Evidence map›Paper›PMID 41021838›Full record

ArticleChemistry, an Asian journal2025

Cobalt-Catalyzed Decarbonylation of Aromatic Acylsilanes via the Cleavage of Carbon-Silicon Bonds.

Akihisa Matsuura, Ryoichi Tabata, Mamoru Tobisu

Abstract read
In one paragraph

Article in Chemistry, an Asian journal, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

3 authors.

Akihisa MatsuuraDepartment of Applied Chemistry, Graduate School of Engineering, The University of Osaka, Suita, Osaka, 565-0871, Japan.
Ryoichi TabataDepartment of Applied Chemistry, Graduate School of Engineering, The University of Osaka, Suita, Osaka, 565-0871, Japan.
Mamoru TobisuDepartment of Applied Chemistry, Graduate School of Engineering, The University of Osaka, Suita, Osaka, 565-0871, Japan.ORCID https://orcid.org/0000-0002-8415-2225

Funding

Japan Society for the Promotion of Science 24H02207JSPS KAKENHI 24H02207JSPS Research 23KJ1433
6 · The paper itself

Abstract

The catalytic decarbonylation of acylsilanes provides a unique entry to arylsilanes through C─Si bond activation. Here we describe a cobalt-catalyzed protocol that enables this transformation. A range of benzoylsilanes bearing trimethylsilyl, triethylsilyl, or dimethylphenylsilyl groups were converted into the corresponding arylsilanes, while functional groups such as esters, nitriles, ethers, and acetals were tolerated. Control experiments using mixed acylsilanes revealed that the cobalt catalyst operates without generating crossover products, suggesting a pathway distinct from that of rhodium catalysts and mechanistically closer to nickel. Comparative studies further demonstrated that the cobalt system exhibits higher activity than the nickel counterpart. In addition, the method allows post-modification of acylsilane directing groups, as illustrated by the sequential ortho-C─H functionalization and subsequent cobalt-catalyzed decarbonylation.

Indexed as

AcylsilaneCobaltC─Si bond activationDecarbonylationHomogeneous catalysis

Identifiers

PMID41021838
PMCPMC12624382

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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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.