| Literature DB >> 27633484 |
Linping Liao1, Jingjing Zhou1, Zhengshuang Xu2, Tao Ye3.
Abstract
Nannocystin A, a structurally unique 21-membered macrocyclic depsipeptide with low nanomolar inhibitory activity against elongation factor 1A, was synthesized according to a strategy involving the vinylogous Mukaiyama aldol reaction, Sharpless epoxidation, olefin metathesis, the Mitsunobu reaction, and a palladium-catalyzed intramolecular Suzuki coupling of a highly complex cyclization substrate. The overall synthesis is efficient and paves the way for preparation of analogues for drug development efforts.Entities:
Keywords: anticancer agents; cyclodepsipeptides; nannocystin A; natural products; total synthesis
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Year: 2016 PMID: 27633484 DOI: 10.1002/anie.201606679
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336