Adelaide Research & Scholarship
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https://hdl.handle.net/2440/68627
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| Type: | Journal article |
| Title: | Total Synthesis of (+)-Azinothricin and (+)-Kettapeptin |
| Author: | Hale, K. Manaviazar, S. George, J. Walters, M. Dalby, S. |
| Citation: | Organic Letters, 2009; 11(3):733-736 |
| Publisher: | Amer Chemical Soc |
| Issue Date: | 2009 |
| ISSN: | 1523-7060 1523-7052 |
| Statement of Responsibility: | Karl J. Hale, Soraya Manaviazar, Jonathan H. George, Marcus A. Walters, and Stephen M. Dalby |
| Abstract: | Asymmetric total syntheses of (+)-azinothricin and (+)-kettapeptin have been completed through a common new pathway that exploits a highly chemoselective coupling reaction between the fully elaborated cyclodepsipeptide 5 and the glycal activated esters 3 and 4 at the final stages of both respective syntheses. |
| Keywords: | Esters Depsipeptides Peptides Molecular Structure Stereoisomerism |
| Rights: | Copyright © 2009 American Chemical Society |
| DOI: | 10.1021/ol802817t |
| Published version: | http://dx.doi.org/10.1021/ol802817t |
| Appears in Collections: | Aurora harvest Chemistry publications |
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