| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5285266 | Tetrahedron Letters | 2008 | 4 Pages |
Abstract
Under near neutral and mildly basic conditions, primary N4-(α-aminoacyl)cytidines (4a-g) undergo a facile rearrangement to form N-(4-cytidinyl)amino acid amides (5a-g). Secondary aminoacyl derivatives rearrange with other competing pathways. Tertiary aminoacyl derivatives do not rearrange.
Keywords
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Deyi Zhang, David M. Bender, Frantz Victor, Jeffrey A. Peterson, Robert D. Boyer, Gregory A. Stephenson, Adam Azman, James R. McCarthy,