Issue 4, 2014

Palladium-catalysed regioselective hydroamination of 1,3-dienes: synthesis of allylic amines

Abstract

Catalytic hydroamination of unactivated 1,3-dienes represents a sustainable and atom-economic C–N bond forming process. Here, we present a novel catalytic system consisting of Pd(cod)Cl2 in combination with DPEphos for the selective 1,4-hydroamination (anti-Markovnikov reaction) of a series of acyclic and cyclic dienes. The reactions proceed in good yields and allow for the exclusive formation of allylic amines with high regioselectivity and do not need any additives.

Graphical abstract: Palladium-catalysed regioselective hydroamination of 1,3-dienes: synthesis of allylic amines

Supplementary files

Article information

Article type
Research Article
Submitted
21 ربيع الأول 1435
Accepted
24 ربيع الثاني 1435
First published
17 جمادى الأولى 1435

Org. Chem. Front., 2014,1, 368-372

Palladium-catalysed regioselective hydroamination of 1,3-dienes: synthesis of allylic amines

D. Banerjee, K. Junge and M. Beller, Org. Chem. Front., 2014, 1, 368 DOI: 10.1039/C4QO00023D

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