Enantioselective hydrogenation Bppfa

Analogues of BPPFA and BPPFOH have been prepared, but for many applications these two ligands still prove to be the best for enantioselective hydrogenations [125]. The introduction of another functional group into the side chain, as in 31, provided the first catalysts capable of hydrogenating the tetra-substi-tuted a,/ -unsaturated acids with high enantioselectivity, even though the activity was very low (turnover frequency, TOF, 2 h-1) [132, 133],... 

Somewhat surprisingly, the Pd-bppfa complex 24 tethered to a macroporous silica was shown to be moderately active for the enantioselective hydrogenation of ethyl nicotinate (25) (a rare example of a homogeneous Pd-catalyzed hydrogenation), but ee s were very low (Scheme 15.1).10a... 

Bppfoh and bppfa derivatives have been applied most successfully for the Rh-catalyzed hydrogenation of dehydro amino acid derivatives such as MAC (ee 97%) and of functionalized ketones [7]. The nature of the amino group has a significant effect on enantioselectivity and often also on activity, and is used to tailor the ligand for a particular substrate. Rh-bppfa complexes were among the first catalysts able to hydrogenate tetrasubstituted C=C bonds, albeit with relatively low activity (Table 25.2, entries 2.1-2.3). Ferrophos, one of the very few li-... 

Ferrocene-based complexes have some potential for the enantioselective reduction of ketones, but compared to other ligand classes this is relatively limited [3]. Rh complexes of bppfa, bophoz and josiphos are among the most selective catalysts for the hydrogenation of a-functionalized ketones (Table 25.9 Fig. 25.18, 30-32). Ru complexes of walphos and ferrotane are quite effective for... 

In addition, a Rh-(R,R)-NORPHOS catalyst has been used to promote enantioselective transfer hydrogenation of the C=C double bond in (Z)-a-(acetylamino)cinnamic acid and in (Z)-a- and ( )-a-(benzoylamino)-2-butenoate by using 80% aqueous formic acid as the source of H2. Optical yields were improved by the addition of sodium formate representative results are presented in Table 2. Comparable, but generally somewhat lower, optical yields were obtained by using other Rh-(biphosphine ligand) catalysts, e.g., biphosphine ligand = (R,S)-(+)-BPPFA (2), (R)-(+)-PROPHOS(3), ot(R,R)-... 

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