Asymmetric hydroformylation and hydrogenation catalyzed by chiral rhodium and ruthenium complexes of phosphorylated 2,2 '-bis(diphenyl-phosphino)-1,1'-binaphthyls
A. Kockritz et al., Asymmetric hydroformylation and hydrogenation catalyzed by chiral rhodium and ruthenium complexes of phosphorylated 2,2 '-bis(diphenyl-phosphino)-1,1'-binaphthyls, J MOL CAT A, 174(1-2), 2001, pp. 119-126
In situ-generated rhodium complexes of mono- and bisphosphorylated enantiop
ure BINAP ligands have been used for the asymmetric hydroformylation of sty
rene and vinylacetate. Corresponding Ru-complexes have been investigated in
the homogeneous and biphasic asymmetric hydrogenation of dimethyl itaconat
e. An increase in the enantioselectivity of about 6-9% compared to BINAP wa
s observed in the vinylacetate hydroformylation. For the aqueous biphasic h
ydroformylation of styrene the most enantio selective rhodium diphosphine c
atalyst (27% e.e.) up to now has been found. (C) 2001 Elsevier Science B.V.
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