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METHOD FOR ASYMMETRICLY HYDRATING (ALPHA) KETOCARBONYL COMPOUNDS TO OPTICALLY ACTIVE (ALPHA) HYDROXYCARBONYL COMPOUNDS

机译:不对称氢化(α)酮碳化合物为光学活性(α)羟基羰基化合物的方法

摘要

The process is aimed at the asymmetric hydrogenation of alpha -ketocarbonyl compounds, in particular alpha -ketolactones, to give the corresponding optically active alpha -hydroxycarbonyl compounds in the presence of platinum metal diphosphine complexes as catalyst and is characterised by the use of chiral iridium complexes containing an optically active 1,2-diphosphine ligand (1,2-DP) of the general formulae …IMAGE… and a cocatalyst from the group of cyclic dicarboximides, preferably succinimide. …??By using cationic or neutral Ir complexes of the formula [Ir(en)2(1,2-DP]+A- or [Ir(Z)(en)2(1,2-DP)] and succinimide in a molar ratio of 1:1 to 1:50, alpha -ketopantolactone can be hydrogenated with a high optical yield to give (R)-(-)-pantolactone.
机译:该方法旨在α-酮羰基化合物,特别是α-酮内酯的不对称氢化,以在铂金属二膦配合物作为催化剂存在下得到相应的旋光α-羟基羰基化合物,其特征在于使用手性铱配合物。含有通式……的旋光的1,2-二膦配体(1,2-DP),以及环二羧酰亚胺,优选琥珀酰亚胺中的助催化剂。 …通过使用式[Ir(en)2(1,2-DP)+ A-或[Ir(Z)(en)2(1,2- DP)]和琥珀酰亚胺的摩尔比为1:1至1:50,可以高光学产率将α-酮基内酯内酯氢化,得到(R)-(-)-泛内酯。

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