Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5267705 | Tetrahedron Letters | 2012 | 4 Pages |
Abstract
An efficient three-step strategy for the synthesis of functionalized flavans, starting from readily available 2-bromoiodobenzenes and aryl vinyl alcohols, is presented and successfully extended to benzoxepine. An intermolecular [Pd]-catalyzed C-C and an intramolecular [Cu]-catalyzed C-O bond formations have been employed as key transformations of the strategy.
Related Topics
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Chemistry
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Authors
B. Suchand, J. Krishna, B. Venkat Ramulu, D. Dibyendu, A. Gopi Krishna Reddy, L. Mahendar, G. Satyanarayana,