Evidence map›Paper›PMID 42356945›Full record

ArticlePolymers2026

Highly Selective Interfacial Route to Eight-Functional Sucrose Methacrylate for Biocompatible Scaffold Fabrication.

Vladislav Kaplin, Nikolay Glagolev, Nikita Minaev, Evgenii Epifanov, Nadezhda Aksenova, Anastasiia Akovantseva, Tatyana Zarkhina, Olga Vasileva, Elena Kiseleva, Marina Zimens and 3 more

Abstract read
In one paragraph

Article in Polymers, 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

13 authors.

Vladislav KaplinSemenov Federal Research Center of Chemical Physics, Russian Academy of Sciences, Moscow 119991, Russia.ORCID 0000-0003-4751-6437
Nikolay GlagolevSemenov Federal Research Center of Chemical Physics, Russian Academy of Sciences, Moscow 119991, Russia.
Nikita MinaevNational Research Centre "Kurchatov Institute", Moscow 123182, Russia.ORCID 0000-0002-9931-0118
Evgenii EpifanovNational Research Centre "Kurchatov Institute", Moscow 123182, Russia.
Nadezhda AksenovaSemenov Federal Research Center of Chemical Physics, Russian Academy of Sciences, Moscow 119991, Russia.ORCID 0000-0003-0527-8899
Anastasiia AkovantsevaSemenov Federal Research Center of Chemical Physics, Russian Academy of Sciences, Moscow 119991, Russia.
Tatyana ZarkhinaSemenov Federal Research Center of Chemical Physics, Russian Academy of Sciences, Moscow 119991, Russia.
Olga VasilevaTranslational Medicine Research Center, Sirius University of Science and Technology, Sochi 354340, Russia.
Elena KiselevaSemenov Federal Research Center of Chemical Physics, Russian Academy of Sciences, Moscow 119991, Russia.
Marina ZimensA.V. Topchiev Institute of Petrochemical Synthesis, Russian Academy of Sciences, Moscow 119991, Russia.
Anastasia KuryanovaSemenov Federal Research Center of Chemical Physics, Russian Academy of Sciences, Moscow 119991, Russia.ORCID 0000-0002-9791-1745
Gulnaz MukhametovaSemenov Federal Research Center of Chemical Physics, Russian Academy of Sciences, Moscow 119991, Russia.
Anna SolovievaSemenov Federal Research Center of Chemical Physics, Russian Academy of Sciences, Moscow 119991, Russia.

Funding

Russian Government assignment 125012200641-2
6 · The paper itself

Abstract

The synthesis of reactive sucrose derivatives is of significant interest for the development of novel biocompatible polymers. In this study, an octa-substituted sucrose derivative containing isocyanate groups was synthesized via a urethane-forming reaction carried out in an aprotic solvent at the phase interface. This approach exhibits high selectivity and provides a target product yield of up to 60%. Subsequently, using the same reaction mechanism, the isocyanate derivative was converted into an octa-functional methacrylate derivative capable of forming three-dimensional cross-linked networks. The structures of both the intermediate and final products were confirmed by IR,

Indexed as

biopolymersucrosetissue engineeringurethane formation

Identifiers

PMID42356945
PMCPMC13306284

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.