Mononuclear heterocyclic rearrangements. Effect of the structure of the side chain on the reactivity. Part 1. Rearrangement of some 3-arylureines of 5-pheny-1,2,4-oxadiazole into 1-aryl-3-benzoylamino-1,2,4-triazolin-5-ones in acetonitrile, benzene, and dioxane–water

Vincenzo Frenna, Domenico Spinelli and Giovanni Consiglio

J. Chem. Soc., Perkin Trans. 2, 1990, 1289
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On the structure of 3‐acetylamino‐5‐methyl‐1,2,4‐oxadiazole and on the fully degenerate rearrangements (FDR) of its anion: a stimulating comparison between the results of ‘in‐silicon chemistry’ and ‘laboratory chemistry’

Angelo Mugnoli, Giampaolo Barone, Silvestre Buscemi, Camilla Zaira Lanza, Andrea Pace, Marcella Pani and Domenico Spinelli

J of Physical Organic Chem, 2009, 22, 1086
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Theoretical study of degenerate Boulton–Katritzky rearrangements. Semiempirical and ab initio procedures

Gianfranco La Manna, Silvestre Buscemi and Nicolò Vivona

Journal of Molecular Structure: THEOCHEM, 1998, 452, 67
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The Boulton–Katritzky Reaction: A Kinetic Study of the Effect of 5‐Nitrogen Substituents on the Rearrangement of Some (Z)‐Phenylhydrazones of 3‐Benzoyl‐1,2,4‐oxadiazoles

Vincenzo Frenna, Antonio Palumbo Piccionello, Barbara Cosimelli, Franco Ghelfi and Domenico Spinelli

Eur J Org Chem, 2014, 2014, 7006
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Mononuclear Rearrangement of theZ-Phenylhydrazones of Some 3-Acyl-1,2,4-oxadiazoles: Effect of Substituents on the Nucleophilic Character of the >C═N–NH–C6H5Chain and on the Charge Density of N-2 of the 1,2,4-Oxadiazole Ring (Electrophilic Counterpart)

Gabriele Micheletti, Vincenzo Frenna, Gabriella Macaluso, Carla Boga and Domenico Spinelli

J. Org. Chem., 2019, 84, 2462
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THE SYNTHESIS OF FLUORINATED HETEROAROMATIC COMPOUNDS. PART 2. FIVE-MEMBERED RINGS WITH TWO HETEROATOMS. A REVIEW

Andrea Pace, Silvestre Buscemi and Nicolò Vivona

Organic Preparations and Procedures International, 2007, 39, 1
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On the application of the extended Fujita–Nishioka equation to polysubstituted systems. A kinetic study of the rearrangement of several poly-substituted Z-arylhydrazones of 3-benzoyl-5-phenyl-1,2,4-oxadiazole into 2-aryl-4-benzoylamino-5-phenyl-1,2,3-triazoles in dioxane/water

Francesca D'Anna, Fiammetta Ferroni, Vincenzo Frenna, Susanna Guernelli, Camilla Zaira Lanza, Gabriella Macaluso, Vitalba Pace, Giovanni Petrillo, Domenico Spinelli and Raffaella Spisani

Tetrahedron, 2005, 61, 167
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On the rearrangement of some Z -arylhydrazones of 3-benzoyl-5-phenylisoxazoles into 2-aryl-4-phenacyl-2 H -1,2,3-triazoles: a kinetic study of the substituent effects in Boulton–Katritzky reactions

Vincenzo Frenna, Antonio Palumbo Piccionello, Domenico Spinelli and Franco Ghelfi

Tetrahedron, 2015, 71, 7315
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A deep insight into the mechanism of the acid‐catalyzed rearrangement of the Z‐phenylhydrazone of 5‐amino‐3‐benzoyl‐1,2,4‐oxadiazole in a non‐polar solvent

Francesca D'Anna, Gianfranco Fontana, Vincenzo Frenna, Gabriella Macaluso, Salvatore Marullo and Domenico Spinelli

J of Physical Organic Chem, 2011, 24, 185
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ChemInform Abstract: Mononuclear Heterocyclic Rearrangements. Part 14. Rearrangement of Some Z‐Arylhydrazones (I) of 3‐Benzoyl‐5‐phenylisoxazole to 2‐Aryl‐4‐phenacyl‐1,2,3‐triazoles (II) in Dioxane‐Water

V. FRENNA, N. VIVONA, G. MACALUSO, D. SPINELLI and G. CONSIGLIO

ChemInform, 1987, 18
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Unexpected Substituent Effects in the Iso-Heterocyclic Boulton–Katritzky Rearrangement of 3-Aroylamino-5-methyl-1,2,4-oxadiazoles: A Mechanistic Study

Vincenzo Frenna, Paolo Lo Meo, Antonio Palumbo Piccionello and Domenico Spinelli

J. Phys. Chem. A, 2019, 123, 10004
DOI: 10.1021/acs.jpca.9b08675

Effects of Nonionic Micelles on the Rate of Mononuclear Heterocyclic Rearrangement of (Z)-Phenylhydrazones of 5-Substituted 3-Benzoyl-1,2,4-oxadiazoles

Susanna Guernelli, Renato Noto, Carmelo Sbriziolo, Domenico Spinelli and Maria Liria Turco Liveri

Journal of Colloid and Interface Science, 2001, 239, 217
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