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BRENNA, MARIA ELISABETTA

BRENNA, MARIA ELISABETTA  

Istituto di Scienze e Tecnologie Chimiche "Giulio Natta" - SCITEC  

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Risultati 1 - 15 di 15 (tempo di esecuzione: 0.036 secondi).
Titolo Data di pubblicazione Autore(i) File
Biocatalytic Approach to Chiral -Nitroalcohols by Enantioselective Alcohol Dehydrogenase-Mediated Reduction of -Nitroketones 1-gen-2018 Tentori, Francesca; Brenna, Elisabetta; Id, ; Colombo, Danilo; Crotti, Michele; Francesco, G Gatti ID; Chiara Ghezzi, Maria; Pedrocchifantoni, Giuseppe
Asymmetric bioreduction of ?-acylaminonitroalkenes: easy access to chiral building blocks with two vicinal nitrose-containing functional groups 1-gen-2017 E. Brenna; M. Crotti; F.G. Gatti; D. Monti; F. Parmeggiani; S. Santangelo
Fungal oxidoreductases as biocatalysts for fine chemicals transformations 1-gen-2016 Romagnolo, A; Spina, F; Risso, S; Crotti, M; Monti, D; Brenna, E; Lanfranco, L; C Varese, G
Lipase-mediated resolution of both diastereoisomeric forms of linalool oxide (pyranoid) 1-gen-2016 D. De Simeis; S. SERRA; E. Brenna
Oxidation of apocarotenoids mediated by fungi 1-gen-2016 D. DE SIMEIS; S. Serra; E. Brenna
Productivity improvement of the bioreduction of ?,?-unsaturated aldehydes by coupling the in situ substrate feeding product removal (SFPR) strategy with isolated enzymes 1-gen-2016 Brenna, E; G Gatti, F; Monti, D; Parmeggiani, F; Sacchetti, A
A rapid and high-throughput assay for the estimation of conversion values of ene-reductases-catalyzed reactions 1-gen-2015 Forchin, Mc; Crotti, M; Gatti, F; Parmeggiani, F; Brenna, E; Monti, D
Opposite enantioselectivity in the bioreduction of (Z)-?-aryl-?-cyanoacrylates mediated by the Trp 116 mutants of Old Yellow Enzyme 1 1-gen-2015 Brenna, E; Crotti, M; Gatti, F; Monti, D; Parmeggiani, F; W Powell III, R; Santangelo, S; D Stewart, J
Enzymatic-organo-catalysis: metal-free preparation of fragrances by a laccase/ene-reductase/oxa-ammonium catalytic system 1-gen-2014 Brenna, E; Crotti, M; G GATTI, F; Monti, D; Manenti, G; Sacchetti, A
Multi-enzyme stereoselective procedures for fragrance chemistry 1-gen-2014 E. Brenna; M. CROTTI; F. G. Gatti; D. Monti; F. Parmeggiani; A. Pugliese; S. Santangelo
Substrate scope and synthetic applications of the enantioselective reduction of ?-alkyl-?-arylenones mediated by Old Yellow Enzymes 1-gen-2014 Monti, D; Brenna, E; E Ferrandi, E; G Gatti, F; Parmeggiani, F; Sacchetti, A
Old Yellow Enzyme-mediated reduction of b-cyano-a,bunsaturated esters for the synthesis of chiral building blocks: stereochemical analysis of the reaction 1-gen-2013 Brenna, Elisabetta; G Gatti, Francesco; Manfredi, Alessia; Monti, Daniela; Parmeggiani, Fabio
Intermittent simulated moving bed chromatographic separation of (RS,RS)-2-(2,4-difluorophenyl)butane-1,2,3-triol 1-gen-2010 Acetti, Daniela; Langel, Christian; Brenna, Elisabetta; Fuganti, Claudio; Mazzotti, Marco
Synthesis, olfactory evaluation, determination of the absolute configuration of the 3,4-dehydroionone stereoisomers 1-gen-2006 S. SERRA; C. FUGANTI; E. BRENNA
Chirality and fragrance chemistry: Stereoisomers of the commercial chiral odorants Muguesia and Pamplefleur 1-gen-2005 Abate, Agnese; Brenna, Elisabetta; Fuganti, Claudio; G Gatti, Francesco; Giovenzana, Tommaso; Malpezzi, Luciana; Serra, Stefano