| Cyclohexylcarbamic acid 3 ‘-or 4 ‘-substituted biphenyl-3-yl esters as fatty acid amide hydrolase inhibitors: synthesis, quantitative structure− activity relationships, and … M Mor, S Rivara, A Lodola, PV Plazzi, G Tarzia, A Duranti, A Tontini, ... Journal of medicinal chemistry 47 (21), 4998-5008, 2004 | 327 | 2004 |
| Design, synthesis, and structure− activity relationships of alkylcarbamic acid aryl esters, a new class of fatty acid amide hydrolase inhibitors G Tarzia, A Duranti, A Tontini, G Piersanti, M Mor, S Rivara, PV Plazzi, ... Journal of medicinal chemistry 46 (12), 2352-2360, 2003 | 207 | 2003 |
| 2-n-Butyl-9-methyl-8-[1,2,3]triazol-2-yl-9H-purin-6-ylamine and Analogues as A2A Adenosine Receptor Antagonists. Design, Synthesis, and Pharmacological … P Minetti, MO Tinti, P Carminati, M Castorina, MA Di Cesare, S Di Serio, ... Journal of medicinal chemistry 48 (22), 6887-6896, 2005 | 110 | 2005 |
| Enantioselective Total Synthesis of (−)‐Acylfulvene and (−)‐Irofulven M Movassaghi, G Piizzi, DS Siegel, G Piersanti Angewandte Chemie 118 (35), 5991-5995, 2006 | 83 | 2006 |
| Switchable reactivity of acylated α, β-dehydroamino ester in the Friedel− Crafts alkylation of indoles by changing the Lewis acid E Angelini, C Balsamini, F Bartoccini, S Lucarini, G Piersanti The Journal of Organic Chemistry 73 (14), 5654-5657, 2008 | 81 | 2008 |
| Synthesis and quantitative structure− activity relationship of fatty acid amide hydrolase inhibitors: Modulation at the N-portion of biphenyl-3-yl alkylcarbamates M Mor, A Lodola, S Rivara, F Vacondio, A Duranti, A Tontini, S Sanchini, ... Journal of medicinal chemistry 51 (12), 3487-3498, 2008 | 78 | 2008 |
| Synthesis of tryptamine derivatives via a direct, one-pot reductive alkylation of indoles M Righi, F Topi, S Bartolucci, A Bedini, G Piersanti, G Spadoni The Journal of Organic Chemistry 77 (14), 6351-6357, 2012 | 75 | 2012 |
| Synthesis and structure–activity relationships of FAAH inhibitors: cyclohexylcarbamic acid biphenyl esters with chemical modulation at the proximal phenyl ring G Tarzia, A Duranti, G Gatti, G Piersanti, A Tontini, S Rivara, A Lodola, ... ChemMedChem: Chemistry Enabling Drug Discovery 1 (1), 130-139, 2006 | 73 | 2006 |
| Iridium-catalyzed direct synthesis of tryptamine derivatives from indoles: exploiting N-protected β-amino alcohols as alkylating agents S Bartolucci, M Mari, A Bedini, G Piersanti, G Spadoni The Journal of Organic Chemistry 80 (6), 3217-3222, 2015 | 67 | 2015 |
| Enantioselective total synthesis of (−)-Acylfulvene and (−)-Irofulven DS Siegel, G Piizzi, G Piersanti, M Movassaghi The Journal of organic chemistry 74 (24), 9292-9304, 2009 | 66 | 2009 |
| Synthesis of (E)-8-(3-Chlorostyryl)caffeine Analogues Leading to 9-Deazaxanthine Derivatives as Dual A2A Antagonists/MAO-B Inhibitors S Rivara, G Piersanti, F Bartoccini, G Diamantini, D Pala, T Riccioni, ... Journal of Medicinal Chemistry 56 (3), 1247-1261, 2013 | 60 | 2013 |
| Quantifying amino acid conformational preferences and side-chain–side-chain interactions in β-hairpins ST Phillips, G Piersanti, PA Bartlett Proceedings of the National Academy of Sciences 102 (39), 13737-13742, 2005 | 59 | 2005 |
| Synthesis of (−)-Epi-Indolactam V by an intramolecular Buchwald–Hartwig C–N coupling cyclization reaction M Mari, F Bartoccini, G Piersanti The Journal of Organic Chemistry 78 (15), 7727-7734, 2013 | 58 | 2013 |
| A Novel One-Pot Approach of Hexahydropyrrolo[2,3-b]indole Nucleus by a cascade addition/cyclization strategy: Synthesis of (±)-Esermethole S Lucarini, F Bartoccini, F Battistoni, G Diamantini, G Piersanti, M Righi, ... Organic Letters 12 (17), 3844-3847, 2010 | 53 | 2010 |
| A Trans-Stereoselective Synthesis of 3-Halo-4-alkyl (aryl)-NH-azetidin-2-ones E Bandini, G Favi, G Martelli, M Panunzio, G Piersanti Organic Letters 2 (8), 1077-1079, 2000 | 49 | 2000 |
| Iron-Catalyzed Direct C3-Benzylation of Indoles with Benzyl Alcohols through Borrowing Hydrogen G Di Gregorio, M Mari, F Bartoccini, G Piersanti The Journal of Organic Chemistry 82 (16), 8769-8775, 2017 | 47 | 2017 |
| Tricyclic alkylamides as melatonin receptor ligands with antagonist or inverse agonist activity V Lucini, M Pannacci, F Scaglione, F Fraschini, S Rivara, M Mor, F Bordi, ... Journal of medicinal chemistry 47 (17), 4202-4212, 2004 | 45 | 2004 |
| Palladium (II)-Catalyzed Cross-Dehydrogenative Coupling (CDC) of N-Phthaloyl Dehydroalanine Esters with Simple Arenes: Stereoselective Synthesis of Z-Dehydrophenylalanine … F Bartoccini, DM Cannas, F Fini, G Piersanti Organic letters 18 (11), 2762-2765, 2016 | 44 | 2016 |
| Direct, Regioselective, and Chemoselective Preparation of Novel Boronated Tryptophans by Friedel–Crafts Alkylation S Bartolucci, F Bartoccini, M Righi, G Piersanti Organic letters 14 (2), 600-603, 2012 | 41 | 2012 |
| New branched macrocyclic ligand and its side-arm, two urea-based receptors for anions: synthesis, binding studies and crystal structure M Formica, V Fusi, E Macedi, P Paoli, G Piersanti, P Rossi, G Zappia, ... New Journal of Chemistry 32 (7), 1204-1214, 2008 | 41 | 2008 |
Francesca BartocciniDipartimento Scienze BiomolecolariVerified email at uniurb.it
