Title of article
Tandem reduction + cyclization of ortho-substituted cinnamic esters
Author/Authors
Sass، نويسنده , , Daiane Cristina and de Lucca Jr.، نويسنده , , Emيlio Carlos and da Silva Barbosa، نويسنده , , Jader and de Oliveira، نويسنده , , Kleber Thiago and Constantino، نويسنده , , Mauricio Gomes، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2011
Pages
4
From page
5371
To page
5374
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.
Keywords
Aldol-type cyclization , Tandem reduction + cyclization , Stryker’s reagent , Indanes , Tetralins
Journal title
Tetrahedron Letters
Serial Year
2011
Journal title
Tetrahedron Letters
Record number
1879367
Link To Document