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A synthesis of oseltamivir (Tamiflu) starting from D-mannitol
1Department of Chemistry, Ewha Womans University, Seoul 120-750, Korea.
The Journal of Organic Chemistry
|September 28, 2010
Abstract:
A synthesis of oseltamivir (Tamiflu) was achieved starting from D-mannitol. A unique feature of the synthetic route is that an acyclic precursor was constructed, which was then cyclized in an intramolecular aldol reaction to form the Tamiflu skeleton. Throughout the synthesis, well-established, highly efficient reactions were employed, and no protection/deprotection sequence was needed.
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