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Diastereoselective hydroformylation 3-pinene

Scheme 4.53 Diastereoselective hydroformylation of (-)-a-pinene as a function of the metal catalyst used. Scheme 4.53 Diastereoselective hydroformylation of (-)-a-pinene as a function of the metal catalyst used.
Figure 1.9 Examples of a chemoselectivity and diastereoselectivity in the oxidation of a-pinene, b regioselectivity in the hydroformylation of 1-octene, and cenantioselectivityin the hydrogenation of the prochiral isopropyl (2-methoxyisopropyl) imine ( indicates the asymmetric carbon atoms). Figure 1.9 Examples of a chemoselectivity and diastereoselectivity in the oxidation of a-pinene, b regioselectivity in the hydroformylation of 1-octene, and cenantioselectivityin the hydrogenation of the prochiral isopropyl (2-methoxyisopropyl) imine ( indicates the asymmetric carbon atoms).
Barros HJV, Ospina ML, Arguello E, Rocha WR, Gusevskaya EV, dos Santos EN (2003) Rhodium catalyzed hydroformylation of [P]-pinene and camphene effect of phosphorous ligands and reaction conditions on diastereoselectivity. J Organomet Chem 671 (1-2) 150-157. doi 10.1016/s0022-328x(03)00098-6... [Pg.126]

See other pages where Diastereoselective hydroformylation 3-pinene is mentioned: [Pg.307]    [Pg.919]    [Pg.101]   
See also in sourсe #XX -- [ Pg.329 ]



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