New chiral (cyclopentadienone) iron complexes as catalysts for ketone asymmetric hydrogenation

In recent years, Fe-cyclopentadienone complexes (1 in Figure 1) [1] have become a hot research topic for a series of reasons: a) firstly, they are a demonstration on how a \u2018non-innocent ligand\u2019 can influence and modify the reactivity of a metal: analogously to what reported for the Shvo\u2019s Ru complexes,[2] their ligand, swinging between the cyclopentadienone (2) and the hydroxycyclopentadienyl form (3), enables a Fe(0)/Fe(II) catalytic cycle which does not belong to the typical reactivity of Fe-complexes (Figure 1).[3] b) Secondly, they rely on a cheap, non-toxic and environmentally benign metal such as Fe, which is nowadays increasingly considered for developing sustainable catalysts.[4] c) Last, they are perfectly stable to air, moisture and even chromatography, which simplifies their isolation and purification. Activation (by creation of a vacant coordination site) can be performed in situ. As efficient chiral Fe-cyclopentadienones for enantioselective reductions are currently missing, we recently developed a new class of (R)-BINOL-derived complexes (Figure 2).[5] Considering the previously reported BINOL-derived catalysts and the above-mentioned mechanism,[3] we envisioned that 3,3\u2019-substituents on the binaphthyl moiety would be needed to ensure an efficient transfer of stereochemical information from the catalyst\u2019s stereoaxis to the substrate. We thus prepared the complexes CK1, CK2 and CK3 (Figure 2), which were screened in the asymmetric hydrogenation (AH) of ketones after in situ activation by reaction with Me3NO. As expected, complex CK2, bearing the biggest 3,3\u2019-substituents on the binaphthyl system, allowed to obtain the best enantiomeric excess with acetophenone (50% e.e.) and was thus screened on a series of other ketones reaching up to 77% e.e.. Starting from 3,3\u2019-dihydroxysubstituted complex CK3, the synthesis of new complexes bearing bulkier 3,3\u2019-substituents (esters, ethers, aryl rings) has been undertaken. The obtained second-generation pre-catalysts will be tested in the AH of ketones and imines, as well as in hydrogen borrowing processes