Evidence map›Paper›PMID 34123160›Full record

ArticleChemical science2020

Selective α,δ-hydrocarboxylation of conjugated dienes utilizing CO

Ahmed M Sheta, Mohammad A Mashaly, Samy B Said, Saad S Elmorsy, Andrei V Malkov, Benjamin R Buckley

Open access · diamondAbstract read
In one paragraph

Article in Chemical science, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
4.3field-weighted citation impact, top 4% 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

16 citing papers in PubMed, 91 citations in OpenAlex.

  1. Article
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  9. Review
  10. Recent Advances in C(spACS organic & inorganic Au · 2022
    Review
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  12. Article
  13. Article
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  15. Electrochemical Dehydrogenative C(spChemistry (Weinheim an der Bergstrasse, Germany) · 2021
    Article
  16. 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

6 authors at 3 institutions in 2 countries.

Ahmed M ShetaDepartment of Chemistry Loughborough University Ashby Road Loughborough Leicestershire LE11 3TU UK b.r.buckley@lboro.ac.uk.ORCID https://orcid.org/0000-0002-9389-6349
Mohammad A MashalyDepartment of Chemistry, Damietta University Damietta El-Gadeeda City, Kafr Saad Damietta Governorate 34511 Egypt.
Samy B SaidDepartment of Chemistry, Damietta University Damietta El-Gadeeda City, Kafr Saad Damietta Governorate 34511 Egypt.
Saad S ElmorsyDepartment of Chemistry, Mansoura University 25 El Gomhouria St Dakahlia Governorate 35516 Egypt.
Andrei V MalkovDepartment of Chemistry Loughborough University Ashby Road Loughborough Leicestershire LE11 3TU UK b.r.buckley@lboro.ac.uk.ORCID https://orcid.org/0000-0001-6072-2353
Benjamin R BuckleyDepartment of Chemistry Loughborough University Ashby Road Loughborough Leicestershire LE11 3TU UK b.r.buckley@lboro.ac.uk.ORCID https://orcid.org/0000-0002-8028-0828
Damietta University · EGLoughborough University · GBMansoura University · EG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

To date the majority of diene carboxylation processes afford the α,δ-dicarboxylated product, the selective mono-carboxylation of dienes is a significant challenge and the major product reported under transition metal catalysis arises from carboxylation at the α-carbon. Herein we report a new electrosynthetic approach, that does not rely on a sacrificial electrode, the reported method allows unprecedented direct access to carboxylic acids derived from dienes at the δ-position. In addition, the α,δ-dicarboxylic acid or the α,δ-reduced alkene can be easily accessed by simple modification of the reaction conditions.

Identifiers

PMID34123160
PMCPMC8163448
OpenAlexW3042899046

What OpenQuestion holds

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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.