A convenient method for the preparation of substituted naphtho[2,3-b]-1,4-dioxin by the Diels-Alder reaction

Article abstract of DOI:10.1080/00397919608002612

The naphtho-fused systems 3 and 4 were synthesized from the hydroxy-acetal 1 through deacetylation, formation of unstable diene 2 and Diels-Alder cycloaddition with the appropriate dienophile in acidic media.

Full text of DOI:10.1080/00397919608002612

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Synthetic Communications: An
International Journal for Rapid
Communication of Synthetic
Organic Chemistry
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A Convenient Method for the
Preparation of Substituted
Naphtho[2,3-b]-1,4-dioxin by
the Diels-Alder Reaction.
A. S. Capilla a & M. D. Pujol a
a Laboratori de Química Farmacèutica, Facultat de
Farmàcia , Universitat de Barcelona , Av. Diagonal
643, 08028, Barcelona, Spain E-mail:
Published online: 21 Aug 2006.
To cite this article: A. S. Capilla & M. D. Pujol (1996) A Convenient Method for the
Preparation of Substituted Naphtho[2,3-b]-1,4-dioxin by the Diels-Alder Reaction.,
Synthetic Communications: An International Journal for Rapid Communication of
Synthetic Organic Chemistry, 26:9, 1729-1738, DOI: 10.1080/00397919608002612
To link to this article: http://dx.doi.org/10.1080/00397919608002612
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