Biocatalytic approaches for a more sustainable synthesis of sandalwood fragrances MC Cancellieri, D Maggioni, L Di Maio, D Fiorito, E Brenna, ... Green Chemistry, 2024 | | 2024 |
Towards compact laser-driven accelerators: exploring the potential of advanced double-layer targets A Maffini, F Mirani, M Galbiati, K Ambrogioni, F Gatti, MSG De Magistris, ... EPJ Techniques and Instrumentation 10 (1), 15, 2023 | 3 | 2023 |
Role of magnetic field and bias configuration on hipims deposition of w films D Vavassori, F Mirani, F Gatti, D Dellasega, M Passoni Surface and Coatings Technology 458, 129343, 2023 | 6 | 2023 |
Stereoselective synthesis of whisky lactone isomers catalyzed by bacteria in the genus Rhodococcus D Hernik, F Gatti, E Brenna, E Szczepańska, T Olejniczak, F Boratyński Frontiers in Microbiology 14, 1117835, 2023 | | 2023 |
Dependence of 1 H-NMR T 1 relaxation time of trimethylglycine betaine deep eutectic solvents on the molar composition and on the presence of water C Allegretti, P D'Arrigo, FG Gatti, LAM Rossato, E Ruffini RSC advances 13 (5), 3004-3007, 2023 | 2 | 2023 |
Thermal stabilization of diverse biologics using reversible hydrogels B Marco-Dufort, JR Janczy, T Hu, M Lütolf, F Gatti, M Wolf, A Woods, ... Science Advances 8 (31), eabo0502, 2022 | 9 | 2022 |
Chemoenzymatic Synthesis of Enantioenriched (R)‐ and (S)‐Aryloxyalkanoic Herbicides D Colombo, A Albergati, EE Ferrandi, D Tessaro, FG Gatti, E Brenna, ... European Journal of Organic Chemistry 2022 (25), e202200609, 2022 | | 2022 |
Chemoenzymatic synthesis of the most pleasant stereoisomer of Jessemal S Venturi, M Trajkovic, D Colombo, E Brenna, MW Fraaije, FG Gatti, ... The Journal of Organic Chemistry 87 (9), 6499-6503, 2022 | 1 | 2022 |
“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 | 27 | 2022 |
Exploitation of soybean oil acid degumming waste: Biocatalytic synthesis of high value phospholipids C Allegretti, A Bono, P D'Arrigo, FG Gatti, S Marzorati, LAM Rossato, ... ChemistrySelect 6 (34), 9157-9163, 2021 | 3 | 2021 |
Reactive Deep Eutectic Solvents (RDESs): A new tool for phospholipase D-catalyzed preparation of phospholipids C Allegretti, FG Gatti, S Marzorati, LAM Rossato, S Serra, A Strini, ... Catalysts 11 (6), 655, 2021 | 15 | 2021 |
Studies of novel trifluoroacetylated diaryl hydrazone molecular photoswitches in solution and in the solid state G Accorsi, AL Capodilupo, RM Claramunt, GJ Clarkson, A Farrán, ... New Journal of Chemistry 45 (28), 12471-12478, 2021 | 3 | 2021 |
Chemo-enzymatic oxidative cleavage of isosafrole for the synthesis of piperonal F Tentori, E Brenna, C Ferrari, FG Gatti, MC Ghezzi, F Parmeggiani Reaction Chemistry & Engineering 6 (9), 1591-1600, 2021 | 2 | 2021 |
11.9 Ene-Reductase-Mediated Reduction of C= C Double Bonds in the Presence of Conjugated C≡ C Triple Bonds: Synthesis of (S)-2-Methyl-5-Phenylpent-4-yn-1-ol D Colombo, E Brenna, FG Gatti, M Chiara Applied Biocatalysis, 468, 2021 | | 2021 |
Multienzymatic stereoselective reduction of tetrasubstituted cyclic enones to halohydrins with three contiguous stereogenic centers S Venturi, E Brenna, D Colombo, MW Fraaije, FG Gatti, P Macchi, D Monti, ... ACS Catalysis 10 (21), 13050-13057, 2020 | 19 | 2020 |
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 | 48 | 2020 |
Synthesis of polycyclic fused indoline scaffolds through a substrate-guided reactivity switch C Ciccolini, G Mari, FG Gatti, G Gatti, G Giorgi, F Mantellini, G Favi The Journal of Organic Chemistry 85 (17), 11409-11425, 2020 | 17 | 2020 |
Conversion of oleic acid into azelaic and pelargonic acid by a chemo-enzymatic route E Brenna, D Colombo, G Di Lecce, FG Gatti, MC Ghezzi, F Tentori, ... Molecules 25 (8), 1882, 2020 | 32 | 2020 |
Development of non-conventional targets for laser-driven particle sources F Gatti | 1 | 2020 |
Chemoselective Biohydrogenation of Alkenes in the Presence of Alkynes for the Homologation of 2‐Alkynals/3‐Alkyn‐2‐ones into 4‐Alkynals/Alkynols D Colombo, E Brenna, FG Gatti, MC Ghezzi, D Monti, F Parmeggiani, ... Advanced Synthesis & Catalysis 361 (11), 2638-2648, 2019 | 12 | 2019 |