1257329-16-0Relevant articles and documents
A highly stereoselective total synthesis of (+)-9-epi-dictyostatin
Zanato, Chiara,Pignataro, Luca,Ambrosi, Andrea,Hao, Zhongyan,Gennari, Cesare
, p. 5767 - 5771 (2010)
The total synthesis of (+)-9-epi-dictyostatin (1b), a diastereomer of the antimitotic marine-sponge-derived macrolide (-)-dictyostatin (1a), was achieved by creating 11 stereogenic centers and 4 stereogenic double bonds with a high level of stereocontrol.
Highly stereoselective total synthesis of (+)-9-epi-Dictyostatin and (-)-12,13-Bis-epi-dictyostatin
Zanato, Chiara,Pignataro, Luca,Ambrosi, Andrea,Hao, Zhongyan,Trigili, Chiara,Diaz, Jose Fernando,Barasoain, Isabel,Gennari, Cesare
, p. 2643 - 2661 (2011/06/25)
The total syntheses of (+)-9-epi-dictyostatin (1a) and (-)-12,13-bis-epi- dictyostatin (1b), diastereomers of the antimitotic marine sponge-derived macrolide (-)-dictyostatin (1), were achieved by creating 11 stereogenic centers and 4stereogenic double bonds with a high level of stereocontrol. The yield for the 29-step longest linear sequence from Roche ester was 1.53 and 1.52%, respectively. The final key steps to these unnatural products were the addition of vinylzincates C10-C26 to aldehyde C1-C9 (leading surprisingly to complete stereoselectivity for the 9R-configuration in 28a and for the 9S-configuration in 12,13-bis-epimeric 28b), followed by Yamaguchi macrolactonization and global deprotection. (-)-12,13-Bis-epi-dictyostatin (1b) displayed a dramatic decrease of cytotoxicity and of the affinity toward the paclitaxel binding site of microtubules. Eleven stereogenic centers and fourstereogenic double bonds were obtained with a high level of stereocontrol in the total synthesis of (+)-9-epi-dictyostatin and(-)-12,13-bis-epi-dictyostatin, diastereomers of the antimitotic marine sponge-derived macrolide (-)-dictyostatin.