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Results: 1-6 |
Results: 6

Authors: Fabbrini, M Galli, C Gentili, P Macchitella, D Petride, H
Citation: M. Fabbrini et al., Aromatic iodination: a new investigation on the nature of the mechanism, J CHEM S P2, (9), 2001, pp. 1516-1521

Authors: Fabbrini, M Galli, C Gentili, P Macchitella, D
Citation: M. Fabbrini et al., An oxidation of alcohols by oxygen with the enzyme laccase and mediation by TEMPO, TETRAHEDR L, 42(43), 2001, pp. 7551-7553

Authors: Campiani, G Aiello, F Fabbrini, M Morelli, E Ramunno, A Armaroli, S Nacci, V Garofalo, A Greco, G Novellino, E Maga, G Spadari, S Bergamini, A Ventura, L Bongiovanni, B Capozzi, M Bolacchi, F Marini, S Coletta, M Guiso, G Caccia, S
Citation: G. Campiani et al., Quinoxalinylethylpyridylthioureas (QXPTs) as potent non-nucleoside HIV-1 reverse transcriptase (RT) inhibitors. Further SAR studies and identification of a novel orally bioavailable hydrazine-based antiviral agent, J MED CHEM, 44(3), 2001, pp. 305-315

Authors: Baciocchi, E Fabbrini, M Lanzalunga, O Manduchi, L Pochetti, G
Citation: E. Baciocchi et al., Prochiral selectivity in H2O2-promoted oxidation of arylalkanols catalysedby chloroperoxidase - The role of the interactions between the OH group and the amino-acid residues in the enzyme active site, EUR J BIOCH, 268(3), 2001, pp. 665-672

Authors: Campiani, G Fabbrini, M Morelli, E Nacci, V Greco, G Novellino, E Maga, G Spadari, S Bergamini, A Faggioli, E Uccella, I Bolacchi, F Marini, S Coletta, M Fracasso, C Caccia, S
Citation: G. Campiani et al., Non-nucleoside HIV-1 reverse transcriptase inhibitors: synthesis and biological evaluation of novel quinoxalinylethylpyridylthioureas as potent antiviral agents, ANTIVIR CHE, 11(2), 2000, pp. 141-155

Authors: Campiani, G Morelli, E Fabbrini, M Nacci, V Greco, G Novellino, E Ramunno, A Maga, G Spadari, S Caliendo, G Bergamini, A Faggioli, E Uccella, I Bolacchi, F Marini, S Coletta, M Nacca, A Caccia, S
Citation: G. Campiani et al., Pyrrolobenzoxazepinone derivatives as non-nucleoside HIV-1 RT inhibitors: Further structure-activity relationship studies and identification of more potent broad-spectrum HIV-1 RT inhibitors with antiviral activity, J MED CHEM, 42(21), 1999, pp. 4462-4470
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