Silvia Terreni

发表

1,2,4-Triazol-3-yl-thiopropyl-tetrahydrobenzazepines: A Series of Potent and Selective Dopamine D3 Receptor Antagonists

J. Hagan, A. Schwarz, A. Capelli, 2007 .

Isoindolone derivatives, a new class of 5-HT2C antagonists: synthesis and biological evaluation.

G. Tedesco, M. Wood, D. Donati, 2007, Bioorganic & medicinal chemistry letters.

A novel ketolide class: Synthesis and antibacterial activity of a lead compound.

S. Lociuro, A. Pozzan, E. Ratti, 2007, Bioorganic & medicinal chemistry letters.

Pyrrolo[1,2-a]pyrazine and pyrazolo[1,5-a]pyrazine: novel, potent, and selective series of Vasopressin 1b receptor antagonists.

A. Pozzan, F. Micheli, R. Di Fabio, 2010, Bioorganic & medicinal chemistry letters.

[3-azabicyclo[3.1.0]hex-1-yl]phenyl-benzenesulfonamides as selective dopamine D3 antagonists.

A. Prandi, C. Heidbreder, D. Donati, 2010, Bioorganic & medicinal chemistry letters.

Triazolyl Azabicyclo[3.1.0]hexanes: a Class of Potent and Selective Dopamine D3 Receptor Antagonists

A. Capelli, G. Tedesco, A. Worby, 2010, ChemMedChem.

Novel analogues of ketamine and phencyclidine as NMDA receptor antagonists.

E. Bettini, A. Paio, P. Zarantonello, 2011, Bioorganic & medicinal chemistry letters.

Silylformylation of Chiral 1‐Alkynes, Catalysed by Solvated Rhodium Atoms

P. Salvadori, A. Caporusso, L. Aronica, 2001 .

Diaryl substituted pyrrolidinones and pyrrolones as 5-HT2C inhibitors: synthesis and biological evaluation.

G. Tedesco, G. Riley, M. Wood, 2006, Bioorganic & medicinal chemistry letters.

1-(Aryl)-6-[alkoxyalkyl]-3-azabicyclo[3.1.0]hexanes and 6-(aryl)-6-[alkoxyalkyl]-3-azabicyclo[3.1.0]hexanes: a new series of potent and selective triple reuptake inhibitors.

K. Read, G. Tedesco, D. Minick, 2010, Journal of medicinal chemistry.

6-(3,4-dichlorophenyl)-1-[(methyloxy)methyl]-3-azabicyclo[4.1.0]heptane: a new potent and selective triple reuptake inhibitor.

K. Read, G. Tedesco, R. Carletti, 2010, Journal of medicinal chemistry.

1,2,4-Triazolyl azabicyclo[3.1.0]hexanes: a new series of potent and selective dopamine D(3) receptor antagonists.

A. Capelli, G. Tedesco, F. Blaney, 2010, Journal of medicinal chemistry.

5-HT2C antagonists based on fused heterotricyclic templates: design, synthesis and biological evaluation.

G. Tedesco, M. Wood, D. Donati, 2007, Bioorganic & medicinal chemistry letters.

Exploration of the amine terminus in a novel series of 1,2,4-triazolo-3-yl-azabicyclo[3.1.0]hexanes as selective dopamine D3 receptor antagonists.

A. Capelli, G. Tedesco, C. Heidbreder, 2010, Journal of medicinal chemistry.