Evidence map›Paper›PMID 36704615›Full record

ArticleFrontiers in chemistry2022

Novel pH-sensitive catechol dyes synthesised by a three component one-pot reaction.

Juan José Calmels, Leandro Aguilar, Juan Mancebo-Aracil, Gabriel Radivoy, Claudia Domini, Mariano Garrido, Miguel D Sánchez, Fabiana Nador

Abstract read
In one paragraph

Article in Frontiers in chemistry, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

8 authors.

Juan José CalmelsInstituto de Química del Sur (INQUISUR-CONICET)-Grupo de Nanocatálisis y Síntesis Orgánica del Sur Departamento de Química, Universidad Nacional del Sur (UNS), Bahía Blanca, Buenos Aires, Argentina.
Leandro AguilarInstituto de Química del Sur (INQUISUR-CONICET)-Grupo de Nanocatálisis y Síntesis Orgánica del Sur Departamento de Química, Universidad Nacional del Sur (UNS), Bahía Blanca, Buenos Aires, Argentina.
Juan Mancebo-AracilInstituto de Química del Sur (INQUISUR-CONICET)-Grupo de Nanocatálisis y Síntesis Orgánica del Sur Departamento de Química, Universidad Nacional del Sur (UNS), Bahía Blanca, Buenos Aires, Argentina.
Gabriel RadivoyInstituto de Química del Sur (INQUISUR-CONICET)-Grupo de Nanocatálisis y Síntesis Orgánica del Sur Departamento de Química, Universidad Nacional del Sur (UNS), Bahía Blanca, Buenos Aires, Argentina.
Claudia DominiInstituto de Química del Sur (INQUISUR-CONICET), Departamento de Química, Universidad Nacional del Sur (UNS), Bahía Blanca, Argentina.
Mariano GarridoInstituto de Química del Sur (INQUISUR-CONICET), Departamento de Química, Universidad Nacional del Sur (UNS), Bahía Blanca, Argentina.
Miguel D SánchezInstituto de Física del Sur (IFISUR-CONICET), Departamento de Física, Universidad Nacional del Sur (UNS), Bahía Blanca, Argentina.
Fabiana NadorInstituto de Química del Sur (INQUISUR-CONICET)-Grupo de Nanocatálisis y Síntesis Orgánica del Sur Departamento de Química, Universidad Nacional del Sur (UNS), Bahía Blanca, Buenos Aires, Argentina.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The synthesis and characterisation of new dyes based on indolizines bearing catechol groups in their structure is presented. The preparation was carried out through a simple three component one-pot reaction promoted by CuNPs/C, between pyridine-2-carbaldehyde, an aromatic alkyne and a tetrahydroisoquinoline (THIQ) functionalized with catechol groups. The products were isolated in 30%-34% yield, which was considered more than acceptable considering that the catechol hydroxyl groups were not protected prior to reaction. In view of the colour developed by the products and their response to the acidic and basic conditions of the medium, product

Indexed as

catecholdyeindolizinenanoparticlespH indicator

Identifiers

PMID36704615
PMCPMC9871305

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.