Ligand -controlled nickel-catalyzed C–O bond cleavage of silyl enol ether for the divergent synthesis of aryl alkenes and silicon-containing product

Silyl enol ethers are easily prepared from available ketones that are widely used as α-carbon nucleophiles in organic synthesis.

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Publication Details

Journal
Organic Chemistry Frontiers
Published
2024-11-27
DOI
https://doi.org/10.1039/d4qo01906g
Citations
1
Primary Topic
Catalytic Cross-Coupling Reactions
Type
article
Field-Weighted Citation Impact
0.25
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article

Ligand -controlled nickel-catalyzed C–O bond cleavage of silyl enol ether for the divergent synthesis of aryl alkenes and silicon-containing product

Yueping Lin, Liangbin Huang, Pei Gu, Changhui Lu et al.
1 citations
Organic Chemistry Frontiers
Catalytic Cross-Coupling Reactions
0.25
article

Ligand -controlled nickel-catalyzed C–O bond cleavage of silyl enol ether for the divergent synthesis of aryl alkenes and silicon-containing product

Yueping Lin, Liangbin Huang, Pei Gu, Changhui Lu, Minyan Wang, Shun-Qin Chang
article en
1 citations

Abstract

Silyl enol ethers are easily prepared from available ketones that are widely used as α-carbon nucleophiles in organic synthesis.

Organic Chemistry FrontiersVol. 12(2)
State Key Laboratory of Pulp and Paper Engineering, Nanjing University (CN), South China University of Technology (CN)
Openalex Percentile: Top 46%
Catalytic Cross-Coupling Reactions
0.25
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