For a novel family of oxanorbornene -peptides, density functional theory computations of the three-dimensional structure and 1H NMR chemical shifts predict that the dimer and trimer form consecutive 8-membered hydrogen-bonded ring helices, which is supported by excellent agreement with experimental solution NMR data
Revised: January 23, 2012 |
Published: October 22, 2003
Citation
Doerksen R., B. Chen, J. Yuan, J.D. Winkler, and M. Klien. 2003.Novel Conformationally-Constrained Beta-Peptides Characterized by 1H NMR Chemical Shifts.Chemical Communications 20.