A Concise Synthesis of (−)‐Oseltamivir
- 28 April 2008
- journal article
- research article
- Published by Wiley in Angewandte Chemie International Edition
- Vol. 47 (20), 3759-3761
- https://doi.org/10.1002/anie.200800282
Abstract
No abstract availableKeywords
This publication has 26 references indexed in Scilit:
- Synthetic Strategies for Oseltamivir PhosphateEuropean Journal of Organic Chemistry, 2008
- Second Generation Catalytic Asymmetric Synthesis of Tamiflu: Allylic Substitution RouteOrganic Letters, 2006
- Tamiflu: The Supply ProblemAngewandte Chemie International Edition, 2006
- Tamiflu: Das VersorgungsproblemAngewandte Chemie, 2006
- Ring-Closing Metathesis-Based Synthesis of (3R,4R,5S)-4-Acetylamino-5-amino-3-hydroxy- cyclohex-1-ene-carboxylic Acid Ethyl Ester: A Functionalized Cycloalkene Skeleton of GS4104The Journal of Organic Chemistry, 2006
- De Novo Synthesis of Tamiflu via a Catalytic Asymmetric Ring-Opening of meso-Aziridines with TMSN3Journal of the American Chemical Society, 2006
- A Short Enantioselective Pathway for the Synthesis of the Anti-Influenza Neuramidase Inhibitor Oseltamivir from 1,3-Butadiene and Acrylic AcidJournal of the American Chemical Society, 2006
- The Synthetic Development of the Anti-Influenza Neuraminidase Inhibitor Oseltamivir Phosphate (Tamiflu®): A Challenge for Synthesis & Process ResearchChimia, 2004
- Practical Total Synthesis of the Anti-Influenza Drug GS-4104The Journal of Organic Chemistry, 1998
- Influenza Neuraminidase Inhibitors Possessing a Novel Hydrophobic Interaction in the Enzyme Active Site: Design, Synthesis, and Structural Analysis of Carbocyclic Sialic Acid Analogues with Potent Anti-Influenza ActivityJournal of the American Chemical Society, 1997