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

IF 4 2区 化学 Q2 CHEMISTRY, APPLIED Advanced Synthesis & Catalysis Pub Date : 2025-03-19 DOI:10.1002/adsc.202500200
Yuntong Hu, Jian Qin, Shengqing Zhu, Lingling Chu
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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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镍催化以异腈为亲核CN源的三氟乙烯酯氰化反应
我们报道了用异丁基叔丁基腈作为亲核CN源镍催化的三氟乙烯酯氰化反应。该反应采用简单的Ni(OTf) 2作为催化剂,无需外源配体或还原剂。该方法能够选择性和有效地获得广泛的环和无环烯基腈,容纳不同的官能团和底物,包括天然产物和药物。
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来源期刊
Advanced Synthesis & Catalysis
Advanced Synthesis & Catalysis 化学-应用化学
CiteScore
9.40
自引率
7.40%
发文量
447
审稿时长
1.8 months
期刊介绍: Advanced Synthesis & Catalysis (ASC) is the leading primary journal in organic, organometallic, and applied chemistry. The high impact of ASC can be attributed to the unique focus of the journal, which publishes exciting new results from academic and industrial labs on efficient, practical, and environmentally friendly organic synthesis. While homogeneous, heterogeneous, organic, and enzyme catalysis are key technologies to achieve green synthesis, significant contributions to the same goal by synthesis design, reaction techniques, flow chemistry, and continuous processing, multiphase catalysis, green solvents, catalyst immobilization, and recycling, separation science, and process development are also featured in ASC. The Aims and Scope can be found in the Notice to Authors or on the first page of the table of contents in every issue.
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