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Davide Tessaro
Davide Tessaro
CMIC "G.Natta" Department, Politecnico di Milano
Verified email at polimi.it
Title
Cited by
Cited by
Year
Chemo-enzymatic deracemization methods for the preparation of enantiopure non-natural α-amino acids
S Servi, D Tessaro, G Pedrocchi-Fantoni
Coordination Chemistry Reviews 252 (5-7), 715-726, 2008
962008
Characterization of a novel amine transaminase from Halomonas elongata
L Cerioli, M Planchestainer, J Cassidy, D Tessaro, F Paradisi
Journal of Molecular Catalysis B: Enzymatic 120, 141-150, 2015
922015
Enzymatic Conversion of Unnatural Amino Acids by Yeast D‐Amino Acid Oxidase
A Caligiuri, P D'Arrigo, E Rosini, D Tessaro, G Molla, S Servi, L Pollegioni
Advanced Synthesis & Catalysis 348 (15), 2183-2190, 2006
672006
A practical selective synthesis of mixed short/long chains glycerophosphocholines
P D’Arrigo, E Fasoli, G Pedrocchi-Fantoni, C Rossi, C Saraceno, ...
Chemistry and physics of lipids 147 (2), 113-118, 2007
472007
A thermostable L-aspartate oxidase: a new tool for biotechnological applications
D Bifulco, L Pollegioni, D Tessaro, S Servi, G Molla
Applied microbiology and biotechnology 97, 7285-7295, 2013
432013
Systems biocatalysis: an artificial metabolism for interconversion of functional groups
D Tessaro, L Pollegioni, L Piubelli, P D’Arrigo, S Servi
ACS Catalysis 5 (3), 1604-1608, 2015
412015
Naphthyl-l-α-amino acids via chemo-enzymatic dynamic kinetic resolution
P D’Arrigo, L Cerioli, A Fiorati, S Servi, F Viani, D Tessaro
Tetrahedron: Asymmetry 23 (13), 938-944, 2012
382012
A Continuous‐Flow Cascade Reactor System for Subtilisin A‐ Catalyzed Dynamic Kinetic Resolution of Ntert‐Butyloxycarbonylphenylalanine Ethyl Thioester with …
P Falus, L Cerioli, G Bajnóczi, Z Boros, D Weiser, J Nagy, D Tessaro, ...
Advanced Synthesis & Catalysis 358 (10), 1608-1617, 2016
352016
Chemo‐enzymatic dynamic kinetic resolution of amino acid thioesters
D Arosio, A Caligiuri, P D'Arrigo, G Pedrocchi‐Fantoni, C Rossi, ...
Advanced Synthesis & Catalysis 349 (8‐9), 1345-1348, 2007
332007
Conversion of oleic acid into azelaic and pelargonic acid by a chemo-enzymatic route
E Brenna, D Colombo, G Di Lecce, FG Gatti, MC Ghezzi, F Tentori, ...
Molecules 25 (8), 1882, 2020
322020
Deracemization and Stereoinversion of α‐Amino Acids by l‐Amino Acid Deaminase
E Rosini, R Melis, G Molla, D Tessaro, L Pollegioni
Advanced Synthesis & Catalysis 359 (21), 3773-3781, 2017
292017
Potential Application of N-Carbamoyl-β-Alanine Amidohydrolase from Agrobacterium tumefaciens C58 for β-Amino Acid Production
AI Martínez-Gómez, S Martínez-Rodríguez, J Pozo-Dengra, D Tessaro, ...
Applied and environmental microbiology 75 (2), 514-520, 2009
282009
“A study in yellow”: Investigations in the stereoselectivity of ene‐reductases
F Parmeggiani, E Brenna, D Colombo, FG Gatti, F Tentori, D Tessaro
ChemBioChem 23 (1), e202100445, 2022
272022
Improvements in the enzymatic synthesis of phosphatidylserine employing ionic liquids
P D’Arrigo, L Cerioli, C Chiappe, W Panzeri, D Tessaro, A Mele
Journal of Molecular Catalysis B: Enzymatic 84, 132-135, 2012
272012
Enzymatic approach to both enantiomers of N-Boc hydrophobic amino acids
E Agosta, A Caligiuri, P D’Arrigo, S Servi, D Tessaro, R Canevotti
Tetrahedron: Asymmetry 17 (13), 1995-1999, 2006
262006
The biocatalyzed stereoselective preparation of polycyclic cyanohydrins
MMC Silva, MLS e Melo, M Parolin, D Tessaro, S Riva, B Danieli
Tetrahedron: Asymmetry 15 (1), 21-27, 2004
252004
Synthesis and antiproliferative activity of alkylphosphocholines
M Agresta, P D’Arrigo, E Fasoli, D Losi, G Pedrocchi-Fantoni, S Riva, ...
Chemistry and physics of lipids 126 (2), 201-210, 2003
252003
Enzymatic methods for the manipulation and valorization of soapstock from vegetable oil refining processes
B Casali, E Brenna, F Parmeggiani, D Tessaro, F Tentori
Sustainable Chemistry 2 (1), 74-91, 2021
242021
Base catalyzed racemization of amino acid derivatives
P D’Arrigo, D Arosio, L Cerioli, D Moscatelli, S Servi, F Viani, D Tessaro
Tetrahedron: Asymmetry 22 (8), 851-856, 2011
232011
Tandem Tetrahydroisoquinoline‐4‐carboxylic Acid/β‐alanine as a new construct able to induce a flexible turn
R Bucci, A Bonetti, F Clerici, A Contini, D Nava, S Pellegrino, D Tessaro, ...
Chemistry–A European Journal 23 (45), 10822-10831, 2017
212017
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Articles 1–20