Pubblicazioni

1. 2021 L. Cicco, J.A. Hernández-Fernández, A. Salomone, P. Vitale, M. Ramos-Martín, J. González-Sabín, A. Presa Soto, F.M. Perna, V. Capriati, J. García-Álvarez. Copper-catalyzed Goldberg-type C-N coupling in deep eutectic solvents (DESs) and water under aerobic conditions. Organic and Biomolecular Chemistry 2021, 19, 1773, doi: 10.1039/d0ob02501a.
2. 2021 L. Cicco, G. Dilauro, F.M. Perna, P. Vitale, V. Capriati. Advances in deep eutectic solvents and water: Applications in metal- And biocatalyzed processes, in the synthesis of APIs, and other biologically active compounds. Organic and Biomolecular Chemistry 2021, 19, 2558, doi: 10.1039/d0ob02491k.
3. 2021 G. Dilauro, C.S. Azzollini, P. Vitale, F.M. Perna, V. Capriati. Scalable Negishi Coupling between Organozinc Compounds and (Hetero)Aryl Bromides under Aerobic Conditions when using Bulk Water or Deep Eutectic Solvents with no Additional Ligands. Angewandte Chemie - International Edition doi: 10.1002/anie.202101571.
4. 2021 A.F. Quivelli. G. D’Addato, P. Vitale, J. García-Álvarez, F.M. Perna, V. Capriati. Expeditious and practical synthesis of tertiary alcohols from esters enabled by highly polarized organometallic compounds under aerobic conditions in Deep EutecticSolvents or bulk water. Tetrahedron 2020, 81, 131898, doi: 10.1016/j.tet.2020.131898.
5. 2020 L. Cicco, A. Fombona-Pascual, A. Sánchez-Condado, G.A. Carriedo, F.M. Perna, V. Capriati, A. Presa Soto, J. García-Álvarez, Fast and Chemoselective Addition of Highly Polarized Lithium Phosphides Generated in Deep Eutectic Solvents to Aldehydes and Epoxides. ChemSusChem 2020, 13, 4967, doi: 10.1002/cssc.202001449.
6. 2020 V. Pelliccioli, G. Dilauro, S. Grecchi, S. Arnaboldi, C. Graiff, F.M. Perna, P. Vitale, E. Licandro, A. Aliprandi, S. Cauteruccio, V. Capriati. Ligand‐Free Suzuki–Miyaura Cross‐Coupling Reactions in Deep Eutectic Solvents: Synthesis of Benzodithiophene Derivatives and Study of their Optical and Electrochemical Performance. European Journal of Organic Chemistry, 2020, 6981, doi: 10.1002/ejoc.202000889.
7. 2020 Perna F.M., Vitale P., Capriati, V. Deep eutectic solvents and their applications as green solvents. Current Opinion in Green and Sustinable Chemistry2020, 21, 27, DOI: 10.1016/j.cogsc.2019.09.004.
8. 2020 L. Cicco, A. Salomone, P. Vitale, N. Ríos-Lombardía, J. González-Sabín, J. García-Álvarez, F.M. Perna, V. Capriati. Addition of Highly Polarized Organometallic Compounds to N-tert-Butanesulfinyl Imines in Deep Eutectic Solvents under Air: Preparation of Chiral Amines of Pharmaceutical Interest. ChemSusChem 2020, 13, 3583, doi: 10.1002/cssc.202001142. “Cover Feature” Issue 14, ChemSusChem 2020, 13, 3541, doi: 10.1002/cssc.202001513.
9. 2020 P. Vitale, L. Cicco, I. Cellamare, F.M. Perna, A. Salomone, V. Capriati. Regiodivergent synthesis of functionalized pyrimidines and imidazoles through phenacyl azides in deep eutectic solvents. Beilstein Journal of Organic Chemistry 2020, 16, 1915, doi: 10.3762/bjoc.16.158.
10. 2020 M. Dell’Aera, F.M. Perna, P. Vitale, A. Altomare, A. Palmieri, L.C.H. Maddock, L.J. Bole, A.R. Kennedy, E. Hevia, V. Capriati, Boosting Conjugate Addition to Nitroolefins Using Lithium Tetraorganozincates: Synthetic Strategies and Structural Insights. Chemistry -A European Journal 2020, 26, 8742, doi: 10.1002/chem.202001294. “Cover Feature” Issue 40, Chemistry -A European Journal 2020, 26, 8666, doi: 10.1002/chem.202001521.
11. 2020 P. Vitale, F. Lavolpe, F. Valerio, M. Di Biase, F.M. Perna, E. Messina, G. Agrimi, I. Pisano, V. Capriati. Sustainable chemo-enzymatic preparation of enantiopure (R)-β-hydroxy-1,2,3-triazoles via lactic acid bacteria-mediated bioreduction of aromatic ketones and a heterogeneous "click" cycloaddition reaction in deep eutectic solvents. Reaction Chemistry and Engineering 2020, 5, 859, doi: 10.1039/d0re00067a.
12. 2020 F. Messa, G. Dilauro, F.M. Perna, P. Vitale, V. Capriati, A. Salomone. Sustainable Ligand-Free Heterogeneous Palladium-Catalyzed Sonogashira Cross-Coupling Reaction in Deep Eutectic Solvents, ChemCatChem 2020, 12, 1979, doi: 10.1002/cctc.201902380.
13. 2020 C.L. Boldrini, N. Manfredi, F.M. Perna, V. Capriati, A. Abbotto. Eco-Friendly Sugar-Based Natural Deep Eutectic Solvents as Effective Electrolyte Solutions for Dye-Sensitized Solar Cells. ChemElectroChem 2020, 7, 1707, doi: 10.1002/celc.202000376.
14. 2020 L. Piemontese, R. Sergio, F. Rinaldo, L. Brunetti, F.M. Perna, M. Amélia Santos, V. Capriati. Deep Eutectic Solvents as Effective Reaction Media for the Synthesis of 2‐Hydroxyphenylbenzimidazole-based Scaffolds en Route to Donepezil‐Like Compounds. Molecules 2020, 25, 574, doi: 10.3390/molecules25030574
15. 2019 Grande M., Bianco G.V., Perna F.M., Capriati V., Capezzuto P., Scalora M., Bruno G., D’Orazio A. Reconfigurable and optically transparent microwave absorbers based on deep eutectic solvent-gated graphene. Scientific Reports 2019, 9, 5463, DOI: 10.1038/s41598-019-41806-w.
16. 2019 Quivelli A.F. Vitale P., Perna F.M., Capriati V. Reshaping Ullmann Amine Synthesis in Deep Eutectic Solvents: A Mild Approach for Cu-Catalyzed C–N Coupling Reactions with No Additional Ligands. Frontiers in Chemistry 2019, 7, 723, DOI: 10.3389/fchem.2019.00723.
17. 2019 Lentini G., Cavalluzzi M.M., Degennaro L., Fracchiolla G., Perna F., Scilimati A. (S)-ethyl 2-(tert-butoxycarbonylamino)-3-(2-iodo-4,5-methylenedioxyphenyl)propanoate. Molbank, 2019, M1049, DOI: 10.3390/M1049.
18. 2019 Dilauro G., Quivelli A.F., Vitale P., Capriati V., Perna F.M. Water and Sodium Chloride: Essential Ingredients for Robust and Fast Pd-Catalysed Cross-Coupling Reactions between Organolithium Reagents and (Hetero)aryl Halides. Angewandte Chemie - International Edition 2019, 58, 1799, DOI: 10.1002/anie.201812537. (Angew. Chem. 2019, 131, 1813)
19. 2019 Vitale P., Cicco L., Messa F., Perna F.M., Salomone A., Capriati V. Streamlined Routes to Phenacyl Azides and 2,5-Diarylpyrazines Enabled by Deep Eutectic Solvents. European Journal of Organic Chemistry, 2019, 5557, DOI: 10.1002/ejoc.201900722.
20. 2019 Ghinato S., Dilauro G., Perna F.M., Capriati V., Blangetti M., Prandi C. Directed: Ortho-metalation-nucleophilic acyl substitution strategies in deep eutectic solvents: The organolithium base dictates the chemoselectivity. Chemical Communications 2019, 55, 7741, doi: 10.1039/c9cc03927a.
21. 2019 Perna F.M., Falcicchio A., Salomone A., Milet A., Rizzi R., Hamdoun G., Barozzino-Consiglio G., Stalke D., Oulyadi H., Capriati, V. First Direct Evidence of an ortho-Lithiated Aryloxetane: Solid and Solution Structure, and Dynamics. European Journal of Organic Chemistry, 2019, 5549, doi: 10.1002/ejoc.201900949.
22. 2018 Boldrini C.L., Manfredi N., Perna F.M., Capriati V., Abbotto A. Designing Eco-Sustainable Dye-Sensitized Solar Cells by the Use of a Menthol-Based Hydrophobic Eutectic Solvent as an Effective Electrolyte Medium. Chemistry - A European Journal 2018, 24, 17656, doi: 10.1002/chem.201803668.
23. 2018 Dilauro G., García S.M., Tagarelli D., Vitale P., Perna F.M., Capriati V. Ligand-Free Bioinspired Suzuki–Miyaura Coupling Reactions using Aryltrifluoroborates as Effective Partners in Deep Eutectic Solvents. ChemSusChem 2018, 11, 3495, DOI: 10.1002/cssc.201801382.
24. 2018 Savino S., Toscano A., Purgatorio R., Profilo E., Laghezza A., Tortorella P., Angelelli M., Cellamarea S., Scala R., Tricarico D., Thomas Marobbio C.M., Perna F., Vitale P., Agamennone M., Dimiccoli V., Tolomeo A., Scilimati A. Novel bisphosphonates with antiresorptive effect in bone mineralization and osteoclastogenesis. European Journal of Medicinal Chemistry 2018, 158, 184, doi: 10.1016/j.ejmech.2018.08.044.
25. 2018 Millia L., Dall'Asta V., Ferrara C., Berbenni V., Quartarone E., Perna F.M., Capriati V., Mustarelli P. Bio-inspired choline chloride-based deep eutectic solvents as electrolytes for lithium-ion batteries. Solid State Ionics 2018, 323, 44, DOI: 10.1016/j.ssi.2018.05.016.
26. 2018 Piemontese L., Vitucci G., Catto M., Laghezza A., Perna F.M., Rullo M., Loiodice F., Capriati V., Solfrizzo, M. Natural scaffolds with multi-target activity for the potential treatment of Alzheimer’s disease. Molecules 2018, 23, 2182, DOI: 10.3390/molecules23092182.
27. 2018 Vitale P., Perna F.M., Agrimi G., Pisano I., Mirizzi F., Capobianco R.V., Capriati V. Whole-cell biocatalyst for chemoenzymatic total synthesis of rivastigmine. Catalysts 2018, 8, 55, DOI: 10.3390/catal8020055.
28. 2018 Cicco L., Ríos-Lombardía N., Rodríguez-Álvarez M.J., Morís, F., Perna F.M., Capriati V., García-Álvarez J., González-Sabín J. Programming cascade reactions interfacing biocatalysis with transition-metal catalysis in: Deep Eutectic Solvents as biorenewable reaction media. Green Chemistry 20, 3468-3475, DOI: 10.1039/c8gc00861b.
29. 2017 Milano F., Giotta L., Guascito M.R., Agostiano A., Sblendorio S., Valli L., Perna F.M., Cicco L., Trotta M., Capriati V. Functional Enzymes in Nonaqueous Environment: The Case of Photosynthetic Reaction Centers in Deep Eutectic Solvents. ACS Sustainable Chemistry and Engineering 2017, 5, 7768, doi: 10.1021/acssuschemeng.7b01270.
30. 2017 Dilauro G., Dell'Aera M., Vitale P., Capriati V., Perna F.M. Unprecedented Nucleophilic Additions of Highly Polar Organometallic Compounds to Imines and Nitriles Using Water as a Non-Innocent Reaction Medium. Angewandte Chemie - International Edition 2017, 56, 10200, doi: 10.1002/anie.201705412. (Angew. Chem. 2017, 129, 10334). Highlighted in Synfacts doi: 10.1002/9783527667512.ch6
31. 2017 Cicco L., Rodríguez-Álvarez M.J., Perna F.M., García-Álvarez J., Capriati V. One-Pot Sustainable Synthesis of Tertiary Alcohols by Combining Ruthenium-Catalysed Isomerisation of Allylic Alcohols and Chemoselective Addition of Polar Organometallic Reagents in Deep Eutectic Solvents. Green Chemistry 2017, 19, 3069, doi: 10.1039/C7GC00458C.
32. 2017 Perna F.M., Vitale P., Summa S., Capriati V. 2-(tert-Butyl)-4-phenyloxetane. Molbank, vol 2017, M930, doi:10.3390/M930.
33. 2017 Dilauro G., Cicco L., Perna F.M., Vitale P., Capriati V. Solvent-catalyzed umpolung carbonsulfur bond-forming reactions by nucleophilic addition of thiolate and sulfinate ions to in situ-derived nitrosoalkenes in deep eutectic solvents. Comptes Rendus Chimie 2017, 20, 617, doi: 10.1016/j.crci.2017.01.008.
34. 2017 Vitale P., Abbinante V.M., Perna F.M., Salomone A., Cardellicchio C., Capriati V. Unveiling the Hidden Performance of Whole Cells in the Asymmetric Bioreduction of Aryl-containing Ketones in Aqueous Deep Eutectic Solvents. Advanced Synthesis and Catalysis 2017, 359, 1049, doi: 10.1002/adsc.201601064.
35. 2017 Piemontese L., Perna F.M., Logrieco A., Capriati V., Solfrizzo M. Deep eutectic solvents as novel and effective extraction media for quantitative determination of Ochratoxin A in wheat and derived products. Molecules 2017, 22, 121, doi: 10.3390/molecules22010121.
36. 2017 Vitale P., Digeo A., Perna F.M., Agrimi G., Salomone A., Scilimati A., Cardellicchio C., Capriati V. Stereoselective chemoenzymatic synthesis of optically active aryl-substituted oxygen-containing heterocycles. Catalysts 2017, 7, 37, 20734344, doi: 10.3390/catal7020037.
37. 2017 Abbotto A., Boldrini C. L., Manfredi N., Perna F.M., Capriati V., Trifiletti V. Dye-sensitized solar cells using an aqueous choline chloride-based deep eutectic solvent as an effective electrolyte solution. Energy Technology, 5, 345, doi: 10.1002/ente.201600420.
38. 2016 Vitale P., Capriati V., Florio S., Perna F.M., Salomone A. Conjugate Additions of Organolithiums to Electron-poor Olefins: A Simple and Useful Approach to the Synthesis of Complex Molecules. Current Organic Chemistry 2016, 21, 190, doi: 10.2174/1385272820666161021161644.
39. 2016 Vitale P., Perna F.M., Agrimi G., Scilimati A., Salomone A., Cardellicchio C., Capriati V. Asymmetric Chemoenzymatic Synthesis of 1,3-Diols and 2,4-Disubstituted Aryloxetanes by Using Whole Cell Biocatalysts. Organic and Biomolecular Chemistry, 14, 11438, doi: 10.1039/C6OB02320G.
40. 2016 Cicco L., Sblendorio S., Mansueto R., Perna F.M., Salomone A., Florio S., Capriati V. Water opens the door to organolithiums and Grignard reagents: exploring and comparing the reactivity of highly polar organometallic compounds in unconventional reaction media towards the synthesis of tetrahydrofurans. Chemical Science 2016, 7, 1192, doi: 10.1039/c5sc03436a. Highlighted in ChemInform doi: 10.1002/chin.201623120 and Synfacts, 2016, 12, 0081; doi: 10.1055/s-0035-1561029.
41. 2016 Cicco L., Addante V., Temperini A., Donau C. A., Karaghiosoff K., Perna F.M., Capriati V. Toward Customized Tetrahydropyran Derivatives through Regioselective α-Lithiation and Functionalization of 2-Phenyltetrahydropyran. European Journal of Organic Chemistry 2016, 3157, doi: 10.1002/ejoc.201600365. Front Cover: Issue 19, Eur. J. Org, 2016, 3130, doi: 10.1002/ejoc.201670191. Highlighted in ChemInform doi: 10.1002/chin.201646154 and Synfacts, 2016, 12, 0965, doi: 10.1055/s-0035-1561871
42. 2016 Mancuso R., Maner A., Cicco L., Perna F.M., Capriati V., Gabriele B. Synthesis of thiophenes in a deep eutectic solvent: heterocyclodehydration and iodocyclization of 1-mercapto-3-yn-2-ols in a choline chloride/glycerol medium. Tetrahedron 2016, 72, 4239, doi: 10.1016/j.tet.2016.05.062. Highlighted in ChemInform doi: 10.1002/chin.201643103.
43. 2016 Massolo E, Palmieri S, Benaglia M, Capriati V, Perna F.M. Stereoselective organocatalysed reactions in deep eutectic solvents: highly tunable and biorenewable reaction media for sustainable organic synthesis. Green Chemistry 2016, 18, 792, doi: 10.1039/C5GC01855B.
44. 2016 Perna F.M., Ricci M.A., Scilimati A., Mena M.C., Pisano I., Palmieri L., Agrimi G., Vitale P. Cheap and environmentally sustainable stereoselective arylketones reduction by Lactobacillus reuteri whole cells. Journal of Molecular catalysis B: Enzymatic 2016, 124, 29, doi: 10.1016/j.molcatb.2015.11.025.
45. 2016 Capua M., Perrone S., Perna F.M., Vitale P., Troisi L., Salomone A., Capriati V. An expeditious and greener synthesis of 2-aminoimidazoles in deep eutectic solvents. Molecules 2016, 21, 924, doi: 10.3390/molecules21070924.
46. 2015 Falcicchio A., Nilsson Lill S.O., Perna F.M., Salomone A., Coppi D.I., Cuocci C., Stalke D., Capriati V. Organotrifluoroborates as attractive self-assembling systems: the case of bifunctional dipotassium phenylene-1,4-bis(trifluoroborate). Dalton Transactions 2015, 44, p. 19447-19450, doi: 10.1039/c5dt02020d.
47. 2015 Sassone F.C., Perna F.M., Salomone A., Florio S., Capriati V. Unexpected lateral-lithiation-induced alkylative ring opening of tetrahydrofurans in deep eutectic solvents: Synthesis of functionalised primary alcohols. Chemical Communications 2015, 51, 9459, doi: 10.1039/c5cc02884a.
48. 2015 Rocchetti M.T., Abbotto A., Perna F.M., Salomone A., Florio S., Capriati V. Regio- and stereochemical aspects in the functionalisation of a lithiated 2-(3-chloro-2-methyl-1-propenyl)-2-oxazoline: electrophile and temperature effects. Tetrahedron 2015, 71, 7451, doi: 10.1016/j.tet.2015.06.034.
49. 2014, Salomone A., Perna F.M., Falcicchio A., Nilsson Lill S.O., Moliterni A., Florio S., Stalke D., Michel R.G., Capriati V. Direct Observation of a Lithiated Oxirane: A Synergistic Study Using Spectroscopic, Crystallographic, and Theoretical Methods on the Structure and Stereodynamics of Lithiated ortho-Trifluoromethyl Styrene Oxide. Chemical Science 2014, 5, 528, doi: 10.1039/C3SC52099D.
50. 2014 Mansueto R., Perna F.M., Salomone A., Perrone S., Florio S., Capriati V. Efficient Regioselective Synthesis of 3,4,5-Trisubstituted 1,2,4-Triazoles on the Basis of a Lithiation–Trapping Sequence. European Journal of Organic Chemistry 2014, 6653, doi: 10.1002/ejoc.201403016. Highlighted in ChemInform doi: 10.1002/chin.201514175.
51. 2014 V. Mallardo, R. Rizzi, F.C. Sassone, R. Mansueto, Perna F.M., A. Salomone, V. Capriati. Regioselective desymmetrization of diaryltetrahydrofurans via directed ortho-lithiation: an unexpected help from green chemistry. Chemical Communications 2014, 50, 8655, doi: 10.1039/c4cc03149k.
52. 2014 Capriati V., Perna F.M., Salomone A. “The Great Beauty” of organolithium chemistry: a land still worth exploring. Dalton Transactions 2014, 43, 14204, doi: 10.1039/c4dt01004c. Highlighted in ChemInform doi: 10.1002/chin.201448255.
53. 2013 Mansueto R., Perna F.M., Salomone A., Florio S., Capriati V. Dynamic resolution of lithiated ortho-trifluoromethyl styrene oxide and the effect of chiral diamines on the barrier to enantiomerisation. Chemical Communications 2013, 49, 4911, doi: 10.1039/c3cc40988k.
54. 2013 Mansueto R., Mallardo V., Perna F.M., Salomone A., Capriati V. Gated access to a-lithiated phenyltetrahydrofuran: functionalisation via direct lithiation of the parent oxygen heterocycle. Chemical Communications 2013, 49, 10160, doi: 10.1039/c3cc45499a. Highlighted in ChemInform doi: 10.1002/chin.201409112.
55. 2013 Vitale P., D'Introno C., Perna F.M., Perrone M.G., Scillimati A. Kluyveromyces marxianus CBS 6556 growing cells as a new biocatalyst in the asymmetric reduction of substituted acetophenones. Tetrahedron Asymmetry 2013, 24, 389, doi: 10.1016/j.tetasy.2013.02.001. Highlighted in ChemInform doi. 10.1002/chin.201335063.
56. 2013 Salomone A., Perna F.M., Sassone F.C., Falcicchio A., Bezenšek J., Svete J., Stanovnik B., Florio S., Capriati V. Preparation of Polysubstituted Isochromanes by Addition of ortho-Lithiated Aryloxiranes to Enaminones. Journal of Organic Chemistry 2013, 78, 11059, doi: 10.1021/jo401689e. Highlighted in ChemInform DOI: 10.1002/chin.201412137.
57. 2012 Coppi D.I., Salomone A., Perna F.M., Capriati V. Exploiting the Lithiation-Directing Ability of Oxetane for the Regioselective Preparation of Functionalized 2-Aryloxetane Scaffolds under Mild Conditions. Angewandte Chemie - International Edition 2012, 51, 7532, doi: 10.1002/anie.201109113 (Angew. Chem. 2012, 124, 7650). Highlighted in ChemInform doi: 10.1002/chin.201301092 and in Synfacts doi: 10.1055/s-0032-1317429
58. 2011 Coppi D.I., Salomone A., Perna F.M., Capriati V. 2-Lithiated-2-phenyloxetane: a new attractive synthon for the preparation of oxetane derivatives. Chemical Communications 2011, 47, 9918, doi: 10.1039/c1cc13670d. Highlighted in ChemInform doi: 10.1002/chin.201202100.
59. 2011 Vitale P., Perna F.M., Perrone M.G., Scilimati A. Screening on the use of Kluyveromyces marxianus CBS 6556 growing cells as enantioselective biocatalysts for ketone reductions. Tetrahedron Asymmetry2011, 22, 1985, doi: 10.1016/j.tetasy.2011.11.014.
60. 2011 Perna F.M., Salomone A, Dammacco M, Florio S, Capriati V. Solvent and TMEDA Effects on the Configurational Stability of Chiral Lithiated Aryloxiranes. Chemistry -A European Journal 2011, 17, 8216, doi: 10.1002/chem.201100351.
61. 2011 Salomone A., Petrera M., Coppi D.I., Perna F.M., Florio S., Capriati V. Synthesis of Conjugated Tri(hetero)aryl Derivatives Based on One-Pot Double Suzuki–Miyaura Couplings Using Bifunctional Dipotassium Phenylene-1,4- Bis(Trifluoroborate). SYNLETT 2011, 12, 1761, doi: 10.1055/s-0030-1260581. Highlighted in ChemInform doi: 10.1002/chin.201151072.
62. 2010 V. Capriati, S. Florio, F.M. Perna, A. Salomone. Lithiated Fluorinated Styrene Oxides: Configurational Stability, Synthetic Applications, and Mechanistic Insight. Chemistry -A European Journal 2010, 16, 9778, doi: 10.1002/chem.201000897. INSIDE COVER Issue 32 Chem. Eur. J. 2010, 16, 9778.
63. 2009 Capriati V., Florio S., Perna F.M., Salomone A., Abbotto A., Amedjkouh M., Nilsson Lill S.O. On the Dichotomic Reactivity of Lithiated Styrene Oxide: A Computational and Multinuclear Magnetic Resonance Investigation. Chemistry -A European Journal 2009, 15, 7958, doi: 10.1002/chem.200900834.
64. 2009 Caccamese S., Chillemi R., Perna F.M., Florio S. Resolution of phthalans obtained by ortho-litiathion of aryloxiranes by enantioselective high-performance liquid chromatography: Performances of various chiral stationary phases. Journal of Chromatography A 2009, 1216, 3048, doi: 10.1016/j.chroma.2009.01.052.
65. 2008 Capriati V., Florio S., Luisi R., Perna F.M., Spina A. 2-Lithio-3,3-dimethyl-2-oxazolinyloxirane: Carbanion or Azaenolate? Structure, Configurational Stability, and Stereodynamics in Solution. Journal of Organic Chemistry 2008, 73, 9552, doi: 10.1021/jo801646e.
66. 2007 Capriati V., Florio S., Luisi R., Perna F.M. Synthesis of 2,3-Dihydro-10bH-oxazolo[2,3-a]isoquinolines from ortho-Lithiated Phenyloxazilinyloxiranes. Journal of Organic Chemistry 2007, 72, 6316, doi: 10.1021/jo070708x. Highlighted in ChemInform doi: 10.1002/chin.200751180.
67. 2006 Capriati V., Florio S., Luisi R., Perna F.M., Salomone A. Synthesis of 1,3-Dihydrobenzo[c]furans from Ortho-Lithiated Aryloxiranes. Journal of Organic Chemistry 2006, 71, 3984, doi: 10.1021/jo052645t. Highlighted in ChemInform doi: 10.1002/chin.200640099
68. 2005 Capriati V., Florio S., Luisi R., Perna F.M., Salomone A., Gasparrini F. An Efficient Route to Tetrahydronaphthols via Addition of Ortho-Lithiated Stilbene Oxides to α,β-Unsaturated Fischer Carbene Complexes. Organic Letters 2005, 7, 4895, doi: 10.1021/ol0518176. Highlighted in ChemInform doi: 10.1002/chin.200608074.
69. 2005 Capriati V., Florio S., Luisi R., Perna F.M., Barluenga J. Asymmetric Synthesis of Cyclopropanes from Lithiated Aryloxiranes and α,β-Unsaturated Fischer Carbene Complexes. Journal of Organic Chemistry 2005, 70, 5852, doi: 10.1021/jo050443r. Highlighted in ChemInform doi: 0.1002/chin.200549073.
70. 2004 Florio S., Perna F.M., Luisi R., Barluenga J., Fananas F.J, Rodriguez F. Stereoselective Synthesis of Pentacarbonyl(3-oxa-2-bicyclo[3.1.0]hexylidene)- and Pentacarbonyl (cyclopropylmethoxymethylene)tungsten Compounds on the Route to Cyclopropane-γ-lactones and -carboxylates. Journal of Organic Chemistry 2004, 69, 9204, doi: 10.1021/jo048731v. Highlighted in ChemInform doi: 10.1002/chin.200521079.
71. 2004 Florio S., Perna F.M., Capriati V., Luisi R., Martina C.F. Barluenga J., Fananas F., Rodriguez F. Synthesis of alpha-Oxazolinylalkanamides. Tetrahedron Letters 2004, 45, 8027, doi: 10.1016/j.tetlet.2004.09.006. Highlighted in ChemInform doi: 10.1002/chin.200506125.
72. 2004 Florio S., Perna F.M., Luisi R., Barluenga J., Fananas F., Rodriguez F. Synthetic Approach To Substituted Cyclopropanes Based on the Coupling Reaction of Lithiated Chloroalkyloxazolines with Fischer Carbene Complexes. Journal of Organic Chemistry 2004, 69, 5480, doi: 10.1021/jo049613a. Highlighted in ChemInform doi: 10.1002/chin.200448065.
73. 2003 Perna F.M., Capriati V., Florio S., Luisi R. Isomerization of Oxazolinyl Allylic Alcohols: Synthesis of 3-Alkylidene-2-Iminooxetanes. Tetrahedron Letters 2003, 44, 3477, doi: 10.1016/S0040-4039(03)00669-5. Highlighted in ChemInform doi: 10.1002/chin.200330131.
74. 2002 Perna F.M., Capriati V., Florio S., Luisi R. An Unexpected Base-Promoted Isomerization of Oxazolinylaryl Oxiranes: Synthesis of Oxazolinylaryl Alkanones. Tetrahedron Letters 2002, 43, 7739, doi: 10.1016/S0040-4039(02)01837-3, 7739-7742. Highlighted in ChemInform doi: 10.1002/chin.200302101.
75. 2002 Perna F.M., Capriati V., Florio S., Luisi R. Synthesis of Allylic Alcohols from Oxazolinyloxiranes. Journal of Organic Chemistry 2002, 67, 8351, doi: 10.1021/jo026234d. Highlighted in ChemInform doi: 10.1002/chin.200318105.
76. 1999 C. Cardellicchio, G. Ciccarella, F. Naso, F. Perna, P. Tortorella. Use of Readily Available Chiral Compounds Related to the Betti Base in the Enantioselective Addition of Diethylzinc to Aryl Aldehydes. Tetrahedron 1999, 55, 14685, doi: 10.1016/S0040-4020(99)00914-X. Highlighted in ChemInform doi: 10.1002/chin.200010040.

Conference Paper

1. 2014 Florio S., Degennaro L., Mansueto R., Musio B., Perna F.M., Salomone A. Lithiated oxazolinyloxiranes and oxazolinylaziridines: key players in organic synthesis. Pure and Applied Chemistry 2014, 86, 913, doi: 10.1515/pac-2013-1103. Highlighted in ChemInform doi: 10.1002/chin.201540259.
2. 2011 V. Capriati, M. Dammacco, S. Florio, F.M. Perna, A. Salomone. On the Configurational Stabilty of α-Lithiated Sulfurated Styrene Oxides: Synthetic and Mechanistic Aspects. Phosphorus Sulfur and Silicon and the Related Elements 2011, 186, 1274, doi: 10.1080/10426507.2010.524180.
3. 2003 Perna F.M., Capriati V., Florio S., Luisi R. Synthesis and Reactivity of Oxazolinyl Allylic Alcohols. La Chimica e L’Industria, vol. 85, p. 9, ISSN: 0009-4315.

CONTRIBUTI IN VOLUME (Capitoli di Libro) 

1)      F.M. Perna, P. Vitale, V. Capriati. (2020) Organic Synthesis in DESs. Chapter 7, pages:111-134. In Deep Eutectic Solvents: Synthesis, Properties, and Applications. Book Editor(s): Diego J. Ramón, Gabriela Guillena. Wiley‐VCH Verlag GmbH & Co. KGaA. Doi: 10.1002/9783527818488.ch7.

2)      Perna F.M., Salomone A., Capriati V. (2015) Recent Developments in the Lithiation Reactions of Oxygen Heterocycles. In: Scriven E.F.V.;Ramsden C. A.. ADVANCES IN HETEROCYCLIC CHEMISTRY. vol. 118, p. 91-127, Academic Press Inc., doi: 10.1016/bs.aihch.2015.10.003

3)      F.M. Perna, A. Salomone, V. Capriati (2014) Oxygen-Bearing Lithium Compounds in Modern Synthesis in: Lithium Compounds in Organic Synthesis - From Fundamentals to Applications Edited by: Renzo Luisi and Vito Capriati. pp. 153-190, Wiley-VCH, ISBN:978-3-527-33343-1.

4)      Florio S., Perna F.M., Salomone A., Vitale P. (2014) Reduction of Epoxides in: Comprehensive Organic Synthesis, Second Edition, edited by: P. Knochel, Chapter 8, pp. 1086-1122. ISBN: 978-0080977423

5)      Florio S., Perna F.M., Salomone A., Vitale P. (2014) Oxygen-Stabilized Carbanions in: Comprehensive Organic Synthesis, Second Edition, edited by: P. Knochel, Chapter 1, pp. 471-515, ISBN: 978-0080977423

6)      F.M. Perna, A. Salomone, V. Capriati (2012) Critical Surveys Covering the Year 2011: Organometallic Compounds in Organic Synthesis In: Seminars in Organic Synthesis - XXXVII "A. Corbella" Summer School Edited by: Enrico Marcatoni, Gabriele Renzi. pp. 304-330 Società Chimica Italiana, ISBN:978-88-86208-71-0. Highlighted in ChemInform doi: 10.1002/chin.201342257.

7)      Perna F.M., Degennaro L., Florio S. (2012) Syntheses Mediated by alpha-lithiated Epoxides and Aziridines. In: SCIENCE OF SYNTHESIS. knowledge Updates 2012/1. vol. 2012/1, p. 115-214. Edited by Molander G A, STUTTGAR T:Georg Thieme Verlag, ISBN: 978-3-13-167181-3.

8)      S. Florio, V. Capriati, L. Degennaro, R. Luisi, Perna F.M. (2003). Novel Oxazoline-Mediated Synthesis of Heterocycles. In: V.G. KARTSEV. Oxygen-and Sulfur-Containing Heterocycles, The Chemistry and Biological Activity of Synthetic and Natural Compounds. vol. 1, p. 66-71, MOSCOW:IBI PRESS, ISBN: 5-902545-03-X