Synthesis of L-tricholomic acid analogues and pharmacological characterization at ionotropic glutamate receptors

The synthesis of analogues of the natural compound ltricholomic acid and of its threo diastereoisomer was accomplished in order to explore their affinity for glutamate ionotropic receptors. In this study, fourteen new unnatural amino acids, characterized by a 3-hydroxy-~2 -isoxazoline or 3- hydroxy-~2 -pyrazoline-skeleton, were obtained exploiting, as key reaction, a 1,3-dipolar cycloaddition or an intramolecular cyclization.