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Issue 5, 2013
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Regioselective Pd-catalyzed hydroamination of substituted dienes

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Abstract

The regioselective addition of hydrazones and related N-nucleophiles to substituted terpene-based substrates can be steered to either 1,2- or 1,4-addition products, making this a potentially powerful protocol for the preparation of amines from biorelevant feedstocks via C–N bond formation.

Graphical abstract: Regioselective Pd-catalyzed hydroamination of substituted dienes

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Article information


Submitted
09 Jan 2013
Accepted
18 Feb 2013
First published
19 Feb 2013

This article is Open Access

Catal. Sci. Technol., 2013,3, 1375-1379
Article type
Paper

Regioselective Pd-catalyzed hydroamination of substituted dienes

A. Perrier, M. Ferreira, J. N. H. Reek and J. I. van der Vlugt, Catal. Sci. Technol., 2013, 3, 1375
DOI: 10.1039/C3CY00024A

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