Modular synthesis of cyclic peptidomimetics inspired by gamma-turns

TitleModular synthesis of cyclic peptidomimetics inspired by gamma-turns
Publication TypeJournal Article
Year of Publication2005
AuthorsRamanathan, SK, Keeler, J, Lee, HL, D. Reddy, S, Lushington, G, Aube, J
JournalOrganic Letters
Volume7
Issue6
Pagination1059-1062
Date PublishedMAR
AbstractA 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.
DOI10.1021/ol047323a
Type of Journal (Indian or Foreign)Foreign
Impact Factor (IF)6.732
Divison category: 
Organic Chemistry