Total Synthesis of (+)-Azinothricin and (+)-Kettapeptin
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...
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| Veröffentlicht in: | Organic letters 2009-02, Vol.11 (3), p.733-736 |
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| container_issue | 3 |
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| container_title | Organic letters |
| container_volume | 11 |
| creator | Hale, Karl J Manaviazar, Soraya George, Jonathan H Walters, Marcus A Dalby, Stephen M |
| description | 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. |
| doi_str_mv | 10.1021/ol802817t |
| format | Article |
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| fulltext | fulltext |
| identifier | ISSN: 1523-7060 |
| ispartof | Organic letters, 2009-02, Vol.11 (3), p.733-736 |
| issn | 1523-7060 1523-7052 |
| language | eng |
| recordid | cdi_proquest_miscellaneous_66859372 |
| source | MEDLINE; ACS Publications |
| subjects | Depsipeptides - chemical synthesis Depsipeptides - chemistry Esters Molecular Structure Peptides - chemical synthesis Peptides - chemistry Stereoisomerism |
| title | Total Synthesis of (+)-Azinothricin and (+)-Kettapeptin |
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