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Updated: Jan 20, 2026
Acid-Catalyzed Hydration of Alkynes: Keto-Enol Tautomerism
Ni-Catalyzed deaminative hydroalkylation of internal alkynes
Ze-Fan Zhu1, Jia-Lin Tu, Feng Liu
1Jiangsu Key Laboratory of Neuropsychiatric Diseases and Department of Medicinal Chemistry, College of Pharmaceutical Sciences, Soochow University, 199 Ren-Ai Road, Suzhou, Jiangsu 215123, People's Republic of China. fliu2@suda.edu.cn.
Abstract:
A regioselective cis-hydroalkylation of internal alkynes with readily prepared Katritzky pyridinium salts for the synthesis of tri-substituted alkenes is described. This reaction is the first example of a metal-catalyzed hydroalkylation of an alkyne via C-N bond activation of an amine. The reaction demonstrates broad scope and functional group tolerance, allowing access to desired products with high diversity. Preliminary mechanistic studies indicate that a combination of an SET-initiated radical process and Ni-catalyzed alkylation could engage in the reaction, which makes it possible to bypass the traditional open-shell addition pathway.
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