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Issue 14, 2017
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Palladium-catalyzed highly regioselective hydroaminocarbonylation of aromatic alkenes to branched amides

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Abstract

Pd(t-Bu3P)2 has been successfully identified as an efficient catalyst for the hydroaminocarbonylation of aromatic alkenes to branched amides under relatively mild reaction conditions. With hydroxylamine hydrochloride as an additive, both aliphatic and aromatic amines could be used as coupling partners for the present reaction, leading to production of branched amides in high yields with excellent regioselectivities.

Graphical abstract: Palladium-catalyzed highly regioselective hydroaminocarbonylation of aromatic alkenes to branched amides

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Supplementary files

Article information


Submitted
15 Feb 2017
Accepted
13 Mar 2017
First published
22 Mar 2017

Org. Biomol. Chem., 2017,15, 2910-2913
Article type
Communication

Palladium-catalyzed highly regioselective hydroaminocarbonylation of aromatic alkenes to branched amides

J. Zhu, B. Gao and H. Huang, Org. Biomol. Chem., 2017, 15, 2910
DOI: 10.1039/C7OB00371D

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