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Propiophenone diasteroselective

Furthermore, the diasteroselectivity observed using catalyst (S,S)-62 depends on the nature of the latent trichlorosilyl enolates. Thus, propiophenone-derived enolate 65 possessing the Z-configuration reacts with benzaldehyde in presence of 15 mol% of (SyS) 62 to afford the syn adduct 66 with very high enantioselectivity. [Pg.102]


See other pages where Propiophenone diasteroselective is mentioned: [Pg.254]    [Pg.254]   
See also in sourсe #XX -- [ Pg.2 , Pg.244 ]

See also in sourсe #XX -- [ Pg.244 ]

See also in sourсe #XX -- [ Pg.244 ]

See also in sourсe #XX -- [ Pg.244 ]




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