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A Practical Synthesis of (−)‐Oseltamivir

Identifieur interne : 004D68 ( Main/Exploration ); précédent : 004D67; suivant : 004D69

A Practical Synthesis of (−)‐Oseltamivir

Auteurs : Nobuhiro Satoh [Japon] ; Takahiro Akiba [Japon] ; Satoshi Yokoshima [Japon] ; Tohru Fukuyama [Japon]

Source :

RBID : ISTEX:1230607F34D6DAF85F327AC19FE752349EB75943

English descriptors

Abstract

Keep it simple: Still in hot demand, the influenza drug (−)‐oseltamivir phosphate (tamiflu; see scheme) has now been synthesized from pyridine by using inexpensive reagents. A strict minimum of purification steps are required in a synthetic route which features an asymmetric Diels–Alder reaction, a bromolactonization, a Hofmann rearrangement, and a domino transformation of a bicyclo[2.2.2] system into an aziridine intermediate.

Url:
DOI: 10.1002/anie.200701754


Affiliations:


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Le document en format XML

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