Syntheses of racemic and optically active 4-hydroxy-2-hydroxymethyl-1,7-dioxaspiro[5.5]undecanes

Article abstract of DOI:10.1080/00397919308009841

Racemic and optically active 4-hydroxy-2-hydroxymethyl-1,7-dioxaspiro[5.5]undecanes were prepared in six steps from butane-1,2,4-triol and valerolactone with the longest linear sequence being four steps.

Full text of DOI:10.1080/00397919308009841

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Synthetic Communications: An
International Journal for Rapid
Communication of Synthetic
Organic Chemistry
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Syntheses of Racemic
and Optically Active 4-
Hydroxy-2-hydroxymethyl-1,7-
dioxaspiro[5.5]undecanes
Girts Kaugars a , Stephen J. Nelson a , Fred E.
Dutton a & Scott E. Martin a
a Animal Health Therapeutics, Upjohn Laboratories ,
The Upjohn Company , Kalamazoo, Michigan, 49001
Published online: 23 Sep 2006.
To cite this article: Girts Kaugars , Stephen J. Nelson , Fred E. Dutton &
Scott E. Martin (1993) Syntheses of Racemic and Optically Active 4-Hydroxy-2-
hydroxymethyl-1,7-dioxaspiro[5.5]undecanes, Synthetic Communications: An
International Journal for Rapid Communication of Synthetic Organic Chemistry, 23:6,
797-809
To link to this article: http://dx.doi.org/10.1080/00397919308009841
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