SYNTHESIS OF NEW CHIRAL PHOSPHINEPHOSPHITES HAVING 2-DIPHENYLPHOSPHINOBIPHENYL-2'-YL BACKBONE AND THEIR USE IN RH(I)-CATALYZED ASYMMETRIC HYDROFORMYLATIONS
T. Higashizima et al., SYNTHESIS OF NEW CHIRAL PHOSPHINEPHOSPHITES HAVING 2-DIPHENYLPHOSPHINOBIPHENYL-2'-YL BACKBONE AND THEIR USE IN RH(I)-CATALYZED ASYMMETRIC HYDROFORMYLATIONS, Tetrahedron letters, 35(13), 1994, pp. 2023-2026
New chiral phosphinephosphites l-2'-yl)((S)-1,1'-binaphthalen-2,2'-diy
l)phosphite [abbreviated (R,S)-BIPHEMPHOS] and its enantiomer (S,R)-BI
PHEMPHOS have been synthesized from '-dichloro-4,4',6,6'-tetramethyl-2
,2'-biphenyldiol in enantiomerically pure form. Their Rh(I) complexes
have been shown to be highly efficient catalysts for asymmetric hydrof
ormylations of a variety of olefinic substrates. The corresponding pho
sphinephosphites derived from 2,2'-biphenyldiol were also tested as li
gands for asymmetric hydroformylation.