| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5267639 | Tetrahedron Letters | 2012 | 5 Pages |
Abstract
Palladium-catalyzed intramolecular arylation at the C-6 position of uracil moiety was examined. Morita-Baylis-Hillman adducts bearing an uracil moiety at the primary position served an efficient way to a benzo[c]pyrimido[1,6-a]azepine scaffold.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Hyun Seung Lee, Ko Hoon Kim, Se Hee Kim, Jae Nyoung Kim,
![First Page Preview: Palladium-catalyzed synthesis of benzo[c]pyrimido[1,6-a]azepine scaffold from Morita-Baylis-Hillman adducts: intramolecular 6-arylation of uracil nucleus Palladium-catalyzed synthesis of benzo[c]pyrimido[1,6-a]azepine scaffold from Morita-Baylis-Hillman adducts: intramolecular 6-arylation of uracil nucleus](/preview/png/5267639.png)