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Asymmetric hydrogenation of ketones using Ir(III) complexes of N-alkyl-N '-tosyl-1,2-ethanediamine ligands

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Martins, Jose E. D., Morris, David J., 1974- and Wills, Martin. (2009) Asymmetric hydrogenation of ketones using Ir(III) complexes of N-alkyl-N '-tosyl-1,2-ethanediamine ligands. Tetrahedron Letters, Vol.50 (No.6). pp. 688-692. ISSN 0040-4039

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Official URL: http://dx.doi.org/10.1016/j.tetlet.2008.11.101

Abstract

The combination of an enantiomerically pure N'-alkylated derivative of N-4-toluenesulfonyl-1,2-diphenylethane-1,2-diamine (TsDPEN) with iridium trichloride results in the formation of a catalyst with high selectivity for ketone hydrogenation. Products with enantiomeric excesses of up to 84% were formed. The best results were obtained using a ligand with an n-alkyl chain and ortho-substituted acetophenone derivatives and other hindered derivatives. (C) 2008 Elsevier Ltd. All rights reserved.

Item Type: Journal Article
Subjects: Q Science > QD Chemistry
Divisions: Faculty of Science > Chemistry
Library of Congress Subject Headings (LCSH): Hydrogenation, Ketones, Iridium, Catalysis, Acetophenone, Ligands
Journal or Publication Title: Tetrahedron Letters
Publisher: Elsevier
ISSN: 0040-4039
Date: 11 February 2009
Volume: Vol.50
Number: No.6
Number of Pages: 5
Page Range: pp. 688-692
Identification Number: 10.1016/j.tetlet.2008.11.101
Status: Peer Reviewed
Publication Status: Published
Funder: Engineering and Physical Sciences Research Council (EPSRC), Brazil. Coordenação do Aperfeiçoamento de Pessoal de Nível Superior (CAPES)
Grant number: EP/D031168/1 (EPSRC)
URI: http://wrap.warwick.ac.uk/id/eprint/28502

Data sourced from Thomson Reuters' Web of Knowledge

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