| The emergence of quinone methides in asymmetric organocatalysis L Caruana, M Fochi, L Bernardi Molecules 20 (7), 11733-11764, 2015 | 322 | 2015 |
| Organocatalytic asymmetric Povarov reactions with 2-and 3-vinylindoles G Bergonzini, L Gramigna, A Mazzanti, M Fochi, L Bernardi, A Ricci Chemical communications 46 (2), 327-329, 2010 | 166 | 2010 |
| Catalytic asymmetric aza-Diels–Alder reactions: The Povarov cycloaddition reaction M Fochi, L Caruana, L Bernardi Synthesis 46 (02), 135-157, 2014 | 150 | 2014 |
| Organocatalytic Asymmetric Mannich Reactions with N‐Boc and N‐Cbz Protected α‐Amido Sulfones (Boc: tert‐Butoxycarbonyl, Cbz: Benzyloxycarbonyl) O Marianacci, G Micheletti, L Bernardi, F Fini, M Fochi, D Pettersen, ... Chemistry–A European Journal 13 (29), 8338-8351, 2007 | 134 | 2007 |
| Organocatalytic enantioselective decarboxylative addition of malonic half thioesters to imines A Ricci, D Pettersen, L Bernardi, F Fini, M Fochi, RP Herrera, V Sgarzani Advanced Synthesis & Catalysis 349 (7), 1037-1040, 2007 | 134 | 2007 |
| Bioinspired organocatalytic asymmetric reactions L Bernardi, M Fochi, MC Franchini, A Ricci Organic & Biomolecular Chemistry 10 (15), 2911-2922, 2012 | 128 | 2012 |
| Sulfoxonium ylides: simple compounds with chameleonic reactivity GD Bisag, S Ruggieri, M Fochi, L Bernardi Organic & Biomolecular Chemistry 18 (43), 8793-8809, 2020 | 110 | 2020 |
| Catalytic Asymmetric Addition of Meldrum’s Acid, Malononitrile, and 1,3‐Dicarbonyls to ortho‐Quinone Methides Generated In Situ Under Basic Conditions L Caruana, M Mondatori, V Corti, S Morales, A Mazzanti, M Fochi, ... Chemistry–A European Journal 21 (16), 6037-6041, 2015 | 109 | 2015 |
| Aziridin-2-yl methanols as organocatalysts in Diels–Alder reactions and Friedel–Crafts alkylations of N-methyl-pyrrole and N-methyl-indole BF Bonini, E Capito, M Comes-Franchini, M Fochi, A Ricci, B Zwanenburg Tetrahedron: Asymmetry 17 (22), 3135-3143, 2006 | 102 | 2006 |
| Nucleophilic dearomatization of activated pyridines G Bertuzzi, L Bernardi, M Fochi Catalysts 8 (12), 632, 2018 | 99 | 2018 |
| Organocatalyzed solvent-free aza-Henry reaction: a breakthrough in the one-pot synthesis of 1, 2-diamines L Bernardi, BF Bonini, E Capito, G Dessole, M Comes-Franchini, M Fochi, ... The Journal of Organic Chemistry 69 (23), 8168-8171, 2004 | 88 | 2004 |
| Catalytic Enantioselective Addition of Indoles to Activated N-Benzylpyridinium Salts: Nucleophilic Dearomatization of Pyridines with Unusual C-4 Regioselectivity G Bertuzzi, A Sinisi, L Caruana, A Mazzanti, M Fochi, L Bernardi ACS Catalysis 6 (10), 6473-6477, 2016 | 79 | 2016 |
| Newly designed acylsilanes as versatile tools in organic synthesis BF Bonini, M Comes-Franchini, M Fochi, G Mazzanti, A Ricci Journal of organometallic chemistry 567 (1-2), 181-189, 1998 | 73 | 1998 |
| Central‐to‐Axial Chirality Conversion Approach Designed on Organocatalytic Enantioselective Povarov Cycloadditions: First Access to Configurationally Stable Indole–Quinoline … GD Bisag, D Pecorari, A Mazzanti, L Bernardi, M Fochi, G Bencivenni, ... Chemistry–A European Journal 25 (68), 15694-15701, 2019 | 66 | 2019 |
| Catalytic highly enantioselective vinylogous Povarov reaction L Caruana, M Fochi, S Ranieri, A Mazzanti, L Bernardi Chemical Communications 49 (9), 880-882, 2013 | 64 | 2013 |
| Organocatalytic asymmetric aza-Michael reaction: enantioselective addition of O-benzylhydroxylamine to chalcones D Pettersen, F Piana, L Bernardi, F Fini, M Fochi, V Sgarzani, A Ricci Tetrahedron letters 48 (44), 7805-7808, 2007 | 62 | 2007 |
| Nucleophilic Dearomatization of Pyridines under Enamine Catalysis: Regio-, Diastereo-, and Enantioselective Addition of Aldehydes to Activated N-Alkylpyridinium … G Bertuzzi, A Sinisi, D Pecorari, L Caruana, A Mazzanti, L Bernardi, ... Organic letters 19 (4), 834-837, 2017 | 59 | 2017 |
| Synthesis of ferrocenyl-oxazolines by ring expansion of N-ferrocenoyl-aziridine-2-carboxylic esters BF Bonini, M Fochi, M Comes-Franchini, A Ricci, L Thijs, B Zwanenburg Tetrahedron: Asymmetry 14 (21), 3321-3327, 2003 | 59 | 2003 |
| Catalytic Asymmetric Inverse‐Electron‐Demand (IED)[4+ 2] Cycloaddition of Salicylaldimines: Preparation of Optically Active 4‐Aminobenzopyran Derivatives L Bernardi, M Comes‐Franchini, M Fochi, V Leo, A Mazzanti, A Ricci Advanced Synthesis & Catalysis 352 (18), 3399-3406, 2010 | 58 | 2010 |
| Catalytic asymmetric reactions of 4‐substituted indoles with nitroethene: a direct entry to ergot alkaloid structures S Romanini, E Galletti, L Caruana, A Mazzanti, F Himo, S Santoro, ... Chemistry–A European Journal 21 (49), 17578-17582, 2015 | 52 | 2015 |
