhotoGreen Lab, Department of Chemistry, University of Pavia, V. Le Taramelli 12, Pavia 27100, Italy.ORCID http://orcid.org/0000-0002-5313-5692

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The number of research papers that report photocatalyst-free protocols is currently increasing. Among the different approaches proposed, the conversion of a strong C-X bond of a stable substrate into a photolabile reactive moiety has been recently proposed. In this Synopsis, we introduce the so-dubbed

Identifiers

PMID32956584
PMCPMC8011925

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.