Evidence map›Paper›PMID 36447519›Full record

ArticleBeilstein journal of organic chemistry2022

An alternative C-P cross-coupling route for the synthesis of novel V-shaped aryldiphosphonic acids.

Stephen J I Shearan, Enrico Andreoli, Marco Taddei

Open access · diamondAbstract read
In one paragraph

Article in Beilstein journal of organic chemistry, 2022. 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
0.4field-weighted citation impact, top 44% 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, 4 citations in OpenAlex.

  1. Article
  2. Organophosphorus chemistry: from model to application.Beilstein journal of organic chemistry · 2023
    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 at 2 institutions in 2 countries.

Stephen J I ShearanEnergy Safety Research Institute, Swansea University, Fabian Way, Crymlyn Burrows, Skewen, Swansea SA1 8EN, UK.ORCID https://orcid.org/0000-0002-0605-016X
Enrico AndreoliEnergy Safety Research Institute, Swansea University, Fabian Way, Crymlyn Burrows, Skewen, Swansea SA1 8EN, UK.
Marco TaddeiEnergy Safety Research Institute, Swansea University, Fabian Way, Crymlyn Burrows, Skewen, Swansea SA1 8EN, UK.ORCID https://orcid.org/0000-0003-2805-6375
Swansea University · GBUniversity of Pisa · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The synthesis of phosphonate esters is a topic of interest for various fields, including the preparation of phosphonic acids to be employed as organic linkers for the construction of metal phosphonate materials. We report an alternative method that requires no solvent and involves a different order of addition of reactants to perform the transition-metal-catalyzed C-P cross-coupling reaction, often referred to as the Tavs reaction, employing NiCl

Indexed as

arylphosphonic acidscross-coupling reactionphosphonate esterstransition-metal catalysis

Identifiers

PMID36447519
PMCPMC9663968
OpenAlexW4308438525

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.