RE.PUBLIC@POLIMI pubblicazioni di ricerca del Politecnico di Milano

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Biocatalytic approaches for a more sustainable synthesis of sandalwood fragrances 1-gen-2024 Cancellieri, Maria CristinaMaggioni, DavideFiorito, DanieleBrenna, ElisabettaParmeggiani, FabioGatti, Francesco +
Dependence of 1H-NMR T1 relaxation time of trimethylglycine betaine deep eutectic solvents on the molar composition and on the presence of water 1-gen-2023 Allegretti, ChiaraD'Arrigo, PaolaGatti, Francesco G.Rossato, LetiziaRuffini, Eleonora
Stereoselective synthesis of whisky lactone isomers catalyzed by bacteria in the genus Rhodococcus 1-gen-2023 F. G. GattiE. Brenna +
Chemoenzymatic Synthesis of the Most Pleasant Stereoisomer of Jessemal 1-gen-2022 Venturi, SilviaColombo, DaniloBrenna, ElisabettaGatti, Francesco GMacchi, Piero +
“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 +
Reactive Deep Eutectic Solvents (RDESs): A New Tool for Phospholipase D-Catalyzed Preparation of Phospholipids 1-gen-2021 Allegretti, ChiaraGatti, Francesco G.Rossato, Letizia Anna MariaSerra, StefanoD’Arrigo, Paola +
Exploitation of Soybean Oil Acid Degumming Waste: Biocatalytic Synthesis of High Value Phospholipids 1-gen-2021 Allegretti, ChiaraBono, AndreaD'Arrigo, PaolaGatti, Francesco G.Rossato, Letizia Anna MariaSerra, StefanoTessaro, Davide +
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. +
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. +
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 +
Synthesis of Polycyclic Fused Indoline Scaffolds through a Substrate-Guided Reactivity Switch 1-gen-2020 Gatti F. G. +
Exploiting the vicinal disubstituent effect on the diastereoselective synthesis of γ and δ lactones 1-gen-2019 Brenna, ElisabettaGatti, Francesco G.Tessaro, Davide +
Experimental Methods in Chemical Engineering: Nuclear Magnetic Resonance 1-gen-2019 Gatti F. G. +
Chemoselective Biohydrogenation of Alkenes in the Presence of Alkynes for the Homologation of 2-Alkynals/3-Alkyn-2-ones into 4-Alkynals/Alkynols 1-gen-2019 Colombo D.Brenna E.Gatti F. G.Ghezzi M. C.Monti D.Parmeggiani F.Tentori F.
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. +
Biocatalytic approach to chiral beta-nitroalcohols by enantioselective alcohol dehydrogenase-mediated reduction of alpha-nitroketones 1-gen-2018 TENTORI, FRANCESCAE. BrennaCOLOMBO, DANILOM. CrottiF. G. GattiGHEZZI, MARIA CHIARA +
Chemo-Enzymatic Oxidative Rearrangement of Tertiary Allylic Alcohols: Synthetic Application and Integration into a Cascade Process 1-gen-2018 Brenna E.Crotti M.Gatti F. G. +
Biocatalytic synthesis of chiral cyclic gamma-oxoesters by sequential C-H hydroxylation, alcohol oxidation and alkene reduction 1-gen-2017 Elisabetta BrennaMichele CrottiFrancesco G. GattiFabio ParmeggianiAndrea PuglieseTENTORI, FRANCESCA +
Substituent and catalyst effects on GAC lactonization of gamma-hydroxy esters 1-gen-2017 BRENNA, MARIA ELISABETTAGATTI, FRANCESCO GILBERTO +
Exploitation of a Multienzymatic Stereoselective Cascade Process in the Synthesis of 2-Methyl-3-Substituted Tetrahydrofuran Precursors 1-gen-2017 BRENNA, MARIA ELISABETTACROTTI, MICHELEGATTI, FRANCESCO GILBERTOQUAIATO, SARA +
One-pot multi-enzymatic synthesis of the four stereoisomers of 4-methylheptan-3-ol 1-gen-2017 E. BrennaM. CrottiF. G. GattiF. ParmeggianiA. Pugliese +
Asymmetric Bioreduction of beta-Acylaminonitroalkenes: Easy Access to Chiral Building Blocks with Two Vicinal Nitrogen-Containing Functional Groups 1-gen-2017 Elisabetta BrennaMichele CrottiFrancesco G. GattiFabio ParmeggianiSara Santangelo +
Substrate Scope Evaluation of the Enantioselective Reduction of β-Alkyl-β-arylnitroalkenes by Old Yellow Enzymes 1-3 for Organic Synthesis Applications 1-gen-2016 BERTOLOTTI, MATTIABRENNA, MARIA ELISABETTACROTTI, MICHELEGATTI, FRANCESCO GILBERTOPARMEGGIANI, FABIOSANTANGELO, SARA +
Synthesis of Enantiomerically Enriched 2-Hydroxymethylalkanoic Acids by Oxidative Desymmetrisation of Achiral 1,3-Diols Mediated by Acetobacter aceti 1-gen-2016 BRENNA, MARIA ELISABETTACANNAVALE, FLAVIACROTTI, MICHELEGATTI, FRANCESCO GILBERTOPARMEGGIANI, FABIO +
Productivity Improvement of the Bioreduction of α,β-Unsaturated Aldehydes by Coupling of the In Situ Substrate Feeding Product Removal (SFPR) Strategy with Isolated Enzymes 1-gen-2015 BRENNA, MARIA ELISABETTAGATTI, FRANCESCO GILBERTOPARMEGGIANI, FABIOSACCHETTI, ALESSANDRO +
Stereoselective synthesis of hernandulcin, peroxylippidulcine A, lippidulcines A, B and C and taste evaluation 1-gen-2015 GATTI, FRANCESCO GILBERTO +
Multi-enzyme cascade synthesis of the most odorous stereoisomers of the commercial odorant Muguesia 1-gen-2015 BRENNA, MARIA ELISABETTACROTTI, MICHELEGATTI, FRANCESCO GILBERTOPARMEGGIANI, FABIOSANTANGELO, SARA +
Cascade Coupling of Ene-Reductases and w-Transaminases for the Stereoselective Synthesis of Diastereomerically Enriched Amines 1-gen-2015 CROTTI, MICHELEPARMEGGIANI, FABIOGATTI, FRANCESCO GILBERTOBRENNA, MARIA ELISABETTA +
Substrate-engineering approach to the stereoselective chemo-multienzymatic cascade synthesis of Nicotiana tabacum lactone 1-gen-2015 BRENNA, MARIA ELISABETTAGATTI, FRANCESCO GILBERTOPARMEGGIANI, FABIOSACCHETTI, ALESSANDRO +
Opposite Enantioselectivity in the Bioreduction of (Z)-beta-Aryl-eta-cyanoacrylates Mediated by the Tryptophan 116 Mutants of Old Yellow Enzyme 1: Synthetic Approach to (R)- and (S)-beta-Aryl-gamma-lactams 1-gen-2015 BRENNA, MARIA ELISABETTACROTTI, MICHELEGATTI, FRANCESCO GILBERTOPARMEGGIANI, FABIOSANTANGELO, SARA +
A Rapid and High-Throughput Assay for the Estimation of Conversions of Ene-Reductase-Catalysed Reactions 1-gen-2015 CROTTI, MICHELEGATTI, FRANCESCO GILBERTOPARMEGGIANI, FABIOBRENNA, MARIA ELISABETTA +
First stereoselective acylation of a primary diol possessing a prochiral quaternary center mediated by lipase TL from Pseudomonas stutzeri 1-gen-2015 GATTI, FRANCESCO GILBERTO +
Multi-enzymatic stereoselective synthesis of chiral synthons and pharmaceutical intermediates 1-gen-2014 BRENNA, MARIA ELISABETTAGATTI, FRANCESCO GILBERTOPARMEGGIANI, FABIOSACCHETTI, ALESSANDRO +
p-Menthandiol-vanillin acetals: Synthesis and study of their chemo-sensorial properties 1-gen-2014 GATTI, FRANCESCO GILBERTO +
Rationalisation of the stereochemical outcome of ene-reductase-mediated bioreduction of α,β-difunctionalised alkenes 1-gen-2014 BRENNA, MARIA ELISABETTAGATTI, FRANCESCO GILBERTOPARMEGGIANI, FABIO +
Enantioselective Synthesis of (R)-2-Arylpropanenitriles Catalysed by Ene-Reductases in Aqueous Media and in Biphasic Ionic Liquid–Water Systems 1-gen-2014 BRENNA, MARIA ELISABETTAGATTI, FRANCESCO GILBERTOPARMEGGIANI, FABIO +
ENE-REDUCTASE-MEDIATED REDUCTION OF beta-CYANO-alpha,beta-UNSATURATED ESTERS FOR THE SYNTHESIS OF CHIRAL BUILDING BLOCKS 1-gen-2013 BRENNA, MARIA ELISABETTAGATTI, FRANCESCO GILBERTOPARMEGGIANI, FABIO +
Old Yellow Enzyme – mediated reduction of unsaturated diesters and cyanoesters for applications in organic synthesis: stereochemical analysis of the reaction 1-gen-2013 BRENNA, MARIA ELISABETTAGATTI, FRANCESCO GILBERTOPARMEGGIANI, FABIO +
Substrate scope and synthetic applications of the enantioselective reduction of α-alkyl-β-arylenones mediated by Old Yellow Enzymes 1-gen-2013 BRENNA, MARIA ELISABETTAGATTI, FRANCESCO GILBERTOPARMEGGIANI, FABIOSACCHETTI, ALESSANDRO +
Old Yellow Enzyme-mediated reduction of β-cyano-α,β- unsaturated esters for the synthesis of chiral building blocks: Stereochemical analysis of the reaction 1-gen-2013 BRENNA, MARIA ELISABETTAGATTI, FRANCESCO GILBERTOPARMEGGIANI, FABIO +
Synthesis of Robalzotan, Ebalzotan, and Rotigotine Precursors via the Stereoselective Multienzymatic Cascade Reduction of α,β-Unsaturated Aldehydes 1-gen-2013 BRENNA, MARIA ELISABETTAGATTI, FRANCESCO GILBERTOMALPEZZI, LUCIANAPARMEGGIANI, FABIOSACCHETTI, ALESSANDRO +
Enoate Reductases for Reduction of Electron Deficient Alkenes 1-gen-2012 BRENNA, MARIA ELISABETTAGATTI, FRANCESCO GILBERTOF. Parmeggiani +
Enoate Reductase-Mediated Preparation of Methyl (S)-2-Bromobutanoate, a Useful Key Intermediate for the Synthesis of Chiral Active Pharmaceutical Ingredients 1-gen-2012 BRENNA, MARIA ELISABETTAGATTI, FRANCESCO GILBERTOPARMEGGIANI, FABIO +
Steric Effects on the Stereochemistry of Old Yellow Enzyme-Mediated Reductions of Unsaturated Diesters: Flipping of the Substrate within the Enzyme Active Site Induced by Structural Modifications 1-gen-2012 BRENNA, MARIA ELISABETTAGATTI, FRANCESCO GILBERTOPARMEGGIANI, FABIO +
On the stereochemistry of the Baker's Yeast-mediated reduction of regioisomeric unsaturated aldehydes: Examples of enantioselectivity switch promoted by substrate-engineering 1-gen-2012 BRENNA, MARIA ELISABETTAFUGANTI, CLAUDIOGATTI, FRANCESCO GILBERTOPARMEGGIANI, FABIO +
Cascade Coupling of Ene Reductases with Alcohol Dehydrogenases: Enantioselective Reduction of Prochiral Unsaturated Aldehydes 1-gen-2012 BRENNA, MARIA ELISABETTAGATTI, FRANCESCO GILBERTOPARMEGGIANI, FABIOSACCHETTI, ALESSANDRO +
Productivity enhancement of C=C bioreductions by coupling the in situ substrate feeding product removal technology with isolated enzymes. 1-gen-2012 BRENNA, MARIA ELISABETTAGATTI, FRANCESCO GILBERTOPARMEGGIANI, FABIOSACCHETTI, ALESSANDRO +
Stereochemical outcome of the biocatalyzed reduction of activated tetrasubstituted olefins by old yellow enzymes 1-3 1-gen-2012 BRENNA, MARIA ELISABETTAGATTI, FRANCESCO GILBERTOPARMEGGIANI, FABIO +
Biotechnological Development of a Practical Synthesis of Ethyl (S)-2-Ethoxy-3-(p-methoxyphenyl)propanoate (EEHP): Over 100-Fold Productivity Increase from Yeast Whole Cells to Recombinant Isolated Enzymes 1-gen-2012 BRENNA, MARIA ELISABETTAGATTI, FRANCESCO GILBERTOPARMEGGIANI, FABIOSACCHETTI, ALESSANDRO +
Mostrati risultati da 1 a 50 di 101
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