Oxygenated dihydrophenanthrenes via quinol acetals: A brief synthesis of orchinol

Article abstract of DOI:10.1080/00397919908086083

The dihydrophenanthrene phytoalexin Orchinol was synthesized in 5 steps from commercially available 3,5-dimethoxybenzaldehyde. The approach utilized a new synthon, p-benzoquinone dibenzylmonoacetal, which served as a phenol 3,4-dication equivalent in an a

Full text of DOI:10.1080/00397919908086083

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Synthetic Communications: An
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Oxygenated
Dihydrophenanthrenes
Via Quinol Acetals: A Brief
Synthesis of Orchinol
Teresa J. Broering a & Gary W. Morrow a
a Department of Chemistry , The University of
Dayton , Dayton, Ohio, 45469, USA
Published online: 17 Sep 2007.
To cite this article: Teresa J. Broering & Gary W. Morrow (1999) Oxygenated
Dihydrophenanthrenes Via Quinol Acetals: A Brief Synthesis of Orchinol, Synthetic
Communications: An International Journal for Rapid Communication of Synthetic
Organic Chemistry, 29:7, 1135-1142, DOI: 10.1080/00397919908086083
To link to this article: http://dx.doi.org/10.1080/00397919908086083
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