Francesca Bartoccini
Francesca Bartoccini
Dipartimento Scienze Biomolecolari
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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
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
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
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
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
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
Organocatalytic synthesis of α-quaternary amino acid derivatives via aza-Friedel–Crafts alkylation of indoles with simple α-amidoacrylates
M Righi, F Bartoccini, S Lucarini, G Piersanti
Tetrahedron 67 (41), 7923-7928, 2011
Synthesis of (±)-cis-Clavicipitic Acid by a Rh(I)-Catalyzed Intramolecular Imine Reaction
F Bartoccini, M Casoli, M Mari, G Piersanti
The Journal of organic chemistry 79 (7), 3255-3259, 2014
Synthesis of benzo [1, 2-d; 3, 4-d′] diimidazole and 1H-pyrazolo [4, 3-b] pyridine as putative A 2A receptor antagonists
G Piersanti, L Giorgi, F Bartoccini, G Tarzia, P Minetti, G Gallo, F Giorgi, ...
Organic & biomolecular chemistry 5 (16), 2567-2571, 2007
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
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
Synthesis of Boron‐and Silicon‐Containing Amino Acids through Copper‐Catalysed Conjugate Additions to Dehydroalanine Derivatives
F Bartoccini, S Bartolucci, S Lucarini, G Piersanti
European Journal of Organic Chemistry 2015 (15), 3352-3360, 2015
Synthesis and Biological Evaluation of Metabolites of 2-n-Butyl-9-methyl-8-[1, 2, 3] triazol-2-yl-9 H-purin-6-ylamine (ST1535), A Potent Antagonist of the A2A Adenosine …
G Piersanti, F Bartoccini, S Lucarini, W Cabri, MA Stasi, T Riccioni, ...
Journal of medicinal chemistry 56 (13), 5456-5463, 2013
Synthesis of 2-substituted tryptophans via a C3-to C2-alkyl migration
M Mari, S Lucarini, F Bartoccini, G Piersanti, G Spadoni
Beilstein journal of organic chemistry 10 (1), 1991-1998, 2014
A simple, modular synthesis of C4-substituted tryptophan derivatives
F Bartoccini, S Bartolucci, M Mari, G Piersanti
Organic & Biomolecular Chemistry 14, 10095-10110, 2016
Direct B-Alkyl Suzuki−Miyaura Cross-Coupling of 2-Halopurines. Practical Synthesis of ST1535, a Potent Adenosine A2A Receptor Antagonist
F Bartoccini, W Cabri, D Celona, P Minetti, G Piersanti, G Tarzia
The Journal of organic chemistry 75 (15), 5398-5401, 2010
Development of a practical and sustainable strategy for the synthesis of ST1535 by an iron-catalyzed Kumada cross-coupling reaction
F Bartoccini, G Piersanti, S Armaroli, A Cerri, W Cabri
Tetrahedron Letters 55 (7), 1376-1378, 2014
Improved synthesis of γ-nitro-α-amino ester and acid derivatives
R Ballini, C Balsamini, F Bartoccini, M Gianotti, C Martinelli, N Savoretti
Synthesis 2005 (02), 296-300, 2005
Synthesis of new C-6 alkyliden penicillin derivatives as β-lactamase inhibitors
B Di Giacomo, G Tarzia, A Bedini, G Gatti, F Bartoccini, C Balsamini, ...
Il Farmaco 57 (4), 273-283, 2002
Divergent reactions of oxindoles with amino alcohols via the borrowing hydrogen process: oxindole ring opening vs. C3 alkylation
G Di Gregorio, M Mari, S Bartolucci, F Bartoccini, G Piersanti
Organic Chemistry Frontiers 5 (10), 1622-1627, 2018
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