Oseltamivir total synthesis

Oseltamivir

Oseltamivir total synthesis concerns the total synthesis of the antiinfluenza drug oseltamivir[1] marketed by Hoffmann-La Roche under the trade name Tamiflu. Its commercial production starts from the biomolecule shikimic acid harvested from Chinese star anise and from recombinant E. coli.[2][3] Control of stereochemistry is important: the molecule has three stereocenters and the sought-after isomer is only 1 of 8 stereoisomers.[citation needed]

  1. ^ Classics in Total Synthesis III: Further Targets, Strategies, Methods K. C. Nicolaou, Jason S. Chen ISBN 978-3-527-32957-1 2011
  2. ^ Farina V, Brown JD (November 2006). "Tamiflu: the supply problem". Angewandte Chemie. 45 (44): 7330–4. doi:10.1002/anie.200602623. PMID 17051628.
  3. ^ Rawat G, Tripathi P, Saxena RK (May 2013). "Expanding horizons of shikimic acid. Recent progresses in production and its endless frontiers in application and market trends". Applied Microbiology and Biotechnology. 97 (10): 4277–87. doi:10.1007/s00253-013-4840-y. PMID 23553030. S2CID 17660413.