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Synfacts 2008(9): 0947-0947
DOI: 10.1055/s-2008-1078003
DOI: 10.1055/s-2008-1078003
Metal-Catalyzed Asymmetric Synthesis and Stereoselective Reactions
© Georg Thieme Verlag
Stuttgart ˙ New York
Asymmetric Transfer Hydrogenation in Aqueous Media of Acetophenone
N. A. Cortez, G. Aguirre, M. Parra-Hake, R. Somanathan*
Instituto Technológico de Tijuana, Mexico
Further Information
Publication History
Publication Date:
22 August 2008 (online)
Significance
Asymmetric transfer hydrogenation (ATH) of ketones using montosylated diamines and 1,2-aminoalcohols has been extensively studied by Noyori and co-workers. Several studies for increasing the reactivity and enantioselectivity of the reaction have been done to improve this method. This work extends those studies to show the importance of electron attractors and donors on the ArSO2 moiety of the diamine ligand. The recent report of ATH in aqueous media under non-inert atmospheric conditions extends the utility and industrial application of this system.