2013•Journal of Natural ProductsRequires access

Total Synthesis of the Marine Cyclic Depsipeptide Viequeamide A

Dongyu Wang, Shanshan Song, Ye Tian, Youjun Xu, Ze‐Hong Miao, Ao Zhang

Open publisher page 19 citations

Abstract

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.

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What this paper is about

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.

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OpenAlex reports 19 citations for this work. Citation counts describe recorded attention and do not establish research quality.

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Available abstract

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.

Key concepts: Depsipeptide, Natural product, Total synthesis, Cyclic peptide, Stereochemistry, Chemistry, Peptide, Combinatorial chemistry

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