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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 23, 1993 - Issue 3
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Original Articles

The Still-Wittig Rearrangement in the Preparation of a Synthetically Useful 4C-Hydroxymethyl-hex-2-eno-pyranoside

Andrew G. Wee Department of Chemistry, University of Regina, Regina, Saskatchewan, S4S 0A2, Canada
&
Lin Zhang Department of Chemistry, University of Regina, Regina, Saskatchewan, S4S 0A2, Canada
Pages 325-334 | Received 12 Aug 1992, Published online: 23 Sep 2006
 
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Abstract

The Still-Wittig rearrangement of the stannyl-ether 9 is successfully carried out under optimal reaction conditions to give the 4C-hydroxymethy-hex-2-enopyranoside 10 in good yields (70–74%).

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