Bernardi, Luca; Caruana, Lorenzo; Pistilli, Dalila; Bussolari, Alessio; Toderi, Edoardo; Nalin, Arnaldo; Osti, Sergio; Fontana, Francesco; Paio, Alfredo; Santarelli, Nicolò; Fochi, Mariafrancesca, Reductive Synthesis of Azoxypyridines from Nitropyridines Using Hydroxides in Alcoholic Media, «SYNTHESIS», 2025, 57, pp. 846 - 854 [articolo]
Pecchini, Pietro; Aguilera, Daniel Antonio; Soccio, Alberto; Lombardi, Alessio; Sanz Azcona, Fátima; Santarelli, Nicolò; Fochi, Mariafrancesca; Gaudin, Pierrick; Tanchoux, Nathalie; Bernardi, Luca, Barium Alginate Gel Beads: A Homochiral Porous Material from Brown Algae for Heterogeneous Asymmetric Catalysis, «ACS CATALYSIS», 2024, 14, pp. 8096 - 8104 [articolo]Open Access
Pecchini, Pietro; Fochi, Mariafrancesca; Bartoccini, Francesca; Piersanti, Giovanni; Bernardi, Luca, Enantioselective organocatalytic strategies to access noncanonical α-amino acids, «CHEMICAL SCIENCE», 2024, 15, pp. 5832 - 5868 [articolo]Open Access
Bisag G.D.; Viola P.; Bernardi L.; Fochi M., Divergent Reactivity of D-A Cyclopropanes under PTC Conditions, Ring-Opening vs. Decyanation Reaction, «CATALYSTS», 2023, 13, Article number: 760, pp. 1 - 20 [articolo]Open Access
Sonsona I.G.; Vicenzi A.; Guidotti M.; Bisag G.D.; Fochi M.; Herrera R.P.; Bernardi L., Investigation of Squaramide Catalysts in the Aldol Reaction En Route to Funapide, «EUROPEAN JOURNAL OF ORGANIC CHEMISTRY», 2022, 2022, Article number: e202101254, pp. 1 - 6 [articolo]Open Access
Bisag, Giorgiana Denisa; Pecchini, Pietro; Mancinelli, Michele; Fochi, Mariafrancesca; Bernardi, Luca, Sulfoxonium Ylides in Aminocatalysis: An Enantioselective Entry to Cyclopropane-Fused Chromanol Structures, «ORGANIC LETTERS», 2022, 24, pp. 5468 - 5473 [articolo]Open Access
Giorgiana D. Bisag; Ruggieri S.; Fochi M.; Bernardi L., Catalyst- and Substrate-Dependent Chemodivergent Reactivity of Stabilised Sulfur Ylides with Salicylaldehydes, «ADVANCED SYNTHESIS & CATALYSIS», 2021, 363, pp. 3053 - 3059 [articolo]Open Access
Corti V.; Riccioli R.; Martinelli A.; Sandri S.; Fochi M.; Bernardi L., Stereodivergent entry to β-branched β-trifluoromethyl α-amino acid derivatives by sequential catalytic asymmetric reactions, «CHEMICAL SCIENCE», 2021, 12, pp. 10233 - 10241 [articolo]Open Access
Aguilera D.A.; Tanchoux N.; Fochi M.; Bernardi L., Blue Chemistry. Marine Polysaccharide Biopolymers in Asymmetric Catalysis: Challenges and Opportunities, «EUROPEAN JOURNAL OF ORGANIC CHEMISTRY», 2020, 2020, pp. 3779 - 3795 [articolo]Open Access
Bertuzzi G.; Silvestrini F.; Moimare P.; Pecorari D.; Mazzanti A.; Bernardi L.; Fochi M., Chemodivergent Preparation of Various Heterocycles via Phase-Transfer Catalysis: Enantioselective Synthesis of Functionalized Piperidines, «ADVANCED SYNTHESIS & CATALYSIS», 2020, 362, pp. 1167 - 1175 [articolo]Open Access
Bisag G.D.; Ruggieri S.; Fochi M.; Bernardi L., Sulfoxonium ylides: Simple compounds with chameleonic reactivity, «ORGANIC & BIOMOLECULAR CHEMISTRY», 2020, 18, pp. 8793 - 8809 [articolo]Open Access
Corti V.; Marcantonio E.; Mamone M.; Giungi A.; Fochi M.; Bernardi L., Synergistic palladium-phosphoric acid catalysis in (3 + 2) cycloaddition reactions between vinylcyclopropanes and imines, «CATALYSTS», 2020, 10, Article number: 150, pp. 1 - 14 [articolo]Open Access
Aguilera D.A.; Spinozzi Di Sante L.; Pettignano A.; Riccioli R.; Roeske J.; Albergati L.; Corti V.; Fochi M.; Bernardi L.; Quignard F.; Tanchoux N., Adsorption of a Chiral Amine on Alginate Gel Beads and Evaluation of its Efficiency as Heterogeneous Enantioselective Catalyst, «EUROPEAN JOURNAL OF ORGANIC CHEMISTRY», 2019, 2019, pp. 3842 - 3849 [articolo]
Bisag G.D.; Pecorari D.; Mazzanti A.; Bernardi L.; Fochi M.; Bencivenni G.; Bertuzzi G.; Corti V., Central-to-Axial Chirality Conversion Approach Designed on Organocatalytic Enantioselective Povarov Cycloadditions: First Access to Configurationally Stable Indole–Quinoline Atropisomers, «CHEMISTRY-A EUROPEAN JOURNAL», 2019, 25, pp. 15694 - 15701 [articolo]Open Access
Bertuzzi, Giulio; Pecorari, Daniel; Bernardi, Luca; Fochi, Mariafrancesca, An organocatalytic enantioselective direct alpha-heteroarylation of aldehydes with isoquinoline N-oxides, «CHEMICAL COMMUNICATIONS», 2018, 54, pp. 3977 - 3980 [articolo]
