Journal
TETRAHEDRON
Volume 65, Issue 31, Pages 6083-6089Publisher
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tet.2009.05.054
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Funding
- MIUR (PRIN 2007, Rome)
- Universita degli Studi di Milano (PUR)
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An efficient stereoselective preparation of the two enantionnerically pure diasteroisomers of gamma-benzyloxy-S-glutamic acid was performed using trans-4-hydroxy-L-proline as a source of chirality, while the erythro and threo isomers of D-benzyloxy-S-glutamic acid were prepared starting from (R)-Garner's aldehyde. All new derivatives were tested for their inhibitory activity against excitatory amino acid transporters in a rat synaptosomal preparation and their IC50 values were compared to that of TBOA, a one carbon lower homologue commonly used as the reference blocker of glutamate transporters. (C) 2009 Elsevier Ltd. All rights reserved.
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