Giovanni Fronza

Tecnologie Avanzate (Italy) — Italy

Chemistry · Physical Sciences

32h-index4.0kcitations301works0.02yr avg
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Research Topics

Carbohydrate Chemistry and Synthesis(54), Analytical Chemistry and Chromatography(51), Enzyme Catalysis and Immobilization(46), Fluorine in Organic Chemistry(41), Microbial Metabolic Engineering and Bioproduction(27)

Publications301 total

“Novel chemo-enzymatic synthesis, structural elucidation and first antiprotozoal activity profiling of the atropoisomeric dimers of trans-8-Hydroxycalamenene”
Bioorganic Chemistry·2024Open Access
Studies on the Oxidation of Aromatic Amines Catalyzed by Trametes versicolor Laccase
International Journal of Molecular Sciences·2023· 8 citedOpen Access
Synthesis of ω‐Muricholic Acid by One‐Pot Enzymatic Mitsunobu Inversion using Hydroxysteroid Dehydrogenases
ChemCatChem·2021· 2 citedOpen Access
Studies on the Laccase‐Catalyzed Oxidation of 4‐Hydroxy‐Chalcones
Advanced Synthesis & Catalysis·2019· 13 citedOpen Access
Response of Pediculus humanus capitis (Phthiraptera: Pediculidae) to Volatiles of Whole and Individual Components of the Human Scalp
Journal of Medical Entomology·2018· 24 citedOpen Access
The Co-identity of Lipiarmycin A3 and Tiacumicin B
Natural Product Communications·2016· 3 cited
Deoxycholic acid transformations catalyzed by selected filamentous fungi
Steroids·2015· 24 cited
Laccase‐Catalyzed Dimerization of Piceid, a Resveratrol Glucoside, and its Further Enzymatic Elaboration
Advanced Synthesis & Catalysis·2015· 21 cited
Investigation of the stereochemical course of ene reductase-catalysed reactions by deuterium labelling
Isotopes in Environmental and Health Studies·2015· 7 citedOpen Access
Investigation of the stereochemical course of ene reductase-catalysed reactions by deuterium labelling
Figshare·2015Open Access
Investigation of the stereochemical course of ene reductase-catalysed reactions by deuterium labelling
Figshare·2015Open Access
Enzymatic oxidative dimerization of silymarin flavonolignans
Journal of Molecular Catalysis B Enzymatic·2014· 28 cited
The Co-identity of Lipiarmycin A3 and Tiacumicin B
Natural Product Communications·2014· 17 citedOpen Access
Unambiguous Characterization of the Sesquiterpene (7<i>R</i>,9<i>E</i>)‐1,2,11‐Trihydroxy‐1,3,5,9‐bisabolatetraene through Its Enantioselective Synthesis
European Journal of Organic Chemistry·2012· 8 cited
Biotransformation of spirolaxine by Absidia cuneospora and Trametes hirsuta: Formation of β-glycosyl and β-xylosyl derivatives
Journal of Molecular Catalysis B Enzymatic·2012· 3 cited
On the stereochemistry of the Baker's Yeast-mediated reduction of regioisomeric unsaturated aldehydes: Examples of enantioselectivity switch promoted by substrate-engineering
Journal of Molecular Catalysis B Enzymatic·2012· 16 cited
Enantioselective C C bond reduction of unsaturated α-chloro esters by old yellow enzymes
Journal of Molecular Catalysis B Enzymatic·2011· 22 cited
Enzymatic Baeyer-Villiger oxidation of steroids with cyclopentadecanone monooxygenase
Journal of Biotechnology·2010
Stereochemical Analysis of the Enzymic Reduction of the Double Bond of α‐ and β‐Substituted Nitrostyrenes and α‐Ethoxycinnamaldehyde through Deuterium Labelling Experiments
European Journal of Organic Chemistry·2010· 17 cited
Microbial Transformations of the Taxan Ring of 10-DAB by Some Strains of the Fungus <i>Curvularia lunata</i>: Formation of the Bis-abeotaxanes Wallifoliol and 4-Deacylwallifoliol
Journal of Natural Products·2010· 19 cited
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Frequent Co-authors

Claudio Fuganti(15), Piero Grasselli(9), Andrea Mele(8), Pierfrancesco Bravo(7), María De Bernardi(7), Giovanni Vidari(7), Paola Vita Finzi(7), Enrico Redenti(4), Paolo Ventura(4), Francesco Minisci(4), Giuseppe Pedrocchi‐Fantoni(4), Domenico Acquotti(4), Sandro Sonnino(4), G. Mellerio(4), Stefano Serra(4), Enzio Ragg(3), Anna Bravo(3), Francesca Fontana(3), C. TICOZZI(3), Guido Tettamanti(3)