| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5225174 | Tetrahedron | 2007 | 9 Pages |
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.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Mandar Deodhar, David StC Black, Naresh Kumar,