Issue 7, 1984

A convenient synthesis of substituted chiral tetrahydrofurans from sugar γ-lactones

Abstract

Sugar γ-lactones react with hexamethylphosphorous triamide–tetrachloromethane to give dichloro-olefins in one step; these are then reduced to optically active tetrahydrofurans.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1984, 449-450

A convenient synthesis of substituted chiral tetrahydrofurans from sugar γ-lactones

Y. Chapleur, J. Chem. Soc., Chem. Commun., 1984, 449 DOI: 10.1039/C39840000449

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