“…[2,3,6] To improve an asymmetric catalytic reaction for a new substrate is not trivial, however, possible approaches being mainly restricted either by the availability of a library of chiral ligands, [3,6] or to the easy structure modification of an efficient lead series such as BINAP, [16,17] DUPHOS, [18] PHOX, [19] monophos, [20] etc. In particular, the phosphorus and phosphinous derivatives usually prepared by treatment of PCl 3 or chlorophosphanes with available chiral diols, [21,22] binaphthol, [23][24][25] or amino alcohols [26][27][28][29][30][31] offer an efficient and easy route to new chiral ligands. Notably, the phosphorus ligands are by far the most commonly used ones, [16][17][18][19][20][21][22][23][24][25][26][27][28][29][30][31] because they offer far more possibilities for modification of the structure (mono-, di-, multidendate, hemilabile, hybrids, etc.…”