6-Carboxy-3,4-methanoprolines were prepared by reacting ethyl diazoacetate with the suitable 3,4-didehydroproline derivative in the presence of rhodium(II)acetate dimer as catalyst. The affinities of the title compounds for displacement of receptor binding to ionotropic and metabotropic (mGluR1 alpha) glutamate receptors were also determined.

Synthesis and Biological Evaluation of 6-Carboxy-3,4-methanoprolines, New Rigid Glutamate Analogs / M., Marinozzi; B., Natalini; C., Thomsen; M. H., Ni; Costantino, Gabriele; R., Pellicciari. - In: IL FARMACO. - ISSN 0014-827X. - 50:(1995), pp. 327-331.

Synthesis and Biological Evaluation of 6-Carboxy-3,4-methanoprolines, New Rigid Glutamate Analogs

COSTANTINO, Gabriele;
1995

Abstract

6-Carboxy-3,4-methanoprolines were prepared by reacting ethyl diazoacetate with the suitable 3,4-didehydroproline derivative in the presence of rhodium(II)acetate dimer as catalyst. The affinities of the title compounds for displacement of receptor binding to ionotropic and metabotropic (mGluR1 alpha) glutamate receptors were also determined.
Synthesis and Biological Evaluation of 6-Carboxy-3,4-methanoprolines, New Rigid Glutamate Analogs / M., Marinozzi; B., Natalini; C., Thomsen; M. H., Ni; Costantino, Gabriele; R., Pellicciari. - In: IL FARMACO. - ISSN 0014-827X. - 50:(1995), pp. 327-331.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11381/2437257
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