Evidence map›Paper›PMID 29629128›Full record

ArticleChemical science2018

Direct sulfonylation of anilines mediated by visible light.

Tarn C Johnson, Bryony L Elbert, Alistair J M Farley, Timothy W Gorman, Christophe Genicot, Bénédicte Lallemand, Patrick Pasau, Jakub Flasz, José L Castro, Malcolm MacCoss and 5 more

Abstract read
In one paragraph

Article in Chemical science, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

  1. Article
  2. Red-Light-Driven C(spJournal of the American Chemical Society · 2025
    Article
  3. Article
  4. Article
  5. Article
  6. Determination of Aniline in Soil by ASE/GC-MS.Molecules (Basel, Switzerland) · 2022
    Article
  7. Review
  8. Article
  9. Review
  10. Article
  11. Article
  12. 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

15 authors.

Tarn C JohnsonDepartment of Chemistry , University of Oxford , Chemical Research Laboratory , Mansfield Road , Oxford , OX1 3TA , UK . Email: darren.dixon@chem.ox.ac.uk ; Email: robert.paton@chem.ox.ac.uk ; Email: christopher.schofield@chem.ox.ac.uk ; Email: martin.smith@chem.ox.ac.uk ; Email: michael.willis@chem.ox.ac.uk.
Bryony L ElbertDepartment of Chemistry , University of Oxford , Chemical Research Laboratory , Mansfield Road , Oxford , OX1 3TA , UK . Email: darren.dixon@chem.ox.ac.uk ; Email: robert.paton@chem.ox.ac.uk ; Email: christopher.schofield@chem.ox.ac.uk ; Email: martin.smith@chem.ox.ac.uk ; Email: michael.willis@chem.ox.ac.uk.
Alistair J M FarleyDepartment of Chemistry , University of Oxford , Chemical Research Laboratory , Mansfield Road , Oxford , OX1 3TA , UK . Email: darren.dixon@chem.ox.ac.uk ; Email: robert.paton@chem.ox.ac.uk ; Email: christopher.schofield@chem.ox.ac.uk ; Email: martin.smith@chem.ox.ac.uk ; Email: michael.willis@chem.ox.ac.uk.
Timothy W GormanDepartment of Chemistry , University of Oxford , Chemical Research Laboratory , Mansfield Road , Oxford , OX1 3TA , UK . Email: darren.dixon@chem.ox.ac.uk ; Email: robert.paton@chem.ox.ac.uk ; Email: christopher.schofield@chem.ox.ac.uk ; Email: martin.smith@chem.ox.ac.uk ; Email: michael.willis@chem.ox.ac.uk.
Christophe GenicotGlobal Chemistry , UCB New Medicines , UCB BioPharma sprl , 1420 Braine-L'Alleud , Belgium.
Bénédicte LallemandGlobal Chemistry , UCB New Medicines , UCB BioPharma sprl , 1420 Braine-L'Alleud , Belgium.
Patrick PasauGlobal Chemistry , UCB New Medicines , UCB BioPharma sprl , 1420 Braine-L'Alleud , Belgium.
Jakub FlaszGlobal Chemistry , UCB , 261 Bath Road, Slough , SL1 3WE , UK.
José L CastroGlobal Chemistry , UCB , 261 Bath Road, Slough , SL1 3WE , UK.
Malcolm MacCossBohicket Pharma Consulting LLC , 2556 Seabrook Island Road , Seabrook Island , South Carolina 29455 , USA.
Darren J DixonDepartment of Chemistry , University of Oxford , Chemical Research Laboratory , Mansfield Road , Oxford , OX1 3TA , UK . Email: darren.dixon@chem.ox.ac.uk ; Email: robert.paton@chem.ox.ac.uk ; Email: christopher.schofield@chem.ox.ac.uk ; Email: martin.smith@chem.ox.ac.uk ; Email: michael.willis@chem.ox.ac.uk.ORCID 0000-0003-2456-5236
Robert S PatonDepartment of Chemistry , University of Oxford , Chemical Research Laboratory , Mansfield Road , Oxford , OX1 3TA , UK . Email: darren.dixon@chem.ox.ac.uk ; Email: robert.paton@chem.ox.ac.uk ; Email: christopher.schofield@chem.ox.ac.uk ; Email: martin.smith@chem.ox.ac.uk ; Email: michael.willis@chem.ox.ac.uk.ORCID 0000-0002-0104-4166
Christopher J SchofieldDepartment of Chemistry , University of Oxford , Chemical Research Laboratory , Mansfield Road , Oxford , OX1 3TA , UK . Email: darren.dixon@chem.ox.ac.uk ; Email: robert.paton@chem.ox.ac.uk ; Email: christopher.schofield@chem.ox.ac.uk ; Email: martin.smith@chem.ox.ac.uk ; Email: michael.willis@chem.ox.ac.uk.ORCID 0000-0002-0290-6565
Martin D SmithDepartment of Chemistry , University of Oxford , Chemical Research Laboratory , Mansfield Road , Oxford , OX1 3TA , UK . Email: darren.dixon@chem.ox.ac.uk ; Email: robert.paton@chem.ox.ac.uk ; Email: christopher.schofield@chem.ox.ac.uk ; Email: martin.smith@chem.ox.ac.uk ; Email: michael.willis@chem.ox.ac.uk.ORCID 0000-0002-8849-488X
Michael C WillisDepartment of Chemistry , University of Oxford , Chemical Research Laboratory , Mansfield Road , Oxford , OX1 3TA , UK . Email: darren.dixon@chem.ox.ac.uk ; Email: robert.paton@chem.ox.ac.uk ; Email: christopher.schofield@chem.ox.ac.uk ; Email: martin.smith@chem.ox.ac.uk ; Email: michael.willis@chem.ox.ac.uk.ORCID 0000-0002-0636-6471

Funding

Wellcome Trust
6 · The paper itself

Abstract

Sulfones feature prominently in biologically active molecules and are key functional groups for organic synthesis. We report a mild, photoredox-catalyzed reaction for sulfonylation of aniline derivatives with sulfinate salts, and demonstrate the utility of the method by the late-stage functionalization of drugs. Key features of the method are the straightforward generation of sulfonyl radicals from bench-stable sulfinate salts and the use of simple aniline derivatives as convenient readily available coupling partners.

Identifiers

PMID29629128
PMCPMC5868301

What OpenQuestion holds

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Read underepoch 390

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.