Total Synthesis of the Marine Cyclic Depsipeptide Viequeamide A
journal contributionposted on 24.05.2013 by Dongyu Wang, Shanshan Song, Ye Tian, Youjun Xu, Zehong Miao, Ao Zhang
Any type of content formally published in an academic journal, usually following a peer-review process.
The first total synthesis of viequeamide A, a natural cyclic depsipeptide isolated from a marine button cyanobacterium, was achieved with the N-Me-Val–Thr peptide bond as the final macrocyclization site. The synthetic product gave nearly identical spectroscopic data to that reported for the natural product.