Evidence map›Paper›PMID 25088979›Full record

ArticleAngewandte Chemie (International ed. in English)2014

Simple sulfinate synthesis enables C-H trifluoromethylcyclopropanation.

Ryan Gianatassio, Shuhei Kawamura, Cecil L Eprile, Klement Foo, Jason Ge, Aaron C Burns, Michael R Collins, Phil S Baran

Abstract read
In one paragraph

Article in Angewandte Chemie (International ed. in English), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing 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

35 citing papers in PubMed.

  1. Article
  2. Harnessing COJournal of the American Chemical Society · 2026
    Article
  3. Article
  4. Article
  5. CFJACS Au · 2024
    Article
  6. Article
  7. Alcohol-alcohol cross-coupling enabled by SScience (New York, N.Y.) · 2024
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Review
  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

8 authors.

Ryan GianatassioDepartment of Chemistry, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, CA 92037 (USA).
Shuhei Kawamura
Cecil L Eprile
Klement Foo
Jason Ge
Aaron C Burns
Michael R Collins
Phil S Baran

Funding

Preparative Radical Chemistry for Biomedical ResearchR01GM106210 · NIGMS · SCRIPPS RESEARCH INSTITUTE, THE · PI BARAN, PHIL S · 2013 to 2016
$2.1M
NIGMS NIH HHS GM-106210NIGMS NIH HHS R01 GM106210
6 · The paper itself

Abstract

A simple method to convert readily available carboxylic acids into sulfinate salts by employing an interrupted Barton decarboxylation reaction is reported. A medicinally oriented panel of ten new sulfinate reagents was created using this method, including a key trifluoromethylcyclopropanation reagent, TFCS-Na. The reactivity of six of these salts towards C-H functionalization was field-tested using several different classes of heterocycles.

Indexed as

Acids, HeterocyclicCatalysisModels, MolecularMolecular StructureSulfinic AcidsAcids, HeterocyclicSulfinic Acidsanalogue synthesisbioisosteresCH functionalizationheterocyclessulfinate salts

Identifiers

PMID25088979
PMCPMC4186797

What OpenQuestion holds

Textmetadata
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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.