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Luca Bernardi

Professore associato

Dipartimento di Chimica Industriale "Toso Montanari"

Settore scientifico disciplinare: CHEM-05/A Chimica organica

Pubblicazioni

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

Emilie, Martinelli; Anna Chiara, Vicini; Mancinelli, Michele; Mazzanti, Andrea; Zani, Paolo; Bernardi, Luca; Fochi, Mariafrancesca, Catalytic highly enantioselective transfer hydrogenation of β-trifluoromethyl nitroalkenes. An easy and general entry to optically active β-trifluoromethyl amines, «CHEMICAL COMMUNICATIONS», 2015, 51, pp. 658 - 660 [articolo]Open Access

Luca Bernardi; Mariafrancesca Fochi; Riccardo Carbone; Ada Martinelli; Martin E. Fox; Christopher J. Cobley; Bhaskar Kandagatla; Srinivas Oruganti; Vilas H. Dahanukar; Armando Carlone, Organocatalytic asymmetric conjugate additions to cyclopent-1-enecarbaldehyde: a critical assessment of organocatalytic approaches towards the telaprevir bicyclic core, «CHEMISTRY», 2015, 21, pp. 19208 - 19222 [articolo]

Caruana, Lorenzo; Fochi, Mariafrancesca; Bernardi, Luca, The emergence of quinone methides in asymmetric organocatalysis, «MOLECULES», 2015, 20, pp. 11733 - 11764 [articolo]Open Access

Lorenzo Caruana;Mariafrancesca Fochi;Mauro Comes Franchini;Silvia Ranieri;Andrea Mazzanti;Luca Bernardi, Asymmetric synthesis of 3,4-annulated indoles through an organocatalytic cascade approach, «CHEMICAL COMMUNICATIONS», 2014, 50, pp. 445 - 447 [articolo]

Mariafrancesca Fochi; Lorenzo Caruana; Luca Bernardi, Catalytic Asymmetric Aza-Diels–Alder Reactions: The Povarov Cycloaddition Reaction, «SYNTHESIS», 2014, 46, pp. 135 - 157 [articolo]

Matea Vlatkovic; Luca Bernardi; Edwin Otten; Ben L. Feringa, Dual stereocontrol over the Henry reaction using a light- and heat-triggered organocatalyst, «CHEMICAL COMMUNICATIONS», 2014, 50, pp. 7773 - 7775 [articolo]

Luca Bernardi; Alfredo Ricci, Third component enolizable carbonyl compound (Mannich reaction), in: Science of Synthesis: Multicomponent reactions 1, Stuttgart, Georg Thieme Verlag, 2014, pp. 123 - 164 [capitolo di libro]

L. Caruana; M. Fochi; S. Ranieri; A. Mazzanti; L. Bernardi, Catalytic highly enantioselective vinylogous Povarov reaction, «CHEMICAL COMMUNICATIONS», 2013, 49, pp. 880 - 882 [articolo]

C. Gioia; A. Ricci; L. Bernardi; K. Bourahla; N. Tanchoux; M. Robitzer; F. Quignard, Chitosan Aerogel Beads as a Heterogeneous Organocatalyst for the Asymmetric Aldol Reaction in the Presence of Water: an Assessment of the Effect of Additives, «EUROPEAN JOURNAL OF ORGANIC CHEMISTRY», 2013, 2013, pp. 588 - 594 [articolo]

P. Blas González; J. Z. Chandanshive; M. Fochi; B. F. Bonini; A. Mazzanti; L. Bernardi; E. Locatelli; L. Caruana; C. Monasterolo; M. Comes Franchini., Experimental and Computational Investigation of the 1,3-Dipolar Cycloaddition of the ynamide tert-butyl-ethynyl-phenyl carbamate with C-carboxymethyl-N-phenyl nitrilimine, «EUROPEAN JOURNAL OF ORGANIC CHEMISTRY», 2013, 36, pp. 8108 - 8114 [articolo]

Brevetto n. IN2013CH04788A, Process for preparation of pregabalin.

L. Bernardi; M. Fochi; M. Comes Franchini; A. Ricci, Bioinspired organocatalytic asymmetric reactions, «ORGANIC & BIOMOLECULAR CHEMISTRY», 2012, 10, pp. 2911 - 2922 [articolo]

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