α-C−H Alkylation of α-Silyl Alcohols: Hydrogen Atom Transfer Catalysis Preserving Labile C−Si Bonds
α-Silyl alcohols are organosilicon motifs that serve as precursors to carbanions and carbon-centered radicals for the construction of silicon-containing molecules and complex carbon frameworks. Despite their synthetic utility, facile methods for preparing structurally diverse α-silyl alcohols remain underdeveloped. Herein, we report a photocatalytic strategy for upgrading readily available, structurally simple α-silyl alcohols into functionalized derivatives via hydrogen atom transfer (HAT) catalysis. The use of phosphonium ylide as a highly tunable HAT catalyst, in combination with a visible-light photoredox catalyst, enables selective α-C−H alkylation without cleavage of the labile C−Si bond, providing access to diverse α-silyl alcohols with good functional group compatibility. Furthermore, orthogonal transformations of the C−H, C−O, and C−Si bonds in α-silyl alcohols demonstrate their utility as versatile building blocks.
Authors
- Keiichi Hirano (ORCID: https://orcid.org/0000-0002-2702-9183)
- Akira Matsumoto (ORCID: https://orcid.org/0000-0002-3719-8597)
- Chao Wang (ORCID: https://orcid.org/0000-0002-9165-7758)
- Shunsuke Ogura
- Yuto Arai
- Shota Kamasaki
Institutions
- Kanazawa University (JP)
Publication Details
- Journal
- ACS Catalysis
- Published
- 2026-07-02
- DOI
- https://doi.org/10.1021/acscatal.6c03020
- Primary Topic
- Radical Photochemical Reactions
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Suzuken Memorial Foundation
- Takeda Science Foundation
- Asahi Glass Foundation
- Uehara Memorial Foundation
- Ministry of Education, Culture, Sports, Science and Technology
- Astellas Foundation for Research on Metabolic Disorders
- Japan Society for the Promotion of Science
- Fusion Oriented REsearch for disruptive Science and Technology