Evidence map›Paper›PMID 37638101›Full record

ArticleFrontiers in chemistry2023

Highly efficient morpholine-based organocatalysts for the 1,4-addition reaction between aldehydes and nitroolefins: an unexploited class of catalysts.

Francesco Vaghi, Giorgio Facchetti, Isabella Rimoldi, Matteo Bottiglieri, Alessandro Contini, Maria Luisa Gelmi, Raffaella Bucci

Abstract read
In one paragraph

Article in Frontiers in chemistry, 2023. 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

7 authors.

Francesco VaghiDipartimento di Scienze Farmaceutiche, DISFARM, Sezione Chimica Generale e Organica "A. Marchesini", Università degli Studi di Milano, Milan, Italy.
Giorgio FacchettiDipartimento di Scienze Farmaceutiche, DISFARM, Sezione Chimica Generale e Organica "A. Marchesini", Università degli Studi di Milano, Milan, Italy.
Isabella RimoldiDipartimento di Scienze Farmaceutiche, DISFARM, Sezione Chimica Generale e Organica "A. Marchesini", Università degli Studi di Milano, Milan, Italy.
Matteo BottiglieriDipartimento di Scienze Farmaceutiche, DISFARM, Sezione Chimica Generale e Organica "A. Marchesini", Università degli Studi di Milano, Milan, Italy.
Alessandro ContiniDipartimento di Scienze Farmaceutiche, DISFARM, Sezione Chimica Generale e Organica "A. Marchesini", Università degli Studi di Milano, Milan, Italy.
Maria Luisa GelmiDipartimento di Scienze Farmaceutiche, DISFARM, Sezione Chimica Generale e Organica "A. Marchesini", Università degli Studi di Milano, Milan, Italy.
Raffaella BucciDipartimento di Scienze Farmaceutiche, DISFARM, Sezione Chimica Generale e Organica "A. Marchesini", Università degli Studi di Milano, Milan, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Many studies have demonstrated how the pyrrolidine nucleus is more efficient than the corresponding piperidine or morpholine as organocatalysts in the condensation of aldehydes with electrophiles

Indexed as

enamine catalysisMichael additionmorpholinenon-coded amino acidsorganocatalysisß-amino acids

Identifiers

PMID37638101
PMCPMC10451084

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.