Evidence map›Paper›PMID 25146415›Full record

ArticleOrganic letters2014

Cobalt-catalyzed direct carbonylation of aminoquinoline benzamides.

Liene Grigorjeva, Olafs Daugulis

Abstract read
In one paragraph

Article in Organic letters, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing 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

23 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. Review
  8. Article
  9. Co-catalyzedRSC advances · 2019
    Article
  10. Article
  11. Article
  12. Aminoquinoline-directed, cobalt-catalyzed carbonylation of sulfonamide spChemical communications (Cambridge, England) · 2017
    Article
  13. 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

2 authors.

Liene GrigorjevaDepartment of Chemistry, University of Houston , Houston, Texas 77204-5003, United States.
Olafs Daugulis

Funding

New Methods for Direct Carbon-Hydrogen Bond FunctionalizationR01GM077635 · NIGMS · UNIVERSITY OF HOUSTON · PI DAUGULIS, OLAFS · 2007 to 2020
$3.6M
NIGMS NIH HHS R01 GM077635NIGMS NIH HHS R01GM077635
6 · The paper itself

Abstract

A method for direct carbonylation of aminoquinoline benzamides has been developed. Reactions proceed at room temperature in trifluoroethanol solvent, use oxygen from air as an oxidant, and require Mn(OAc)3 as a cocatalyst. Benzoic and acrylic acid derivatives can be carbonylated by carbon monoxide affording imides in good yields. Halogen, nitro, ether, cyano, and ester functional groups are tolerated. The directing group can be removed under mild conditions affording phthalimides.

Indexed as

AminoquinolinesBenzamidesCatalysisCobaltMolecular StructureOxidation-ReductionPhthalimidesAminoquinolinesBenzamidesCobaltPhthalimides

Identifiers

PMID25146415
PMCPMC4156261

What OpenQuestion holds

Textmetadata
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.