| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5283798 | Tetrahedron Letters | 2007 | 4 Pages |
Abstract
Bromodimethylsulfonium bromide has been found to be an efficient catalyst for the Michael addition of a wide variety of amines to electron deficient alkenes at room temperature. The protocol is very simple and chemoselective. Aliphatic and benzylic amines undergo conjugate addition within a very short period under solvent-free conditions and provide excellent yields of products.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Abu T. Khan, Tasneem Parvin, Sarifuddin Gazi, Lokman H. Choudhury,