Evidence map›Paper›PMID 38711590›Full record

ArticleBeilstein journal of organic chemistry2024

Synthesis and properties of 6-alkynyl-5-aryluracils.

Ruben Manuel Figueira de Abreu, Till Brockmann, Alexander Villinger, Peter Ehlers, Peter Langer

Abstract read
In one paragraph

Article in Beilstein journal of organic chemistry, 2024. 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
–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

2 citing papers in PubMed.

  1. Synthesis of pyrrolo[3,2-Beilstein journal of organic chemistry · 2025
    Article
  2. Synthesis of benzo[Beilstein journal of organic chemistry · 2024
    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

5 authors.

Ruben Manuel Figueira de AbreuUniversität Rostock, Institut für Chemie, A.-Einstein-Str.3a, 18059 Rostock, Germany.
Till BrockmannUniversität Rostock, Institut für Chemie, A.-Einstein-Str.3a, 18059 Rostock, Germany.
Alexander VillingerUniversität Rostock, Institut für Chemie, A.-Einstein-Str.3a, 18059 Rostock, Germany.ORCID https://orcid.org/0000-0002-0868-9987
Peter EhlersUniversität Rostock, Institut für Chemie, A.-Einstein-Str.3a, 18059 Rostock, Germany.ORCID https://orcid.org/0000-0001-6444-7563
Peter LangerUniversität Rostock, Institut für Chemie, A.-Einstein-Str.3a, 18059 Rostock, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The development of a new and straightforward chemoselective method for the synthesis of uracil-based structures by combining Suzuki-Miyaura and Sonogashira-Hagihara cross-coupling is reported. The methodology was applied to synthesize a series of novel compounds. The tolerance of the combination of different functional groups was tested. The influence of different functional groups on the physical properties was studied by ultraviolet-visible (UV-vis) and fluorescence spectroscopy, providing new insights into the potential applications of uracil-based structures.

Indexed as

catalysiscross-couplingfluorescenceheterocyclesregioselectivity

Identifiers

PMID38711590
PMCPMC11070962

What OpenQuestion holds

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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.