| abstract |
A process for preparing a-L-aspartyl-L-phenylalanine methyl ester:in which:a) the compound methyl N(a-L-aspartyl)a-aminocinn- amate, protected at the nitrogen, of formula:where R is a protector group at the nitrogen, is subjected to hydrogenation at the olefin bond by means of gaseous hydrogen in the presence of a hydrogenation catalyst, to give the compound of formula:where R has the aforesaid meaning, in the form of a mixture of a-L-aspartyl-L-phenylalanine methyl ester protected at the nitrogen, and α-αL-aspartyl-D-phenylalanine methyl ester protected at the nitrogen;b) the protector group is removed from said a-L-aspartyl-L-phenylalanine and a-L-aspartyl-D-phenylalanine methyl esters protected at the nitrogen;c) the a-L-aspartyl-L-phenylalanine methyl ester is separated and recovered from said deprotection reaction product. |