| 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 | 50 | 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 | 49 | 2015 |
| Asymmetric Synthetic Strategies of (R)-(–)-Baclofen: An Antispastic Drug P Ramesh, D Suman, KSN Reddy Synthesis 50 (02), 211-226, 2018 | 37 | 2018 |
| Peroxygenase‐Catalyzed Enantioselective Sulfoxidations I Bassanini, EE Ferrandi, M Vanoni, G Ottolina, S Riva, M Crotti, E Brenna, ... European Journal of Organic Chemistry 2017 (47), 7186-7189, 2017 | 36 | 2017 |
| Enantiocomplementary Epoxidation Reactions Catalyzed by an Engineered Cofactor‐Independent Non‐natural Peroxygenase G Xu, M Crotti, T Saravanan, KM Kataja, GJ Poelarends Angewandte Chemie 132 (26), 10460-10464, 2020 | 33 | 2020 |
| Chemo‐Enzymatic oxidative rearrangement of tertiary allylic alcohols: synthetic application and integration into a cascade process E Brenna, M Crotti, M De Pieri, FG Gatti, G Manenti, D Monti Advanced Synthesis & Catalysis 360 (19), 3677-3686, 2018 | 31 | 2018 |
| Biocatalytic synthesis of chiral cyclic γ-oxoesters by sequential C–H hydroxylation, alcohol oxidation and alkene reduction E Brenna, M Crotti, FG Gatti, D Monti, F Parmeggiani, A Pugliese, ... Green chemistry 19 (21), 5122-5130, 2017 | 29 | 2017 |
| Enantioselective Synthesis of (R)‐2‐Arylpropanenitriles Catalysed by Ene‐Reductases in Aqueous Media and in Biphasic Ionic Liquid–Water Systems E Brenna, M Crotti, FG Gatti, A Manfredi, D Monti, F Parmeggiani, ... ChemCatChem 6 (8), 2425-2431, 2014 | 27 | 2014 |
| Exploitation of a multienzymatic stereoselective cascade process in the synthesis of 2-methyl-3-substituted tetrahydrofuran precursors E Brenna, M Crotti, FG Gatti, L Marinoni, D Monti, S Quaiato The Journal of Organic Chemistry 82 (4), 2114-2122, 2017 | 26 | 2017 |
| Multi-enzyme cascade synthesis of the most odorous stereoisomers of the commercial odorant Muguesiaź E Brenna, M Crotti, FG Gatti, D Monti, F Parmeggiani, A Pugliese, ... Journal of Molecular Catalysis B: Enzymatic 114, 37-41, 2015 | 25 | 2015 |
| Comprehensive Structure–Activity Profiling of Micheliolide and its Targeted Proteome in Leukemia Cells via Probe-Guided Late-Stage C–H Functionalization H Alwaseem, S Giovani, M Crotti, K Welle, CT Jordan, S Ghaemmaghami, ... ACS Central Science 7 (5), 841-857, 2021 | 20 | 2021 |
| One-pot multi-enzymatic synthesis of the four stereoisomers of 4-methylheptan-3-ol E Brenna, M Crotti, FG Gatti, D Monti, F Parmeggiani, A Pugliese Molecules 22 (10), 1591, 2017 | 19 | 2017 |
| Substrate Scope Evaluation of the Enantioselective Reduction of β‐Alkyl‐β‐arylnitroalkenes by Old Yellow Enzymes 1–3 for Organic Synthesis Applications M Bertolotti, E Brenna, M Crotti, FG Gatti, D Monti, F Parmeggiani, ... ChemCatChem 8 (3), 577-583, 2016 | 19 | 2016 |
| Biocatalysed reduction of carboxylic acids to primary alcohols in aqueous medium: A novel synthetic capability of the zygomycete fungus Syncephalastrum racemosum E Brenna, F Cannavale, M Crotti, F Parmeggiani, A Romagnolo, F Spina, ... Journal of molecular catalysis B: enzymatic 116, 83-88, 2015 | 19 | 2015 |
| Stereoselectivity switch in the reduction of α-alkyl-β-arylenones by structure-guided designed variants of the ene reductase OYE1 M Crotti, F Parmeggiani, EE Ferrandi, FG Gatti, A Sacchetti, S Riva, ... Frontiers in Bioengineering and Biotechnology 7, 89, 2019 | 18 | 2019 |
| Rationalisation of the stereochemical outcome of ene-reductase-mediated bioreduction of α, β-difunctionalised alkenes E Brenna, M Crotti, FG Gatti, A Manfredi, D Monti, F Parmeggiani, ... Journal of Molecular Catalysis B: Enzymatic 101, 67-72, 2014 | 17 | 2014 |
| Gene Fusion and Directed Evolution to Break Structural Symmetry and Boost Catalysis by an Oligomeric C− C Bond‐Forming Enzyme G Xu, A Kunzendorf, M Crotti, HJ Rozeboom, AMWH Thunnissen, ... Angewandte Chemie 134 (8), e202113970, 2022 | 16 | 2022 |
| Identification of fungal ene-reductase activity by means of a functional screening A Romagnolo, F Spina, E Brenna, M Crotti, F Parmeggiani, GC Varese Fungal biology 119 (6), 487-493, 2015 | 16 | 2015 |
| Asymmetric Bioreduction of β‐Acylaminonitroalkenes: Easy Access to Chiral Building Blocks with Two Vicinal Nitrogen‐Containing Functional Groups E Brenna, M Crotti, FG Gatti, D Monti, F Parmeggiani, S Santangelo ChemCatChem 9 (13), 2480-2487, 2017 | 15 | 2017 |
| Biocatalytic approach to chiral β-nitroalcohols by enantioselective alcohol dehydrogenase-mediated reduction of α-nitroketones F Tentori, E Brenna, D Colombo, M Crotti, FG Gatti, MC Ghezzi, ... Catalysts 8 (8), 308, 2018 | 14 | 2018 |
