Evidence map›Paper›PMID 38638215›Full record

ArticleChemical science2024

From propenolysis to enyne metathesis: tools for expedited assembly of 4

Federica Rulli, Guillem Sanz-Liarte, Pol Roca, Nina Martínez, Víctor Medina, Raimon Puig de la Bellacasa, Alexandr Shafir, Ana B Cuenca

Abstract read
In one paragraph

Article in Chemical science, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Article
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

8 authors.

Federica RulliBISi-Bonds/CRISOL Group, Dept. 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/0000-0001-8450-3294
Guillem Sanz-LiarteBISi-Bonds Group, Dept. Química Biológica. 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
Pol RocaBISi-Bonds Group, Dept. Química Biológica. Institut de Química Avançada de Catalunya, IQAC-CSIC C/Jordi Girona 20 08034 Barcelona Spain alexandr.shafir@iqac.csic.es.
Nina MartínezBISi-Bonds/CRISOL Group, Dept. of Organic and Pharmaceutical Chemistry. Institut Químic de Sarrià, Universitat Ramon Llull Vía Augusta 390 08017 Barcelona Spain anabelen.cuenca@iqs.url.edu.
Víctor MedinaBISi-Bonds Group, Dept. Química Biológica. Institut de Química Avançada de Catalunya, IQAC-CSIC C/Jordi Girona 20 08034 Barcelona Spain alexandr.shafir@iqac.csic.es.
Raimon Puig de la BellacasaBISi-Bonds/CRISOL Group, Dept. 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/0000-0001-8349-4082
Alexandr ShafirBISi-Bonds Group, Dept. Química Biológica. 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
Ana B CuencaBISi-Bonds/CRISOL Group, Dept. 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

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The synthesis of BN-containing molecules, which have an interesting isosteric relationship to their parent all-C cores, has drawn a great deal of attention as an avenue to alter and tune molecular function. Nevertheless, many cores with embedded BN are still hard to synthesize, and thus, further effort is required in this direction. Herein, we present an integrated approach to BN-containing polycycles rooted in an exceptionally clean B-N condensation of amines with a tri-allylborane. Having released propene as the only byproduct, the resulting BN precursors are seamlessly telescoped into BN-containing polycyclic cores

Identifiers

PMID38638215
PMCPMC11023045

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.