VACCARO, Luigi

VACCARO, Luigi  

DIPARTIMENTO DI CHIMICA, BIOLOGIA E BIOTECNOLOGIE  

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Titolo Data di pubblicazione Autore(i) File
(R,R)-6,6′-Bis(1-hydroxy-2,2-dimethylpropyl)-2,2′-bipyridine (S,S)-6,6′-Bis(1-hydroxy-2,2-dimethylpropyl)-2,2′-bipyridineEncyclopedia of Reagents for Organic Synthesis 2013 Bonollo, Simona; Lanari, Daniela; Vaccaro, Luigi
2-tert-butylimino-2-diethylamino-1,3-dimethylperhydro-1,3,2- diazaphosphorine supported on polystyrene (PS-BEMP) as an efficient recoverable and reusable catalyst for the phenolysis of epoxides under solvent-free conditions 2010 A., Zvagulis; Bonollo, Simona; Lanari, Daniela; Pizzo, Ferdinando; Vaccaro, Luigi
3-Nitrocoumarins as Dienophiles in the Diels-Alder Reaction in Water. An Approach to the Synthesis of Nitrotetrahydrobenzo[c]chromenones and Dihydrodibenzo[b,d]furans 2003 Amantini, D.; Fringuelli, Francesco; Piermatti, Oriana; Pizzo, Ferdinando; Vaccaro, Luigi
3-Nitrocumarine come accettori di Michael in condizioni di solvent-free 2004 Fringuelli, Francesco; Girotti, Rugiada; Pizzo, Ferdinando; Vaccaro, Luigi
[2]Catenanes on Surfaces as Candidates for Nanoelectronic Devices 2012 Lanari, Daniela; Bonollo, Simona; Vaccaro, Luigi
[AlCl3+2THF]: a new and efficient catalytic system for Diels-Alder cycloaddition of α,β-unsaturated carbonyl compounds under solvent-free condition 2006 Fringuelli, Francesco; Girotti, Rugiada; Pizzo, Ferdinando; Vaccaro, Luigi
A biomass-derived safe medium to replace toxic dipolar solvents and access cleaner Heck coupling reactions 2015 Strappaveccia, Giacomo; Ismalaj, Ermal; Petrucci, Chiara; Lanari, Daniela; Marrocchi, Assunta; Drees, Martin; Facchetti, Antonio; Vaccaro, Luigi
A catalytic approach to the base-promoted reaction of epoxides with activated methylenes 2010 Angelini, Tommaso; Fringuelli, Francesco; Lanari, Daniela; Pizzo, Ferdinando; Vaccaro, Luigi
A catalytic approach to the metal-free reaction of epoxides with ketene silyl acetals for accessing γ-lactones 2014 Bonollo, Simona; Ahmady, Amanollah Zarei; Petrucci, Chiara; Marrocchi, Assunta; Pizzo, Ferdinando; Vaccaro, Luigi
A Catalytic Peterson-like Synthesis of Alkenyl Nitriles 2016 Lanari, Daniela; Alonzi, Matteo; Ferlin, Francesco; Santoro, Stefano; Vaccaro, Luigi
A comparative approach to the most sustainable protocol for the β-azidation of α,β-unsaturated ketones and acids 2015 Andraos, John; Ballerini, Eleonora; Vaccaro, Luigi
A continuous flow approach for the C-H functionalization of 1,2,3-triazoles in γ-valerolactone as a biomass-derived medium 2018 Ferlin, Francesco; Luciani, Lorenzo; Santoro, Stefano; Marrocchi, Assunta; Lanari, Daniela; Bechtoldt, Alexander; Ackermann, Lutz; Vaccaro, Luigi
A General Enantioselective C−H Arylation Using an Immobilized Recoverable Palladium Catalyst 2023 Salameh, N.; Valentini, F.; Baudoin, O.; Vaccaro, L.
A green route to β-amino alcohols via the uncatalyzed aminolysis of 1,2-epoxides by alkyl- and arylamines 2006 Bonollo, Simona; Fringuelli, Francesco; Pizzo, Ferdinando; Vaccaro, Luigi
A green synthesis of a novel class of biphenyls via Diels-Alder cycloaddition of (E)-2-aryl-1-cyano-1-nitroethenes under SFC 2005 Fringuelli, Francesco; Girotti, Rugiada; Pizzo, Ferdinando; Vaccaro, Luigi
A heterogeneous and recoverable palladium catalyst to access the regioselective C-H alkenylation of quinoline N -oxides 2020 Sciosci, D.; Valentini, F.; Ferlin, F.; Chen, S.; Gu, Y.; Piermatti, O.; Vaccaro, L.
A high-valent Ru-PCP pincer catalyst for hydrosilylation reactions 2024 Mujahed, S.; Gandolfo, D.; Vaccaro, L.; Kirillov, E.; Gelman, D.
A New One-Pot Synthesis of Polysubstituted Indoles fromPyrroles and b-Nitroacrylates 2011 A., Palmieri; S., Gabrielli; Lanari, Daniela; Vaccaro, Luigi; R., Ballini
A Polymer-Supported Phosphazene Catalyst for Phospha-Michael Additions 2016 Strappaveccia, Giacomo; Ziarelli, S.; Pizzo, Ferdinando; Santoro, Stefano; Lanari, Daniela; Vaccaro, Luigi
A Protocol for Accessing the beta‑Azidation of alpha,beta-Unsaturated Carboxylic Acids 2012 Angelini, T.; Bonollo, Simona; Lanari, Daniela; Pizzo, Ferdinando; Vaccaro, Luigi