Unsupported Nanoporous Copper Catalyzed Insertion of Carbenes from α‐Diazo Compounds into Hydrosilanes

Abstract The insertion of diazo carbene into Si−H bonds with unsupported nanoporous copper (CuNPore) catalyst has been developed. α‐Aryl diazoesters, diazophosphonates, and unstable aryl diazoalkyls can be used as carbene precursors to exquisitely insert into the Si−H bond of silanes. A variety of α‐silylesters, silylphosphonate, and functionalized arylsilane were obtained in 35–82% yields. The reusability feature of the CuNPore catalyst for this insertion reaction demonstrated its high heterogeneous catalytic activity and practicality. Further, mechanistic studies revealed that the insertion of carbene from diazo compounds into the Si−H bond may include a three‐center concerted transition state on CuNPore.

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Publication Details

Journal
Advanced Synthesis & Catalysis
Published
2024-10-24
DOI
https://doi.org/10.1002/adsc.202401036
Citations
1
Primary Topic
Asymmetric Hydrogenation and Catalysis
Type
article
Field-Weighted Citation Impact
0.16

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article

Unsupported Nanoporous Copper Catalyzed Insertion of Carbenes from α‐Diazo Compounds into Hydrosilanes

Yuhui Zhao, Wanguo Wei, Ruyi Jiang, Xiaojun Zheng et al.
1 citations
Advanced Synthesis & Catalysis
Asymmetric Hydrogenation and Catalysis
0.16
article

Unsupported Nanoporous Copper Catalyzed Insertion of Carbenes from α‐Diazo Compounds into Hydrosilanes

Yuhui Zhao, Wanguo Wei, Ruyi Jiang, Xiaojun Zheng, Cuiping Wang, Tienan Jin
article en
1 citations

Abstract

Abstract The insertion of diazo carbene into Si−H bonds with unsupported nanoporous copper (CuNPore) catalyst has been developed. α‐Aryl diazoesters, diazophosphonates, and unstable aryl diazoalkyls can be used as carbene precursors to exquisitely insert into the Si−H bond of silanes. A variety of α‐silylesters, silylphosphonate, and functionalized arylsilane were obtained in 35–82% yields. The reusability feature of the CuNPore catalyst for this insertion reaction demonstrated its high heterogeneous catalytic activity and practicality. Further, mechanistic studies revealed that the insertion of carbene from diazo compounds into the Si−H bond may include a three‐center concerted transition state on CuNPore.

Advanced Synthesis & CatalysisVol. 367(5)
University of Science and Technology Liaoning (CN), Tohoku University (JP), Educational Department of Liaoning Province (CN), Roche (China) (CN)
National Natural Science Foundation of China
Openalex Percentile: Top 57%
Asymmetric Hydrogenation and Catalysis
0.16
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Unsupported Nanoporous Copper Catalyzed Insertion of Carbenes from α‐Diazo Compounds into Hydrosilanes — Yuhui Zhao, Wanguo Wei, et al. · Advanced Synthesis & Catalysis (2024) | TGRS Research Map | TGRS