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Titolo Data di pubblicazione Autori File
Valorisation of the industrial hemp residue from essential oil production by recovery of cannabidiol and chemo-enzymatic conversion to cannabielsoin 1-gen-2024 Daniele FioritoDavide TessaroFabio SangalliCeleste NobbioElisabetta BrennaFabio Parmeggiani +
Stereoselective synthesis of whisky lactone isomers catalyzed by bacteria in the genus Rhodococcus 1-gen-2023 F. G. GattiE. Brenna +
Insight into the Stereoselective Synthesis of (1S)‐Nor(pseudo)ephedrine Analogues by a Two‐Steps Biocatalytic Process 1-gen-2023 Fracchiolla, NoemiSangalli, FabioParmeggiani, FabioBrenna, ElisabettaTessaro, Davide +
Lipase-Mediated Synthesis of Oleoyl Ethanolamide Starting from High-Oleic Sunflower Oil Soapstock 1-gen-2023 Brenna, EDe Fabritiis, VParmeggiani, FTentori, FTessaro, D
Multi-step chemo-enzymatic synthesis of azelaic and pelargonic acids from the soapstock of high-oleic sunflower oil refinement 1-gen-2022 Casali, BeatriceBrenna, ElisabettaParmeggiani, FabioTentori, FrancescaTessaro, Davide
Development of a flow process for an easy and fast access to 2-pyrone derivatives 1-gen-2022 Righetti, Grazia Isa C.Tentori, FrancescaBrenna, ElisabettaGambarotti, Cristian
“A Study in Yellow”: Investigations in the Stereoselectivity of Ene-Reductases 1-gen-2022 Parmeggiani F.Brenna E.Colombo D.Gatti F. G.Tentori F.Tessaro D.
Chemoenzymatic Synthesis of Enantioenriched (R)‐ and (S)‐Aryloxyalkanoic Herbicides 1-gen-2022 Colombo, DaniloTessaro, DavideGatti, Francesco G.Brenna, ElisabettaParmeggiani, Fabio +
Chemoenzymatic Synthesis of the Most Pleasant Stereoisomer of Jessemal 1-gen-2022 Venturi, SilviaColombo, DaniloBrenna, ElisabettaGatti, Francesco GMacchi, Piero +
Enzymatic Methods for the Manipulation and Valorization of Soapstock from Vegetable Oil Refining Processes 1-gen-2021 Casali, BeatriceBrenna, ElisabettaParmeggiani, FabioTessaro, DavideTentori, Francesca
Oxidation of threo-9,10-Dihydroxystearic Acid Mediated by Micrococcus luteus as a Key Step in the Conversion of Oleic Acid into Pelargonic and Azelaic Acids 1-gen-2021 Colombo D.Brenna E.Casali B.Ghezzi M. C.Parmeggiani F.Tentori F.Tessaro D. +
Ene-reductase transformation of massoia lactone to δ-decalactone in a continuous-flow reactor 1-gen-2021 Colombo D.Tentori F.Brenna E. +
Chemo-enzymatic oxidative cleavage of isosafrole for the synthesis of piperonal 1-gen-2021 Tentori F.Brenna E.Gatti F. G.Ghezzi M. C.Parmeggiani F. +
Immobilization of old yellow enzymes via covalent or coordination bonds 1-gen-2020 F. TentoriE. BrennaD. Colombo +
Bacterial biotransformation of oleic acid: new findings on the formation of γ-dodecalactone and 10-ketostearic acid in the culture of Micrococcus luteus 1-gen-2020 E. Brenna +
Multienzymatic Stereoselective Reduction of Tetrasubstituted Cyclic Enones to Halohydrins with Three Contiguous Stereogenic Centers 1-gen-2020 Venturi, SilviaBrenna, ElisabettaColombo, DaniloGatti, Francesco G.Macchi, Piero +
Conversion of oleic acid into azelaic and pelargonic acid by a chemo-enzymatic route 1-gen-2020 Brenna E.Colombo D.Gatti F. G.Ghezzi M. C.Tentori F.Tessaro D.Viola M. +
Continuous-Flow Biocatalytic Process for the Synthesis of the Best Stereoisomers of the Commercial Fragrances Leather Cyclohexanol (4-Isopropylcyclohexanol) and Woody Acetate (4-(Tert-Butyl)Cyclohexyl Acetate) 1-gen-2020 Tentori, FrancescaBrenna, ElisabettaCrotti, MicheleGhezzi, Maria ChiaraTessaro, Davide +
Stereoselectivity switch in the reduction of α-Alkyl-β-arylenones by structure-guided designed variants of the ene reductase OYE1 1-gen-2019 Crotti M.Parmeggiani F.Gatti F. G.Sacchetti A.Brenna E. +
Exploiting the vicinal disubstituent effect on the diastereoselective synthesis of γ and δ lactones 1-gen-2019 Brenna, ElisabettaGatti, Francesco G.Tessaro, Davide +
Mostrati risultati da 1 a 20 di 183
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