BARTOCCINI, FRANCESCA
BARTOCCINI, FRANCESCA
Dipartimento di Scienze Biomolecolari (DISB)
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 Characterization
2005 Minetti, P; Tinti, M. O.; Carminati, P; Castorina, M; DI CESARE, M. A.; DI SERIO, S; Gallo, G; Ghirardi, O; Giorgi, F; Giorgi, Luca; Piersanti, Giovanni; Bartoccini, Francesca; Tarzia, Giorgio
2-n-butyl-9-methyl-8-(1,2,3)triazol-2yl-9H-purin-6-yl-amine (ST 1535) and analogs as A2a Adenosine receptor antagonists. Design, synthesis and pharmacological characterization
2003 Bartoccini, Francesca; Castorina, M.; DI CESARE, M. A.; Gallo, G; Ghirardi, O.; Giorgi, F. GIORGI L.; Minetti, P.; Piersanti, Giovanni; Tarzia, Giorgio; Tinti, M. O.
A Novel One-Pot Approach of Hexahydropyrrolo[2,3-b]indole Nucleus by a cascade addition/cyclization strategy: Synthesis of (±)-Esermethole
2010 Lucarini, Simone; Bartoccini, Francesca; Battistoni, F; Diamantini, Giuseppe; Piersanti, Giovanni; Righi, M; Spadoni, Gilberto
A Short Synthesis of (−)‐6,7‐Secoagroclavine via Metal‐Free Reductive Coupling
2024 Diotallevi, Francesca; Bartoccini, Francesca; Piersanti, Giovanni
A simple, modular synthesis of C4-substituted tryptophan derivatives
2016 Bartoccini, Francesca; Bartolucci, Silvia; Mari, Michele; Piersanti, Giovanni
A synthetic thiol molecule releasing N-acetyl-l-cysteine and cysteamine drives early up-regulation of immunoproteasome subunits in the lymph nodes of mice infected with LP-BM5 leukemia retrovirus
2024 Crinelli, Rita; Monittola, Francesca; Masini, Sofia; Diotallevi, Aurora; Bartoccini, Francesca; Smietana, Michaël; Galluzzi, Luca; Magnani, Mauro; Fraternale, Alessandra
Asymmetric Alkylation of Cyclic Ketones with Dehydroalanine via H-Bond-Directing Enamine Catalysis: Straightforward Access to Enantiopure Unnatural α-Amino Acids
2022 Retini, Michele; Bartolucci, Silvia; Bartoccini, Francesca; Piersanti, Giovanni
Asymmetric Synthesis and Biological Evaluation of Both Enantiomers of 5- and 6-Boronotryptophan as Potential Boron Delivery Agents for Boron Neutron Capture Therapy
2024 Retini, Michele; Järvinen, Juulia; Bahrami, Katayun; Tampio, Janne; Bartoccini, Francesca; Riihelä, Petri; Pehkonen, Henna; Värä, Arina; Laitinen, Tuomo; Huttunen, Kristiina M.; Rautio, Jarkko; Piersanti, Giovanni; Timonen, Juri M.
Asymmetric Total Synthesis of All Rugulovasine Stereoisomers and Preliminary Evaluation of Their Biological Properties
2022 Bartoccini, Francesca; Regni, Alessio; Retini, Michele; Piersanti, Giovanni
C3-Alkylation of indoles and oxindoles by alcohols by means of borrowing hydrogen methodology
2020 Bartoccini, Francesca; Retini, Michele; Piersanti, Giovanni
Concise and Convergent Enantioselective Total Syntheses of (+)- and (-)-Fumimycin
2019 Retini, Michele; Bartolucci, Silvia; Bartoccini, Francesca; Mari, Michele; Piersanti, Giovanni
Concise catalytic asymmetric synthesis of (R)-4-amino Uhle's ketone
2021 Bartoccini, Francesca; Regni, Alessio; Retini, Michele; Piersanti, Giovanni
Development of a practical and sustainable strategy for the synthesis of ST1535 by an iron-catalyzed Kumada cross-coupling reaction
2014 Bartoccini, Francesca; Piersanti, Giovanni; Silvia, Armaroli; Alberto, Cerri; Walter, Cabri
Direct B-alkyl Suzuki-Miyaura cross-coupling of 2-halopurines. Practical synthesis os ST1535, a potent adenosine A2A receptor antagonist
2010 Bartoccini, Francesca; Cabri, W; Celona, D; Minetti, P; Piersanti, Giovanni; G., Tarzia
Direct, Regioselective, and Chemoselective Preparation of Novel Boronated Tryptophans by Friedel–Crafts Alkylation
2012 Bartolucci, Silvia; Bartoccini, Francesca; Righi, M.; Piersanti, Giovanni
Dithiol Based on L-Cysteine and Cysteamine as a Disulfide-Reducing Agent
2022 Bartoccini, Francesca; Retini, Michele; Crinelli, Rita; Menotta, Michele; Fraternale, Alessandra; Piersanti, Giovanni
Divergent reactions of oxindoles with amino alcohols via the borrowing hydrogen process: oxindole ring opening vs. C3 alkylation
2018 Di Gregorio, Giovanni; Mari, Michele; Bartolucci, Silvia; Bartoccini, Francesca; Piersanti, Giovanni
Divergent synthesis of novel 9-deazaxanthine derivatives via late-stage cross-coupling reactions
2012 Bartoccini, Francesca; Piersanti, Giovanni; Marco, Mor; Tarzia, Giorgio; Patrizia, Minetti; Walter, Cabri
Enantioselective organocatalytic strategies to noncanonical α‐amino acids
2024 Pecchini, Pietro; Fochi, Mariafrancesca; Bartoccini, Francesca; Piersanti, Giovanni; Bernardi, Luca
General Access to Clavine Alkaloids via a Rhodium(I)‐Catalyzed Diastereoselective Hayashi‐Miyaura Reaction
2024 Leoni, Giovanni; Bartoccini, Francesca; Piersanti, Giovanni
Titolo | Data di pubblicazione | Autore(i) | File |
---|---|---|---|
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 Characterization | 1-gen-2005 | Minetti, P; Tinti, M. O.; Carminati, P; Castorina, M; DI CESARE, M. A.; DI SERIO, S; Gallo, G; Ghirardi, O; Giorgi, F; Giorgi, Luca; Piersanti, Giovanni; Bartoccini, Francesca; Tarzia, Giorgio | |
2-n-butyl-9-methyl-8-(1,2,3)triazol-2yl-9H-purin-6-yl-amine (ST 1535) and analogs as A2a Adenosine receptor antagonists. Design, synthesis and pharmacological characterization | 1-gen-2003 | Bartoccini, Francesca; Castorina, M.; DI CESARE, M. A.; Gallo, G; Ghirardi, O.; Giorgi, F. GIORGI L.; Minetti, P.; Piersanti, Giovanni; Tarzia, Giorgio; Tinti, M. O. | |
A Novel One-Pot Approach of Hexahydropyrrolo[2,3-b]indole Nucleus by a cascade addition/cyclization strategy: Synthesis of (±)-Esermethole | 1-gen-2010 | Lucarini, Simone; Bartoccini, Francesca; Battistoni, F; Diamantini, Giuseppe; Piersanti, Giovanni; Righi, M; Spadoni, Gilberto | |
A Short Synthesis of (−)‐6,7‐Secoagroclavine via Metal‐Free Reductive Coupling | 1-gen-2024 | Diotallevi, Francesca; Bartoccini, Francesca; Piersanti, Giovanni | |
A simple, modular synthesis of C4-substituted tryptophan derivatives | 1-gen-2016 | Bartoccini, Francesca; Bartolucci, Silvia; Mari, Michele; Piersanti, Giovanni | |
A synthetic thiol molecule releasing N-acetyl-l-cysteine and cysteamine drives early up-regulation of immunoproteasome subunits in the lymph nodes of mice infected with LP-BM5 leukemia retrovirus | 1-gen-2024 | Crinelli, Rita; Monittola, Francesca; Masini, Sofia; Diotallevi, Aurora; Bartoccini, Francesca; Smietana, Michaël; Galluzzi, Luca; Magnani, Mauro; Fraternale, Alessandra | |
Asymmetric Alkylation of Cyclic Ketones with Dehydroalanine via H-Bond-Directing Enamine Catalysis: Straightforward Access to Enantiopure Unnatural α-Amino Acids | 1-gen-2022 | Retini, Michele; Bartolucci, Silvia; Bartoccini, Francesca; Piersanti, Giovanni | |
Asymmetric Synthesis and Biological Evaluation of Both Enantiomers of 5- and 6-Boronotryptophan as Potential Boron Delivery Agents for Boron Neutron Capture Therapy | 1-gen-2024 | Retini, Michele; Järvinen, Juulia; Bahrami, Katayun; Tampio, Janne; Bartoccini, Francesca; Riihelä, Petri; Pehkonen, Henna; Värä, Arina; Laitinen, Tuomo; Huttunen, Kristiina M.; Rautio, Jarkko; Piersanti, Giovanni; Timonen, Juri M. | |
Asymmetric Total Synthesis of All Rugulovasine Stereoisomers and Preliminary Evaluation of Their Biological Properties | 1-gen-2022 | Bartoccini, Francesca; Regni, Alessio; Retini, Michele; Piersanti, Giovanni | |
C3-Alkylation of indoles and oxindoles by alcohols by means of borrowing hydrogen methodology | 1-gen-2020 | Bartoccini, Francesca; Retini, Michele; Piersanti, Giovanni | |
Concise and Convergent Enantioselective Total Syntheses of (+)- and (-)-Fumimycin | 1-gen-2019 | Retini, Michele; Bartolucci, Silvia; Bartoccini, Francesca; Mari, Michele; Piersanti, Giovanni | |
Concise catalytic asymmetric synthesis of (R)-4-amino Uhle's ketone | 1-gen-2021 | Bartoccini, Francesca; Regni, Alessio; Retini, Michele; Piersanti, Giovanni | |
Development of a practical and sustainable strategy for the synthesis of ST1535 by an iron-catalyzed Kumada cross-coupling reaction | 1-gen-2014 | Bartoccini, Francesca; Piersanti, Giovanni; Silvia, Armaroli; Alberto, Cerri; Walter, Cabri | |
Direct B-alkyl Suzuki-Miyaura cross-coupling of 2-halopurines. Practical synthesis os ST1535, a potent adenosine A2A receptor antagonist | 1-gen-2010 | Bartoccini, Francesca; Cabri, W; Celona, D; Minetti, P; Piersanti, Giovanni; G., Tarzia | |
Direct, Regioselective, and Chemoselective Preparation of Novel Boronated Tryptophans by Friedel–Crafts Alkylation | 1-gen-2012 | Bartolucci, Silvia; Bartoccini, Francesca; Righi, M.; Piersanti, Giovanni | |
Dithiol Based on L-Cysteine and Cysteamine as a Disulfide-Reducing Agent | 1-gen-2022 | Bartoccini, Francesca; Retini, Michele; Crinelli, Rita; Menotta, Michele; Fraternale, Alessandra; Piersanti, Giovanni | |
Divergent reactions of oxindoles with amino alcohols via the borrowing hydrogen process: oxindole ring opening vs. C3 alkylation | 1-gen-2018 | Di Gregorio, Giovanni; Mari, Michele; Bartolucci, Silvia; Bartoccini, Francesca; Piersanti, Giovanni | |
Divergent synthesis of novel 9-deazaxanthine derivatives via late-stage cross-coupling reactions | 1-gen-2012 | Bartoccini, Francesca; Piersanti, Giovanni; Marco, Mor; Tarzia, Giorgio; Patrizia, Minetti; Walter, Cabri | |
Enantioselective organocatalytic strategies to noncanonical α‐amino acids | 1-gen-2024 | Pecchini, Pietro; Fochi, Mariafrancesca; Bartoccini, Francesca; Piersanti, Giovanni; Bernardi, Luca | |
General Access to Clavine Alkaloids via a Rhodium(I)‐Catalyzed Diastereoselective Hayashi‐Miyaura Reaction | 1-gen-2024 | Leoni, Giovanni; Bartoccini, Francesca; Piersanti, Giovanni |