The preparations of the hexapeptides (3) and (6) derived from the antibiotic vancomycin (1), are described. The conformation of the N-terminal regions of (3) and (6) are discussed and compared to previous observations made on vancomycin. The hexapeptides lack any significant binding capability relative to vancomycin, and the reasons for this are discussed.
P. M. Booth and D. H. Williams, J. Chem. Soc., Perkin Trans. 1, 1989, 2335 DOI: 10.1039/P19890002335
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...