Modular synthesis of cyclic peptidomimetics inspired by gamma-turns
Title | Modular synthesis of cyclic peptidomimetics inspired by gamma-turns |
Publication Type | Journal Article |
Year of Publication | 2005 |
Authors | Ramanathan, SK, Keeler, J, Lee, HL, D. Reddy, S, Lushington, G, Aube, J |
Journal | Organic Letters |
Volume | 7 |
Issue | 6 |
Pagination | 1059-1062 |
Date Published | MAR |
Abstract | A series of peptidomimetics based on a gamma-turn motif were synthesized using a modular approach, in which N-protected piperidones were reacted with a selection of 2-hydroxyalkyl azides derived from common L-amino acids. Hydrolysis of the initially formed iminium ethers afforded the targeted series of substituted 1,4-diazepin-5-ones. |
DOI | 10.1021/ol047323a |
Type of Journal (Indian or Foreign) | Foreign |
Impact Factor (IF) | 6.732 |
Divison category:
Organic Chemistry