Evidence map›Paper›PMID 35011236›Full record

ArticleMolecules (Basel, Switzerland)2021

Highly Selective Synthesis of 6-Glyoxylamidoquinoline Derivatives via Palladium-Catalyzed Aminocarbonylation.

Sami Chniti, László Kollár, Attila Bényei, Attila Takács

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.3field-weighted citation impact, top 43% of its field
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

2 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. 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

4 authors at 2 institutions in 1 country.

Sami ChnitiDepartment of Inorganic Chemistry, University of Pécs, Ifjúság útja 6, H-7624 Pecs, Hungary.ORCID 0000-0003-2125-0220
László KollárDepartment of Inorganic Chemistry, University of Pécs, Ifjúság útja 6, H-7624 Pecs, Hungary.
Attila BényeiDepartment of Pharmaceutical Chemistry, University of Debrecen, Egyetem tér 1, H-4032 Debrecen, Hungary.ORCID 0000-0002-0617-6264
Attila TakácsDepartment of Inorganic Chemistry, University of Pécs, Ifjúság útja 6, H-7624 Pecs, Hungary.ORCID 0000-0003-2773-8788
University of Pecs · HUUniversity of Debrecen · HU

Funding

European Union, co-financed by the European Social Fund Grant EFOP-3.6.1.-16-2016-00004National Research, Development, and Innovation Office 2020-4.1.1-TKP2020National Research, Development, and Innovation Office PD-132403
6 · The paper itself

Abstract

The aminocarbonylation of 6-iodoquinoline has been investigated in the presence of large series of amine nucleophiles, providing an efficient synthetic route for producing various quinoline-6-carboxamide and quinoline-6-glyoxylamide derivatives. It was shown, after detailed optimization study, that the formation of amides and ketoamides is strongly influenced by the reaction conditions. Performing the reactions at 40 bar of carbon monoxide pressure in the presence of Pd(OAc)

Indexed as

6-iodoquinolineaminocarbonylationcarbon monoxidedouble carbonylationpalladium

Identifiers

PMID35011236
PMCPMC8746719
OpenAlexW4200483554

What OpenQuestion holds

Textmetadata
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.