Issue 24, 2022

Copper-catalyzed aerobic nitrogen-migration cyanation and oxygenation of unsaturated ketoximes via the C[double bond, length as m-dash]C bond cleavage: facile access to 4-oxobutanenitriles

Abstract

A new copper-catalyzed aerobic synthesis of 4-oxobutanenitriles by the nitrogen-migration cyanation and oxygenation of γ,δ-unsaturated ketoximes at room temperature is developed. By means of a copper(0) powder catalyst, the nitrogen-migration cyanation and oxygenation of unsaturated ketoximes with O2via a radical intramolecular 5-exo-trig cyclization, C[double bond, length as m-dash]C double bond cleavage and ring-opening process efficiently execute to assemble 4-oxobutanenitriles. Mechanistic studies indicate that these processes include radicals initiating the reaction from the oxime side and the superoxide radical formation.

Graphical abstract: Copper-catalyzed aerobic nitrogen-migration cyanation and oxygenation of unsaturated ketoximes via the C [[double bond, length as m-dash]] C bond cleavage: facile access to 4-oxobutanenitriles

Supplementary files

Article information

Article type
Research Article
Submitted
03 Oct 2022
Accepted
27 Oct 2022
First published
29 Oct 2022

Org. Chem. Front., 2022,9, 6920-6925

Copper-catalyzed aerobic nitrogen-migration cyanation and oxygenation of unsaturated ketoximes via the C[double bond, length as m-dash]C bond cleavage: facile access to 4-oxobutanenitriles

X. Liu, Y. Li, M. Hu, Q. Wang and J. Li, Org. Chem. Front., 2022, 9, 6920 DOI: 10.1039/D2QO01553F

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