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.
Original language | English |
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Pages (from-to) | 733-736 |
Number of pages | 4 |
Journal | Organic Letters |
Volume | 11 |
Issue number | 3 |
Early online date | 06 Jan 2009 |
DOIs | |
Publication status | Published - 05 Feb 2009 |
ASJC Scopus subject areas
- Organic Chemistry
- Physical and Theoretical Chemistry
- Biochemistry