Evidence map›Paper›PMID 38313473›Full record

ArticleACS omega2024

A Highly Efficient Strategy for One-Pot and Pseudo-Six-Component Synthesis of Hexahydroquinolines.

Parvin Mohammadikia, Sorour Ramezanpour, Pezhman Shiri, Wim Dehaen, Linde Achten

Abstract read
In one paragraph

Article in ACS omega, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

5 authors.

Parvin MohammadikiaDepartment of Chemistry, K. N. Toosi University of Technology, P.O. Box 15875-4416, Tehran 19697, Iran.
Sorour RamezanpourDepartment of Chemistry, K. N. Toosi University of Technology, P.O. Box 15875-4416, Tehran 19697, Iran.ORCID https://orcid.org/0000-0002-3901-0391
Pezhman ShiriDepartment of Chemistry, K. N. Toosi University of Technology, P.O. Box 15875-4416, Tehran 19697, Iran.
Wim DehaenMolecular Design and Synthesis, Department of Chemistry, KU Leuven, Leuven 3000, Belgium.ORCID https://orcid.org/0000-0002-9597-0629
Linde AchtenMolecular Design and Synthesis, Department of Chemistry, KU Leuven, Leuven 3000, Belgium.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In this study, a homogeneous acid-catalyzed reaction of a series of benzaldehydes, benzylamines, and Meldrum's acid was presented, allowing the novel one-pot and multicomponent synthesis of hexahydroquinolines with high stereoselectivity. The current strategy has advantages including high regioselectivity, good efficiency, reasonable diversity, utilization of an inexpensive and safe catalyst, and easy purification of products by simple recrystallization. The current reaction utilizes 2 equiv of Meldrum's acid, 3 equiv of benzaldehyde derivatives, and one equiv of amine derivatives to yield (4'S,5'S,7'S)-1'-benzyl-2,2-dimethyl-4',5',7'-triphenyl-3',4',7',8'-tetrahydro-1'

Identifiers

PMID38313473
PMCPMC10832005

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Registered trials

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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.