A focus on the asymmetric synthesis of a novel threo-ß-benzyl-ß-hydroxy aspartate analogue - Archive ouverte HAL
Article Dans Une Revue Tetrahedron: Asymmetry Année : 2012

A focus on the asymmetric synthesis of a novel threo-ß-benzyl-ß-hydroxy aspartate analogue

Résumé

Considering the biological activity of b-alkyl-b-hydroxyaspartate derivatives as potent blockers of glutamate transporters (EAATs) impacting on glutamatergic synapses activity, we have developed a concise, asymmetric synthesis of enantiomerically pure threo-b-benzyl-b-hydroxyaspartates. The key step is a regiospecific and stereoselective Sharpless asymmetric aminohydroxylation (SAA) on previously synthesized benzyl fumarate.

Domaines

Chimie organique

Dates et versions

hal-00668879 , version 1 (10-02-2012)

Identifiants

Citer

Sofiane Mekki, Salima Bellahouel, Nicolas Vanthuyne, Marc Rolland, Aïcha Derdour, et al.. A focus on the asymmetric synthesis of a novel threo-ß-benzyl-ß-hydroxy aspartate analogue. Tetrahedron: Asymmetry, 2012, 23, pp.94-99. ⟨10.1016/j.tetasy.2012.01.004⟩. ⟨hal-00668879⟩
79 Consultations
0 Téléchargements

Altmetric

Partager

More