Colloidal and Nanosized Catalysts in Organic Synthesis: XXIII. Reductive Amination of Carbonyl Compounds Catalyzed by Nickel Nanoparticles in a Plug-Flow Reactor
作者:V. M. Mokhov、Yu. V. Popov、A. N. Paputina、D. N. Nebykov、E. V. Shishkin
DOI:10.1134/s1070363219120016
日期:2019.12
Reductive amination of aldehydes and ketones with primary and secondary amines under catalysis with nickel nanoparticles supported on zeolite X, MgO, or activated carbon in the gas phase or in the gas-liquid system in a plug-flow reactor proceeds at atmospheric pressure of hydrogen with the formation of secondary or tertiary amines in high yield.
N-alkyl(cycloalkyl)benzylamines, p-fluorobenzylamines, (1-phenylethyl)amines, [1-(p-fluorophenyl)ethyl]amines were synthesized by hydroamination of aldehydes and ketones with oximes.
A Highly Enantioselective Organocatalytic Method for Reduction of Aromatic
<i>N</i>
‐Alkyl Ketimines