Andrea Temperini

Prof.

University of Perugia

Italy

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Professor Andrea Temperini is a faculty member at the University of Perugia, Italy. His research focuses on synthetic organic chemistry, particularly in the development of metal-free reactions and functionalized compounds. Recent contributions include advancements in the synthesis of γ-lactams and the preparation of new intermediates such as alkynyl phenyl selenides. He has also explored innovative approaches for the synthesis of various organic compounds including benzo[c]chromenes and 2,3-diaminopropanol derivatives.

Articles (10)

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2025

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2025

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2023

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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

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2020

Collaborators (3)

Donatella Aiello

University of Calabria

ITALY

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Marco Ballarotto

Ph.D. student in Organic Chemistry under the supervision of Prof. Andrea Temperini

Università degli Studi di Napoli Federico II

ITALY

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Bruno Cerra

Assistant Professor (Tenure track - RTDb)

University of Perugia

ITALY

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Andrea Temperini

Research Interests

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Articles (10)

A Versatile Preparation of (2R,3S)‐ and (2R,3R)‐2‐Benzyloxy(allyloxy)‐3‐Hydroxybutyrolactones as Useful C4‐Synthons

Alkynyl Phenyl Selenides as Intermediates in the Metal‐Free Cyclisation of N‐Tosyl Homopropargyl Amides to γ‐Lactams

Multicomponent and Metal‐Free Diels–Alder/Aromatization Approach to the Stereospecific Synthesis of E‐(Hetero)Stilbenes and Diarylacetylenes

(Phenylseleno)acetic acid based precursor for the regiospecific synthesis of 1-phenylseleno-2-alkanones*

Metal‐Free Synthesis of Alkyl Phenyl Selenides by Reaction of Activated Alcohols with the O‐(tert‐ Butyl) Se ‐Phenyl Selenocarbonate/HI System

A straightforward synthesis of functionalized 6H-benzo[c]chromenes from 3-alkenyl chromenes by intermolecular Diels–Alder/aromatization sequence

Metal-Free Hyperbaric Multicomponent Approach to 4-Aryl[2.2]Paracyclophanes

O-(tert-butyl) Se-phenyl selenocarbonate: A convenient, bench-stable and metal-free precursor of benzeneselenol

2,3-Diaminopropanols Obtained from d-Serine as Intermediates in the Synthesis of Protected 2,3-l-Diaminopropanoic Acid (l-Dap) Methyl Esters

Chemoselective and metal-free reduction of α,β-unsaturated ketones by in situ produced benzeneselenol from O-(tert-butyl) Se-phenyl selenocarbonate

Collaborators (3)

Donatella Aiello

Marco Ballarotto

Bruno Cerra

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