3913-68-6Relevant articles and documents
Stereoselective synthesis of γ-hydroxy-α-amino acids through aldolase-transaminase recycling cascades
Guérard-Hélaine, Christine,Heuson, Egon,Ndiaye, Moussa,Gourbeyre, Léa,Lemaire, Marielle,Hélaine, Virgil,Charmantray, Franck,Petit, Jean-Louis,Salanoubat, Marcel,De Berardinis, Véronique,Gefflaut, Thierry
supporting information, p. 5465 - 5468 (2017/07/06)
Efficient bi-enzymatic cascades combining aldolases and α-transaminases were designed for the synthesis of γ-hydroxy-α-amino acids. These recycling cascades provide high stereoselectivity, atom economy, and an equilibrium shift of the transamination. l-syn or anti-4-hydroxyglutamic acid and d-anti-4,5-dihydroxynorvaline were thus prepared in 83-95% yield in one step from simple substrates.
Synthesis and properties of 4-haloglutamates
Krasnow,Bukrina,Zhdanova,Kodess,Korolyova
, p. 961 - 964 (2007/10/02)
Synthesis of stereoisomers of 4-bromo- and 4-iodo-N-phthaloylglutamates based on the bromination of N-phthaloylglutamic acid followed by separation of diastereoisomers is described.
STEREOSPECIFIC SYNTHESIS OF ENANTIOMERS OF 4-HYDROXYGLUTAMIC ACID AND STUDY OF THEIR INHIBITING PROPERTIES WITH RESPECT TO GLUTAMINE SYNTHETASE
Krasnov, V. P.,Alekseeva, L. V.,Firsova, N. A.,Kodess, I. K.,Burde, N. L.
, p. 369 - 372 (2007/10/02)
-