| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5275633 | Tetrahedron Letters | 2011 | 4 Pages |
Abstract
The total synthesis of argyrins A and E were accomplished using a convergent strategy by condensation of one tripeptide and two dipeptide fragments. The synthesis strategy, which was developed for the protection of peptide fragments and identification of the optimum macrocylization site, can be applied to further synthetic studies involving other members of the argyrin family.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Wenbin Wu, Zheng Li, Guangbiao Zhou, Sheng Jiang,