P‐Directed and Lewis Acid‐Assisted Pd‐Catalyzed Si─Me Bond Activation Enabling Alkyl Exchange at Silicon

ABSTRACT A novel mode of Si─Me bond activation has been unveiled through the cooperative action of a P‐directing group, a palladium catalyst and a Lewis acid. The pivotal role of the Lewis acid in enabling the activation of the strong and low‐polarity Si─Me bond was elucidated via stoichiometric experiments. According to DFT calculations, the Lewis acid acts as a Me − acceptor and triggers the formation of the key cationic silyl Pd complex responsible for the alkyl exchange at Si. This unprecedented Si─Me bond transformation has been demonstrated in a four‐step sequence, enabling the stepwise upgrading of Me 3 SiCl into silanols bearing diverse organic substituents.

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Publication Details

Journal
Angewandte Chemie
Published
2026-08-24
DOI
https://doi.org/10.1002/ange.1850136
Primary Topic
Organoboron and organosilicon chemistry
Type
article
Field-Weighted Citation Impact
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article

P‐Directed and Lewis Acid‐Assisted Pd‐Catalyzed Si─Me Bond Activation Enabling Alkyl Exchange at Silicon

Hajime Kameo, Keitaro Yamanaka, Akihiro Mushiake, Hiroyuki Matsuzaka et al.
Angewandte Chemie
Organoboron and organosilicon chemistry
article

P‐Directed and Lewis Acid‐Assisted Pd‐Catalyzed Si─Me Bond Activation Enabling Alkyl Exchange at Silicon

Hajime Kameo, Keitaro Yamanaka, Akihiro Mushiake, Hiroyuki Matsuzaka, Didier Bourissou, Kanta OISHI
article en

Abstract

ABSTRACT A novel mode of Si─Me bond activation has been unveiled through the cooperative action of a P‐directing group, a palladium catalyst and a Lewis acid. The pivotal role of the Lewis acid in enabling the activation of the strong and low‐polarity Si─Me bond was elucidated via stoichiometric experiments. According to DFT calculations, the Lewis acid acts as a Me − acceptor and triggers the formation of the key cationic silyl Pd complex responsible for the alkyl exchange at Si. This unprecedented Si─Me bond transformation has been demonstrated in a four‐step sequence, enabling the stepwise upgrading of Me 3 SiCl into silanols bearing diverse organic substituents.

Angewandte Chemie
Centre National de la Recherche Scientifique (FR), Laboratoire Hétérochimie Fondamentale et Appliquée (FR), Tokyo Metropolitan University (JP)
Openalex Percentile: Top 18%
Organoboron and organosilicon chemistry
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