ASYMMETRIC-SYNTHESIS .1. ENANTIOSELECTIVE CONJUGATE ADDITIONS OF GRIGNARD-REAGENTS TO CINNAMAMIDES DERIVED FROM N-METHYL, N-BUTYL AND N-BENZYL DERIVATIVES OF (R)-(-)-2-AMINOBUTAN-1-OL
J. Touet et al., ASYMMETRIC-SYNTHESIS .1. ENANTIOSELECTIVE CONJUGATE ADDITIONS OF GRIGNARD-REAGENTS TO CINNAMAMIDES DERIVED FROM N-METHYL, N-BUTYL AND N-BENZYL DERIVATIVES OF (R)-(-)-2-AMINOBUTAN-1-OL, Journal of chemical research. Synopses, (5), 1996, pp. 224-225
The reaction of simple Grignard reagents with (R)-(-)-2-aminobutan-1-o
l are shown to afford the corresponding conjugate adducts; acidic hydr
olysis of these adducts yielded beta-phenylalkanoic acids with enantio
meric excesses generally in the range 72-98%.