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.
Authors
- Hajime Kameo (ORCID: https://orcid.org/0000-0002-6901-6372)
- Keitaro Yamanaka
- Akihiro Mushiake
- Hiroyuki Matsuzaka (ORCID: https://orcid.org/0000-0001-6494-034X)
- Didier Bourissou (ORCID: https://orcid.org/0000-0002-0249-1769)
- Kanta OISHI
Institutions
- Centre National de la Recherche Scientifique (FR)
- Laboratoire Hétérochimie Fondamentale et Appliquée (FR)
- Tokyo Metropolitan University (JP)
Publication Details
- Journal
- Angewandte Chemie International Edition
- Published
- 2026-08-24
- DOI
- https://doi.org/10.1002/anie.1850136
- Primary Topic
- Organoboron and organosilicon chemistry
- Type
- article
- Field-Weighted Citation Impact
- 0.00