Evidence map›Paper›PMID 40453118›Full record

ArticleRSC advances2025

Multicomponent Hosomi-Sakurai reaction on chiral, bio-based, alcohols.

Chiara Lambruschini, Asunción Barbero, Alberto Cherubin, Lisa Moni, Lorenzo Palio, Renata Riva, Luca Banfi

Abstract read
In one paragraph

Article in RSC advances, 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

7 authors.

Chiara LambruschiniDepartment of Chemistry and Industrial Chemistry, University of Genova via Dodecaneso 31 16146 Genova Italy chiara.lambruschini@unige.it luca.banfi@unige.it.ORCID https://orcid.org/0000-0003-1447-2650
Asunción BarberoDepartment of Organic Chemistry, University of Valladolid Paseo de Belen, 7 Valladolid 47011 Spain.
Alberto CherubinDepartment of Chemistry and Industrial Chemistry, University of Genova via Dodecaneso 31 16146 Genova Italy chiara.lambruschini@unige.it luca.banfi@unige.it.
Lisa MoniDepartment of Chemistry and Industrial Chemistry, University of Genova via Dodecaneso 31 16146 Genova Italy chiara.lambruschini@unige.it luca.banfi@unige.it.ORCID https://orcid.org/0000-0001-5149-2963
Lorenzo PalioDepartment of Chemistry and Industrial Chemistry, University of Genova via Dodecaneso 31 16146 Genova Italy chiara.lambruschini@unige.it luca.banfi@unige.it.
Renata RivaDepartment of Chemistry and Industrial Chemistry, University of Genova via Dodecaneso 31 16146 Genova Italy chiara.lambruschini@unige.it luca.banfi@unige.it.ORCID https://orcid.org/0000-0002-0829-9444
Luca BanfiDepartment of Chemistry and Industrial Chemistry, University of Genova via Dodecaneso 31 16146 Genova Italy chiara.lambruschini@unige.it luca.banfi@unige.it.ORCID https://orcid.org/0000-0001-7605-0993

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The multicomponent Hosomi-Sakurai reaction, which gives homoallyl ethers from aldehydes, trimethylsilyl ethers and allyltrimethylsilane, was thoroughly studied using a bio-based aldehyde (protected 5-(hydroxymethyl)tetrahydrofuran-2-carboxyaldehyde) along with trimethylsilyl ethers derived from a variety of (mainly bio-based) alcohols. For comparison, a reactive aromatic aldehyde was also employed. These studies helped to identify the optimal conditions for each aldehyde and provided insight into the scope and limitations of this relatively underexplored multicomponent reaction, one of the few that can incorporate alcohols as diversity inputs.

Identifiers

PMID40453118
PMCPMC12120932

What OpenQuestion holds

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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.