Evidence map›Paper›PMID 42038273›Full record

ArticleRSC advances2026

Copper-catalyzed one-pot synthesis of isoquinolines

Ali Akbari, Danial Zand Hoseinshahi

Abstract read
In one paragraph

Article in RSC advances, 2026. 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

2 authors.

Ali AkbariDepartment of Chemistry, Faculty of Science, University of Jiroft Jiroft Iran P. O. Box 8767161167 a.akbari@ujiroft.ac.ir +98-344-334-7065 +98-344-334-7061.ORCID https://orcid.org/0000-0002-0891-8620
Danial Zand HoseinshahiDepartment of Chemistry, Faculty of Science, University of Jiroft Jiroft Iran P. O. Box 8767161167 a.akbari@ujiroft.ac.ir +98-344-334-7065 +98-344-334-7061.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A copper-catalyzed multicomponent protocol is described for the synthesis of structurally diverse isoquinolines from readily available phenylacetaldehyde derivatives, benzaldehydes, and ammonia. A commercially available 4 M solution of ammonia in methanol serves as a practical and comparatively benign nitrogen source, avoiding the use of prefunctionalized amine substrates. The transformation proceeds at room temperature

Identifiers

PMID42038273
PMCPMC13108578

What OpenQuestion holds

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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.