Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5281579 | Tetrahedron Letters | 2010 | 5 Pages |
Abstract
A general and efficient procedure for the synthesis of 1,1,3-triheteroaryl compounds in good to excellent yield at room temperature is developed. The reaction proceeds via mixed Michael and Friedel-Crafts reactions of α,β-enals or α,β-enones and indoles, 2-methylfuran or 2-methylthiophene in the presence of a catalytic amount of AlCl3.
Graphical abstractA general and efficient procedure for the synthesis of 1,1,3-triheteroaryl compounds is developed.Download full-size image
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Morteza Shiri, Mohammad Ali Zolfigol, Roya Ayazi-Nasrabadi,