Search Results - "Artuso, Emma"

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  1. 1

    Fungal Anticancer Metabolites: Synthesis Towards Drug Discovery by Barbero, Margherita, Artuso, Emma, Prandi, Cristina

    Published in Current medicinal chemistry (01-01-2018)
    “…Fungi are a well-known and valuable source of compounds of therapeutic relevance, in particular of novel anticancer compounds. Although seldom obtainable…”
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    Recent advances in the synthesis of analogues of phytohormones strigolactones with ring-closing metathesis as a key step by Lombardi, Chiara, Artuso, Emma, Grandi, Eleonora, Lolli, Marco, Spyrakis, Francesca, Priola, Emanuele, Prandi, Cristina

    Published in Organic & biomolecular chemistry (04-10-2017)
    “…In this paper, we synthesized and evaluated the biological activity of structural analogues of natural strigolactones in which the butenolide D-ring has been…”
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    Structure-activity relationships of strigolactones via a novel, quantitative in planta bioassay by Sanchez, Elena, Artuso, Emma, Lombardi, Chiara, Visentin, Ivan, Lace, Beatrice, Saeed, Wajeeha, Lolli, Marco L, Kobauri, Piermichele, Ali, Zahid, spyrakis, Francesca, Cubas, Pilar, Cardinale, Francesca, Prandi, Cristina

    Published in Journal of experimental botany (23-04-2018)
    “…The biological activity of natural and novel strigolactone D-lactam analogues is assessed using a novel bioassay based on Arabidopsis transgenic lines…”
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    Tailoring fluorescent strigolactones for in vivo investigations: a computational and experimental study by Prandi, Cristina, Ghigo, Giovanni, Occhiato, Ernesto G, Scarpi, Dina, Begliomini, Stefano, Lace, Beatrice, Alberto, Gabriele, Artuso, Emma, Blangetti, Marco

    Published in Organic & biomolecular chemistry (14-05-2014)
    “…Strigolactones (SLs) are a new class of plant hormones whose role has been recently defined in shoot branching, root development and architecture, and…”
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    Synthesis and properties of cationic surfactants with tuned hydrophylicity by Quagliotto, Pierluigi, Barbero, Nadia, Barolo, Claudia, Artuso, Emma, Compari, Carlotta, Fisicaro, Emilia, Viscardi, Guido

    Published in Journal of colloid and interface science (15-12-2009)
    “…Cationic surfactants having different hydrophobic moieties on the headgroup were prepared and characterized by conductivity and surface tension. The solution…”
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    Rationalization of Dye Uptake on Titania Slides for Dye-Sensitized Solar Cells by a Combined Chemometric and Structural Approach by Gianotti, Valentina, Favaro, Giada, Bonandini, Luca, Palin, Luca, Croce, Gianluca, Boccaleri, Enrico, Artuso, Emma, van Beek, Wouter, Barolo, Claudia, Milanesio, Marco

    Published in ChemSusChem (01-11-2014)
    “…A model photosensitizer (D5) for application in dye‐sensitized solar cells has been studied by a combination of XRD, theoretical calculations, and…”
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    Characterization of monomeric and gemini cationic amphiphilic molecules by fluorescence intensity and anisotropy. Part 2 by Barbero, Nadia, Quagliotto, Pierluigi, Barolo, Claudia, Artuso, Emma, Buscaino, Roberto, Viscardi, Guido

    Published in Dyes and pigments (01-12-2009)
    “…Four fluorophores of different nature, structure and properties were employed as probes for the characterization of a series of…”
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    A Simple Synthetic Route to Obtain Pure Trans-Ruthenium(II) Complexes for Dye-Sensitized Solar Cell Applications by Barolo, Claudia, Yum, Jun-Ho, Artuso, Emma, Barbero, Nadia, Di Censo, Davide, Lobello, Maria Grazia, Fantacci, Simona, De Angelis, Filippo, Grätzel, Michael, Nazeeruddin, Mohammed Khaja, Viscardi, Guido

    Published in ChemSusChem (01-11-2013)
    “…We report a facile synthetic route to obtain functionalized quaterpyridine ligand and its trans‐dithiocyanato ruthenium complex, based on a microwave‐assisted…”
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  12. 12

    Arenediazonium o-benzenedisulfonimides as efficient reagents for Heck-type arylation reactions by Artuso, Emma, Barbero, Margherita, Degani, Iacopo, Dughera, Stefano, Fochi, Rita

    Published in Tetrahedron (27-03-2006)
    “…Arenediazonium o-benzenedisulfonimides can be used as new and efficient reagents for Heck-type arylation reactions of some common substrates containing C–C…”
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