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Acid catalyzed stereoselective rearrangement and dimerization of flavenes: synthesis of dependensin
Authors:Mandar Deodhar
Affiliation:School of Chemistry, University of New South Wales, UNSW, Sydney, NSW 2052, Australia
Abstract:Appropriately substituted flavenes undergo stereoselective rearrangement and dimerization when treated with methanolic hydrochloric acid to give benzopyranobenzopyrans. A rationale for the rearrangement is proposed. This synthetic methodology has been used for a high yield synthesis of the natural product dependensin.
Keywords:Dimers   Dependensin   Acid catalyzed dimerization   Benzopyranobenzopyran
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