Evidence map›Paper›PMID 41214752›Full record

ArticleBMC research notes2025

A three-step, one-pot strategy to unsymmetrical 1,1-diarylalkenes.

Vijayaragavan Elumalai, Hanna Bähr, Karoline Nordli, Stian R Martinsen, Cole Funk, Jørn H Hansen

Abstract read
In one paragraph

Article in BMC research notes, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

6 authors.

Vijayaragavan ElumalaiDepartment of Chemistry, UiT The Arctic University of Norway, Chemical Synthesis and Analysis Group, 9037, Tromsø, Norway.
Hanna BährDepartment of Chemistry, UiT The Arctic University of Norway, Chemical Synthesis and Analysis Group, 9037, Tromsø, Norway.
Karoline NordliDepartment of Chemistry, UiT The Arctic University of Norway, Chemical Synthesis and Analysis Group, 9037, Tromsø, Norway.
Stian R MartinsenDepartment of Chemistry, UiT The Arctic University of Norway, Chemical Synthesis and Analysis Group, 9037, Tromsø, Norway.
Cole FunkDepartment of Chemistry, UiT The Arctic University of Norway, Chemical Synthesis and Analysis Group, 9037, Tromsø, Norway.
Jørn H HansenDepartment of Chemistry, UiT The Arctic University of Norway, Chemical Synthesis and Analysis Group, 9037, Tromsø, Norway. jorn.h.hansen@uit.no.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveDevelop a one-pot, three-step procedure for effective access to diverse unsymmetrical 1,1-diarylalkenes from readily accessible reagents, catalysts and substrates.

resultsA three-step, one-pot procedure for the synthesis of unsymmetrical 1,1-diarylalkenes via a dibromination-elimination-Suzuki Miyaura coupling sequence has been designed and a range of reaction conditions have been screened. Although high selectivities can be achieved in some cases, the overall reaction typically proceeds in low to moderate isolated yields albeit up to 70% was observed. The reaction is compatible with a range of substituent patterns on the arylboronic acid and different styrenes.

Indexed as

AlkenesBoronic AcidsCatalysisAlkenesBoronic Acids1,1-DiarylalkenesDibrominationOne-pot procedureSuzuki-Miyaura coupling

Identifiers

PMID41214752
PMCPMC12604287

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.