GIANFRANCO FAVI

Associate Professor

University of Urbino

Italy

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About

Gianfranco Favi is an Associate Professor at the University of Urbino in Italy. His research focuses on synthetic methodologies, particularly in the development of heterocycles and novel organic compounds. Recent publications include explorations of carbonyl umpolung reactivity, as well as the synthesis of multifunctionalized indole-pyrrole hybrids and various heterocyclic scaffolds.

Articles (16)

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2025

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2025

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2024

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2024

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2024

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2024

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2023

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2022

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2022

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2022

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2021

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2021

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2021

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2020

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2020

Collaborators (6)

Fabio Mantellini

ITALY

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Giacomo Mari

University of Urbino Carlo Bo

ITALY

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yolanda perez-pertejo

Profesora Titular de Universidad

Universidad de León

SPAIN

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Stefania Santeusanio

ITALY

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Michele Mancinelli

University of Bologna

ITALY

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Simone Lucarini

Associate Professor of Medicinal Chemistry

Università degli Studi di Udine

ITALY

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GIANFRANCO FAVI

Research Interests

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Articles (16)

A Noncarbenoid Approach to Imidazolidines via ZnCl2-Catalyzed Annulation of 4-Alkoxycarbonyl-1,2-diaza-1,3-dienes with 1,3,5-Triazinanes

Redrawing the Mannich‐Type Reaction through Carbonyl Umpolung Reactivity

Challenge N- versus O-six-membered annulation: FeCl3-catalyzed synthesis of heterocyclic N,O-aminals

Useful Access to Uncommon Thiazolo[3,2-a]indoles

Easy one-pot synthesis of multifunctionalized indole–pyrrole hybrids as a new class of antileishmanial agents

1,2‐Diaza‐1,3‐Dienes as a Multifaceted Synthons for the Synthesis of Heterocycles: A Fifteen‐Years Update

A Metal‐Free C−H Amination‐Based Strategy for N‐Amino Indole Synthesis

Straightforward Access to Pyrazine‐(2,3)‐diones through Sequential Three‐Component Reaction

Easy Access to Indole‐based Bi‐Sulfurylate‐Heterocyclic Scaffolds

A facile protocol for the preparation of 2-carboxylated thieno [2,3-b] indoles: a de novo access to alkaloid thienodolin

Practical and sustainable preparation of pyrrolo[2,3-b]indoles by Cu/Fe catalyzed intramolecular C(sp2)–H amination

Synthesis of Azacarbolines via PhIO2-Promoted Intramolecular Oxidative Cyclization of α-Indolylhydrazones

Experimental and Theoretical DFT Investigations in the [2,3]-Wittig-Type Rearrangement of Propargyl/Allyl-Oxy-Pyrazolones

Phenotype Screening of an Azole-bisindole Chemical Library Identifies URB1483 as a New Antileishmanial Agent Devoid of Toxicity on Human Cells

Metal and Oxidant Free Construction of Substituted‐ and/or Polycyclic Indoles: A Useful Alternative to Bischler and Related Syntheses

Construction of Unusual Indole-Based Heterocycles from Tetrahydro-1H-pyridazino[3,4-b]indoles

Collaborators (6)

Fabio Mantellini

Giacomo Mari

yolanda perez-pertejo

Stefania Santeusanio

Michele Mancinelli

Simone Lucarini

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