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Updated: Jul 11, 2026

Light-driven Enzymatic Decarboxylation
Published on: May 22, 2016
Amines made easily: a highly selective hydroaminomethylation of olefins
Moballigh Ahmed1, Abdul Majeed Seayad, Ralf Jackstell
1Leibniz-Institut für Organische Katalyse an der Universität Rostock e.V., Buchbinderstrasse 5-6, D-18055 Rostock, Germany.
Abstract:
A highly chemo- and regioselective hydroaminomethylation of simple as well as functionalized alpha-olefins using a cationic rhodium precatalyst together with Xantphos as ligand is reported. Studies of the influence of ligands and reaction conditions led to an unprecedented selective hydroaminomethylation procedure. The novel procedure constitutes an economically attractive and environmentally favorable synthesis of secondary and tertiary aliphatic amines.
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