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镍催化 Zn(CN) 对未活化的烷基磺酸盐的氰化作用。

Nickel-Catalyzed Cyanation of Unactivated Alkyl Sulfonates with Zn(CN).

机构信息

State Key Laboratory of Organometallic Chemistry, Center for Excellence in Molecular Synthesis, Shanghai Institute of Organic Chemistry, University of Chinese Academy of Sciences, Chinese Academy of Sciences, 345 Lingling Lu, Shanghai 200032, People's Republic of China.

出版信息

Org Lett. 2020 Oct 16;22(20):7842-7847. doi: 10.1021/acs.orglett.0c02722. Epub 2020 Oct 2.

Abstract

Cyanation of unactivated primary and secondary alkyl mesylates with Zn(CN) catalyzed by nickel has been developed. The reaction provides an efficient route for the synthesis of alkyl nitriles with wide substrate scope, good functional group tolerance, and compatibility with heterocyclic compounds. Mechanistic studies indicate that alkyl iodide generated in situ serves as the reactive intermediate and the gradual release of alkyl iodide is crucial for the success of the reaction.

摘要

镍催化未活化的伯、仲烷基甲磺酸酯与 Zn(CN) 的氰化反应已经被开发出来。该反应为合成具有广泛底物范围、良好官能团耐受性以及与杂环化合物相容性的烷基腈提供了一种有效的途径。机理研究表明,原位生成的碘化烷基作为反应中间体,碘化烷基的逐渐释放对于反应的成功至关重要。

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