Evidence map›Paper›PMID 40696877›Full record

ArticleThe Journal of organic chemistry2025

One-Pot Metal-Free Synthesis of Diarylamines from Aromatic Aldehydes and Anilines.

Piotr Szcześniak, Bartłomiej Furman

Abstract read
In one paragraph

Article in The Journal of organic chemistry, 2025. 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.

Piotr SzcześniakInstitute of Organic Chemistry, Polish Academy of Sciences, Kasprzaka 44/52, 01-224 Warsaw, Poland.ORCID 0000-0001-7144-3405
Bartłomiej FurmanInstitute of Organic Chemistry, Polish Academy of Sciences, Kasprzaka 44/52, 01-224 Warsaw, Poland.ORCID 0000-0001-5459-8026

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A novel and environmentally friendly method has been developed for the synthesis of a broad range of diarylamines from inexpensive and readily available starting materials, such as aromatic aldehydes and amines. The process follows a one-pot strategy in which imine formation is succeeded by an oxidative rearrangement analogous to the Meinwald reaction and concludes with a light-induced deformylation step. This efficient transformation proceeds in a single vessel with a high atom economy under mild, metal-free conditions. The methodology was further demonstrated as a key step in the synthesis of phentolamine, a reversible, nonselective α-adrenergic blocker used in the treatment of hypertensive emergencies.

Identifiers

PMID40696877
PMCPMC12442086

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.