The Still-Wittig rearrangement in the preparation of a synthetically useful 4C-hydroxymethyl-hex-2-enopyranoside

Article abstract of DOI:10.1080/00397919308009784

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

Full text of DOI:10.1080/00397919308009784

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Synthetic Communications: An
International Journal for Rapid
Communication of Synthetic
Organic Chemistry
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The Still-Wittig Rearrangement
in the Preparation of a
Synthetically Useful 4C-
Hydroxymethyl-hex-2-eno-
pyranoside
Andrew G. Wee a & Lin Zhang a
a Department of Chemistry , University of Regina ,
Regina, Saskatchewan, S4S 0A2, Canada
Published online: 23 Sep 2006.
To cite this article: Andrew G. Wee & Lin Zhang (1993) The Still-Wittig
Rearrangement in the Preparation of a Synthetically Useful 4C-Hydroxymethyl-
hex-2-eno-pyranoside, Synthetic Communications: An International Journal
for Rapid Communication of Synthetic Organic Chemistry, 23:3, 325-334, DOI:
10.1080/00397919308009784
To link to this article: http://dx.doi.org/10.1080/00397919308009784
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