Iridium complexes of planar-chiral ferrocenyl phosphine-thioether ligands were tested in the hydrogenation of simple ketones. Optimization of the conditions led to a highly active catalytic system with turnover numbers up to 915 and turnover frequencies up to ca. 250 h-1. Furthermore, very high enantioselectivities (up to >99%) together with complete conversions were obtained for the asymmetric hydrogenation of various acetophenones at 10 °C.

Highly efficient asymmetric hydrogenation of alkyl aryl ketones catalyzed by iridium complexes with chiral planar ferrocenyl phosphino-thioether ligands

Gonsalvi Luca;Peruzzini Maurizio
2007

Abstract

Iridium complexes of planar-chiral ferrocenyl phosphine-thioether ligands were tested in the hydrogenation of simple ketones. Optimization of the conditions led to a highly active catalytic system with turnover numbers up to 915 and turnover frequencies up to ca. 250 h-1. Furthermore, very high enantioselectivities (up to >99%) together with complete conversions were obtained for the asymmetric hydrogenation of various acetophenones at 10 °C.
2007
Istituto di Chimica dei Composti OrganoMetallici - ICCOM -
alkyl aryl ketones
asymmetric catalysis
ferrocene ligands
hydrogenation
iridium
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/171028
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