Evidence map›Paper›PMID 41210287›Full record

ArticleChemical science2025

B-N axis as a facilitating agent for the synthesis of 3D structures: the paradigmatic case of BN-[4.4.4]propellane.

Guillem Sanz-Liarte, Josep Saurí, Pau Nolis, Ana B Cuenca, Alexandr Shafir

Abstract read
In one paragraph

Article in Chemical science, 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

5 authors.

Guillem Sanz-LiarteBISi-Bonds group, Department of Biological Chemistry, Institut de Química Avançada de Catalunya, IQAC-CSIC c/Jordi Girona 20 08034 Barcelona Spain alexandr.shafir@iqac.csic.es.ORCID https://orcid.org/0009-0004-2022-8819
Josep SauríBISi-Bonds/CRISOL group, Department of Organic and Pharmaceutical Chemistry, Institut Químic de Sarrià, Universitat Ramon Llull Vía Augusta 390 08017 Barcelona Spain anabelen.cuenca@iqs.url.edu.ORCID https://orcid.org/0000-0002-2706-2426
Pau NolisServei de Ressonància Magnètica Nuclear, Universitat Autònoma de Barcelona Bellaterra 08193 Barcelona Spain.ORCID https://orcid.org/0000-0003-2360-1709
Ana B CuencaBISi-Bonds/CRISOL group, Department of Organic and Pharmaceutical Chemistry, Institut Químic de Sarrià, Universitat Ramon Llull Vía Augusta 390 08017 Barcelona Spain anabelen.cuenca@iqs.url.edu.ORCID https://orcid.org/0000-0002-6842-1261
Alexandr ShafirBISi-Bonds group, Department of Biological Chemistry, Institut de Química Avançada de Catalunya, IQAC-CSIC c/Jordi Girona 20 08034 Barcelona Spain alexandr.shafir@iqac.csic.es.ORCID https://orcid.org/0000-0002-8127-2299

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Flat aromatic compounds containing a boron-nitrogen (BN) fragment have gained significant attention in the field of organic optoelectronics. Unsurprisingly, therefore, an increasing number of synthetic methodology groups have devoted efforts and creativity to developing new strategies for accessing diverse structures incorporating a B[double bond, length as m-dash]N unit, which is isosteric with the olefinic C[double bond, length as m-dash]C bond. In contrast, the potential of BN isosterism to expand the structural diversity of three-dimensional architectures based on sp

Identifiers

PMID41210287
PMCPMC12593829

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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.