Journal
ORGANIC LETTERS
Volume 11, Issue 3, Pages 733-736Publisher
AMER CHEMICAL SOC
DOI: 10.1021/ol802817t
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Funding
- Novartis Pharma AG
- Queen's University Belfast
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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.
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