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Items: 1 to 20 of 22

1.

Directed ortho-metalation-nucleophilic acyl substitution strategies in deep eutectic solvents: the organolithium base dictates the chemoselectivity.

Ghinato S, Dilauro G, Perna FM, Capriati V, Blangetti M, Prandi C.

Chem Commun (Camb). 2019 Jul 11;55(54):7741-7744. doi: 10.1039/c9cc03927a. Epub 2019 Jun 6.

PMID:
31168546
2.

Reconfigurable and optically transparent microwave absorbers based on deep eutectic solvent-gated graphene.

Grande M, Bianco GV, Perna FM, Capriati V, Capezzuto P, Scalora M, Bruno G, D'Orazio A.

Sci Rep. 2019 Apr 2;9(1):5463. doi: 10.1038/s41598-019-41806-w.

3.

Water and Sodium Chloride: Essential Ingredients for Robust and Fast Pd-Catalysed Cross-Coupling Reactions between Organolithium Reagents and (Hetero)aryl Halides.

Dilauro G, Francesca Quivelli A, Vitale P, Capriati V, Perna FM.

Angew Chem Int Ed Engl. 2019 Feb 4;58(6):1799-1802. doi: 10.1002/anie.201812537. Epub 2019 Jan 17.

PMID:
30516878
4.

Designing Eco-Sustainable Dye-Sensitized Solar Cells by the Use of a Menthol-Based Hydrophobic Eutectic Solvent as an Effective Electrolyte Medium.

Boldrini CL, Manfredi N, Perna FM, Capriati V, Abbotto A.

Chemistry. 2018 Dec 3;24(67):17656-17659. doi: 10.1002/chem.201803668. Epub 2018 Oct 30.

PMID:
30230651
5.

Natural Scaffolds with Multi-Target Activity for the Potential Treatment of Alzheimer's Disease.

Piemontese L, Vitucci G, Catto M, Laghezza A, Perna FM, Rullo M, Loiodice F, Capriati V, Solfrizzo M.

Molecules. 2018 Aug 29;23(9). pii: E2182. doi: 10.3390/molecules23092182.

6.

Unprecedented Nucleophilic Additions of Highly Polar Organometallic Compounds to Imines and Nitriles Using Water as a Non-Innocent Reaction Medium.

Dilauro G, Dell'Aera M, Vitale P, Capriati V, Perna FM.

Angew Chem Int Ed Engl. 2017 Aug 14;56(34):10200-10203. doi: 10.1002/anie.201705412. Epub 2017 Jul 26.

PMID:
28695616
7.

Deep Eutectic Solvents as Novel and Effective Extraction Media for Quantitative Determination of Ochratoxin A in Wheat and Derived Products.

Piemontese L, Perna FM, Logrieco A, Capriati V, Solfrizzo M.

Molecules. 2017 Jan 12;22(1). pii: E121. doi: 10.3390/molecules22010121.

8.

Asymmetric chemoenzymatic synthesis of 1,3-diols and 2,4-disubstituted aryloxetanes by using whole cell biocatalysts.

Vitale P, Perna FM, Agrimi G, Scilimati A, Salomone A, Cardellicchio C, Capriati V.

Org Biomol Chem. 2016 Dec 28;14(48):11438-11445. Epub 2016 Nov 23.

PMID:
27878162
9.

An Expeditious and Greener Synthesis of 2-Aminoimidazoles in Deep Eutectic Solvents.

Capua M, Perrone S, Perna FM, Vitale P, Troisi L, Salomone A, Capriati V.

Molecules. 2016 Jul 16;21(7). pii: E924. doi: 10.3390/molecules21070924.

10.

Preparation of polysubstituted isochromanes by addition of ortho-lithiated aryloxiranes to enaminones.

Salomone A, Perna FM, Sassone FC, Falcicchio A, Bezenšek J, Svete J, Stanovnik B, Florio S, Capriati V.

J Org Chem. 2013 Nov 1;78(21):11059-65. doi: 10.1021/jo401689e. Epub 2013 Oct 24.

PMID:
24083540
11.

Gated access to α-lithiated phenyltetrahydrofuran: functionalisation via direct lithiation of the parent oxygen heterocycle.

Mansueto R, Mallardo V, Perna FM, Salomone A, Capriati V.

Chem Commun (Camb). 2013 Oct 3;49(86):10160-2. doi: 10.1039/c3cc45499a.

PMID:
24051990
12.

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.

Chem Commun (Camb). 2013 May 28;49(43):4911-3. doi: 10.1039/c3cc40988k.

PMID:
23478355
13.

Exploiting the lithiation-directing ability of oxetane for the regioselective preparation of functionalized 2-aryloxetane scaffolds under mild conditions.

Coppi DI, Salomone A, Perna FM, Capriati V.

Angew Chem Int Ed Engl. 2012 Jul 23;51(30):7532-6. doi: 10.1002/anie.201109113. Epub 2012 Jun 13. No abstract available.

PMID:
22696451
14.

2-Lithiated-2-phenyloxetane: a new attractive synthon for the preparation of oxetane derivatives.

Coppi DI, Salomone A, Perna FM, Capriati V.

Chem Commun (Camb). 2011 Sep 21;47(35):9918-20. doi: 10.1039/c1cc13670d. Epub 2011 Aug 4.

PMID:
21814695
15.

Solvent and TMEDA effects on the configurational stability of chiral lithiated aryloxiranes.

Perna FM, Salomone A, Dammacco M, Florio S, Capriati V.

Chemistry. 2011 Jul 11;17(29):8216-25. doi: 10.1002/chem.201100351. Epub 2011 May 25.

PMID:
21618297
16.

Lithiated fluorinated styrene oxides: configurational stability, synthetic applications, and mechanistic insight.

Capriati V, Florio S, Perna FM, Salomone A.

Chemistry. 2010 Aug 23;16(32):9778-88. doi: 10.1002/chem.201000897.

PMID:
20645346
17.

On the dichotomic reactivity of lithiated styrene oxide: a computational and multinuclear magnetic resonance investigation.

Capriati V, Florio S, Perna FM, Salomone A, Abbotto A, Amedjkouh M, Nilsson Lill SO.

Chemistry. 2009 Aug 10;15(32):7958-79. doi: 10.1002/chem.200900834.

PMID:
19623585
18.

Resolution of phthalans obtained by ortho-litiathion of aryloxiranes by enantioselective high-performance liquid chromatography: performances of various chiral stationary phases.

Caccamese S, Chillemi R, Perna FM, Florio S.

J Chromatogr A. 2009 Apr 10;1216(15):3048-53. doi: 10.1016/j.chroma.2009.01.052. Epub 2009 Jan 23.

PMID:
19200551
19.

2-Lithio-3,3-dimethyl-2-oxazolinyloxirane: carbanion or azaenolate? Structure, configurational stability, and stereodynamics in solution.

Capriati V, Florio S, Luisi R, Perna FM, Spina A.

J Org Chem. 2008 Dec 19;73(24):9552-64. doi: 10.1021/jo801646e.

PMID:
19006370
20.

Synthesis of 2,3-dihydro-10bh-oxazolo[2,3-a]isoquinolines from ortho-lithiated phenyloxazolinyloxiranes.

Capriati V, Florio S, Luisi R, Perna FM.

J Org Chem. 2007 Aug 3;72(16):6316-9. Epub 2007 Jul 4.

PMID:
17608536

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