Evidence map›Paper›PMID 35099185›Full record

ArticleOrganic letters2022

Cu(I)-Catalyzed Alkynylation of Quinolones.

Aitor Maestro, Sebastien Lemaire, Syuzanna R Harutyunyan

Abstract read
In one paragraph

Article in Organic letters, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. 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.

Aitor MaestroStratingh Institute for Chemistry, University of Groningen, 9747 AG Groningen,The Netherlands.ORCID 0000-0003-4726-9675
Sebastien LemaireJanssen Pharmaceutica, Chemical Process Research & Development, Turnhoutseweg 30, B-2340 Beerse, Belgium.ORCID 0000-0002-9343-0493
Syuzanna R HarutyunyanStratingh Institute for Chemistry, University of Groningen, 9747 AG Groningen,The Netherlands.ORCID 0000-0003-2411-1250

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Herein we report the first alkynylation of quinolones with terminal alkynes under mild reaction conditions. The reaction is catalyzed by Cu(I) salts in the presence of a Lewis acid, which is essential for the reactivity of the system. The enantioselective version of this transformation has also been explored, and the methodology has been applied in the synthesis of the enantioenriched tetrahydroquinoline alkaloid cuspareine.

Identifiers

PMID35099185
PMCPMC8845045

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.