Enzymatic Methods for the Manipulation and Valorization of Soapstock from Vegetable Oil Refining Processes
Davide Tessaro , Elisabetta Brenna , Fabio Parmeggiani , Francesca Tentori
Sustainable Chemistry 2 ( 1) 74 -91
18
2021
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
Davide Tessaro , Elisabetta Brenna , Fabio Parmeggiani , Filip Boratyński
Chemcatchem
3
2021
Chemoselective Biohydrogenation of Alkenes in the Presence of Alkynes for the Homologation of 2‐Alkynals/3‐Alkyn‐2‐ones into 4‐Alkynals/Alkynols
Danilo Colombo , Elisabetta Brenna , Francesco G Gatti , Maria Chiara Ghezzi
Advanced Synthesis & Catalysis 361 ( 11) 2638 -2648
2019
Biocatalytic Approach to Chiral β-Nitroalcohols by Enantioselective Alcohol Dehydrogenase-Mediated Reduction of α-Nitroketones
Francesca Tentori , Elisabetta Brenna , Danilo Colombo , Michele Crotti
Catalysts 8 ( 8) 308
7
2018
Bioprocess Intensification Using Flow Reactors: Stereoselective Oxidation of Achiral 1,3-diols with Immobilized Acetobacter Aceti
Valerio De Vitis , Federica Dall’Oglio , Francesca Tentori , Martina Contente
Catalysts 9 ( 3) 208
9
2019
Biocatalytic synthesis of chiral cyclic γ-oxoesters by sequential C–H hydroxylation, alcohol oxidation and alkene reduction
Elisabetta Brenna , Michele Crotti , Francesco G. Gatti , Daniela Monti
Green Chemistry 19 ( 21) 5122 -5130
26
2017
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)
Francesca Tentori , Elisabetta Brenna , Michele Crotti , Giuseppe Pedrocchi-Fantoni
Catalysts 10 ( 1) 102
9
2020
Conversion of Oleic Acid into Azelaic and Pelargonic Acid by a Chemo-Enzymatic Route
Elisabetta Brenna , Danilo Colombo , Giuseppe Di Lecce , Francesco G Gatti
Molecules 25 ( 8) 1882 -1892
8
2020
Immobilization of Old Yellow Enzymes via Covalent or Coordination Bonds
Francesca Tentori , Teodora Bavaro , Elisabetta Brenna , Danilo Colombo
Catalysts 10 ( 2) 260
2020
Lipase-mediated synthesis of oleoyl ethanolamide starting from high-oleic sunflower oil soapstock
Elisabetta Brenna , Valeria De Fabritiis , Fabio Parmeggiani , Francesca Tentori
ACS Sustainable Chemistry \& Engineering 11 ( 7) 2764 -2772
2023
Chemo-enzymatic oxidative cleavage of isosafrole for the synthesis of piperonal
Francesca Tentori , Elisabetta Brenna , Chiara Ferrari , Francesco G Gatti
Reaction Chemistry \& Engineering 6 ( 9) 1591 -1600
2021
Multi-step chemo-enzymatic synthesis of azelaic and pelargonic acids from the soapstock of high-oleic sunflower oil refinement
Beatrice Casali , Elisabetta Brenna , Fabio Parmeggiani , Francesca Tentori
Green Chemistry 24 ( 5) 2082 -2093
4
2022
“A study in yellow”: Investigations in the stereoselectivity of ene‐reductases
Fabio Parmeggiani , Elisabetta Brenna , Danilo Colombo , Francesco G Gatti
ChemBioChem 23 ( 1) e202100445 -e202100445
30
2022
Multi-step chemo-enzymatic synthesis of azelaic and pelargonic acids from the soapstock of high-oleic sunflower oil refinement
Francesca Tentori , Elisabetta Brenna , Beatrice Casali , Fabio Parmeggiani
Synthesis of biologically active molecules by continuous flow biocatalysis 137 -137
Ene-reductase transformation of massoia lactone to δ-decalactone in a continuous-flow reactor
Ewa Szczepańska , Danilo Colombo , Francesca Tentori , Teresa Olejniczak
Scientific Reports 11 ( 1) 18794 -18794
14
2021
Development of a flow process for an easy and fast access to 2-pyrone derivatives
Grazia Isa C Righetti , Francesca Tentori , Elisabetta Brenna , Cristian Gambarotti
Reaction Chemistry & Engineering 8 ( 1) 199 -204
2023
2021
Enantioselective desymmetrisation of achiral 2-substituted-1, 3-diols by acetobacter aceti: traditional approach and developments
FRANCESCA TENTORI
Politecnico di Milano
2015