Preparation of annulated 2,4-dioxygenated-5-methylfurans

Article abstract of DOI:10.1080/00397919108016771

A concise route from dihydropyran to the furans 12 and 13 has been developed that takes advantage of the regioselective Baeyer-Villiger oxidation of bicyclic ketone 6.

Full text of DOI:10.1080/00397919108016771

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Synthetic Communications: An
International Journal for Rapid
Communication of Synthetic
Organic Chemistry
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Preparation of Annulated 2,4-
Dioxygenated-5-Methylfurans
Leo A. Paquette a & Matthew R. Sivik a
a Evans Chemical Laboratories , The Ohio State
University , Columbus, Ohio, 43210
Published online: 24 Sep 2006.
To cite this article: Leo A. Paquette & Matthew R. Sivik (1991) Preparation of
Annulated 2,4-Dioxygenated-5-Methylfurans, Synthetic Communications: An
International Journal for Rapid Communication of Synthetic Organic Chemistry, 21:3,
467-479, DOI: 10.1080/00397919108016771
To link to this article: http://dx.doi.org/10.1080/00397919108016771
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