G
Giovanni Fronza
Researcher at Instituto Politécnico Nacional
Publications - 189
Citations - 2482
Giovanni Fronza is an academic researcher from Instituto Politécnico Nacional. The author has contributed to research in topics: Ring (chemistry) & Enantioselective synthesis. The author has an hindex of 25, co-authored 188 publications receiving 2404 citations. Previous affiliations of Giovanni Fronza include Polish Academy of Sciences & University of Pavia.
Papers
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The Local Structure of Ionic Liquids: Cation–Cation NOE Interactions and Internuclear Distances in Neat [BMIM][BF4] and [BDMIM][BF4]
Andrea Mele,Greta Romanò,Matteo Giannone,Enzio Ragg,Giovanni Fronza,Guido Raos,Valentina Marcon +6 more
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Molecule-Induced Homolysis versus “Concerted Oxenoid Oxygen Insertion” in the Oxidation of Organic Compounds by Dimethyldioxirane
TL;DR: In this article, evidence for a molecule-induced homolysis of dimethyldioxirane by several classes of organic compounds (alkanes, alkenes, ethers, alcohols, aldehydes, iododerivatives) is reported.
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Proton Nuclear Magnetic Resonance Spectroscopy Studies of the Inclusion Complex of Piroxicam with β‐Cyclodextrin
TL;DR: In this paper, Piroxicam sodium salt forms an inclusion complex with beta-cyclodextrin in aqueous solution and the 1:1 stoichiometry of the complex was determined by the continuous variation method.
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New Versatile Fluorinated Chiral Building Blocks: Synthesis and Reactivity of Optically Pure α-(Fluoroalkyl)-β-sulfinylenamines
Alberto Arnone,Pierfrancesco Bravo,Silvia C. Capelli,Giovanni Fronza,and Stefano V. Meille,Matteo Zanda,Giancarlo Cavicchio and,Marcello Crucianelli +7 more
TL;DR: In this paper, an optically pure α-(fluoroalkyl)-β-sulfinyl enamines has been achieved by aza-Wittig reaction of triphenyliminophosphoranes with the corresponding α-fluorinated-α-Sulfinyl ketones.
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Homolytic acylation of protonated pyridine and pyrazine derivatives
TL;DR: In this paper, the results of homolytic acylation of compounds containing pyridine and pyrazine rings are reported, aldehydes being used as source of acyl radicals.