Evidence map›Paper›PMID 35480011›Full record

ArticleRSC advances2021

Evaluation of P-bridged biaryl phosphine ligands in palladium-catalysed Suzuki-Miyaura cross-coupling reactions.

Jairus L Lamola, Paseka T Moshapo, Cedric W Holzapfel, Munaka Christopher Maumela

Abstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in RSC advances, 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
–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. 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.

Jairus L LamolaResearch Centre for Synthesis and Catalysis, Department of Chemical Sciences University of Johannesburg, Kingsway Campus Auckland Park 2006 South Africa chris.maumela@sasol.com.ORCID https://orcid.org/0000-0002-7633-3966
Paseka T MoshapoResearch Centre for Synthesis and Catalysis, Department of Chemical Sciences University of Johannesburg, Kingsway Campus Auckland Park 2006 South Africa chris.maumela@sasol.com.
Cedric W HolzapfelResearch Centre for Synthesis and Catalysis, Department of Chemical Sciences University of Johannesburg, Kingsway Campus Auckland Park 2006 South Africa chris.maumela@sasol.com.
Munaka Christopher MaumelaResearch Centre for Synthesis and Catalysis, Department of Chemical Sciences University of Johannesburg, Kingsway Campus Auckland Park 2006 South Africa chris.maumela@sasol.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A family of biaryl phosphacyclic ligands derived from phobane and phosphatrioxa-adamantane frameworks is described. The rigid biaryl phosphacycles are efficient for Suzuki-Miyaura cross-coupling of aryl bromides and chlorides. In particular, coupling reactions of the challenging sterically hindered and heterocyclic substrates were viable at room temperature.

Identifiers

PMID35480011
PMCPMC9037619

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.