Evidence map›Paper›PMID 37614524›Full record

ArticleACS catalysis2023

Mechanism of Cu-Catalyzed Iododeboronation: A Description of Ligand-Enabled Transmetalation, Disproportionation, and Turnover in Cu-Mediated Oxidative Coupling Reactions.

Matthew J Andrews, Ambre Carpentier, Alexandra M Z Slawin, David B Cordes, Stuart A Macgregor, Allan J B Watson

Abstract read
In one paragraph

Article in ACS catalysis, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Article
  2. High-Yield Room-Temperature ArylACS organic & inorganic Au · 2026
    Article
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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

6 authors.

Matthew J AndrewsEaStCHEM, School of Chemistry, University of St Andrews, Purdie Building, St Andrews KY16 9ST, U.K.
Ambre CarpentierInstitute of Chemical Sciences, Heriot-Watt University, Edinburgh EH14 4AS, U.K.ORCID https://orcid.org/0000-0001-9507-0463
Alexandra M Z SlawinEaStCHEM, School of Chemistry, University of St Andrews, Purdie Building, St Andrews KY16 9ST, U.K.ORCID https://orcid.org/0000-0002-9527-6418
David B CordesEaStCHEM, School of Chemistry, University of St Andrews, Purdie Building, St Andrews KY16 9ST, U.K.ORCID https://orcid.org/0000-0002-5366-9168
Stuart A MacgregorInstitute of Chemical Sciences, Heriot-Watt University, Edinburgh EH14 4AS, U.K.ORCID https://orcid.org/0000-0003-3454-6776
Allan J B WatsonEaStCHEM, School of Chemistry, University of St Andrews, Purdie Building, St Andrews KY16 9ST, U.K.ORCID https://orcid.org/0000-0002-1582-4286

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We report a combined experimental and computational study of the mechanism of the Cu-catalyzed arylboronic acid iododeboronation reaction. A combination of structural and density functional theory (DFT) analyses has allowed determination of the identity of the reaction precatalyst with insight into each step of the catalytic cycle. Key findings include a rationale for ligand (phen) stoichiometry related to key turnover events-the ligand facilitates transmetalation via H-bonding to an organoboron boronate generated in situ and phen loss/gain is integral to the key oxidative events. These data provide a framework for understanding ligand effects on these key mechanistic processes, which underpin several classes of Cu-mediated oxidative coupling reactions.

Identifiers

PMID37614524
PMCPMC10442916

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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.