| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5275011 | Tetrahedron Letters | 2011 | 4 Pages |
Abstract
Conjugate reduction of ortho-substituted cinnamic esters by Stryker's reagent to form copper enolates, followed by intramolecular aldol-type cyclization, successfully generated indane and tetralin rings in one pot efficiently. This tandem reaction is generally diastereoselective and provides good yields.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Daiane Cristina Sass, EmÃlio Carlos Jr., Jader da Silva Barbosa, Kleber Thiago de Oliveira, Mauricio Gomes Constantino,