| Photoinduction of fast, reversible translational motion in a hydrogen-bonded molecular shuttle AM Brouwer, C Frochot, FG Gatti, DA Leigh, L Mottier, F Paolucci, S Roffia, ... Science 291 (5511), 2124-2128, 2001 | 787 | 2001 |
| Electrochemically switchable hydrogen-bonded molecular shuttles A Altieri, FG Gatti, ER Kay, DA Leigh, D Martel, F Paolucci, AMZ Slawin, ... Journal of the American Chemical Society 125 (28), 8644-8654, 2003 | 291 | 2003 |
| Stiff, and sticky in the right places: The dramatic influence of preorganizing guest binding sites on the hydrogen bond-directed assembly of rotaxanes FG Gatti, DA Leigh, SA Nepogodiev, AMZ Slawin, SJ Teat, JKY Wong Journal of the American Chemical Society 123 (25), 5983-5989, 2001 | 268 | 2001 |
| Influencing intramolecular motion with an alternating electric field V Bermudez, N Capron, T Gase, FG Gatti, F Kajzar, DA Leigh, F Zerbetto, ... Nature 406 (6796), 608-611, 2000 | 268 | 2000 |
| Photoisomerization of a rotaxane hydrogen bonding template: Light-induced acceleration of a large amplitude rotational motion FG Gatti, S Leon, JKY Wong, G Bottari, A Altieri, MAF Morales, SJ Teat, ... Proceedings of the National Academy of Sciences 100 (1), 10-14, 2003 | 139 | 2003 |
| Biocatalytic methods for the synthesis of enantioenriched odor active compounds E Brenna, C Fuganti, FG Gatti, S Serra Chemical Reviews 111 (7), 4036-4072, 2011 | 106 | 2011 |
| Biotechnological Development of a Practical Synthesis of Ethyl (S)-2-Ethoxy-3-(p-methoxyphenyl)propanoate (EEHP): Over 100-Fold Productivity Increase from … M Bechtold, E Brenna, C Femmer, FG Gatti, S Panke, F Parmeggiani, ... Organic Process Research & Development 16 (2), 269-276, 2012 | 88 | 2012 |
| Chirality and fragrance chemistry: stereoisomers of the commercial chiral odorants Muguesia and Pamplefleur A Abate, E Brenna, C Fuganti, FG Gatti, T Giovenzana, L Malpezzi, ... The Journal of Organic Chemistry 70 (4), 1281-1290, 2005 | 81 | 2005 |
| Enoate Reductase-Mediated Preparation of Methyl (S)-2-Bromobutanoate, a Useful Key Intermediate for the Synthesis of Chiral Active Pharmaceutical Ingredients E Brenna, FG Gatti, A Manfredi, D Monti, F Parmeggiani Organic Process Research & Development 16 (2), 262-268, 2012 | 76 | 2012 |
| Cascade coupling of ene reductases with alcohol dehydrogenases: Enantioselective reduction of prochiral unsaturated aldehydes E Brenna, FG Gatti, D Monti, F Parmeggiani, A Sacchetti ChemCatChem 4 (5), 653-659, 2012 | 71 | 2012 |
| Synthesis of robalzotan, ebalzotan, and rotigotine precursors via the stereoselective multienzymatic cascade reduction of α, β-unsaturated aldehydes E Brenna, FG Gatti, L Malpezzi, D Monti, F Parmeggiani, A Sacchetti The Journal of Organic Chemistry 78 (10), 4811-4822, 2013 | 62 | 2013 |
| An ‘off-on-off’fluorescent sensor for pH based on ligand–proton and ligand–metal–proton interactions L Fabbrizzi, F Gatti, P Pallavicini, L Parodi New Journal of Chemistry 22 (12), 1403-1407, 1998 | 61 | 1998 |
| Lipase-catalysed preparation of enantiomerically enriched odorants A Abate, E Brenna, C Fuganti, FG Gatti, S Serra Journal of molecular catalysis B: Enzymatic 32 (1-2), 33-51, 2004 | 58 | 2004 |
| Addition of TMSCN to chiral ketimines derived from isatin. Synthesis of an oxindole-based peptidomimetic and a bioactive spirohydantoin A Sacchetti, A Silvani, FG Gatti, G Lesma, T Pilati, B Trucchi Organic & Biomolecular Chemistry 9 (15), 5515-5522, 2011 | 56 | 2011 |
| Environment controls biomolecule release from dynamic covalent hydrogels B Marco-Dufort, J Willi, F Vielba-Gomez, F Gatti, MW Tibbitt Biomacromolecules 22 (1), 146-157, 2020 | 53 | 2020 |
| Cascade Coupling of Ene‐Reductases and ω‐Transaminases for the Stereoselective Synthesis of Diastereomerically Enriched Amines D Monti, MC Forchin, M Crotti, F Parmeggiani, FG Gatti, E Brenna, S Riva ChemCatChem 7 (19), 3106-3109, 2015 | 52 | 2015 |
| Opposite Enantioselectivity in the Bioreduction of (Z)‐β‐Aryl‐β‐cyanoacrylates Mediated by the Tryptophan 116 Mutants of Old Yellow Enzyme 1: Synthetic Approach to (R)‐and (S … E Brenna, M Crotti, FG Gatti, D Monti, F Parmeggiani, RW Powell III, ... Advanced Synthesis & Catalysis 357 (8), 1849-1860, 2015 | 50 | 2015 |
| Redox‐Driven Intramolecular Anion Translocation between Transition Metal Centres L Fabbrizzi, F Gatti, P Pallavicini, E Zambarbieri Chemistry–A European Journal 5 (2), 682-690, 1999 | 50 | 1999 |
| A general method for the synthesis of the most powerful naturally occurring Maillard flavors C Fuganti, FG Gatti, S Serra Tetrahedron 63 (22), 4762-4767, 2007 | 44 | 2007 |
| “A study in yellow”: Investigations in the stereoselectivity of ene‐reductases F Parmeggiani, E Brenna, D Colombo, FG Gatti, F Tentori, D Tessaro ChemBioChem 23 (1), e202100445, 2022 | 42 | 2022 |
