Caruana, Lorenzo; Fochi, Mariafrancesca*; Bernardi, Luca, Enantioselective Approaches to 3,4-Annulated Indoles Using Organocatalytic Domino Reactions, «SYNLETT», 2017, 28, pp. 1530 - 1543 [articolo]
Bertuzzi, Giulio; Sinisi, Alessandro; Pecorari, Daniel; Caruana, Lorenzo; Mazzanti, Andrea; Bernardi, Luca; Fochi, Mariafrancesca, Nucleophilic Dearomatization of Pyridines under Enamine Catalysis: Regio-, Diastereo-, and Enantioselective Addition of Aldehydes to Activated N-Alkylpyridinium Salts, «ORGANIC LETTERS», 2017, 19, pp. 834 - 837 [articolo]
Corti, Vasco; Camarero Gonzalez, Patricia; Febvay, Julie; Caruana, Lorenzo; Mazzanti, Andrea; Fochi, Mariafrancesca; Bernardi, Luca, Organocatalytic Asymmetric Sulfa-Michael Addition of 2-Aminothiophenols to Chalcones: First Enantioselective Access to 2,3,4,5-Tetrahydro-1,5-benzothiazepines, «EUROPEAN JOURNAL OF ORGANIC CHEMISTRY», 2017, 2017, pp. 49 - 52 [articolo]
Asja Pettignano; Marleen Häring; Luca Bernardi; Nathalie Tanchoux; Fran\ccoise Quignard; David D\'\iaz D\'\iaz, Self-healing alginate-gelatin biohydrogels based on dynamic covalent chemistry: elucidation of key parameters, «MATERIALS CHEMISTRY FRONTIERS», 2017, 1, pp. 73 - 79 [articolo]
Pettignano, Asja; Tanchoux, Nathalie*; Cacciaguerra, Thomas; Vincent, Thierry; Bernardi, Luca; Guibal, Eric; Quignard, Françoise, Sodium and acidic alginate foams with hierarchical porosity: Preparation, characterization and efficiency as a dye adsorbent, «CARBOHYDRATE POLYMERS», 2017, 178, pp. 78 - 85 [articolo]Open Access
Bernardi, Luca; Fochi, Mariafrancesca, A General Catalytic Enantioselective Transfer Hydrogenation Reaction of β,β-Disubstituted Nitroalkenes Promoted by a Simple Organocatalyst, «MOLECULES», 2016, 21, Article number: 1000, pp. 1 - 14 [articolo]
Bernardi, Luca; Bolzoni, Giada; Fochi, Mariafrancesca; Mancinelli, Michele; Mazzanti, Andrea, An Atropisomerically Enforced Phosphoric Acid for Organocatalytic Asymmetric Reactions, «EUROPEAN JOURNAL OF ORGANIC CHEMISTRY», 2016, 2016, pp. 3208 - 3216 [articolo]
Bertuzzi, Giulio; Sinisi, Alessandro; Caruana, Lorenzo; Mazzanti, Andrea; Fochi, Mariafrancesca; Bernardi, Luca, Catalytic Enantioselective Addition of Indoles to Activated N-Benzylpyridinium Salts: Nucleophilic Dearomatization of Pyridines with Unusual C-4 Regioselectivity, «ACS CATALYSIS», 2016, 6, pp. 6473 - 6477 [articolo]Open Access
Luca Bernardi; Mariafrancesca Fochi, Nonquaternised Cinchona Alkaloid Derivatives as Asymmetric Organocatalysts for Carbon-Carbon Bond-Forming Reactions, in: Sustainable Catalysis without metals or other endangered elements-part 2, Cambridge, The Royal Society of Chemistry, 2016, pp. 1 - 43 (RSC GREEN CHEMISTRY SERIES) [capitolo di libro]
Ferraro, Antonino; Bernardi, Luca; Fochi, Mariafrancesca, Organocatalytic Enantioselective Transfer Hydrogenation of β-Amino Nitroolefins, «ADVANCED SYNTHESIS & CATALYSIS», 2016, 358, pp. 1561 - 1565 [articolo]
Brevetto n. WO2017064627, Process for the preparation of eribulin and intermediates thereof.
Foli, Giacomo; D'Elia, Cecilia Sasso; Fochi, Mariafrancesca; Bernardi, Luca, Reversible modulation of the activity of thiourea catalysts with anions: A simple approach to switchable asymmetric catalysis, «RSC ADVANCES», 2016, 6, pp. 66490 - 66494 [articolo]
Pettignano, A.; Bernardi, L.; Fochi, M.; Geraci, L.; Robitzer, M.; Tanchoux, N.; Quignard, F., Alginic acid aerogel: A heterogeneous Brønsted acid promoter for the direct Mannich reaction, «NEW JOURNAL OF CHEMISTRY», 2015, 39, pp. 4222 - 4226 [articolo]
Lorenzo, Caruana; Martina, Mondatori; Vasco, Corti; Sara, Morales; Andrea, Mazzanti; Mariafrancesca, Fochi; Luca, Bernardi, Catalytic Asymmetric Addition of Meldrum's Acid, Malononitrile, and 1,3-Dicarbonyls to ortho-Quinone Methides Generated In Situ under Basic Conditions, «CHEMISTRY-A EUROPEAN JOURNAL», 2015, 21, pp. 6037 - 6041 [articolo]
Romanini, Simone; Galletti, Emilio; Caruana, Lorenzo; Mazzanti, Andrea; Himo, Fahmi; Santoro, Stefano; Fochi, Mariafrancesca; Bernardi, Luca, Catalytic Asymmetric Reactions of 4-Substituted Indoles with Nitroethene: A Direct Entry to Ergot Alkaloid Structures, «CHEMISTRY-A EUROPEAN JOURNAL», 2015, 21, pp. 17578 - 17582 [articolo]Open Access
