Evidence map›Paper›PMID 36432151›Full record

ArticleMolecules (Basel, Switzerland)2022

Green Synthesis of Spiro Compounds with Potential Anticancer Activity through Knoevenagel/Michael/Cyclization Multicomponent Domino Reactions Organocatalyzed by Ionic Liquid and Microwave-Assisted.

Regina Westphal, Eclair Venturini Filho, Laiza Bruzadelle Loureiro, Cláudio Francisco Tormena, Claudia Pessoa, Celina de Jesus Guimarães, Mariana Palmeira Manso, Rodolfo Goetze Fiorot, Vinicius Rangel Campos, Jackson Antônio Lamounier Camargos Resende and 2 more

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.3field-weighted citation impact, top 21% 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

8 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
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  3. Review
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  5. Article
  6. Review
  7. Synthesis of COF-SOScientific reports · 2023
    Article
  8. 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

12 authors at 6 institutions in 2 countries.

Regina WestphalChemistry Department, Federal University of Espírito Santo, Fernando Ferrari Avenue 514, Vitória 29075-910, ES, Brazil.
Eclair Venturini FilhoChemistry Department, Federal University of Espírito Santo, Fernando Ferrari Avenue 514, Vitória 29075-910, ES, Brazil.
Laiza Bruzadelle LoureiroInstitute of Chemistry, University of Campinas, Josué de Castro Street, Campinas 13083-970, SP, Brazil.
Cláudio Francisco TormenaInstitute of Chemistry, University of Campinas, Josué de Castro Street, Campinas 13083-970, SP, Brazil.
Claudia PessoaDepartment of Physiology and Pharmacology, Faculty of Medicine, Federal University of Ceará, Fortaleza 60430-275, CE, Brazil.
Celina de Jesus GuimarãesDepartment of Physiology and Pharmacology, Faculty of Medicine, Federal University of Ceará, Fortaleza 60430-275, CE, Brazil.ORCID 0000-0001-5244-3522
Mariana Palmeira MansoDepartment of Physiology and Pharmacology, Faculty of Medicine, Federal University of Ceará, Fortaleza 60430-275, CE, Brazil.
Rodolfo Goetze FiorotCampus do Valonguinho, Institute of Chemistry, Fluminense Federal University, Niterói 24020-141, RJ, Brazil.
Vinicius Rangel CamposCampus do Valonguinho, Institute of Chemistry, Fluminense Federal University, Niterói 24020-141, RJ, Brazil.ORCID 0000-0003-3676-5964
Jackson Antônio Lamounier Camargos ResendeExact and Earth Sciences Institute, Federal University of Mato Grosso, Campus Universitário do Araguaia, Pontal do Araguaia 78698-000, MT, Brazil.
Fabrizio MediciChemistry Department, University of Milan, Via Golgi 19, 20133 Milan, Italy.ORCID 0000-0003-1356-7244
Sandro José GrecoChemistry Department, Federal University of Espírito Santo, Fernando Ferrari Avenue 514, Vitória 29075-910, ES, Brazil.ORCID 0000-0003-2382-9295
Universidade Federal do Ceará · BRUniversidade Federal do Espírito Santo · BRUniversidade Estadual de Campinas (UNICAMP) · BRUniversidade Federal Fluminense · BRUniversidade Federal de Mato Grosso · BRUniversity of Milan · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In this work a microwave-assisted Knoevenagel/Michael/cyclization multicomponent domino methodology, using ethanol as solvent and the ionic liquid 1-methylimidazolium chloride as catalyst was developed for the synthesis of spiro compounds. The reaction conditions considered ideal were determined from a methodological study varying solvent, catalyst, amount of catalyst, temperature, and heating mode. Finally, the generality of the methodology was evaluated by exploring the scope of the reaction, varying the starting materials (isatin, malononitrile, and barbituric acid). Overall, the twelve spiro compounds were synthesized in good yields (43-98%) and the X-ray structure of compound

Indexed as

CarcinomaIonic LiquidsSpiro CompoundsCyclizationHumansMicrowavesSolventsIonic LiquidsSolventsSpiro Compoundsanticancer activitydomino reactionionic liquidmulticomponent reactionspiro compound

Identifiers

PMID36432151
PMCPMC9697156
OpenAlexW4309449988

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.