Giovanni Loriga

Tricyclic Pyrazoles. 4. Synthesis and Biological Evaluation of Analogues of the Robust and Selective CB₂Cannabinoid Ligand 1-(2‘,4‘-Dichlorophenyl)-6-methyl-<i>N</i>-piperidin-1-yl- 1,4-dihydroindeno[1,2-<i>c</i>]pyrazole-3-carboxamide

Gabriele Murineddu, Paolo Lazzari, Stefania Ruiu et al. · Journal of Medicinal Chemistry · 2006 · 72 citations · Full text

Tricyclic Pyrazoles. Part 1: Synthesis and Biological Evaluation of Novel 1,4-Dihydroindeno[1,2-c]pyrazol-based Ligands for CB1and CB2 Cannabinoid Receptors

Jean‐Mario Mussinu, Stefania Ruiu, Antonio Mulè et al. · Bioorganic & Medicinal Chemistry · 2003 · 59 citations

Cannabis Use, Medicinal Chemistry, Heterocyclic +12

Synthesis and Anti-HIV-1 Activity of New Delavirdine Analogues Carrying Arylpyrrole Moieties.

Gérard A. Pinna, Giovanni Loriga, Gabriele Murineddu et al. · Chemical and Pharmaceutical Bulletin · 2001 · 53 citations · Full text

Immunology, Delavirdine Analogues, Chemistry +18

Synthesis and application in asymmetric copper(I)-catalyzed allylic oxidation of a new chiral 1,10-phenanthroline derived from pinene

Giorgio Chelucci, Giovanni Loriga, Gabriele Murineddu et al. · Tetrahedron Letters · 2002 · 49 citations

Chemical Engineering, Engineering, Allylic Oxidation +7

Tricyclic pyrazoles. Part 2: Synthesis and biological evaluation of novel 4,5-dihydro-1H-benzo[g]indazole-based ligands for cannabinoid receptors

Gabriele Murineddu, Stefania Ruiu, Jean‐Mario Mussinu et al. · Bioorganic & Medicinal Chemistry · 2005 · 49 citations · Full text

Cannabis Use, Medicinal Chemistry, Heterocyclic +10