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

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  • Highly efficient asymmetric hydrogenation of alkyl aryl ketones catalyzed by iridium complexes with chiral planar ferrocenyl phosphino-thioether ligands (Articolo in rivista) (literal)
Anno
  • 2007-01-01T00:00:00+01:00 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
  • 10.1002/adsc.200600350 (literal)
Alternative label
  • Le Roux, Erwan; Malacea, Raluca; Manoury, Eric; Poli, Rinaldo; Gonsalvi, Luca; Peruzzini, Maurizio (2007)
    Highly efficient asymmetric hydrogenation of alkyl aryl ketones catalyzed by iridium complexes with chiral planar ferrocenyl phosphino-thioether ligands
    in Advanced synthesis & catalysis (Internet); Wiley-VCH Verlag, GmbH, Weinheim (Germania)
    (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
  • Le Roux, Erwan; Malacea, Raluca; Manoury, Eric; Poli, Rinaldo; Gonsalvi, Luca; Peruzzini, Maurizio (literal)
Pagina inizio
  • 309 (literal)
Pagina fine
  • 313 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#url
  • http://onlinelibrary.wiley.com/doi/10.1002/adsc.200600350/abstract;jsessionid=300DCC884282D6EBE1BED4DBEC57FF43.d03t03 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
  • 349 (literal)
Rivista
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#pagineTotali
  • 5 (literal)
Note
  • ISI Web of Science (WOS) (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
  • ICCOM-CNR; CNRS-LCC Toulouse Cedex 4, France (literal)
Titolo
  • Highly efficient asymmetric hydrogenation of alkyl aryl ketones catalyzed by iridium complexes with chiral planar ferrocenyl phosphino-thioether ligands (literal)
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. (literal)
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