Evidence map›Paper›PMID 39407692›Full record

ArticleMolecules (Basel, Switzerland)2024

Base-Catalyzed Reaction of Isatins and (3-Hydroxyprop-1-yn-1-yl)phosphonates as a Tool for the Synthesis of Spiro-1,3-dioxolane Oxindoles with Anticancer and Anti-Platelet Properties.

Arina V Murashkina, Andrei V Bogdanov, Alexandra D Voloshina, Anna P Lyubina, Alexandr V Samorodov, Alexander Y Mitrofanov, Irina P Beletskaya, Elena A Smolyarchuk, Kseniya A Zavadich, Zulfiya A Valiullina and 3 more

Abstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 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

13 authors.

Arina V MurashkinaDepartment of Chemistry, M. V. Lomonosov Moscow State University, 119991 Moscow, Russia.ORCID 0000-0002-4288-8912
Andrei V BogdanovA. M. Butlerov Institute of Chemistry, Kazan Federal University, 420008 Kazan, Russia.
Alexandra D VoloshinaArbuzov Institute of Organic and Physical Chemistry, FRC Kazan Scientific Center, Russian Academy of Sciences, 420088 Kazan, Russia.
Anna P LyubinaArbuzov Institute of Organic and Physical Chemistry, FRC Kazan Scientific Center, Russian Academy of Sciences, 420088 Kazan, Russia.ORCID 0000-0002-2816-8142
Alexandr V SamorodovDepartment of Pharmacology, Bashkir State Medical University, 450008 Ufa, Russia.ORCID 0000-0001-9302-499X
Alexander Y MitrofanovDepartment of Chemistry, M. V. Lomonosov Moscow State University, 119991 Moscow, Russia.ORCID 0000-0003-3141-3599
Irina P BeletskayaDepartment of Chemistry, M. V. Lomonosov Moscow State University, 119991 Moscow, Russia.ORCID 0000-0001-9705-1434
Elena A SmolyarchukThe A.P. Nelyubin Institute of Pharmacy, Sechenov First Moscow State Medical University (Sechenov University), 119571 Moscow, Russia.
Kseniya A ZavadichThe A.P. Nelyubin Institute of Pharmacy, Sechenov First Moscow State Medical University (Sechenov University), 119571 Moscow, Russia.ORCID 0000-0002-4792-7132
Zulfiya A ValiullinaDepartment of Pharmacology, Bashkir State Medical University, 450008 Ufa, Russia.ORCID 0009-0006-9107-0435
Kseniya A NazmievaDepartment of Pharmacology, Bashkir State Medical University, 450008 Ufa, Russia.ORCID 0000-0001-6745-219X
Vladislav I KorunasDepartment of Pharmacology, Bashkir State Medical University, 450008 Ufa, Russia.ORCID 0000-0001-6809-5892
Irina D KrylovaDepartment of Pharmacology, Bashkir State Medical University, 450008 Ufa, Russia.

Funding

Russian Science Foundation 23-25-00144
6 · The paper itself

Abstract

An approach to the synthesis of phosphoryl substituted spiro-1,3-dioxolane oxindoles was developed from the base-catalyzed reaction of various isatins with (3-hydroxyprop-1-yn-1-yl)phosphonates. It was found that various aryl-substituted and N-functionalized isatins with the formation of appropriate products with high yields and stereoselectivity when using

Indexed as

Antineoplastic AgentsIsatinOrganophosphonatesOxindolesPlatelet Aggregation InhibitorsAdolescentAnticoagulantsCatalysisCell DeathCell Line, TumorHumansInhibitory Concentration 50MaleYoung AdultAnticoagulantsAntineoplastic AgentsIsatinOrganophosphonatesOxindolesPlatelet Aggregation Inhibitorsanticoagulantscytotoxicityisatinphosphonatesspiro compoundsstereoselectivity

Identifiers

PMID39407692
PMCPMC11477635

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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.