| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5279744 | Tetrahedron Letters | 2007 | 5 Pages |
Abstract
The Katsuki-Jacobsen oxidation-epoxidation of acyclic α-silyloxy sulfinyl dienes, followed by acid-promoted cyclization, leads to 2,5-trans sulfonyl dihydrofurans with good selectivities. As an application, the formal synthesis of (6S,7S,9R,10R)-6,9-epoxynonadec-18-ene-7,10-diol is reported.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Roberto Fernández de la Pradilla, Alejandro Castellanos,