Chiral Ferrocene-based Bisphosphane Ligands

Togni and Spindler introduced non-C2-symmetric ferrocene-based Josiphos-type ligands [47], which are effective for rhodium-catalyzed hydrogenation of a-(acetami-do)cinnamate, dimethyl itaconate, and / -keto esters. The Josiphos-type hgands have been applied as the stereodefming step in a number of industrial processes, as exemplified the use of PPF- Bu2 for the commercial synthesis of (-i-)-biotin [48], and Xyli-Phos for the preparation of the herbicide (S)-metolachlor [49]. 

Two C2-symmetric bisphosphane hgands, namely Kang s FerroPhos [50] and Kno-chel s FFRRIPHOS (MandyPhos) [51], have provided excellent enantioselectivities in 

Marinetti [53] and Burk [54] reported the preparation of chiral l,l -bis(phos-phetano)ferrocenes (FerroTANE) independently, in which Et-FerroTANE demonstrated excellent enantioselectivity in the rhodium-catalyzed hydrogenation of itaconates. Zhang has reported a l,T-bis(phospholanyl)ferrocene hgand (f-KetalPhos) with ketal substituents at 3,4-positions [55], which proved an excellent ligand for the enantioselective hydrogenation of a-dehydroamino acid derivatives [56]. 

A C2-symmetric bisphosphane FerroPhos has been developed by Kang and is found to be efficient for the Rh-catalyzed hydrogenation of a-dehydroamino acid derivatives.86,863 Knochel has independently reported a class of FERRIPHOS (MandyPhos) with similar structural features. All these ligands have provided excellent 

A series of non-f, -symmetrical ferrocene-based 1,5-diphosphane ligands (TaniaPhos) has been developed by Knochel.88,88a,88b The ligands have been effectively used in Rh- or Ru-catalyzed asymmetric hydrogenations. The ligand 39, which has an MeO group at the chiral carbon center, has shown excellent applications in the hydrogenation of several olefin and ketone substrates.89 Weissensteiner and Spindler have reported a series of structurally different 

Mezzetti91 and Leeuwen/Widhal92 have independently reported P-chiral ferrocenyl bisphosphines 42 and 43. These two ligands have shown excellent enantioselectivity (up to 99% ee) for the asymmetric hydrogenation of 

Fu has reported a planar-chiral bisphosphorus ligand 45 with a phosphaferrocene backbone. The ligand has provided enantioselectivity up to 96% ee in the hydrogenation of a-dehydroamino acid derivatives.99 Another planar-chiral ferrocene-based bisphosphorus ligand 46 has been reported by Kagan recently and enantioselectivity up to 95% ee has been obtained in the reduction of dimethyl itaconate.100 

---

Figure 6 Chiral ferrocene-based bisphosphane ligands.

Many chiral ferrocene-based bisphosphane ligands with great structural variations have been developed recently. Togni and Spindler introduced non-Crsymmetric ferrocene-based Josiphos type ligands. Josiphos 38 has been found to be effective for Rh-catalyzed hydrogenation of a-acetamidocinnamate, dimethyl itaconate, and P-keto esters. A class of non-Cj-symmetrical ferrocene-based 1,5-diphosphane ligands (TaniaPhos 39) has also been... 

Fig. 2.10 The ligand universe A stunning breadth of structural variation with members representing various motifs, e.g. atropisomeric biaryls, ferrocene-based bisphosphanes, P-chiral bisphosphanes, bisphosphites, monodentate phosphoramidites, AJ,P-ligands.

---