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

Institutions

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

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

α-C−H Alkylation of α-Silyl Alcohols: Hydrogen Atom Transfer Catalysis Preserving Labile C−Si Bonds

Keiichi Hirano, Akira Matsumoto, Chao Wang, Shunsuke Ogura et al.
ACS Catalysis
Radical Photochemical Reactions
article

α-C−H Alkylation of α-Silyl Alcohols: Hydrogen Atom Transfer Catalysis Preserving Labile C−Si Bonds

Keiichi Hirano, Akira Matsumoto, Chao Wang, Shunsuke Ogura, Yuto Arai, Shota Kamasaki
article en

Abstract

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.

ACS Catalysis
Kanazawa University (JP)
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
Openalex Percentile: Top 14%
Radical Photochemical Reactions
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.