C. Leslie

发表

Central administration of NPY or an NPY-Y5 selective agonist increase in vivo extracellular monoamine levels in mesocorticolimbic projecting areas

R. Carletti, L. Caberlotto, E. Valerio, 2011, Neuropharmacology.

GSK 163090 ) , a Potent , Selective , and Orally Active 5-HT 1 A / B / D Receptor Antagonist

S. Bromidge, S. Ward, A. Jaxa-Chamiec, 2010 .

Discovery and structure-activity relationship of a novel spirocarbamate series of NPY Y5 antagonists.

M. Tessari, L. Caberlotto, G. Merlo, 2010, Bioorganic & medicinal chemistry letters.

Synthesis and structure-activity relationship of N-(3-azabicyclo[3.1.0]hex-6-ylmethyl)-5-(2-pyridinyl)-1,3-thiazol-2-amines derivatives as NPY Y5 antagonists.

L. Caberlotto, R. Di Fabio, C. Seri, 2010, Bioorganic & medicinal chemistry letters.

Novel imidazobenzazepine derivatives as dual H1/5-HT2A antagonists for the treatment of sleep disorders.

M. Wigglesworth, C. Corti, M. Gianotti, 2010, Bioorganic & medicinal chemistry letters.

Diastereoselectivity in the SE2″ reaction of chiral pentadienylsilanes: a test for the relative importance of steric and electronic effects

A. K. Sarkar, I. Fleming, S. Peukert, 1996 .

Total synthesis and semi-synthetic approaches to analogues of antibacterial natural product althiomycin.

W. Kazmierski, P. Zarantonello, R. Ferritto, 2002, Bioorganic & medicinal chemistry letters.

Design and synthesis of novel tricyclic benzoxazines as potent 5-HT(1A/B/D) receptor antagonists leading to the discovery of 6-{2-[4-(2-methyl-5-quinolinyl)-1-piperazinyl]ethyl}-4H-imidazo[5,1-c][1,4]benzoxazine-3-carboxamide (GSK588045).

S. Bromidge, J. Watson, A. Worby, 2010, Journal of medicinal chemistry.

Studies Towards Asymmetric Catalyzed Metallo-ene Reactions

J. Durand, W. Oppolzer, M. Hutzinger, 1997 .

Diastereoselectivity in the SE2′′ Reaction of Chiral Pentadienylsilanes: A Test for the Relative Importance of Steric and Electronic Effects.

A. K. Sarkar, I. Fleming, S. Peukert, 1996 .

Novel carbazole derivatives as NPY Y1 antagonists.

F. Pavone, L. Stasi, D. Donati, 2007, Bioorganic & medicinal chemistry letters.

d‐Glucose as a Regioselectively Addressable Scaffold for Combinatorial Chemistry on Solid Phase

F. Nicotra, P. Seneci, F. Peri, 2003 .

Synthesis and SAR of substituted tetrahydrocarbazole derivatives as new NPY-1 antagonists.

D. Donati, Barbara Bertani, A. Bozzoli, 2006, Bioorganic & medicinal chemistry letters.

Stereospecific synthesis and structure-activity relationships of unsymmetrical 4,4-diphenylbut-3-enyl derivatives of nipecotic acid as GAT-1 inhibitors.

L. Mangiarini, E. Greco, R. Di Fabio, 2011, Bioorganic & medicinal chemistry letters.

Studies on the resorcylates: biomimetic total syntheses of (+)-montagnetol and (+)-erythrin

Andrew J. P. White, A. Barrett, A. White, 2010 .

Total Synthesis and Semi‐Synthetic Approaches to Analogues of Antibacterial Natural Product Althiomycin.

W. Kazmierski, P. Zarantonello, R. Ferritto, 2002 .

Discovery of 1-(3-{2-[4-(2-methyl-5-quinolinyl)-1-piperazinyl]ethyl}phenyl)-2-imidazolidinone (GSK163090), a Potent, selective, and orally active 5-HT1A/B/D receptor antagonist.

S. Bromidge, S. Ward, A. Jaxa-Chamiec, 2010, Journal of medicinal chemistry.