Synthesis of the constrained glutamate analogues (2S,1 ' R,2 ' R)- and (2S,1 ' S,2 ' S)-2- (2 'carboxycyclobutyl)glycines L-CBG-II and L-CBG-I by enzymatic transamination
Résumé
Optically pure trans-cyclobutane analogues of glutamic acid are prepared by highly selective enzymatic transamination of a single racemic trans-cyclobutane α-ketoglutaric acid derivative 5, which is synthesized in five steps from maleic anhydride. (2S,1′R,2′R)- and (2S,1′S,2′S)-2-(2′-carboxycyclobutyl)glycines L-CBG-II and L-CBG-I are obtained using aspartate aminotransferase (AAT) and branched chain aminotransferase (BCAT), respectively.
Domaines
Chimie organique| Origine | Fichiers éditeurs autorisés sur une archive ouverte |
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