| Dioxindole in asymmetric catalytic synthesis: direct access to 3-substituted 3-hydroxy-2-oxindoles via 1, 4-additions to nitroalkenes M Retini, G Bergonzini, P Melchiorre Chemical communications 48 (27), 3336-3338, 2012 | 73 | 2012 |
| Intracellular redox-modulated pathways as targets for effective approaches in the treatment of viral infection A Fraternale, C Zara, M De Angelis, L Nencioni, AT Palamara, M Retini, ... International Journal of Molecular Sciences 22 (7), 3603, 2021 | 37 | 2021 |
| New coumarin-urea based receptor for anions: A selective off–on fluorescence response to fluoride G Ambrosi, M Formica, V Fusi, L Giorgi, E Macedi, G Piersanti, M Retini, ... Tetrahedron 68 (19), 3768-3775, 2012 | 32 | 2012 |
| C3-Alkylation of indoles and oxindoles by alcohols by means of borrowing hydrogen methodology F Bartoccini, M Retini, G Piersanti Tetrahedron letters 61 (22), 151875, 2020 | 26 | 2020 |
| An efficient, economical synthesis of hydroxytyrosol and its protected forms via Baeyer–Villiger oxidation G Piersanti, M Retini, JL Espartero, A Madrona, G Zappia Tetrahedron letters 52 (38), 4938-4940, 2011 | 23 | 2011 |
| Boosting GSH Using the Co-Drug Approach: I-152, a Conjugate of N-acetyl-cysteine and β-mercaptoethylamine AF Rita Crinelli , Carolina Zara, Michaël Smietana, Michele Retini, Mauro ... Nutrients 11 (6), 1291, 2019 | 22 | 2019 |
| Organocatalytic Aza-Friedel–Crafts/Lactonization Domino Reaction of Naphthols and Phenols with 2-Acetamidoacrylate to Naphtho-and Benzofuranones Bearing a Quaternary Center at … F Bartoccini, M Mari, M Retini, S Bartolucci, G Piersanti The Journal of Organic Chemistry 83 (19), 12275-12283, 2018 | 19 | 2018 |
| Concise and convergent enantioselective total syntheses of (+)-and (−)-fumimycin M Retini, S Bartolucci, F Bartoccini, M Mari, G Piersanti The Journal of Organic Chemistry 84 (18), 12221-12227, 2019 | 18 | 2019 |
| Total Synthesis of (-)-Clavicipitic Acid via γ, γ-Dimethylallyltryptophan (DMAT) and Chemoselective C− H Hydroxylation F Bartoccini, S Venturi, M Retini, M Mari, G Piersanti The Journal of organic chemistry 84 (12), 8027-8034, 2019 | 15 | 2019 |
| General synthesis of unnatural 4-, 5-, 6-, and 7-bromo-d-tryptophans by means of a regioselective indole alkylation F Bartoccini, F Fanini, M Retini, G Piersanti Tetrahedron Letters 61 (22), 151923, 2020 | 11 | 2020 |
| Indolizine derivatives as phoshoinositide 3-kinases inhibitors M Biagetti, A Accetta, AM Capelli, M Guala, M Retini US Patent 9,527,869, 2016 | 10 | 2016 |
| Identification of a 2, 4-diaminopyrimidine scaffold targeting Trypanosoma brucei pteridine reductase 1 from the LIBRA compound library screening campaign P Linciano, G Cullia, C Borsari, M Santucci, S Ferrari, G Witt, S Gul, ... European Journal of Medicinal Chemistry 189, 112047, 2020 | 8 | 2020 |
| Targeting SARS‐CoV‐2 by synthetic dual‐acting thiol compounds that inhibit Spike/ACE2 interaction and viral protein production A Fraternale, M De Angelis, R De Santis, D Amatore, S Masini, F Monittola, ... The FASEB Journal 37 (2), 2023 | 7 | 2023 |
| Dithiol Based on l-Cysteine and Cysteamine as a Disulfide-Reducing Agent F Bartoccini, M Retini, R Crinelli, M Menotta, A Fraternale, G Piersanti The Journal of Organic Chemistry 87 (15), 10073-10079, 2022 | 6 | 2022 |
| Novel, Chiral, and Enantiopure C2‐symmetric Thioureas Promote Asymmetric Protio‐Pictet–Spengler Reactions by Anion‐Binding Catalysis M Retini, F Bartoccini, G Zappia, G Piersanti European Journal of Organic Chemistry 2021 (5), 825-829, 2021 | 6 | 2021 |
| Concise catalytic asymmetric synthesis of (R)-4-amino Uhle's ketone F Bartoccini, A Regni, M Retini, G Piersanti Organic & biomolecular chemistry 19 (13), 2932-2940, 2021 | 6 | 2021 |
| Neutral urea-based receptors for phosphates: synthesis and spectrophotometric studies M Formica, V Fusi, L Giorgi, G Piersanti, M Retini, G Zappia Tetrahedron 72 (44), 7039-7049, 2016 | 6 | 2016 |
| Asymmetric total synthesis of all rugulovasine stereoisomers and preliminary evaluation of their biological properties F Bartoccini, A Regni, M Retini, G Piersanti European Journal of Organic Chemistry 2022 (17), e202200315, 2022 | 5 | 2022 |
| Chemical modification of NSC12 leads to a specific FGF-trap with antitumor activity in multiple myeloma R Castelli, S Taranto, L Furiassi, N Bozza, G Marseglia, F Ferlenghi, ... European Journal of Medicinal Chemistry 221, 113529, 2021 | 4 | 2021 |
| Large-Scale Preparation of N-Butanoyl-l-glutathione (C4-GSH) F Bartoccini, M Mari, M Retini, A Fraternale, G Piersanti Organic Process Research & Development 23 (9), 2069-2073, 2019 | 4 | 2019 |
