Evidence map›Paper›PMID 34476053›Full record

ReviewChemical science2021

Expanding organofluorine chemical space: the design of chiral fluorinated isosteres enabled by I(i)/I(iii) catalysis.

Stephanie Meyer, Joel Häfliger, Ryan Gilmour

Abstract readReview
In one paragraph

Review in Chemical science, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing 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

21 citing papers in PubMed.

  1. Direct Regioselective para-Fluorination via I(I)/I(III) Catalysis.Angewandte Chemie (International ed. in English) · 2026
    Article
  2. Organic chemistry frontiers : an international journal of organic chemistry · 2026
    Article
  3. Article
  4. Article
  5. Privileged Chiral Photocatalysts.Angewandte Chemie (International ed. in English) · 2025
    Review
  6. Article
  7. Conformational Analysis of 1,3-Difluorinated Alkanes.The Journal of organic chemistry · 2024
    Article
  8. Article
  9. Chemical science · 2023
    Article
  10. Enyne difluorination.Nature chemistry · 2023
    Article
  11. Article
  12. Article
  13. Catalytic, Regioselective 1,4-Fluorodifunctionalization of Dienes.Angewandte Chemie (International ed. in English) · 2023
    Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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

3 authors.

Stephanie MeyerOrganisch-Chemisches Institut, Westfälische Wilhelms-Universität Münster Correnstraße 36 48149 Münster Germany ryan.gilmour@uni-muenster.de.
Joel HäfligerOrganisch-Chemisches Institut, Westfälische Wilhelms-Universität Münster Correnstraße 36 48149 Münster Germany ryan.gilmour@uni-muenster.de.
Ryan GilmourOrganisch-Chemisches Institut, Westfälische Wilhelms-Universität Münster Correnstraße 36 48149 Münster Germany ryan.gilmour@uni-muenster.de.ORCID https://orcid.org/0000-0002-3153-6065

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Short aliphatic groups are prevalent in bioactive small molecules and play an essential role in regulating physicochemistry and molecular recognition phenomena. Delineating their biological origins and significance have resulted in landmark developments in synthetic organic chemistry: Arigoni's venerable synthesis of the chiral methyl group is a personal favourite. Whilst radioisotopes allow the steric footprint of the native group to be preserved, this strategy was never intended for therapeutic chemotype development. In contrast, leveraging H → F bioisosterism provides scope to complement the chiral, radioactive bioisostere portfolio and to reach unexplored areas of chiral chemical space for small molecule drug discovery. Accelerated by advances in I(i)/I(iii) catalysis, the current arsenal of achiral 2D and 3D drug discovery modules is rapidly expanding to include chiral units with unprecedented topologies and van der Waals volumes. This

Identifiers

PMID34476053
PMCPMC8372324

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.