L. Kollar et al., PLATINUM-CATALYZED ENANTIOSELECTIVE HYDROFORMYLATION OF STYRENE - PLATINUM DIPHOSPHINE TIN(II)FLUORIDE CATALYTIC-SYSTEM - A NOVEL ASYMMETRIC HYDROFORMYLATION CATALYST, Journal of organometallic chemistry, 453(1), 1993, pp. 155-158
Enantioselective hydroformylation of styrene was carried out in the pr
esence of platinum-containing catalysts. Tin(II) fluoride was used as
cocatalyst, giving a catalytic system of unusually high stability. Whe
n the optically active diphosphine 2,4-bis(diphenylphosphino)pentane (
BDPP) was used the absolute configuration of the 2-phenylpropanal form
ed varied with the temperature used. In dichloromethane the enantiomer
ic excess depends strongly on the temperature used. Although the addit
ion of 2-diphenylphosphino-pyridine to the catalytic system strongly r
educes the catalytic activity, the BDPP-2-diphenylphosphino-pyridine '
'mixed-phosphine system'' gave 86.7% e.e.