Evidence map›Paper›PMID 39931416›Full record

ArticleRSC advances2025

Solvent-free synthesis of bio-based

Antoine Fournier, Jean-Moïse Suisse, Pierre de Frémont, Jacques Andrieu

Abstract read
In one paragraph

Article in RSC advances, 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

4 authors.

Antoine FournierInstitut de Chimie Moléculaire de l'Université de Bourgogne, UMR CNRS 6302, Université de Bourgogne 9 Av. Alain Savary 21078 Dijon France jacques.andrieu@u-bourgogne.fr.ORCID https://orcid.org/0000-0003-1563-9926
Jean-Moïse SuisseInstitut de Chimie Moléculaire de l'Université de Bourgogne, UMR CNRS 6302, Université de Bourgogne 9 Av. Alain Savary 21078 Dijon France jacques.andrieu@u-bourgogne.fr.
Pierre de FrémontInstitut de Chimie Moléculaire de l'Université de Bourgogne, UMR CNRS 6302, Université de Bourgogne 9 Av. Alain Savary 21078 Dijon France jacques.andrieu@u-bourgogne.fr.
Jacques AndrieuInstitut de Chimie Moléculaire de l'Université de Bourgogne, UMR CNRS 6302, Université de Bourgogne 9 Av. Alain Savary 21078 Dijon France jacques.andrieu@u-bourgogne.fr.ORCID https://orcid.org/0000-0003-4278-3915

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Oxazolidinones are five-membered N-heterocycle rings containing a carbamate moiety and are known for their industrial applications as antibiotics, herbicides and electrolytes in Li batteries. Considering the projected ecological transition, they have the potential to be recognized as a green solvent according to the European standards for bio-based solvents, if they can be synthesized

Identifiers

PMID39931416
PMCPMC11808357

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.