| Design and synthesis of diselenobisbenzamides (DISeBAs) as nucleocapsid protein 7 (NCp7) inhibitors with anti-HIV activity L Sancineto, A Mariotti, L Bagnoli, F Marini, J Desantis, N Iraci, C Santi, ... Journal of medicinal chemistry 58 (24), 9601-9614, 2015 | 203 | 2015 |
| Asymmetric azidoselenenylation of alkenes: a key step for the synthesis of enantiomerically enriched nitrogen-containing compounds M Tiecco, L Testaferri, C Santi, C Tomassini, F Marini, L Bagnoli, ... Angewandte Chemie International Edition 42 (27), 3131-3133, 2003 | 150 | 2003 |
| Preparation of a New Chiral Non‐Racemic Sulfur‐Containing Diselenide and Applications in Asymmetric Synthesis M Tiecco, L Testaferri, C Santi, C Tomassini, F Marini, L Bagnoli, ... Chemistry–A European Journal 8 (5), 1118-1124, 2002 | 136 | 2002 |
| Stereoselective selenium catalyzed dihydroxylation and hydroxymethoxylation of alkenes C Santi, R Di Lorenzo, C Tidei, L Bagnoli, T Wirth Tetrahedron 68 (51), 10530-10535, 2012 | 101 | 2012 |
| Selenium catalyzed oxidation of aldehydes: green synthesis of carboxylic acids and esters L Sancineto, C Tidei, L Bagnoli, F Marini, EJ Lenardão, C Santi Molecules 20 (6), 10496-10510, 2015 | 93 | 2015 |
| New nitrogen containing chiral diselenides: synthesis and asymmetric addition reactions to olefins M Tiecco, L Testaferri, C Santi, C Tomassini, F Marini, L Bagnoli, ... Tetrahedron: Asymmetry 11 (23), 4645-4650, 2000 | 93 | 2000 |
| Ring-closure reactions of alkenyl oximes induced by persulfate anion oxidation of diphenyl diselenide. Formation of 1, 2-oxazines and cyclic nitrones M Tiecco, L Testaferri, M Tingoli, L Bagnoli, F Marini Journal of the Chemical Society, Perkin Transactions 1, 1989-1993, 1993 | 83 | 1993 |
| Synthesis of Enantiopure 1, 4‐Dioxanes, Morpholines, and Piperazines from the Reaction of Chiral 1, 2‐Diols, Amino Alcohols, and Diamines with Vinyl Selenones L Bagnoli, C Scarponi, MG Rossi, L Testaferri, M Tiecco Chemistry–A European Journal 17 (3), 993-999, 2011 | 78 | 2011 |
| New halogen-containing drugs approved by FDA in 2021: An overview on their syntheses and pharmaceutical use D Benedetto Tiz, L Bagnoli, O Rosati, F Marini, L Sancineto, C Santi Molecules 27 (5), 1643, 2022 | 75 | 2022 |
| A sulfur-containing diselenide as an efficient chiral reagent in asymmetric selenocyclization reactions M Tiecco, L Testaferri, F Marini, S Sternativo, L Bagnoli, C Santi, ... Tetrahedron: Asymmetry 12 (10), 1493-1502, 2001 | 69 | 2001 |
| A new vinyl selenone-based domino approach to spirocyclopropyl oxindoles endowed with anti-HIV RT activity M Palomba, L Rossi, L Sancineto, E Tramontano, A Corona, L Bagnoli, ... Organic & biomolecular chemistry 14 (6), 2015-2024, 2016 | 66 | 2016 |
| Efficient asymmetric selenocyclizations of alkenyl oximes into cyclic nitrones and 1, 2-oxazines promoted by sulfur containing diselenides M Tiecco, L Testaferri, L Bagnoli, V Purgatorio, A Temperini, F Marini, ... Tetrahedron: Asymmetry 12 (23), 3297-3304, 2001 | 66 | 2001 |
| Efficient asymmetric selenomethoxylation and selenohydroxylation of alkenes with a new sulfur containing chiral diselenide M Tiecco, L Testaferri, L Bagnoli, F Marini, A Temperini, C Tomassini, ... Tetrahedron Letters 41 (17), 3241-3245, 2000 | 65 | 2000 |
| Optically active isoxazolidines and 1, 3-amino alcohols by asymmetric selenocyclization reactions of O-allyl oximes M Tiecco, L Testaferri, F Marini, S Sternativo, C Santi, L Bagnoli, ... Tetrahedron: Asymmetry 12 (21), 3053-3059, 2001 | 62 | 2001 |
| A chiral electrophilic selenium reagent to promote the kinetic resolution of racemic allylic alcohols M Tiecco, L Testaferri, C Santi, C Tomassini, R Bonini, F Marini, L Bagnoli, ... Organic Letters 6 (25), 4751-4753, 2004 | 59 | 2004 |
| Selenium promoted synthesis of enantiopure pyrrolidines starting from chiral aminoalcohols M Tiecco, L Testaferri, L Bagnoli, C Scarponi, A Temperini, F Marini, ... Tetrahedron: Asymmetry 18 (23), 2758-2767, 2007 | 58 | 2007 |
| Seleno-Functionalization of Quercetin Improves the Non-Covalent Inhibition of Mpro and Its Antiviral Activity in Cells against SARS-CoV-2 F Mangiavacchi, P Botwina, E Menichetti, L Bagnoli, O Rosati, F Marini, ... International journal of molecular sciences 22 (13), 7048, 2021 | 57 | 2021 |
| Ring‐Closure Reactions through Intramolecular Displacement of the Phenylselenonyl Group by Nitrogen Nucleophiles: A New Stereospecific Synthesis of N‐Tosyl and N‐Benzoyl‐1, 3 … M Tiecco, L Testaferri, A Temperini, L Bagnoli, F Marini, C Santi Chemistry–A European Journal 10 (7), 1752-1764, 2004 | 57 | 2004 |
| Asymmetric selenomethoxylation of alkenes with camphorselenenyl sulfate M Tiecco, L Testaferri, C Santi, F Marini, L Bagnoli, A Temperini Tetrahedron letters 39 (18), 2809-2812, 1998 | 53 | 1998 |
| Asymmetric oxyselenenylation–deselenenylation reactions of alkenes induced by camphor diselenide and ammonium persulfate. A convenient one-pot synthesis of enantiomerically … M Tiecco, L Testaferri, F Marini, C Santi, L Bagnoli, A Temperini Tetrahedron: Asymmetry 10 (4), 747-757, 1999 | 51 | 1999 |
