A, 3-dehydroamino acid derivatives

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... 

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... 

Hydrogenation of ct-dehydroamino acid derivatives has been a typical reaction to test the efficiency of new chiral phosphorus ligands. Indeed, a number of chiral phosphorus ligands with great structural diversity are found to be effective for the Rh-catalyzed hydrogenation of a-dehydroamino acid derivatives. Since (Z)-2-(acetamido)cinnamic... 

Blackmond et al. investigated the influence of gas-liquid mass transfer on the selectivity of various hydrogenations [39]. It could be shown - somewhat impressively - that even the pressure-dependence of enantioselectivity of the asymmetric hydrogenation of a-dehydroamino acid derivatives with Rh-catalysts (as described elsewhere [21b]) can be simulated under conditions of varying influence of diffusion These results demonstrate the importance of knowing the role of transport phenomena while monitoring hydrogenations. 

In general, the choice of counteranion has a minor effect on catalyst performance, with typical examples being selected from BF4, OTD, PFg, or BARF-. In one example, however, it was noted that [(R.R)-Et-DuPhos Rh CODJOTf gave superior selectivity for the reduction of / -/ disubstituted a-dehydroamino acid derivatives than the corresponding BARF complex when performed in a range of solvents, including supercritical carbon dioxide [39]. 

Table 24.1 Phospholanes reported to hydrogenate model a-dehydroamino acid derivatives in >95% ee.

Scheme 24.7 Non-standard a-dehydroamino acid derivatives reduced by Rh-phospholane-based catalysts.

Several accounts have described (Z)-dehydroamino acid esters as being less active than the corresponding (F)-isomer [59c, 143-145]. In fact, Bruneau and Demonchaux reported that when reduction of an (E/Z)-mixture of 73 with Rh-Et-DuPhos in THF was not complete, only unreacted (Z)-73 was detected. These findings conflict, however, with results obtained in MeOH [56 d], where the ligand structure was also found to be significant to the relative reactivity of each stereoisomer. As for a-dehydroamino acid derivatives, preformed metal-diphosphine complexes generally perform in superior fashion to those prepared in situ [56d]. 

Table 26.1 Enantioselective hydrogenation of a-dehydroamino acid derivatives.

Several chiral ligands, such as PYRPHOS [78b], have been shown to be very efficient ligands for the hydrogenation of a-dehydroamino acid derivatives in terms of both high enantioselectivity and reactivity. 

Many synthetic applications of Rh-catalyzed hydrogenation of a-dehydroamino acid derivatives have recently been explored (Scheme 26.2). Takahashi has reported a one-pot sequential enantioseiective hydrogenation utilizing a BINAP-Rh and a BINAP-Ru catalyst to synthesize 4-amino-3-hydroxy-5-phenylpentanoic acids in over 95% ee. The process involves a first step in which the dehydroami-no acid unit is hydrogenated with the BINAP-Rh catalyst, followed by hydrogenation of the / -keto ester unit with the BINAP-Ru catalyst [87]. A hindered pyridine substituted a-dehydroamino acid derivative has been hydrogenated by a... 

The enantioselectivities were found to be relatively independent of the solvent used. In 1998, Zhang reported a bisphosphinite based on a rigid bis-cyclopentyl ring system (BICPO, 95, 96) which induced 45.7 to 95% ee in the hydrogenation of a-dehydroamino acid derivatives [85]. 

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]. 

Pye and Rossen have developed a planar chiral bisphosphine ligand, [2.2]PHANE-PHOS, based on a paracyclophane backbone (Scheme 1.6) [69]. Moreover, the ortho-phenyl substituted NAPHOS ligand, Ph-o-NAPHOS, has been successfully applied for the rhodium-catalyzed hydrogenation of a-dehydroamino acid derivatives [70]. 

Some excellent bisphosphonite ligands have also been developed. For example, Re-etzfs binaphthol-derived ferrocene-based bisphosphonite hgand L12 has demonstrated to have excellent reactivity and enantioselectivity in the rhodium-catalyzed hydrogenation of itaconates and a-dehydroamino acid derivatives [76]. Zanotti-Gerosa s bisphosphonite ligand L13 has also been successfully apphed to the asymmetric hydrogenation of a-dehydroamino acid derivatives with up to 99% ee [77]. 

A few efficient bisphosphite ligands have been used for asymmetric hydrogenation of itaconates or a-dehydroamino acid derivatives. Reetz has developed a series of C2-symmetric bisphosphite ligands such as L14, which are based on the structure of 1,4 3,6-dianhydro-D-mannite [78]. The ligands exhibit excellent reactivity and enantioselectivity for the asymmetric hydrogenation of itaconates. 

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