Evidence derived largely from studies of monamycins D1 and H1 in solution using 1H n.m.r., 13C n.m.r., and i.r. spectroscopy supports a single conformation (Figure 6) for each congener. It incorporates a β-loop with hydrogen bonding of the NH groups of the Val residue to the carbonyl of the hydroxypiperazic acid residue.
C. H. Hassall, W. A. Thomas and M. C. Moschidis, J. Chem. Soc., Perkin Trans. 1, 1977, 2369 DOI: 10.1039/P19770002369
To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.
If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.
If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.
Read more about how to correctly acknowledge RSC content.
Please wait while we load your content...