Colloid and nanosized catalysts in organic synthesis: XIV. Reductive amination and amidation of carbonitriles catalyzed by nickel nanoparticles
- Authors: Popov Y.V.1, Mokhov V.M.1, Shcherbakova K.V.1
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Affiliations:
- Volgograd State Technical University
- Issue: Vol 86, No 4 (2016)
- Pages: 798-805
- Section: Article
- URL: https://journals.rcsi.science/1070-3632/article/view/214595
- DOI: https://doi.org/10.1134/S107036321604006X
- ID: 214595
Cite item
Abstract
Hydrogenation of carbonitriles catalyzed by nickel nanoparticles in the presence of primary amines led to the predominant formation of unsymmetrical secondary amines. In the presence of secondary amines hydrogenation of nitrites provided enamines as main products. Hydrogenation of nitriles in the presence of formamide or acetamide afforded formyl or acetyl derivatives of primary amines.
Keywords
About the authors
Yu. V. Popov
Volgograd State Technical University
Author for correspondence.
Email: tons@vstu.ru
Russian Federation, pr. Lenina 28, Volgograd, 400131
V. M. Mokhov
Volgograd State Technical University
Email: tons@vstu.ru
Russian Federation, pr. Lenina 28, Volgograd, 400131
K. V. Shcherbakova
Volgograd State Technical University
Email: tons@vstu.ru
Russian Federation, pr. Lenina 28, Volgograd, 400131