Evidence map›Paper›PMID 41599288›Full record

ArticleMolecules (Basel, Switzerland)2026

Synthesis of Hydroxyaromatic Carboxylic Acids via Homogeneous Kolbe-Schmitt Carboxylation of Phenoxides.

Dmitriy A Merzliakov, Michael S Alexeev, Maxim A Topchiy, Dmitry G Yakhvarov, Nikolai Yu Kuznetsov, Anton L Maximov, Irina P Beletskaya

Abstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

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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

7 authors.

Dmitriy A MerzliakovA.V. Topchiev Institute of Petrochemical Synthesis, Russian Academy of Sciences, Leninsky Prospect 29, 119991 Moscow, Russia.ORCID 0000-0002-7116-5772
Michael S AlexeevA.V. Topchiev Institute of Petrochemical Synthesis, Russian Academy of Sciences, Leninsky Prospect 29, 119991 Moscow, Russia.ORCID 0000-0002-5419-3990
Maxim A TopchiyA.V. Topchiev Institute of Petrochemical Synthesis, Russian Academy of Sciences, Leninsky Prospect 29, 119991 Moscow, Russia.ORCID 0000-0002-6604-7034
Dmitry G YakhvarovFederal Research Center Kazan Scientific Center of Russian Academy of Sciences, Lobachevskogo st. 2/31, 420111 Kazan, Russia.ORCID 0000-0002-3906-8841
Nikolai Yu KuznetsovA.V. Topchiev Institute of Petrochemical Synthesis, Russian Academy of Sciences, Leninsky Prospect 29, 119991 Moscow, Russia.ORCID 0000-0003-2702-5366
Anton L MaximovA.V. Topchiev Institute of Petrochemical Synthesis, Russian Academy of Sciences, Leninsky Prospect 29, 119991 Moscow, Russia.ORCID 0000-0001-9297-4950
Irina P BeletskayaA.V. Topchiev Institute of Petrochemical Synthesis, Russian Academy of Sciences, Leninsky Prospect 29, 119991 Moscow, Russia.ORCID 0000-0001-9705-1434

Funding

Ministry of Science and Higher Education of the Russian Federation 075-15-2024-646.
6 · The paper itself

Abstract

Homogeneous Kolbe-Schmitt carboxylation of phenoxides offers a mild and effective alternative to the classical high-temperature solid-phase Kolbe-Schmitt reaction. To develop this into a practical synthetic approach, we investigated several fundamental dependencies, particularly the impact of cations (Na, K, Li, Cs, and Rb), phenoxide concentration, and solvents (DMSO or DMF) on the yield and regioisomeric ratio of hydroxyaromatic carboxylic acids (HACAs). We identified optimal conditions for the effective carboxylation of different phenoxides, including a chiral Ellman's sulfinamide derived from

Indexed as

carboxylationCO2DMFDMSOhydroxyaromatic carboxylic acids (HACA)Kolbe–Schmittphenoxides

Identifiers

PMID41599288
PMCPMC12843966

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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.