An improved method for the preparation of both the enantiopure b-amino acids is presented. The diastereomer benzyl b-amino esters, obtained by stereoselective reduction of b-enamino esters, were separated and hydrogenolyzed to the free enantiopure b-amino acids.
An improved synthesis of enantiopure b-amino acids
CIMARELLI, Cristina;PALMIERI, Gianni;
2001-01-01
Abstract
An improved method for the preparation of both the enantiopure b-amino acids is presented. The diastereomer benzyl b-amino esters, obtained by stereoselective reduction of b-enamino esters, were separated and hydrogenolyzed to the free enantiopure b-amino acids.File in questo prodotto:
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