SYNTHESIS OF OPTICALLY-ACTIVE AZETIDINE-2,4-DICARBOXYLIC ACID AND RELATED CHIRAL AUXILLARIES FOR ASYMMETRIC-SYNTHESIS

(S)-1-Phenylethylamine has been used as a chiral auxiliary as well as a nitrogen atom donor in the synthesis of an enantiomeric pair of azet idine-2,4-dicarboxylic acids, the absolute configuration of one of whi ch has been assigned on the basis of the X-ray structure and the known absolute configuration of the (S)-1-phenylethylamine moiety. Chiral a uxiliaries of related C-2-symmetric azetidines have also been prepared and their propionamides have been asymmetrically alkylated. The stere ochemistry of the resulting products was compared with their analogues having different ring sizes.