Search Results - "Cermola, F"

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    A novel autoregulatory loop between the Gcn2-Atf4 pathway and L-Proline metabolism controls stem cell identity by D'Aniello, C, Fico, A, Casalino, L, Guardiola, O, Di Napoli, G, Cermola, F, De Cesare, D, Tatè, R, Cobellis, G, Patriarca, E J, Minchiotti, G

    Published in Cell death and differentiation (01-07-2015)
    “…Increasing evidence indicates that metabolism is implicated in the control of stem cell identity. Here, we demonstrate that embryonic stem cell (ESC) behaviour…”
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    Journal Article
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    Substituent and Solvent Effects on the Photosensitized Oxygenation of 5,6-Dihydro-1,4-oxathiins. Intramolecular Oxygen Transfer vs Normal Cleavage of the Dioxetane Intermediates by Cermola, F, Iesce, M. R

    Published in Journal of organic chemistry (12-07-2002)
    “…The reaction of singlet oxygen with variously substituted oxathiins 1 affords dicarbonyl compounds 4 and/or ketosulfoxides 7 and 8 depending on the nature of…”
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    Erratum: A novel autoregulatory loop between the Gcn2-Atf4 pathway and l-Proline metabolism controls stem cell identity by D'Aniello, C, Fico, A, Casalino, L, Guardiola, O, Di Napoli, G, Cermola, F, De Cesare, D, Tatè, R, Cobellis, G, Patriarca, E J, Minchiotti, G

    Published in Cell death and differentiation (08-06-2015)
    “…Correction to: Cell Death and Differentiation (2015) 22, 1094–1105; doi:10.1038/cdd.2015.24; published online 10 April 2015 Since the publication of this paper…”
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    Dye-Sensitized Photooxygenation of Furanosyl Furans:  Synthesis of a New Pyridazine C-Nucleoside by Cermola, Flavio, Iesce, M. Rosaria, Buonerba, Gianluca

    Published in Journal of organic chemistry (05-08-2005)
    “…The dye-sensitized photooxygenation of furanosyl furans easily affords C- or O-glycosides with cis-α,β-unsaturated 1,4-dioxo aglycones. The reaction, performed…”
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    A novel autoregulatory loop between the Gcn2-Atf4 pathway and (L)-Proline [corrected] metabolism controls stem cell identity by D'Aniello, C, Fico, A, Casalino, L, Guardiola, O, Di Napoli, G, Cermola, F, De Cesare, D, Tatè, R, Cobellis, G, Patriarca, E J, Minchiotti, G

    Published in Cell death and differentiation (01-07-2015)
    “…Increasing evidence indicates that metabolism is implicated in the control of stem cell identity. Here, we demonstrate that embryonic stem cell (ESC) behaviour…”
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    Journal Article
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    A mild photochemical approach to the degradation of phenols from olive oil mill wastewater by Cermola, Flavio, DellaGreca, Marina, Iesce, M.Rosaria, Montella, Stefania, Pollio, Antonino, Temussi, Fabio

    Published in Chemosphere (Oxford) (01-05-2004)
    “…Photooxidation of cathecol ( 1) is carried out in aqueous solution at λ>300 nm using different sensitizers: rose bengal (RB), 9,10-dicyanoanthracene (DCA),…”
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    Phototransformation of Carboxin in Water. Toxicity of the Pesticide and Its Sulfoxide to Aquatic Organisms by DellaGreca, Marina, Iesce, Maria Rosaria, Cermola, Flavio, Rubino, Maria, Isidori, Marina

    Published in Journal of agricultural and food chemistry (06-10-2004)
    “…Sunlight exposure of aqueous suspensions of carboxin (1) causes its phototransformation to sulfoxide 2 and minor components. Similar effects are observed in…”
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    Transformation and ecotoxicity of carbamic pesticides in water by Iesce, Maria Rosaria, della Greca, Marina, Cermolal, Flavio, Rubino, Maria, Isidori, Marina, Pascarella, Luigia

    “…N-methylcarbamate insecticides are widely used chemicals for crop protection. This study examines the hydrolytic and photolytic cleavage of benfuracarb,…”
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    Effects of sensitizers on the photodegradation of the systemic fungicide triadimenol by Iesce, Maria Rosaria, Graziano, Maria Liliana, Cermola, Flavio, Montella, Stefania, di Gioia, Lucrezia, Stasio, Ciriaco

    Published in Chemosphere (Oxford) (01-04-2003)
    “…The photochemical behaviour of triadimenol ( 1) under various conditions has been examined. Significant degradation is obtained only in the presence of…”
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    The first nucleophilic aromatic substitution of suitably activated 2-methoxyfurans with Grignard reagents by Iesce, M.Rosaria, Graziano, M.Liliana, Cermola, Flavio, Montella, Stefania, Di Gioia, Lucrezia

    Published in Tetrahedron letters (28-07-2003)
    “…The reaction of 2-methoxyfuroates 1 with Grignard reagents 2 leads to tertiary alcohols or S NAr products depending on the position of the alkoxycarbonyl…”
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    Bromination and iodination of donor–acceptor cyclopropanes. Evidence for an ET mechanism by Piccialli, Vincenzo, Graziano, M.Liliana, Iesce, M.Rosaria, Cermola, Flavio

    Published in Tetrahedron letters (04-11-2002)
    “…Ethyl 2,2-dimethoxycyclopropanecarboxylates 1a– d react easily with Br 2 and I 2 in CCl 4 or CH 2Cl 2 leading, in high yields, to 1-ethyl-4-methyl…”
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    Sensitized Photooxygenation of the Fungicide Furalaxyl by Iesce, M R, Cermola, F, Graziano, M L, Montella, S, Di Gioia, L, Isidori, M

    “…Background. The photolysis of pesticides is of high current interest since light is one of the most important abiotic factors which are responsible for the…”
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    Photochemical Behaviour of the Systemic Fungicide Carboxin by Iesce, M R, Cermola, F, de Lorenzo, F, Graziano, M L, Caliendo, B

    “…Irradiation or carboxin (1) with a 500W UV lamp (filter pyrex) in CH3CN leads to the products 3, 5-8, 12-14 depending upon the reaction conditions. All…”
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    Unexpected Products via Singlet Oxygen Oxygenation of Functionalized 5,6-Dihydro-1,4-oxathiins by Cermola, Flavio, De Lorenzo, Fulvio, Giordano, Federico, Graziano, M. Liliana, Iesce, M. Rosaria, Palumbo, Giovanni

    Published in Organic letters (04-05-2000)
    “…Singlet oxygen oxygenation of 5,6-dihydro-1,4-oxathiins substituted at C-3 with an electron-withdrawing group leads stereoselectively to ketosulfoxides 5 and…”
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    Photochemical behaviour of the systemic fungicide carboxin by Iesce, Maria Rosaria, Cermola, Flavio, De Lorenzo, Fulvio, Graziano, Maria Liliana, Caliendo, Barbara

    “…Irradiation of carboxin (1) with a 500 W UV lamp (filter Pyrex) in CH3CN leads to the products 3, 5-8, 12-14 depending upon the reaction conditions. All…”
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    Journal Article
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