| 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
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
B. Suchand, J. Krishna, B. Venkat Ramulu, D. Dibyendu, A. Gopi Krishna Reddy, L. Mahendar, G. Satyanarayana,
![First Page Preview: An efficient intermolecular [Pd]-catalyzed C-C and intramolecular [Cu]-catalyzed C-O bonds formation: synthesis of functionalized flavans and benzoxepine An efficient intermolecular [Pd]-catalyzed C-C and intramolecular [Cu]-catalyzed C-O bonds formation: synthesis of functionalized flavans and benzoxepine](/preview/png/5267705.png)