Issue 83, 2019

Palladium-catalyzed decarboxylative ortho-amidation of O-methyl ketoximes with oxamic acids

Abstract

The first palladium-catalyzed ortho-amidation of ketoximes has been developed with readily available, easy to handle and environment-friendly N,N-disubstituted oxamic acids as the amidation sources. When N-monosubstituted oxamic acids are used as the substrates, the formed ortho-amidated ketoximes undergo further intramolecular cyclization to provide 3-methyleneisoindolinones.

Graphical abstract: Palladium-catalyzed decarboxylative ortho-amidation of O-methyl ketoximes with oxamic acids

Supplementary files

Article information

Article type
Communication
Submitted
20 Aug 2019
Accepted
24 Sep 2019
First published
25 Sep 2019

Chem. Commun., 2019,55, 12551-12554

Palladium-catalyzed decarboxylative ortho-amidation of O-methyl ketoximes with oxamic acids

K. Jing, P. Cui and G. Wang, Chem. Commun., 2019, 55, 12551 DOI: 10.1039/C9CC06460E

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