β N-O turns and helices induced by β2-aminoxy peptides: synthesis and conformational studies.

Abstract

Herein, we report an efficient route for the asymmetric synthesis of β(2)-aminoxy acids as well as experimental and theoretical studies of conformations of peptides composed of β(2)-aminoxy acids. The nine-membered-ring intramolecular hydrogen bonds, namely, β N-O turns, are generated between adjacent residues in those peptides, in accordance with our… (More)
DOI: 10.1002/asia.201000933

Topics

Cite this paper

@article{Jiao2011NT, title={β N-O turns and helices induced by β2-aminoxy peptides: synthesis and conformational studies.}, author={Zhi-gang Jiao and Xiao-wei Chang and Wei Ding and Guo-jun Liu and Ke-Sheng Song and Nian-Yong Zhu and Dan-Wei Zhang and D. H. Yang}, journal={Chemistry, an Asian journal}, year={2011}, volume={6 7}, pages={1791-9} }