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Enol phosphinates, asymmetric hydrogenation

Iridium-Catalyzed Asymmetric Hydrogenation of Olefins with Chiral N,P and C,N Ligands 63 Table 12 Asymmetric hydrogenation of enol phosphinates... [Pg.63]

Enantioselective transfer hydrogenation (from propan-2-ol) of some ketones catalysed by iridium(i) complexes with chiral Schifl-base ligands has been reported, giving product alcohol of up to 33% e.e. with propiophenone as substrate. Other new reductive routes to chiral secondary alcohols involve the asymmetric hydrogenation of enol phosphinates (21) catalysed by chiral ferrocenyl-rhodium... [Pg.162]

See other pages where Enol phosphinates, asymmetric hydrogenation is mentioned: [Pg.4]    [Pg.6]    [Pg.240]    [Pg.104]    [Pg.104]    [Pg.172]    [Pg.133]    [Pg.303]    [Pg.40]    [Pg.181]    [Pg.712]    [Pg.712]    [Pg.138]    [Pg.142]    [Pg.357]   
See also in sourсe #XX -- [ Pg.63 ]



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