Evidence map›Paper›PMID 33180241›Full record

ReviewMolecular diversity2022

Current advances in the synthetic strategies of 2-arylbenzothiazole.

Ayushi Sethiya, Nusrat Sahiba, Pankaj Teli, Jay Soni, Shikha Agarwal

Abstract readReview
PubMed Publisher
In one paragraph

Review in Molecular diversity, 2022. 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
–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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. 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

5 authors.

Ayushi SethiyaDepartment of Chemistry, Synthetic Organic Chemistry Laboratory, MLSU, Udaipur, 313001, India.ORCID http://orcid.org/0000-0002-9595-221X
Nusrat SahibaDepartment of Chemistry, Synthetic Organic Chemistry Laboratory, MLSU, Udaipur, 313001, India.
Pankaj TeliDepartment of Chemistry, Synthetic Organic Chemistry Laboratory, MLSU, Udaipur, 313001, India.
Jay SoniDepartment of Chemistry, Synthetic Organic Chemistry Laboratory, MLSU, Udaipur, 313001, India.
Shikha AgarwalDepartment of Chemistry, Synthetic Organic Chemistry Laboratory, MLSU, Udaipur, 313001, India. shikhaagarwal@mlsu.ac.in.ORCID http://orcid.org/0000-0003-2946-0409

Funding

Council of Scientific and Industrial Research, India CSIR [file no. 09/172(0088)2018-EMR-I]Council of Scientific and Industrial Research, India file no. 09/172(0099)2019-EMR-I]University Grants Commission 201819-MANF-2018-19-RAJ-91971
6 · The paper itself

Abstract

Benzothiazole is a privileged scaffold in the field of synthetic and medicinal chemistry. Its derivatives and metal complexes possess a gamut of pharmacological properties and high degree of structural diversity that has proven it vital for the investigation for novel therapeutics. The 2nd position of benzothiazole is the most active site that makes 2-arylbenzothiazole as felicitous scaffolds in pharmaceutical chemistry. The extensive significance of benzo-fused heterocyclic moieties formation has led to broad and valuable different approaches for their synthesis. This review deals with the synthetic approaches developed so far for the synthesis of 2-arylbenzothiazoles. Moreover, this article abridges the publications devoted to the synthesis of this moiety over the last 6 years. This study gives a current precis of research on the fabrication of 2-arylbenzothiazoles through different synthetic pathways and shall be helpful for researchers and scientists who are working in this field to make more potent biologically active benzothiazole-based drugs.

Indexed as

Chemistry, Pharmaceutical2-Aminothiophenol2-ArylbenzothiazoleCatalysisCoupling reactionsGreen chemistry

Identifiers

What OpenQuestion holds

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Registered trials

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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.