e.g. Filippa Pettersson or Cancer Res. 75(6) , 1102-12, (2015) or 10.1002/anie.201600521
Liebigs Annalen der Chemie
Preparative Bioorganic Chemistry, XI Preparation of the Enantiomers of Paraconic Acid Employing Lipase??Mediated Asymmetric Hydrolysis of Prochiral Diacetates as …
K Mori, N Chiba
Index: Mori, Kenji; Chiba, Naoki Liebigs Annalen der Chemie, 1989 , p. 957 - 962
Abstract (S)-(-)-Paraconic acid (1) was prepared from 2-(acetoxymethyl)-3-phenylpropyl acetate (4) by its asymmetric hydrolysis with pig pancreatic lipase as the key step. Similarly,(R)-(+)-1 was prepared from 2-(acetoxymethyl)-4-pentenyl acetate (2) by its asymmetric hydrolysis with lipase MY.