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Toward a Total Synthesis of Okilactomycin (VII). Part 1. A Direct, Enantiocontrolled Route to the Western Sector.

✍ Scribed by Leo A. Paquette; Serge L. Boulet


Publisher
John Wiley and Sons
Year
2010
Weight
29 KB
Volume
33
Category
Article
ISSN
0931-7597

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Model Studies Directed Toward the Total Synthesis of (Β±)-Ribasine. A Tandem Cyclization-Cycloaddition Route Leading to the Core Skeleton. -A tandem cyclization-cycloaddition sequence of model compound (II) represents a useful approach towards the synthesis of the oxabicyclo[3.2.1]octane ring system