Design and synthesis of tubulin ligands based on epothilones: a preliminary study
β Scribed by Sophie Vielle; Eric Raimbaud; Philippe Bertrand; Delphine Quintard; Pierre Renard; Bruno Pfeiffer; Jean-Pierre Gesson
- Book ID
- 104252399
- Publisher
- Elsevier Science
- Year
- 2002
- Tongue
- French
- Weight
- 162 KB
- Volume
- 43
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
Starting from the X-ray structure of epothilone B, an original, non macrocyclic, structure has been designed to mimic the key structural features of this potent anticancer agent; the preparation of a key intermediate incorporating four stereogenic centers is described from cyclohexane-1,3-dione.
π SIMILAR VOLUMES
The synthesis of new unsymmetrical and symmetrical macrocycles based on 2,2'-bipyridine units bearing two or four phenyl groups at the 6 and 6' positions was achieved by an oxidative coupling reaction using 1,2-dibromoethane and organolithium derivatives of bipyridine. Among all new compounds prepar
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