New chiral complexes of platinum(II) as catalysts for the enantioselectiveBaeyer-Villiger oxidation of ketones with hydrogen peroxide: Dissymmetrization of meso-cyclohexanones
C. Paneghetti et al., New chiral complexes of platinum(II) as catalysts for the enantioselectiveBaeyer-Villiger oxidation of ketones with hydrogen peroxide: Dissymmetrization of meso-cyclohexanones, ORGANOMETAL, 18(24), 1999, pp. 5057-5065
The synthesis and characterization of a number of chiral complexes of the t
ype [(P-P)Pt(mu-OH)](2)(2+) (P-P = (R)-binap, (S,S)-diop, (R,R)-pyrphos, (R
,R)-norphos, (R,R)-Me-duphos, (S,S)-bppm) are reported. These are used for
the enantioselective Baeyer-Villiger oxidation of substituted meso-cyclohex
anones using 35% hydrogen peroxide as oxidant. The reaction is performed at
0 degrees C with moderate yields, showing in some cases ee higher than 50%
. Best catalysts are those containing atropoisomeric ligands possessing C-2
symmetry and/or capable of making seven-membered chelate rings with the me
tal. The results represent the first example of dissymmetrization of achira
l cyclohexanones obtained via the Baeyer-Villiger oxidation using a transit
ion metal catalyst.