Evidence map›Paper›PMID 37198143›Full record

ArticleChemistryOpen2023

Mechanochemically-Assisted Passerini Reactions: A Practical and Convenient Method for the Synthesis of Novel α-Acyloxycarboxamide Derivatives.

Sodeeq Aderotimi Salami, Justin Bazibuhe Safari, Vincent J Smith, Rui W M Krause

Abstract read
In one paragraph

Article in ChemistryOpen, 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
–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. Review
  2. Article
  3. Article
  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

4 authors.

Sodeeq Aderotimi SalamiCenter for Chemico- and Biomedicinal Research (CCBR) Rhodes University, Grahamstown, Makhanda, 6139, South Africa.ORCID http://orcid.org/0000-0002-8742-8004
Justin Bazibuhe SafariCenter for Chemico- and Biomedicinal Research (CCBR) Rhodes University, Grahamstown, Makhanda, 6139, South Africa.ORCID http://orcid.org/0000-0002-8940-9552
Vincent J SmithCenter for Chemico- and Biomedicinal Research (CCBR) Rhodes University, Grahamstown, Makhanda, 6139, South Africa.ORCID http://orcid.org/0000-0003-3546-3884
Rui W M KrauseCenter for Chemico- and Biomedicinal Research (CCBR) Rhodes University, Grahamstown, Makhanda, 6139, South Africa.ORCID http://orcid.org/0000-0001-6788-6449

Funding

National Department of Health 116109
6 · The paper itself

Abstract

A carboxylic acid, an aldehyde, and an isonitrile were combined in a single step (Passerini reaction) under mechanochemical activation to produce several α-acyloxycarboxamide derivatives in high to excellent yields within 15 min of milling. Mechanochemistry, when combined with the diversity provided by multicomponent reactions, enables the efficient synthesis of the target compounds, with great atom economy, shorter reaction times, and experimental simplicity. The method allows for the rapid production of a vast library of complex compounds from a limited number of substrates.

Indexed as

liquid-assisted grindingmechanochemistryPasserini reactionsilica sulfuric acidα-acyloxycarboxamide

Identifiers

PMID37198143
PMCPMC10191865

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.