Pubblicazioni su Riviste Scientifiche Internazionali Peer Reviewed
- “Oxiranyllithium based synthesis of α-keto-2-oxazolines”, V. Capriati; S. Florio, R. Luisi, V. Russo, A. Salomone, Tetrahedron Letters 2000, 41, 8835. Highlighted in ChemInform DOI: 10.1002/chin.200109123
- “A stereospecific synthesis of oxazolinyloxiranes”, A. Abbotto, V. Capriati, L. Degennaro, S. Florio, R. Luisi, M. Pierrot, A. Salomone, Journal of Organic Chemistry 2001, 66, 3049. Highlighted in ChemInform DOI: 10.1002/chin.200137132
- “Oxiranyl anion-mediated synthesis of highly enantiomerically enriched styrene oxide derivatives”, V. Capriati, S. Florio, R. Luisi, A. Salomone, Organic Letters 2002, 4, 2445. Highlighted in ChemInform DOI: 10.1002/chin.200249102.
- “Lithiation and reactions of stilbene oxides: synthetic utility”, S. Florio, V. Aggarwal, A. Salomone, Organic Letters 2004, 6, 4191. Highlighted in ChemInform DOI: 10.1002/chin.200509091
- “An Efficient Route to Tetrahydronaphthols via Addition of ortho-Lithiated Stilbene Oxides to α,β-Unsaturated Fischer Carbene Complexes” V. Capriati, S. Florio, R. Luisi, F.M. Perna, A. Salomone, F. Gasparrini, Organic Letters 2005, 7,4895. Highlighted in ChemInform DOI: 10.1002/chin.200608074
- “Synthesis of 1,3-Dihydrobenzo[c]furans from Ortho-Lithiated Aryloxiranes” V. Capriati, S. Florio, R. Luisi, F.M. Perna, A. Salomone, Journal of Organic Chemistry 2006, 71, 3984. Highlighted in ChemInform DOI: 10.1002/chin.200640099
- “Stereoselective Synthesis of Novel β,γ-Epoxyhydroxylamines and 4-Hydroxyalkyl-1,2-oxazetidines” V. Capriati, S. Florio, R. Luisi, A. Salomone, C.Cuocci, Organic Letters 2006, 8, 3923. Highlighted in ChemInform DOI: 10.1002/chin.200702098 and Highlighted in Synfacts DOI: 10.1055/s-2006-949429
- “Crystal Structure of (N-tert-butyl-3,4-diphenyl-1,2-oxazetidin-4-yl)methanol, C19H23NO2” V. Capriati, S. Florio, R. Luisi, A. Salomone, C. Cuocci Zeitschrift fur Kristallographie-New Crystal 2006, 221, 398.
- “Michael Addition of Ortho-Lithiated Aryloxiranes to α,β-Unsaturated Malonates: Synthesis of Tetrahydroindenofuranones” A. Salomone, V. Capriati, S. Florio, R. Luisi Organic Letters 2008, 10, 1947. Highlighted in ChemInform DOI: 10.1002/chin.200841105
- “Influence of an ortho-sulfinyl group on the configurational stability of α-lithiated aryloxiranes: deuteration of tolylsulfinyl styrene oxides” V. Capriati, S. Florio, R. Luisi , A. Salomone, M. G. Tocco, M. Castro, J. L. Garcia Ruano, E. Torrente Tetrahedron 2009, 65, 383.
- “On the Dichotomic Reactivity of Lithiated Styrene Oxide: A Computational and Multinuclear Magnetic Resonance Investigation” V. Capriati, S. Florio, F. M. Perna, A. Salomone, A. Abbotto, M. Amedjkouh, S. O. Nilsson Lill Chemistry: A European Journal 2009, 15, 7958
- “Lithiated Fluorinated Styrene Oxides: Configurational Stability, Synthetic Applications, and Mechanistic Insight” V. Capriati, S. Florio, F. M. Perna, A. Salomone Chemistry: A European Journal 2010, 16, 9778 – 9788.
- “Azodioxy-carbonyl compounds by oxidation of cyclic imines with m-CPBA” S. Perrone, T.Pilati, F. Rosato, A. Salomone, V. Videtta, L. Troisi. Tetrahedron 2011, 67, 2090. Highlighted in ChemInform DOI: 10.1002/chin.201125063
- “Solvent and TMEDA Effects on the Configurational Stability of Chiral Lithiated Aryloxiranes” F. M. Perna, A. Salomone, M. Dammacco, S. Florio, V. Capriati Chemistry: A European Journal 2011, 17, 8216 – 8225.
- “On the Configurational Stability of α-Lithiated Sulfurated Styrene Oxides: Synthetic and Mechanistic Aspects.” V. Capriati, M. Dammacco, S. Florio, F. M. Perna, A. Salomone Phosphorus, Sulfur, and Silicon and the Related Elements, 2011, 186, 1274 - 1277.
- “Synthesis of Conjugated Tri(hetero)aryl Derivatives Based on One-Pot Double Suzuki-Miyaura Couplings Using Bifunctional Dipotassium Phenylene-1,4-Bis(Trifluoroborate)” A. Salomone, M. Petrera, D.I. Coppi, F.M. Perna, S. Florio, V. Capriati Synlett 2011, 12, 1761-1765 Highlighted in ChemInform DOI: 10.1002/chin.201151072
- “2-Lithiated 2-Phenyloxetane: A New Attractive Synthon for the Preparation of Oxetane Derivatives.” I. Coppi, A. Salomone, F.M. Perna, V. Capriati Chemical Communications 2011, 47, 9918–9920. Highlighted in ChemInform DOI: 10.1002/chin.201202100
- “One-Pot Ester Synthesis from Allyl and Benzyl Halides and Alcohols by Palladium-Catalyzed Carbonylation” S. Tommasi, S. Perrone, F. Rosato, A. Salomone, L. Troisi. Synthesis 2012, 3, 423-430. Highlighted in ChemInform DOI: 10.1002/chin.201219043
- “Exploiting the Lithiation-directing Ability of Oxetane for the Regioselective Preparation of Functionalized 2-Aryloxetane Scaffolds under Mild Conditions” D. Coppi, A. Salomone, F. M. Perna, Capriati, Chemie Int. Ed. 2012, 51, 7532-7536 Highlighted in ChemInform DOI: 10.1002/chin.201301092 and Highlighted in SYNFACTS DOI: 10.1055/s-0032-1317429
- “Dynamic resolution of lithiated ortho-trifluoromethyl styrene oxide and the effect of chiral diamines on the barrier to enantiomerisation” Mansueto R, Perna FM, Salomone A, Florio S, Capriati V. Chemical Communications 2013, 49, 4911.
- “Synthesis and reactivity of trifluoromethyl substituted oxaziridines” Perrone S, Rosato F, Salomone A., Troisi L. Tetrahedron 2013, 69, 3878-3884. Highlighted in ChemInform DOI: 10.1002/chin.201341094
- “Gated Access to α-Lithiated Phenyltetrahydrofuran: Functionalisation via Direct Lithiation of the Parent Oxygen Heterocycle” Mansueto R, Mallardo V.; Perna F.M., Salomone A, Capriati V. Chemical Communications 2013, 49, 10160. Highlighted in ChemInform DOI: 10.1002/chin.201409112
- “Preparation of Polysubstituted Isochromanes by Addition of ortho-Lithiated Aryloxiranes to Enaminones” Salomone A, Perna FM, Sassone F., Falcicchio A., BezenŠek J., Stanovnik B., Svete J., Florio S., Capriati V. Journal of Organic Chemistry 2013, 78, 11059-11065 Highlighted in ChemInform DOI: 10.1002/chin.201412137
- “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” Salomone A, Perna M.F., Falcicchio A., S. O. Nilsson Lill, Moliterni A., Reent M., Florio S., Stalke D., Capriati V. Chemical Science 2014, 5, 528-538.
- "Ring opening of heterocycles containing a C-N double bond: A simple synthesis of imides promoted by acyl palladium species" Perrone, S., Cannazza, G., Caroli, A., Salomone, A., Troisi, L. Tetrahedron 2014, 70, 6938-6943. Highlighted in ChemInform DOI: 10.1002/chin.201508081
- "Lithiated oxazolinyloxiranes and oxazolinylaziridines: Key players in organic synthesis" Florio, S., Degennaro, L., Mansueto, R., Musio, B., Perna, F.M., Salomone, A. (2014) Pure and Applied Chemistry, 2014, 86, 913-924.
- "Regioselective desymmetrization of diaryltetrahydrofurans via directed ortho-lithiation: An unexpected help from green chemistry" Mallardo, V., Rizzi, R., Sassone, F.C., Mansueto, R., Perna, F.M., Salomone, A., Capriati, V. Chemical Communications, 2014, 50, 8655-8658.
- "Stereoselective synthesis of α-alkylidene β-oxo amides by palladium-catalyzed carbonylation" Perrone, S., Salomone, A., Caroli, A., Falcicchio, A., Citti, C., Cannazza, G., Troisi, L. European Journal of Organic Chemistry, 2014, 27, 5932-5938. Highlighted in ChemInform DOI: 10.1002/chin.201512119
- "The Great Beauty of organolithium chemistry: A land still worth exploring" Capriati, V., Perna, F.M., Salomone, A. Dalton Transactions, 2014, 43, 14204-14210. Highlighted in ChemInform DOI: 10.1002/chin.201448255
- "Efficient regioselective synthesis of 3,4,5-trisubstituted 1,2,4-triazoles on the basis of a lithiation-trapping sequence" Mansueto, R., Perna, F.M., Salomone, A., Perrone, S., Florio, S., Capriati, V. European Journal of Organic Chemistry, 2014, 30, 6653-6657. Highlighted in ChemInform DOI: 10.1002/chin.201514175
- "3-Aryl-5-vinyl-2-isoxazolines and 3-aryl-5-vinylisoxazoles from aryl nitrile oxides and methyl vinyl ketone lithium enolate: reaction limits and synthetic utility exploitation " Salomone, A.; Scilimati, A.; Vitale, P. Synthesis 2015, 47, 807−
- "A direct synthesis of 3-acyl-4-hydroxy-2-pyranone derivatives via palladium-catalyzed carbonylation of α-chloroketones. A cascade reaction involving acylketenes" S. Perrone, A. Caroli, G. Cannazza, C. Granito, A. Salomone, L. Troisi Tetrahedron Letters 2015, 56, 2773-2776
- "Multicomponent Synthesis of Uracil Analogues Promoted by Pd-Catalyzed Carbonylation of α-Chloroketones in the Presence of Isocyanates and Amines" S. Perrone, M. Capua, A. Salomone, L. Troisi Journal of Organic Chemistry 2015, 80, 8189-8197.
- "Regio-and stereochemical aspects in the functionalisation of a lithiated 2-(3-chloro-2-methyl-1-propenyl)-2-oxazoline: electrophile and temperature effects" M.T. Rocchetti, A. Abbotto, F.M. Perna, A. Salomone, S. Florio, V. Capriati Tetrahedron 2015, 71, 7451-7458
- "Organotrifluoroborates as attractive self-assembling systems: the case of bifunctional dipotassium phenylene-1,4-bis(trifluoroborate)" A. Falcicchio, S.O. Nilsson Lill, F. M. Perna, A. Salomone, D. I. Coppi, C Cuocci, Dalton Transactions 2015, 44, 19447-19450
- "Unexpected lateral-lithiation-induced alkylative ring opening of tetrahydrofurans in deep eutectic solvents: synthesis of functionalised primary alcohols" F.C. Sassone, F.M. Perna, A. Salomone, S. Florio, V. Capriati Chemical Communications 2015, 51, 9459-9462.
- “Heterocycle-Mediated ortho -Functionalization of Aromatic Compounds: The DoM Methodology and Synthetic Utility”, Florio, S., Salomone, A., (2016) Synthesis (Germany), 48 (13), art. no. ss-2016-z0112-sr, pp. 1993-2008. DOI: 10.1055/s-0035-1561596
- “An expeditious and greener synthesis of 2-aminoimidazoles in deep eutectic solvents”, Capua, M., Perrone, S., Perna, F.M., Vitale, P., Troisi, L., Salomone, A., Capriati, V., (2016) Molecules, 21 (7), art. no. 924, . DOI: 10.3390/molecules21070924
- “Synthesis of β-enamino acid and heteroaryl acetic acid derivatives by Pd-catalyzed carbonylation of α-chloroimines and 2-chloromethyl aza-heterocycles”, Perrone, S., Capua, M., Cannazza, G., Salomone, A., Troisi, L., (2016) Tetrahedron Letters, 57 (13), pp. 1421-1424. DOI: 10.1016/j.tetlet.2016.02.035
- “Enhanced solubility and antibacterial activity of lipophilic fluoro-substituted N-benzoyl-2-aminobenzothiazoles by complexation with β-cyclodextrins”, Trapani, A., De Laurentis, N., Armenise, D., Carrieri, A., Defrenza, I., Rosato, A., Mandracchia, D., Tripodo, G., Salomone, A., Capriati, V., Franchini, C., Corbo, F., (2016) International Journal of Pharmaceutics, 497 (1-2), pp. 18-22. DOI: 10.1016/j.ijpharm.2015.11.024
- “Recent Developments in the Lithiation Reactions of Oxygen Heterocycles”, Perna, F.M., Salomone, A., Capriati, V., (2016) Advances in Heterocyclic Chemistry, 118, pp. 91-127. DOI: 10.1016/bs.aihch.2015.10.003
- “Conjugate additions of organolithiums to electron-poor olefins: A simple and useful approach to the synthesis of complex molecules”, Vitale, P., Capriati, V., Florio, S., Perna, F.M., Salomone, A., (2016) Current Organic Chemistry, 21 (3), pp. 190-217. DOI: 10.2174/1385272820666161021161644
- “Palladium-catalyzed carbonylative coupling of α-chloroketones with hydrazines: a simple route to pyrazolone derivatives”, Capua, M., Granito, C., Perrone, S., Salomone, A., Troisi, L., (2016) Tetrahedron Letters, 57 (30), pp. 3363-3367. DOI: 10.1016/j.tetlet.2016.06.072
- “Asymmetric chemoenzymatic synthesis of 1,3-diols and 2,4-disubstituted aryloxetanes by using whole cell biocatalysts”, Vitale, P., Perna, F.M., Agrimi, G., Scilimati, A., Salomone, A., Cardellicchio, C., Capriati, V., (2016) Organic and Biomolecular Chemistry, 14 (48), pp. 11438-11445. DOI: 10.1039/c6ob02320g
- “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”, Cicco, L., Sblendorio, S., Mansueto, R., Perna, F.M., Salomone, A., Florio, S., Capriati, V., (2016) Chemical Science, 7 (2), pp. 1192-1199. DOI: 10.1039/c5sc03436a
- “A Direct Synthesis of Isocytosine Analogues by Carbonylative Coupling of α-Chloro Ketones and Guanidines”, Capua, M., Perrone, S., Bona, F., Salomone, A., Troisi, L. (2017) European Journal of Organic Chemistry, 2017 (13), pp. 1780-1787. DOI: 10.1002/ejoc.201601654
- “Stereoselective chemoenzymatic synthesis of optically active aryl-substituted oxygen-containing heterocycles”, Vitale, P., Digeo, A., Perna, F.M., Agrimi, G., Salomone, A., Scilimati, A., Cardellicchio, C., Capriati, V., (2017) Catalysts, 7 (2), art. no. 37, . DOI: 10.3390/catal7020037
- “Green synthesis of 2-pyrazinones in deep eutectic solvents: From α-chloro oximes to peptidomimetic scaffolds”, Perrone, S., Capua, M., Messa, F., Salomone, A., Troisi, L., (2017) Tetrahedron, 73 (43), pp. 6193-6198. DOI: 10.1016/j.tet.2017.09.013
- “Unveiling the Hidden Performance of Whole Cells in the Asymmetric Bioreduction of Aryl-containing Ketones in Aqueous Deep Eutectic Solvents”, Vitale, P., Abbinante, V.M., Perna, F.M., Salomone, A., Cardellicchio, C., Capriati, V., (2017) Advanced Synthesis and Catalysis, 359 (6), pp. 1049-1057. DOI: 10.1002/adsc.201601064
- “Towards a sustainable synthesis of amides: chemoselective palladium-catalysed aminocarbonylation of aryl iodides in deep eutectic solvents”, Messa, F., Perrone, S., Capua, M., Tolomeo, F., Troisi, L., Capriati, V., Salomone, A. (2018) Chemical Communications, 2018, vol. 54, no. 58, pp. 8100-8103. DOI: 10.1039/c8cc03858a
- “First Direct Evidence of an ortho-Lithiated Aryloxetane: Solid and Solution Structure, and Dynamics.” Perna, F. M., Falcicchio, A., Salomone, A., Milet, A., Rizzi, R., Hamdoun, G., Capriati, V. (2019). European Journal of Organic Chemistry, 2019 (31–32), 5549–5556. doi: 10.1002/ejoc.201900949
- “Streamlined Routes to Phenacyl Azides and 2,5-Diarylpyrazines Enabled by Deep Eutectic Solvents” Vitale, P., Cicco, L., Messa, F., Perna, F. M., Salomone, A., Capriati, V. (2019). European Journal of Organic Chemistry, 2019 (31–32), 5557–5562. DOI: 10.1002/ejoc.201900722.
- “Heterocycle Synthesis through Pd-Catalyzed Carbonylative Coupling” Perrone, S., Troisi, L., Salomone, A. (2019). European Journal of Organic Chemistry, 2019(29), 4626–4643. https://doi.org/10.1002/ejoc.201900439
- “Bio-based benzoxazines synthesized in a deep eutectic solvent: A greener approach toward vesicular nanosystems” Behalo, M.S., Bloise, E., Mele, G., Salomone, A., Messa, F., Carbone, L., Mazzetto, S.E., Lomonaco, D. (2020) Journal of Heterocyclic Chemistry, 2020, 57, 768- DOI: 10.1002/jhet.3818
- “Sustainable Ligand-Free Heterogeneous Palladium-Catalyzed Sonogashira Cross-Coupling Reaction in Deep Eutectic Solvents” (2020) Messa, F., Dilauro, G., Perna, F.M., Vitale, P., Capriati, V., Salomone, A. ChemCatChem 2020, 12, 1979. DOI: 10.1002/cctc.201902380
- “Regiodivergent synthesis of functionalized pyrimidines and imidazoles through phenacyl azides in deep eutectic solvents” (2020) Beilstein Journal of Organic Chemistry, 16, pp. 1915 – 1923, Vitale P., Cicco L., Cellamare I., Perna F.M., Salomone A., Capriati V. https://doi.org/10.3762/bjoc.16.158
- “Strategies for Reuse of Skins Separated From Grape Pomace as Ingredient of Functional Beverages”, (2020) Frontiers in Bioengineering and Biotechnology, 8, art. no. 645, Gerardi C., D'amico L., Migoni D., Santino A., Salomone A., Carluccio M.A., Giovinazzo G., DOI: 10.3389/fbioe.2020.00645
- "Addition of Highly Polarized Organometallic Compounds to N-tert-Butanesulfinyl Imines in Deep Eutectic Solvents under Air: Preparation of Chiral Amines of Pharmaceutical Interest", (2020) ChemSusChem, 13 (14), pp. 3583 - 3588, Cicco L., Salomone A., Vitale P., Ríos-Lombardía N., González-Sabín J., García-Álvarez J., Perna F.M., Capriati V., DOI: 10.1002/cssc.202001142
- "Cobalt-catalyzed cross-coupling reactions of aryl- And alkylaluminum derivatives with (hetero)aryl and alkyl bromides", (2021) Chemical Communications, 57 (81), pp. 10564 - 10567, Dilauro G., Messa F., Bona F., Perrone S., Salomone A., DOI: 10.1039/d1cc04002b
- "Copper-catalyzed Goldberg-type C-N coupling in deep eutectic solvents (DESs) and water under aerobic conditions", (2021) Organic and Biomolecular Chemistry, 19 (8), pp. 1773 - 1779, Cicco L., Hernández-Fernández J.A., Salomone A., Vitale P., Ramos-Martín M., González-Sabín J., Presa Soto A., Perna F.M., Capriati V., García-Álvarez J., DOI: 10.1039/d0ob02501a
- "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", (2021) Angewandte Chemie - International Edition, 60 (19), pp. 10632 - 10636, Dilauro G., Azzollini C.S., Vitale P., Salomone A., Perna F.M., Capriati V., DOI: 10.1002/anie.202101571
- "Deep eutectic solvents meet safe, scalable and sustainable hydrogenations enabled by aluminum powder and Pd/C", (2022) Green Chemistry, 24 (11), pp. 4388 - 4394, Messa F., Dilauro G., Paparella A.N., Silvestri L., Furlotti G., Iacoangeli T., Perrone S., Salomone A., DOI: 10.1039/d2gc00636g
- "A Glycerol-Based Deep Eutectic Solvent as Natural Medium and Organic Reductant for Homocoupling of (Hetero)Aryl Chlorides: a Green Route to 2,2’-Bipyridine and Biaryl Scaffolds", (2022) ChemistrySelect, 7 (37), art. no. e202203438, Paparella A.N., Messa F., Dilauro G., Troisi L., Perrone S., Salomone A., DOI: 10.1002/slct.202203438
- "1,3-Dipolar Cycloaddition of Alkanone Enolates with Azides in Deep Eutectic Solvents for the Metal-Free Regioselective Synthesis of Densely Functionalized 1,2,3-Triazoles", (2022) European Journal of Organic Chemistry, 2022 (36), art. no. e202200843, Cicco L., Perna F.M., Falcicchio A., Altomare A., Messa F., Salomone A., Capriati V., Vitale P., DOI: 10.1002/ejoc.202200843
- "Highly chemoselective conjugate addition of lithium tetraorganozincates to coumarin derivatives and functionalization with electrophiles", (2023) Arkivoc, 2023 (3), pp. 50 - 61, Dell’Aera M., Perna F.M., Vitale P., Salomone A., Altomare A., Capriati V., DOI: 10.24820/ark.5550190.p011.877
- “3-Cyclohexyl-6-phenyl-1-(p-tolyl)pyrimidine-2,4(1H,3H)-dione”, (2023) MolBank, 2023 (2), art. no. M1611, Messa F., Perrone S., Salomone A., DOI: 10.3390/M1611
- "5-(4-Chlorophenyl)-N,1-di-o-tolyl-1H-imidazole-2-amine", (2023) MolBank, 2023 (2), art. no. M1648, Messa F., Papadia P., Perrone S., Salomone A., DOI: 10.3390/M1648
- "Gas-free alkoxycarbonylation of aryl iodides in a phosphonium-based deep eutectic solvent with Mo(CO)6 as a solid CO source", (2023) Organic and Biomolecular Chemistry, 21 (25), pp. 5164 - 5170, Messa F., Paparella A.N., Perrone S., Salomone A., DOI: 10.1039/d3ob00596h
- "Gas-Free Amino- and Alkoxycarbonylation of Aryl Iodides in a Bioinspired Deep Eutectic Solvent with Mo(CO)6 as a Safe CO Source", (2023) European Journal of Organic Chemistry, 26 (24), art. no. e202300309, Messa F., Paparella A.N., Veselý D., Krajčovič J., Papadia P., Perrone S., Salomone A., DOI: 10.1002/ejoc.202300309
- "A phosphonium-based deep eutectic solvent promotes the stereoselective semi-reduction of internal alkynes to (Z)-alkenes", (2023) Organic and Biomolecular Chemistry, 21 (18), pp. 3770 - 3777, Paparella A.N., Messa F., Perrone S., Salomone A., DOI: 10.1039/d3ob00433c
- "Towards Green Reductions in Bio-Derived Solvents", (2023) European Journal of Organic Chemistry, 26 (14), art. no. e202201494, Perrone S., Messa F., Salomone A., DOI: 10.1002/ejoc.202201494
- "The Sorption of Amoxicillin on Engineered Polyethylene Terephthalate Microplastics", (2023) Journal of Polymers and the Environment, 31 (4), pp. 1383 - 1397, Lionetto F., Esposito Corcione C., Messa F., Perrone S., Salomone A., Maffezzoli A., DOI: 10.1007/s10924-022-02690-0
- "N-, O- and S-Heterocycles Synthesis in Deep Eutectic Solvents", (2023) Molecules, 28 (8), art. no. 3459, Perrone S., Messa F., Troisi L., Salomone A., DOI: 10.3390/molecules28083459
- "Use of Deep Eutectic Solvents in Plastic Depolymerization", (2023) Catalysts, 13 (7), art. no. 1035, Paparella A.N., Perrone S., Salomone A., Messa F., Cicco L., Capriati V., Perna F.M., Vitale P., DOI: 10.3390/catal13071035
- "Use of Deep Eutectic Solvents in Plastic Depolymerization", (2023) Catalysts, 13 (7), art. no. 1035, Paparella A.N., Perrone S., Salomone A., Messa F., Cicco L., Capriati V., Perna F.M., Vitale P., DOI: 10.3390/catal13071035
- "Sustainable Extraction of Hydroxytyrosol from Olive Leaves Based on a Nature-Inspired Deep Eutectic Solvent (NADES)", (2024) ChemistrySelect, 9 (37), art. no. e202403476, Messa F., Giotta L., Troisi L., Perrone S., Salomone A., DOI: 10.1002/slct.202403476
- “Binary mixtures of menthol and alkanoic acids as green solvents for efficient astaxanthin recovery from Aristaeomorpha foliacea shrimp shells“ Mancarella F., Milano F., Semeraro P., Leo V.D., Messa F., Perrone S., Salomone A., Durante M., Lenucci M.S., Benedictis M.D., Santino A., Giotta L., Valli L., (2025) Separation and Purification Technology, 371, art. no. 133261, DOI: 10.1016/j.seppur.2025.133261
- “Reactive Behaviour of Platinum(II) Salts with Ethylenediamine in Sustainable Water/Choline Chloride-Based Deep Eutectic Solvents Mixtures”, Garofalo N., Messa F., Barbanente A., Fanizzi F.P., Salomone A., Margiotta N., Papadia P. (2025) Molecules, 30 (9), art. no. 1890, DOI: 10.3390/molecules30091890
- “Synthesis and characterization of succinylated pectin hydrogels with enhanced swelling performances”, Liotino S., Cometa S., Todisco S., Mastrorilli P., Bengoechea C., Salomone A., De Giglio E., (2025) Reactive and Functional Polymers, 214, art. no. 106331, DOI: 10.1016/j.reactfunctpolym.2025.106331
- “Sustainable Synthesis of α-Glucosidase Inhibitors by Gas-Free Pd-Carbonylation of Nature-Based Hydroxytyrosol”, Messa F., Armenise D., Liturri A., Perrone M.G., Perrone S., Salomone A. (2025) Catalysts, 15 (3), art. no. 202, DOI: 10.3390/catal15030202
- “Bombyx Mori Silk Fibroin as a Sustainable Organocatalyst for Diastereoselective Michael Additions”, Ricciardelli C., Rizzo G., Cotugno P., Salomone A., Trisciuzzi D., Nicolotti O., Colaprico E., Altomare C.D., Farinola G.M., (2025) ChemSusChem, 18 (16), art. no. e202500584, DOI: 10.1002/cssc.202500584
- “Sustainable Synthesis of α-Glucosidase Inhibitors by Gas-Free Pd-Carbonylation of Nature-Based Hydroxytyrosol”, Messa F., Armenise D., Liturri A., Perrone M.G., Perrone S., Salomone A. (2025) Catalysts, 15 (3), art. no. 202, DOI: 10.3390/catal15030202