Evidence map›Paper›PMID 36985628›Full record

ReviewMolecules (Basel, Switzerland)2023

Recent Advances in the Synthesis and Applications of m-Aryloxy Phenols.

Dinara Amankulova, Gulzat Berganayeva, Bates Kudaibergenova, Dinara Zhetpisbay, Ayshagul Sharipova, Moldyr Dyusebaeva

Open access · goldAbstract readReview
In one paragraph

Review in Molecules (Basel, Switzerland), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.6field-weighted citation impact, top 39% 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

4 citing papers in PubMed, 4 citations in OpenAlex.

  1. Review
  2. Synthesis and Auxin-like Activity of Halogenated Alkylphenoxyacetic Acids.International journal of molecular sciences · 2026
    Article
  3. Article
  4. Review
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.

Dinara AmankulovaFaculty of Chemistry and Chemical Technology, Al-Farabi Kazakh National University, 71 al-Farabi Ave., 050042 Almaty, Kazakhstan.ORCID 0009-0001-3364-2910
Gulzat BerganayevaFaculty of Chemistry and Chemical Technology, Al-Farabi Kazakh National University, 71 al-Farabi Ave., 050042 Almaty, Kazakhstan.
Bates KudaibergenovaFaculty of Chemistry and Chemical Technology, Al-Farabi Kazakh National University, 71 al-Farabi Ave., 050042 Almaty, Kazakhstan.
Dinara ZhetpisbayDepartment of Biochemistry, Asfendiyarov Kazakh National Medical University, 94 Tole bi Ave., 050012 Almaty, Kazakhstan.
Ayshagul SharipovaChemical and Technological Faculty, Karakalpak Berdah State University, 1 Ch. Abdirov St., Nukus 230100, Uzbekistan.
Moldyr DyusebaevaFaculty of Chemistry and Chemical Technology, Al-Farabi Kazakh National University, 71 al-Farabi Ave., 050042 Almaty, Kazakhstan.
Al-Farabi Kazakh National University · KZKarakalpak State University · UZKazakh National Medical University · KZ

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Since phenol derivatives have high potential as building blocks for the synthesis of bioactive natural products and conducting polymers, many synthesis methods have been invented. In recent years, innovative synthetic methods have been developed for the preparation of m-aryloxy phenols, which has allowed for the preparation of complex m-aryloxy phenols with functional groups, such as esters, nitriles, and halogens, that impart specific properties of these compounds. This review provides an overview of recent advances in synthetic strategies for m-aryloxy phenols and their potential biological activities. This paper highlights the importance of m-aryloxy phenols in various industries, including plastics, adhesives, and coatings, and it discusses their applications as antioxidants, ultraviolet absorbers, and flame retardants.

Indexed as

electrophilic aromatic substitutionshydroxylation of benzenesm-aryloxy phenolsmetal-catalyzed cross-coupling reactionnucleophilic aromatic substitutionspotential biological activities

Identifiers

PMID36985628
PMCPMC10056990
OpenAlexW4324381448

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.