Walter Cabri
Affiliations: | Ciamician | University of Bologna |
Area:
Organic ChemistryGoogle:
"Walter Cabri"Mean distance: (not calculated yet)
Parents
Sign in to add mentor| Carlo Scolastico | grad student | 1984-1985 | |
| Stephen Hanessian | post-doc | 1998-1999 | University of Montreal (Canada) |
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Publications
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| Ferrazzano L, Martelli G, Fantoni T, et al. (2020) Fast Heck-Cassar-Sonogashira (HCS) Reactions in Green Solvents. Organic Letters. 22: 3969-3973 |
| Ferrazzano L, Corbisiero D, Martelli G, et al. (2019) Green Solvent Mixtures for Solid-Phase Peptide Synthesis:A Dimethylformamide-Free Highly Efficient Synthesis of Pharmaceutical-Grade Peptides Acs Sustainable Chemistry & Engineering. 7: 12867-12877 |
| Guryanov I, Orlandin A, Viola A, et al. (2019) Overcoming Chemical Challenges in the Solid-Phase Synthesis of High-Purity GnRH Antagonist Degarelix. Part 2 Organic Process Research & Development. 24: 274-278 |
| Guryanov I, Bondesan A, Visentini D, et al. (2016) Innovative chemical synthesis and conformational hints on the lipopeptide liraglutide Journal of Peptide Science. 471-479 |
| Giannini G, Vesci L, Battistuzzi G, et al. (2014) ST7612AA1, a thioacetate-ω(γ-lactam carboxamide) derivative selected from a novel generation of oral HDAC inhibitors. Journal of Medicinal Chemistry. 57: 8358-77 |
| Taddei M, Ferrini S, Giannotti L, et al. (2014) Synthesis and evaluation of new Hsp90 inhibitors based on a 1,4,5-trisubstituted 1,2,3-triazole scaffold. Journal of Medicinal Chemistry. 57: 2258-74 |
| Baruchello R, Simoni D, Marchetti P, et al. (2014) 4,5,6,7-Tetrahydro-isoxazolo-[4,5-c]-pyridines as a new class of cytotoxic Hsp90 inhibitors. European Journal of Medicinal Chemistry. 76: 53-60 |
| Taddei M, Cini E, Giannotti L, et al. (2014) Lactam based 7-amino suberoylamide hydroxamic acids as potent HDAC inhibitors. Bioorganic & Medicinal Chemistry Letters. 24: 61-4 |
| Kotoni D, Piras M, Cabri W, et al. (2014) Thermodynamic and kinetic investigation of monoketo-aldehyde-peroxyhemiacetal (MKA), a stereolabile degradation product of dihydroartemisinin Rsc Advances. 4: 32847-32857 |
| Giannini G, Battistuzzi G, Vignola D, et al. (2013) Abstract 1010: New thiol-ω(γ-lactam amide) SAHA analogues as potent histone deacetylase (HDAC) inhibitors.. Cancer Research. 73: 1010-1010 |