Evidence map›Paper›PMID 35873324›Full record

ReviewRSC advances2022

Heterocycles from cyclopropenones.

Ashraf A Aly, Alaa A Hassan, Sara M Mostafa, Asmaa H Mohamed, Esraa M Osman, AbdElAziz A Nayl

Open access · goldAbstract readReview
In one paragraph

Review in RSC advances, 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
2.1field-weighted citation impact, top 13% 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, 22 citations in OpenAlex.

  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

6 authors at 2 institutions in 2 countries.

Ashraf A AlyChemistry Department, Faculty of Science, Minia University El-Minia 61519 Egypt ashrafaly63@yahoo.com ashraf.shehata@mu.edu.eg alaahassan2001@mu.edu.eg sara.ahmed@mu.edu.eg esraamah33@gmail.com asmaa.hamouda@mu.edu.eg.ORCID https://orcid.org/0000-0002-0314-3408
Alaa A HassanChemistry Department, Faculty of Science, Minia University El-Minia 61519 Egypt ashrafaly63@yahoo.com ashraf.shehata@mu.edu.eg alaahassan2001@mu.edu.eg sara.ahmed@mu.edu.eg esraamah33@gmail.com asmaa.hamouda@mu.edu.eg.
Sara M MostafaChemistry Department, Faculty of Science, Minia University El-Minia 61519 Egypt ashrafaly63@yahoo.com ashraf.shehata@mu.edu.eg alaahassan2001@mu.edu.eg sara.ahmed@mu.edu.eg esraamah33@gmail.com asmaa.hamouda@mu.edu.eg.ORCID https://orcid.org/0000-0001-6381-1300
Asmaa H MohamedChemistry Department, Faculty of Science, Minia University El-Minia 61519 Egypt ashrafaly63@yahoo.com ashraf.shehata@mu.edu.eg alaahassan2001@mu.edu.eg sara.ahmed@mu.edu.eg esraamah33@gmail.com asmaa.hamouda@mu.edu.eg.
Esraa M OsmanChemistry Department, Faculty of Science, Minia University El-Minia 61519 Egypt ashrafaly63@yahoo.com ashraf.shehata@mu.edu.eg alaahassan2001@mu.edu.eg sara.ahmed@mu.edu.eg esraamah33@gmail.com asmaa.hamouda@mu.edu.eg.
AbdElAziz A NaylDepartment of Chemistry, College of Science, Jouf University P. O. Box 2014 Sakaka Aljouf Saudi Arabia aanayel@ju.edu.sa aanayl@yahoo.com.
Minia University · EGJouf University · SA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Great attention has been paid to cyclopropenones as they are present in many natural sources. Various synthesized cyclopropenone derivatives also show a wide range of biological activities. The cyclopropenone derivatives undergo a variety of reactions such as ring-opening reactions, isomerization reactions, C-C coupling reactions, C-H activation, cycloaddition reactions, thermal and photo-irradiation reactions, and acid-base-catalyzed reactions under the influence of various chemical reagents (electrophiles, nucleophiles, radicals, and organometallics) and external forces (heat and light). Many previous reviews have dealt with the chemistry and reactions of cyclopropenones. However and to the best of our knowledge, the utility of cyclopropenones in the synthesis of heterocycles has not been reported before. Therefore, it would be interesting to shed light on this new topic. The present review article provides, for the first time, a comprehensive compilation of synthetic methods for the synthesis of various heterocyclic ring systems, as a significant family in the field of organic chemistry.

Identifiers

PMID35873324
PMCPMC9229296
OpenAlexW4285161989

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.