Evidence map›Paper›PMID 31398916›Full record

ArticleMolecules (Basel, Switzerland)2019

Green Synthesis of Privileged Benzimidazole Scaffolds Using Active Deep Eutectic Solvent.

Maria Luisa Di Gioia, Roberta Cassano, Paola Costanzo, Natividad Herrera Cano, Loredana Maiuolo, Monica Nardi, Fiore Pasquale Nicoletta, Manuela Oliverio, Antonio Procopio

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
3.8field-weighted citation impact, top 6% 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

18 citing papers in PubMed, 65 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Organic Named Reactions in Green Deep Eutectic Solvents (DESs).Topics in current chemistry (Cham) · 2025
    Review
  5. Review
  6. Article
  7. Article
  8. Review
  9. Review
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. 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

9 authors at 3 institutions in 2 countries.

Maria Luisa Di GioiaDipartimento di Farmacia e Scienze della Salute e della Nutrizione, Dipartimento di Eccellenza L. 232/2016, Edificio Polifunzionale, Università della Calabria, 87036 Rende (CS), Italy. ml.digioia@unical.it.ORCID 0000-0001-5469-5459
Roberta CassanoDipartimento di Farmacia e Scienze della Salute e della Nutrizione, Dipartimento di Eccellenza L. 232/2016, Edificio Polifunzionale, Università della Calabria, 87036 Rende (CS), Italy.ORCID 0000-0001-6980-6799
Paola CostanzoDepartment of Health Sciences, Magna Græcia University, Viale Europa, 88100 Germaneto CZ, Italy. pcostanzo@unicz.it.ORCID 0000-0002-2205-1541
Natividad Herrera CanoICYTAC, CONICET and Universidad Nacional de Córdoba, Facultad de Ciencias Químicas, Departamento. Química Orgánica. Ciudad Universitaria, Bv. Juan Filloy s/n, 5000 Córdoba, Argentina.
Loredana MaiuoloDipartimento di Chimica e Tecnologie Chimiche, Via P. Bucci, cubo 12C, Università della Calabria, 87036 Rende (CS), Italy.
Monica NardiDepartment of Health Sciences, Magna Græcia University, Viale Europa, 88100 Germaneto CZ, Italy.ORCID 0000-0001-6617-9320
Fiore Pasquale NicolettaDipartimento di Farmacia e Scienze della Salute e della Nutrizione, Dipartimento di Eccellenza L. 232/2016, Edificio Polifunzionale, Università della Calabria, 87036 Rende (CS), Italy.
Manuela OliverioDepartment of Health Sciences, Magna Græcia University, Viale Europa, 88100 Germaneto CZ, Italy.ORCID 0000-0002-1918-5813
Antonio ProcopioDepartment of Health Sciences, Magna Græcia University, Viale Europa, 88100 Germaneto CZ, Italy.
Magna Graecia University · ITUniversity of Calabria · ITConsejo Nacional de Investigaciones Científicas y Técnicas · AR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The exploitation and use of alternative synthetic methods, in the face of classical procedures that do not conform to the ethics of green chemistry, represent an ever-present problem in the pharmaceutical industry. The procedures for the synthesis of benzimidazoles have become a focus in synthetic organic chemistry, as they are building blocks of strong interest for the development of compounds with pharmacological activity. Various benzimidazole derivatives exhibit important activities such as antimicrobial, antiviral, anti-inflammatory, and analgesic activities, and some of the already synthesized compounds have found very strong applications in medicine praxis. Here we report a selective and sustainable method for the synthesis of 1,2-disubstituted or 2-substituted benzimidazoles, starting from

Indexed as

Green Chemistry TechnologyBenzimidazolesMolecular StructureSolventsSpectrum AnalysisbenzimidazoleBenzimidazolesSolventsaromatic aminesbenzimidazolesdeep eutectic solventsgreen chemistryheterocyclic moiety

Identifiers

PMID31398916
PMCPMC6719900
OpenAlexW2964011798

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.