A. Gambacorta

Roma Tre University — Italy

Chemistry · Physical Sciences

40h-index5.0kcitations185works0.02yr avg
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Research Topics

Asymmetric Synthesis and Catalysis(21), Lipid Membrane Structure and Behavior(21), Enzyme Catalysis and Immobilization(16), Enzyme Structure and Function(16), Microbial Metabolic Engineering and Bioproduction(15)

Publications185 total

ChemInform Abstract: First Asymmetric Organocatalyzed Domino Friedel—Crafts/Lactonization Reaction in the Enantioselective Synthesis of the GABAB Receptor Modulator (S)‐BHFF.
ChemInform·2016
First asymmetric organocatalyzed domino Friedel–Crafts/lactonization reaction in the enantioselective synthesis of the GABAB receptor modulator (S)-BHFF
Tetrahedron Letters·2016· 18 cited
ChemInform Abstract: Catalytic Friedel—Crafts/Lactonization Domino Reaction: Facile Access to 3‐Hydroxybenzofuran‐2‐one Scaffold.
ChemInform·2015
Chemical Reactions embedded in Liposomes: First moves toward a novel approach in Organocatalysis
IRIS Research product catalog (Sapienza University of Rome)·2015
Catalytic Friedel–Crafts/Lactonization Domino Reaction: Facile Access to 3‐Hydroxybenzofuran‐2‐one Scaffold
European Journal of Organic Chemistry·2014· 13 cited
Dihydroxytyrosyl Esters Of Dicarboxilic Acids. Synthesis And Structure/Antioxidant Activity Relationships
Iris (Roma Tre University)·2013
Noncovalent organocatalysis:an open door in the asymmetric nucleophilic epoxidation
IRIS Research product catalog (Sapienza University of Rome)·2013
Asymmetric synthesis of Natural-product-inspired Spiro epoxyoxindoles via Hydrogen-Bond Organocatalysis
IRIS Research product catalog (Sapienza University of Rome)·2013
Synthesis and Structure/Antioxidant Activity Relationship of Novel Catecholic Antioxidant Structural Analogues to Hydroxytyrosol and Its Lipophilic Esters
Journal of Agricultural and Food Chemistry·2012· 77 cited
ChemInform Abstract: Noncovalent Organocatalysis: A Powerful Tool for the Nucleophilic Epoxidation of α‐Ylideneoxindoles.
ChemInform·2012
Noncovalent Organocatalysis: A Powerful Tool for the Nucleophilic Epoxidation of α-Ylideneoxindoles
Organic Letters·2011· 91 cited
Organocatalytic nucleophilic epoxidation promoted by prolinol derivatives: a straightforward approach to spiroepoxy esters
IRIS Research product catalog (Sapienza University of Rome)·2011
“Enantioselective synthesis of actractive spiroepoxy-oxindoles by means of organocatalysis”.
2011
Proline Derivatives in Asymmetric NucleophilicEpoxidation: a Novel Organocatalytic Approach to SpiroepoxyEsters
IRIS Research product catalog (Sapienza University of Rome)·2011
Structure/antioxidant activity relationship of hydroxytyrosol analogues and their fatty acid esters
Iris (Roma Tre University)·2011
Hydroxytyrosol analogues and their fatty acid esters. Synthesis and structure/antioxidant activity relationships
Iris (Roma Tre University)·2011
Fatty Acid Hydroxytyrosyl Esters: Structure/Antioxidant Activity Relationship by ABTS and in Cell-Culture DCF Assays
Journal of Agricultural and Food Chemistry·2010· 82 cited
The role of fatty acid esters chain length on the antioxidant capacity of hydroxytyrosyl esters and their analogues. Polar paradox or cut-off effect?
2010
Biological evaluation of the antioxidant activity of novel cathecolic compounds
2010
Synthesis and antioxidant properties of hydroxytyrosyl esters analogues
IRIS Research product catalog (Sapienza University of Rome)·2010
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Frequent Co-authors

Mario De Rosa(28), J. D. Bu’Lock(8), Barbara Nicolaus(7), Alessandra Gliozzi(6), Barbara Nicolaus(5), Licia Lama(5), Daniela Tofani(5), Antonio Trincone(4), Vincenzo Buonocore(3), María Cristina Manca(3), Enrico Esposito(3), William D. Grant(3), Roberta Bernini(3), Wolfram Zillig(2), Paola Giardina(2), Stéphane L’Haridon(2), Daniël Prieur(2), Christian Jeanthon(2), Roberta Improta(2), William D. Grant(2)