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

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.

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Publication Details

Journal
RSC Advances
Published
2025-01-01
DOI
https://doi.org/10.1039/d5ra03165f
Citations
1
Primary Topic
Synthetic Organic Chemistry Methods
Type
article
Field-Weighted Citation Impact
0.94

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

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article

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

Renata Riva, Chiara Lambruschini, Luca Banfi, Alberto Cherubin, Asunción Barbero, Lisa Moni, Lorenzo Palio
article en
1 citations

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.

RSC AdvancesVol. 15(23)
Universidad de Valladolid (ES), University of Genoa (IT)
European Commission, Ministero dell'Università e della Ricerca
Openalex Percentile: Top 25%
Synthetic Organic Chemistry Methods
0.94
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