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|Title:||Total Synthesis of (+)-Azinothricin and (+)-Kettapeptin|
|Citation:||Organic Letters, 2009; 11(3):733-736|
|Publisher:||Amer Chemical Soc|
|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|
|Appears in Collections:||Chemistry publications|
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