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| Research article summary (published 5 Jul 2008): |
Synthesis of enantiomerically pure 1,2,3,4-tetrahydro-beta-carbolines and N-acyl-1-aryl ethylamines by rhodium-catalyzed hydrogenation.
Full Abstract
The rhodium-catalyzed asymmetric hydrogenation of different enamides, in particular, dihydro-beta-carboline derivates, was investigated in the presence of chiral phosphorus ligands. Enantioselectivities of up to 99 % ee were obtained after ligand screening and optimization of the reaction conditions. The scope and limitation of the catalysts were shown in the synthesis of optically active tetrahydro-beta-carbolines and other benchmark N-acyl-1-aryl ethylamines.
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Author information
Author/s: Enthaler, Stephan (S); Erre, Giulia (G); Junge, Kathrin (K); Addis, Daniele (D); Kadyrov, Renat (R); Beller, Matthias (M);
Affiliation: Leibniz-Institut für Katalyse an der Universität Rostock e. V. Albert-Einstein-Str. 29A, D-18059 Rostock, Germany.
Journal and publication information
Publication Type: Journal Article
Journal: Chemistry, an Asian journal (Chem Asian J), published in Germany. (Language: eng)
Reference: 2008-Jul; vol 3 (issue 7) : pp 1104-10
Dates: Created 2008/06/30; Completed 2008/08/13;
PMID: 18496827, status: MEDLINE (last retrieval date: 11/6/2008)
Sourced from the National Library of Medicine. Abstract text and other information may be subject to copyright.
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