Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5227155 | Tetrahedron | 2009 | 7 Pages |
Abstract
Oseltamivir phosphate (Tamiflu®) is a potent inhibitor of neuraminidase, and is used worldwide as a drug for type A or B influenza. The industrial synthesis of oseltamivir uses shikimic acid as a starting material, but the price fluctuates, depending on the supply of star anise. We have developed a practical synthesis of oseltamivir from pyridine, which features an asymmetric Diels-Alder reaction of dihydropyridine using MacMillan's catalyst, a bromolactonization, Hofmann rearrangement with PhI(OAc)2, and a domino transformation of the bicyclo[2.2.2] system into an aziridine compound.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Nobuhiro Satoh, Takahiro Akiba, Satoshi Yokoshima, Tohru Fukuyama,