Chemischer Informationsdienst
 1984
DOI: 10.1002/chin.198434318
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ChemInform Abstract: TOTAL SYNTHESIS OF 2,6‐EPOXY‐2H‐1‐BENZOXOCIN SUGAR ANALOGS

Frank M. Hauser1,
William P. Ellenberger2,
Theodore C. Adams3

Abstract: Aus dem 2‐Furan‐carbonsäure‐p‐kresolester (I) erhält man nach Fries das Umlagerungsprodukt (II), dasnach Addition von Methyllithium zu (III) durch Behandlung mit Brom in Methanol und anschließende Schwefelsäure‐Behandlung in das Cyclisierungsprodukt (V) übergeführt wird.

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