Giovanni Piersanti

Full Professor

Università degli Studi di Udine

Italy

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Giovanni Piersanti is a Full Professor at Università degli Studi di Urbino Carlo Bo in Italy. His research primarily focuses on synthetic chemistry, specifically in the areas of redox modulation, synthesis of cage receptors, and organocatalytic strategies for amino acid derivatives. Recent articles authored by him explore innovative methodologies in organic synthesis and their applications in biochemistry.

Giovanni Piersanti

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Articles (19)

Redox modulation by a synthetic thiol compound reduces LPS-induced pro-inflammatory cytokine expression in macrophages via AP-1/NLRP3 axis and influences the crosstalk with endothelial cells

A New Bis‐Urea Based Cage Receptor for Anions: Synthesis, Solid State Structures and Binding Studies

Front Cover: A New Bis‐Urea Based Cage Receptor for Anions: Synthesis, Solid State Structures and Binding Studies (Chem. Asian J. 2/2025)

Enantioselective organocatalytic strategies to access noncanonical α-amino acids

Practical and Selective Syntheses of S‐Acyl and N‐Acyl Glutathiones with N‐Acyl Imidazoles in Water

A Short Synthesis of (−)‐6,7‐Secoagroclavine via Metal‐Free Reductive Coupling

General Access to Clavine Alkaloids via a Rhodium(I)‐Catalyzed Diastereoselective Hayashi‐Miyaura Reaction

Giese-type alkylation of dehydroalanine derivatives via silane-mediated alkyl bromide activation

Photoredox catalysis enabling decarboxylative radical cyclization of γ,γ-dimethylallyltryptophan (DMAT) derivatives: formal synthesis of 6,7-secoagroclavine

Synthesis and Fluorescence Properties of 4-Cyano and 4-Formyl Melatonin as Putative Melatoninergic Ligands

Targeting <scp>SARS‐CoV</scp> ‐2 by synthetic dual‐acting thiol compounds that inhibit Spike/ <scp>ACE2</scp> interaction and viral protein production

Asymmetric Total Synthesis of All Rugulovasine Stereoisomers and Preliminary Evaluation of Their Biological Properties

Asymmetric Alkylation of Cyclic Ketones with Dehydroalanine via H‐Bond‐Directing Enamine Catalysis: Straightforward Access to Enantiopure Unnatural α‐Amino Acids

Dithiol Based on l-Cysteine and Cysteamine as a Disulfide-Reducing Agent

Novel, Chiral, and Enantiopure C<sub>2</sub>-Symmetric Thioureas Promote Asymmetric Protio-Pictet-Spengler Reactions by Anion-Binding Catalysis

Synthesis and Reactivity of Uhle's Ketone and Its Derivatives

Concise catalytic asymmetric synthesis of (R)-4-amino Uhle's ketone

C3-Alkylation of indoles and oxindoles by alcohols by means of borrowing hydrogen methodology

General synthesis of unnatural 4-, 5-, 6-, and 7-bromo-D-tryptophans by means of a regioselective indole alkylation

Collaborators (9)

Mariele Montanari

Rita Crinelli

Francesco Secci

Francesca BARTOCCINI

Patrizia Rossi

Mauro Magnani

Luca Bernardi

Michele Mari

Michela Bruschi

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