STEREOCONTROLLED ENANTIOSELECTIVE ADDITION OF DIETHYLZINC TO ALDEHYDES USING NEW CHIRAL AMINOALCOHOLS

The new chiral beta-aminoalcohols of indolinylmethanols (1) and their reduced derivatives (2) were synthesized from (S)-indoline-2-carboxylic acid. Both (R) and (S) enantiomers of the optically active secondary alcohols have been successfully obtained in high enantiomeric excess from the stereoselective addition of diethylzinc to the aldehydes catalyzed by the chiral aminoalcohols (1 and 2). The sense of the asymmetric induction and the degrees of enantioselectivities turned out to be highly dependent on the structure of the catalysts: The presence of the catalyst 1 afforded the (S)-configuration of the corresponding alcohols; on the other hand, the presence of 2 afforded the (R)-configuration of the alcohols in high enantiomeric selectivity.