azides has been researched along with oseltamivir in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (66.67) | 29.6817 |
| 2010's | 1 (33.33) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Karpf, M; Trussardi, R | 1 |
| Alymova, IV; Portner, A; Taylor, G | 1 |
| Li, H; Shen, SJ; Xu, H; Zhu, CL | 1 |
1 review(s) available for azides and oseltamivir
| Article | Year |
|---|---|
Neuraminidase inhibitors as antiviral agents.
Topics: Acetamides; Animals; Antiviral Agents; Azides; Drug Design; Enzyme Inhibitors; Guanidines; Hexuronic Acids; HN Protein; Humans; Molecular Structure; Neuraminidase; Orthomyxoviridae; Oseltamivir; Protein Conformation; Pyrans; Respirovirus; Sialic Acids; Zanamivir | 2005 |
2 other study(ies) available for azides and oseltamivir
| Article | Year |
|---|---|
New, azide-free transformation of epoxides into 1,2-diamino compounds: synthesis of the anti-influenza neuraminidase inhibitor oseltamivir phosphate (Tamiflu).
Topics: Acetamides; Amines; Antiviral Agents; Azides; Enzyme Inhibitors; Epoxy Compounds; Molecular Structure; Neuraminidase; Orthomyxoviridae; Oseltamivir; Spectrum Analysis | 2001 |
Enantioselective Synthesis of Oseltamivir Phosphate (Tamiflu) via the Iron-Catalyzed Stereoselective Olefin Diazidation.
Topics: Alkenes; Antiviral Agents; Azides; Calorimetry, Differential Scanning; Catalysis; Iron; Oseltamivir; Stereoisomerism | 2018 |