• Italiano
  • English
ATENEO DI QUALITÀ ACCREDITATO ANVUR - FASCIA A

menu

ATENEO DI QUALITÀ ACCREDITATO ANVUR - FASCIA A

Principali pubblicazioni sull’argomento (2006-2016)

  1. Curti, C.; Zanardi, F.; Battistini, L.; Sartori, A.; Rassu, G.; Auzzas, L.; Roggio, A.; Pinna, L.; Casiraghi, G. New Enantioselective Entry to Cycloheptane Amino Acid Polyols. J. Org. Chem. 2006, 71, 225-230.
  2. Zanardi, F.; Sartori, A.; Curti, C.; Battistini, L.; Rassu, G.; Nicastro, G.; Casiraghi, G. Diastereoselective Synthesis of 4,5'-Bis-Proline Compounds via Reductive Dimerization of N-Acyloxyiminium Ions. J. Org. Chem. 2007, 72, 1814-1817.
  3. Zanardi, F.; Curti, C.; Sartori, A.; Rassu, G.; Roggio, A.; Battistini, L.; Burreddu, P.; Pinna, L.; Pelosi, G.; Casiraghi, G. Further Uses of Pyrrole-Based Dienoxysilane Synthons: A Full Aldol Approach to Azabicyclo[x.2.1]alkane Systems. Eur. J. Org. Chem. 2008, 2273-2287.
  4. Curti, C.; Sartori, A.; Battistini, L.; Rassu, G.; Burreddu, P.; Zanardi, F.; Casiraghi, G. Vicarious Silylative Mukaiyama Aldol Reaction: A Vinylogous Extension. J. Org. Chem. 2008, 73, 5446-5451 (DOI: 10.1021/jo800741c).
  5. Sartori, A.; Curti, C.; Battistini, L.; Burreddu, P.; Rassu, G.; Pelosi, G.; Casiraghi, G.; Zanardi, F. Direct-type vinylogous Mukaiyama-Michael addition reactions involving pyrrolinone donors. Tetrahedron 2008, 64, 11697-11705 (DOI: 10.1016/j.tet.2008.10.007)
  6. Casiraghi, G.; Zanardi, F.; Battistini, L.; Rassu, G. Advances in Exploring Heterocyclic Dienoxysilane Nucleophiles in Asymmetric Synthesis Synlett 2009, 1525-1542.
  7. Curti, C.; Sartori, A.; Battistini, L.; Rassu, G.; Zanardi, F.; Casiraghi, G. Asymmetric, catalytic, vinylogous aldol reactions using pyrrole-based dienoxy silanes. Enantioselective synthesis of α,β-unsaturated γ-butyrolactam synthons. Tetrahedron Lett. 2009, 50, 3428-3431.
  8. Zambrano, V.; Rassu, G.; Roggio, A.; Pinna, L.; Zanardi, F.; Curti, C.; Casiraghi, G.; Battistini, L. Asymmetric Total Synthesis of 1-Deoxy-7,8-di-epi-castanospermine. Org. Biomol. Chem. 2010, 8, 1725-1730. DOI: 10.1039/b924721a.
  9. Curti, C.; Ranieri, B.; Battistini, L.; Gloria Rassu, G.; Zambrano, V.; Pelosi, G.; Casiraghi, G.; Zanardi, F. Catalytic, Asymmetric Vinylogous Mukaiyama Aldol Reactions of Pyrrole- and Furan-Based Dienoxy Silanes: How the Diene Heteroatom Impacts Stereocontrol. Adv. Synth. Catal. 2010, 352, 2011-2022. DOI: 10.1002/adsc.201000189.
  10. Curti, C.; Battistini, L.; Zanardi, F.; Rassu, G.; Zambrano, V.; Pinna, L.; Casiraghi, G. Uncatalyzed, Diastereoselective Vinylogous Mukaiyama Aldol Reactions on Aqueous media: Pyrrole vs Furan 2-Silyloxy Dienes. J. Org. Chem. 2010, 75, 8681-8684. DOI: 10.1021/jo101799e.
  11. Casiraghi, G.; Battistini, L.; Curti, C.; Rassu, G.; Zanardi, F. The Vinylogous Aldol and Related Reactions: Ten Years of Progress. Chem. Rev. 2011, 111, 3076-3154. DOI: 10.1021/cr100304n.
  12. Curti, C.; Battistini, L.; Ranieri, B.; Pelosi, G.; Rassu, G.; Casiraghi, G.; Zanardi, F. anti-Selective, Catalytic Asymmetric Vinylogous Mukaiyama Mannich Reactions of Pyrrole-Based Silyl Dienolates with N-Aryl Aldimines. J. Org. Chem. 2011, 76, 2248-2252. Doi: 10.1021/jo1021234.
  13. Battistini, L.; Dell’Amico L.; Sartori, A.; Curti, C.; Pelosi, G.; Casiraghi, G.; Attanasi, O.A.; Favi, G.; Zanardi, F. On-Water Vinylogous Mukaiyama-Michael Addition of Heterocyclic 2-Silyloxydienes to 1,2-Diaza-1,3-dienes: One-Pot Three-Step Entry to Functionality-Rich Pyrroles. Adv. Synth. Catal. 2011, 353, 1966-1972. DOI: 10.1002/adsc.201100296.
  14. Curti, C.; Battistini, L.; Sartori, A.; Lodola, A.; Mor, M.; Rassu, G.; Pelosi, G.; Zanardi, F.; Casiraghi, G. Catalytic, Asymmetric Hypervinylogous Mukaiyama Aldol Reactions of Extended Furan-Based Silyl Enolates. Org. Lett. 2011, 13, 4738-4741 (DOI: 10.1021/ol2020626).
  15. Sartori, A.; Dell’Amico, L.; Curti, C.; Battistini, L.; Pelosi, G.; Rassu, G.; Casiraghi, G.; Zanardi, F. Aqueous and Solvent-Free Uncatalyzed Three-Component Vinylogous Mukaiyama-Mannich Reactions of Pyrrole-Based Silyl Dienolates. Adv. Synth. Catal. 2011, 353, 3278-3284 (DOI: 10.1002/adsc.201100572).
  16. Ranieri, B.; Curti, C.; Battistini, L.; Sartori, A.; Pinna, L.; Casiraghi, G.; Zanardi, F. Diastereo- and Enantioselective Catalytic Vinylogous Mukaiyama-Mannich Reactions of Pyrrole-Based Silyl Dienolates with Alkyl-Substituted Aldehydes. J. Org. Chem., 2011, 76, 10291-10298 (DOI: 10.1021/jo201875a).
  17. Rassu, G.; Zambrano, V.; Tanca, R.; Sartori, A.; Battistini, L.; Zanardi, F.; Curti, C.; Casiraghi, G. 3-Alkenyl-2-silyloxyindoles: an Enabling, yet Understated Progeny of Vinylogous Carbon Nucleophiles. Eur. J. Org. Chem. 2012, 466-470 (DOI: 10.1002/ejoc.201101446).
  18. Curti, C.; Rassu, G.; Zambrano, V.; Pinna, L.; Pelosi, G.; Sartori, A.; Battistini, L.; Zanardi, F.; Casiraghi, G. Bifunctional Cinchona Alkaloid/Thiourea Catalyzes Direct and Enantioselective Vinylogous Michael Addition of 3-Alkylidene Oxindoles to Nitroolefins. Angew. Chem. Int. Ed. 2012, 51, 6200-6204. DOI: 10.1002/anie.201202027.
  19. Zanardi, F.; Rassu, G.; Battistini, L.; Curti, C.; Sartori, A.; Casiraghi, G. The Principle of Vinylogy as Applied to Heterocyclic Donor Systems. In Targets in Heterocyclic Systems – Chemistry and Properties (Attanasi, O. A., Spinelli, D. Eds.); Società Chimica Italiana: Roma, 2012, Vol. 16, p 56-89.
  20. Rassu, G.; Zambrano, V.; Pinna, L.; Curti, C.; Battistini, L.; Sartori, A.; Pelosi, G.; Zanardi, F.; Casiraghi, G. Direct Regio-, Diastereo-, and Enantioselective Vinylogous Michael Addition of Prochiral 3-Alkylidene Oxindoles to Nitroolefins. Adv. Synth. Catal. 2013, 355, 1881-1886 (DOI: 10.1002/adsc.201300168).
  21. Sartori, A.; Dell’Amico, L.; Battistini, L.; Curti, C.; Rivara, S.; Pala, D.; Kerry, P. S.; Pelosi, G.; Casiraghi, G.; Rassu, G.; Zanardi, F. Synthesis, structure and inhibitory activity of a stereoisomer of oseltamivir carboxylate. Org. Biomol. Chem. 2014, 12, 1561-1569.
  22. Ranieri, B.; Sartori, A.; Curti, C.; Battistini, L.; Rassu, G.; Pelosi, G.; Casiraghi, G.; Zanardi, F. 3-Alkenyl-2-silyloxyindoles in Vinylogous Mannich Reactions: Synthesis of Aminated Indole-Based Scaffolds and Products. Org. Lett. 2014, 16, 932-935 (DOI: 10.1021/ol4036598).
  23. Rassu, G.; Zambrano, V.; Pinna, L.; Curti, C.; Battistini, L.; Sartori, A.; Pelosi, G.; Casiraghi, G.; Zanardi, F. Direct and Enantioselective Vinylogous Michael Addition of α-Alkylidenepyrazolinones to Nitroolefins Catalyzed by Dual Cinchona Alkaloid Thioureas. Adv. Synth. Catal. 2014, 356, 2330-2336 (DOI: 10.1002/adsc.201300964).
  24. Dell’Amico, L.; Rassu, G.; Zambrano, V.; Sartori, A.; Curti, C.; Battistini, L.; Pelosi, G.; Casiraghi, G.; Zanardi, F. Exploring the Reactivity of Cyclohexenylidene Malononitriles: Switchable Regioselectivity in the Organocatalytic Asymmetric Additin to Enals Giving Highly Enantioenriched Carbabicyclic Structures. J. Am. Chem. Soc. 2014, 136, 11107-11114 (DOI: 10.1021/ja5054576l).
  25. Curti, C.; Sartori, A.; Battistini, L.; Brindani, N.; Rassu, G.; Pelosi, G.; Lodola, A.; Mor, M.; Casiraghi, G.; Zanardi, F. Pushing the Boundaries of Vinylogous Reactivity: Catalytic Enantioselective Mukaiyama Aldol Reactions of Highly Unsaturated 2-Silyloxyindoles. Chem. Eur. J. 2015, 21, 6433-6442 (DOI: 10.1002/chem.201500083).
  26. Brindani, N.; Rassu, G.; Dell’Amico, L.; Zambrano, V.; Pinna, L.; Curti, C.; Sartori, A.; Battistini, L.; Casiraghi, G.; Pelosi, G.; Greco, D.; Zanardi, F. Organocatalytic, Asymmetric Eliminative [4+2] Cycloaddition of Allylidene Malononitriles with Enals: Rapid Entry to Cyclohexadiene-Embedding Linear and Angular Polycycles. Angew. Chem. Int. Ed. 2015, 54, 7386-7390 (DOI: 10.1002/anie.201501894).
  27. Curti, C.; Rassu, G.; Zambrano, V.; Pinna, L.; Brindani, N.; Pelosi, G.; Zanardi, F. Exploiting the Distal Reactivity of Indolyl-methylenemalononitriles: an Asymmetric Organocatalyzed [4+2] Cycloaddition with Enals Enables the Assembly of Elusive Dihydrocarbazoles. Chem. Eur. J. 2016, DOI: 10.1002/chem.201602793.
Pubblicato Mercoledì, 11 Giugno, 2014 - 14:29 | ultima modifica Martedì, 10 Gennaio, 2017 - 18:10