Nickel‐Catalyzed Cyanation of Vinyl Triflates with Isonitrile as a Nucleophilic CN Source

Abstract We report a nickel‐catalyzed cyanation of vinyl triflates using tert ‐butyl isonitrile as a nucleophilic CN source. This reaction employs simple Ni(OTf) 2 as the catalyst, operating without exogenous ligands or reductants. The method enables selective and efficient access to a broad range of cyclic and acyclic alkenyl nitriles, accommodating diverse functional groups and substrates, including natural products and pharmaceuticals.

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Publication Details

Journal
Advanced Synthesis & Catalysis
Published
2025-03-19
DOI
https://doi.org/10.1002/adsc.202500200
Citations
1
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
Field-Weighted Citation Impact
0.94
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article

Nickel‐Catalyzed Cyanation of Vinyl Triflates with Isonitrile as a Nucleophilic CN Source

Jian Qin, Lingling Chu, Yuntong Hu, Shengqing Zhu
1 citations
Advanced Synthesis & Catalysis
Catalytic C–H Functionalization Methods
0.94
article

Nickel‐Catalyzed Cyanation of Vinyl Triflates with Isonitrile as a Nucleophilic CN Source

Jian Qin, Lingling Chu, Yuntong Hu, Shengqing Zhu
article en
1 citations

Abstract

Abstract We report a nickel‐catalyzed cyanation of vinyl triflates using tert ‐butyl isonitrile as a nucleophilic CN source. This reaction employs simple Ni(OTf) 2 as the catalyst, operating without exogenous ligands or reductants. The method enables selective and efficient access to a broad range of cyclic and acyclic alkenyl nitriles, accommodating diverse functional groups and substrates, including natural products and pharmaceuticals.

Advanced Synthesis & CatalysisVol. 367(10)
Donghua University (CN)
Openalex Percentile: Top 28%
Catalytic C–H Functionalization Methods
0.94
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