Issue 44, 2016

Palladium-catalysed hydroamidocarbonylation of 1,3-dienes

Abstract

Herein, we report our recent result on the development of the selective catalytic method towards the synthesis of β,γ-unsaturated imides via Pd-catalysed hydroamidocarbonylation of conjugated dienes. Note that this reaction proceeds under acid additive free conditions. Various dienes, including those of high industrial value (e.g. isoprene, 1,3-butadiene), are shown to be compatible with our established method (28 examples, 40–99% yield), which leads to the corresponding β,γ-unsaturated imides in a highly efficient and atom-economic fashion.

Graphical abstract: Palladium-catalysed hydroamidocarbonylation of 1,3-dienes

Supplementary files

Article information

Article type
Communication
Submitted
11 Apr 2016
Accepted
28 Apr 2016
First published
28 Apr 2016

Chem. Commun., 2016,52, 7142-7145

Palladium-catalysed hydroamidocarbonylation of 1,3-dienes

H. Li, X. Fang, R. Jackstell, H. Neumann and M. Beller, Chem. Commun., 2016, 52, 7142 DOI: 10.1039/C6CC03017C

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