Regioselective Carbosilylation of Allenes by Supported Au Catalysts
This manuscript reports the development of supported Au nanoparticle catalysts that promote the regioselective carbosilylation of allenes. Single-electron transfer catalysis of Au nanoparticles enabled the generation of silyl and alkyl radicals from disilanes and redox-active esters, respectively. These radicals were selectively delivered to the β- and γ-positions of the carbonyl group in allenoates, affording the corresponding vinylsilanes. Notably, alkyl acetates could also serve as alkylating agents in the Au-catalyzed carbosilylation, providing access to a broad range of multifunctionalized vinylsilanes. Detailed mechanistic studies revealed that the reaction involves the generation of silyl radicals and alkyl radicals, which enabled this unprecedented regioselectivity. In addition, the high reusability and air tolerance of the supported Au catalysts highlight their potential for practical and sustainable synthetic applications.
Authors
- Hiroki Miura (ORCID: https://orcid.org/0000-0002-2488-4432)
- Tetsuya Shishido (ORCID: https://orcid.org/0000-0002-8475-4226)
- Yoshinori Sato (ORCID: https://orcid.org/0000-0002-2862-7708)
- Kaede Ameyama
Institutions
- Institute for Molecular Science (JP)
- Tokyo Metropolitan University (JP)
Publication Details
- Journal
- The Journal of Organic Chemistry
- Published
- 2025-10-21
- DOI
- https://doi.org/10.1021/acs.joc.5c01882
- Primary Topic
- Organoboron and organosilicon chemistry
- Type
- article
- Field-Weighted Citation Impact
- 0.00