Ernesto Giovanni Occhiato

Professore associato

Università degli Studi di Napoli Federico II

Italy

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About

Ernesto Giovanni Occhiato is an Associate Professor at Università degli Studi di Firenze, Italy. His research areas include the development of gold catalysis methods, asymmetric synthesis, and novel reactions involving carbonyl compounds. Recent articles authored by Professor Occhiato highlight significant advancements in cycloisomerization techniques and the synthesis of various heterocycles. His work contributes to the fields of organic chemistry and catalysis, focusing on innovative approaches to complex molecule construction.

Articles (13)

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2025

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2025

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2024

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2024

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2023

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2022

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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

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2020

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2020

Collaborators (2)

Asier Carral Menoyo

Associate Professor

University of the Basque Country

SPAIN

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Andrea Maranzana

Associate Professor

Università degli Studi di Torino

ITALY

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Ernesto Giovanni Occhiato

Research Interests

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Articles (13)

Central-to-Axial-to-Central Chirality Transfer in the Au(I)-Catalyzed Cycloisomerization of Propargyl Vinyl Ethers to Cyclopentadienes

Recent Advances in the α‐Hydrazination (α‐Amination) of Carbonyl Compounds

Gold(I)-Catalyzed Rautenstrauch/Hetero-Diels–Alder/Retro-aza-Michael Cascade Reaction for the Synthesis of α-Hydrazineyl-2-cyclopentenones

Asymmetric Reduction of Cyclic Imines by Imine Reductase Enzymes in Non‐Conventional Solvents

Synthesis of 5-Hydrazino-2-cyclopentenone Derivatives by a Gold(I)-Catalyzed Cycloisomerization/Hetero-Diels–Alder/Ring-Opening Tandem Reaction of Enynyl Acetates

Gold(I)-Catalyzed Cycloisomerization/Hetero-Diels–Alder Reaction/Ring Opening Cascade to Functionalized Cyclopentadienes

Enantiodivergent Synthesis of Halofuginone by Candida antarctica Lipase B (CAL-B)-Catalyzed Kinetic Resolution in Cyclopentyl Methyl Ether (CPME)

Synthesis of (±)‐epi‐Jungianol by the Gold(I)‐Catalyzed Propargyl Claisen Rearrangement/Hydroarylation Cascade Reaction of Propargyl Vinyl Ethers

Front Cover: Gold(I)‐Catalysed Hydroarylation of Lactam‐Derived Enynes as an Entry to Tetrahydrobenzo[g]quinolines (Eur. J. Org. Chem. 6/2020)

Gold(I)‐Catalysed Hydroarylation of Lactam‐Derived Enynes as an Entry to Tetrahydrobenzo[g]quinolines

Pentannulation of N-heterocycles by a tandem gold-catalyzed [3,3]-rearrangement/Nazarov reaction of propargyl ester derivatives: a computational study on the crucial role of the nitrogen atom

Enantioselective Synthesis of cis and trans 4‐Aminopipecolic Acids as γ‐Amino Acids for the Construction of Cyclic RGD‐Containing Peptidomimetics Antagonists of αVβ3 Integrin

One-Pot Access to 1,7a-Dihydro-1,3a-ethano-indene and 1,8a-Dihydro-1,3a-ethano-azulene Skeletons by a Sequential Gold(I)-Catalyzed Propargyl Claisen Rearrangement/Nazarov Cyclization/[4+2] Cycloaddition Reaction

Collaborators (2)

Asier Carral Menoyo

Andrea Maranzana

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