BRENNA, MARIA ELISABETTA
BRENNA, MARIA ELISABETTA
Istituto di Scienze e Tecnologie Chimiche "Giulio Natta" - SCITEC
Insight into the Stereoselective Synthesis of (1S)- Nor(pseudo)ephedrine Analogues by a Two-Steps Biocatalytic Process
2023 Fracchiolla, Noemi; Patti, Stefania; Sangalli, Fabio; Monti, Daniela; Presini, Francesco; Paolo Giovannini, Pier; Parmeggiani, Fabio; Brenna, Elisabetta; Tessaro, Davide; Ferrandi, ERICA ELISA
Biocatalytic Approach to Chiral -Nitroalcohols by Enantioselective Alcohol Dehydrogenase-Mediated Reduction of -Nitroketones
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
2017 E. Brenna; M. Crotti; F.G. Gatti; D. Monti; F. Parmeggiani; S. Santangelo
Old Yellow Enzyme-mediated reduction of b-cyano-a,bunsaturated esters for the synthesis of chiral building blocks: stereochemical analysis of the reaction
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
2010 Acetti, Daniela; Langel, Christian; Brenna, Elisabetta; Fuganti, Claudio; Mazzotti, Marco
Chirality and fragrance chemistry: Stereoisomers of the commercial chiral odorants Muguesia and Pamplefleur
2005 Abate, Agnese; Brenna, Elisabetta; Fuganti, Claudio; G Gatti, Francesco; Giovenzana, Tommaso; Malpezzi, Luciana; Serra, Stefano
Titolo | Data di pubblicazione | Autore(i) | File |
---|---|---|---|
Insight into the Stereoselective Synthesis of (1S)- Nor(pseudo)ephedrine Analogues by a Two-Steps Biocatalytic Process | 1-gen-2023 | Fracchiolla, Noemi; Patti, Stefania; Sangalli, Fabio; Monti, Daniela; Presini, Francesco; Paolo Giovannini, Pier; Parmeggiani, Fabio; Brenna, Elisabetta; Tessaro, Davide; Ferrandi, ERICA ELISA | |
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 | |
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 | |
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 |