| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5276009 | Tetrahedron Letters | 2012 | 4 Pages |
Abstract
Several 3-substituted pyrido[1,2,5]triazepin-4-ones and their benzo counterparts have been prepared in three steps from commercial starting materials. The key step involves SNAr-type intramolecular nucleophilic aromatic substitution of the appropriate hydrazone substrates.
Graphical abstractDownload full-size image
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
![Rapid access to pyrido[1,2,5]triazepin-4-ones through intramolecular nucleophilic aromatic substitution](/preview/png/5276009.png "First Page Preview: Rapid access to pyrido[1,2,5]triazepin-4-ones through intramolecular nucleophilic aromatic substitution")
Authors
Shujuan Jin, Olivier St-Jean, Sandra I. Baltatu, Vijayaratnam Santhakumar, MirosÅaw J. Tomaszewski,