Evidence map›Paper›PMID 42234543›Full record

ArticleOrganic letters2026

Selective Copper-Catalyzed Cross-Coupling of Cyclopropyl and Cyclobutyl 1,2-Bis(boronates).

Marina Velado, Javier Teresa, Roberto Fernández de la Pradilla, Alma Viso, Mariola Tortosa

Abstract read
In one paragraph

Article in Organic letters, 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

5 authors.

Marina VeladoInstituto de Química Orgánica General (IQOG), CSIC, Juan de la Cierva 3, 28006 Madrid, Spain.
Javier TeresaOrganic Chemistry Department, Universidad Autónoma de Madrid (UAM), 28049 Madrid, Spain.ORCID 0000-0002-7305-0530
Roberto Fernández de la PradillaInstituto de Química Orgánica General (IQOG), CSIC, Juan de la Cierva 3, 28006 Madrid, Spain.
Alma VisoInstituto de Química Orgánica General (IQOG), CSIC, Juan de la Cierva 3, 28006 Madrid, Spain.ORCID 0000-0003-2622-4777
Mariola TortosaOrganic Chemistry Department, Universidad Autónoma de Madrid (UAM), 28049 Madrid, Spain.ORCID 0000-0002-5107-0549

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Herein we disclose an approach to perform the selective copper-catalyzed cross-coupling of 1,2-diborylcyclopropanes and cyclobutanes with different electrophiles. In the case of 1,2-diborylcyclopropanes, a simple alkoxide base was needed to promote the cross-coupling with either allyl halides, propargyl halides, alkynyl halides, or electrophilic amines, which highlights the special reactivity of these diboron compounds. In the case of 1,2-diborylspirocyclobutanes, a site-selective activation of the less hindered boron was observed. Further functionalization of the remaining boryl moiety provides access to highly functionalized stereodefined cyclopropanes and spirocyclobutanes.

Identifiers

PMID42234543
PMCPMC13270634

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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.