@article {43215,
	title = {Modular synthesis of cyclic peptidomimetics inspired by gamma-turns},
	journal = {Organic Letters},
	volume = {7},
	year = {2005},
	month = {MAR},
	pages = {1059-1062},
	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},
	author = {Ramanathan, S. K. and Keeler, J. and Lee, H. L. and Reddy, D. Srinavasa and Lushington, G. and Aube, J.}
}
