Establishment of the absolute configuration of the 34-membered polyol macrolide compound JBIR-129
Author:
Publisher
Springer Science and Business Media LLC
Subject
Drug Discovery,Pharmacology
Link
http://www.nature.com/articles/ja20147.pdf
Reference8 articles.
1. Kawahara, T. et al. JBIR-129 and -139, cytotoxic 34-membered polyol macrolides of microbial origin. J. Nat. Prod. 75, 1814–1818 (2012).
2. Kawahara, T., Izumikawa, M., Takagi, M. & Shin-ya, K. Relative configuration of JBIR-129, a cytotoxic 34-membered glycosidic polyol macrolide from Streptomyces sp. RK74. Org. Lett. 14, 4434–4437 (2012).
3. Park, H.-R., Chijiwa, S., Furihata, K., Hayakawa, Y. & Shin-ya, K. Relative and absolute configuration of versipelostatin, a down-regulator of molecular chaperone GRP78 expression. Org. Lett. 49, 1457–1460 (2007).
4. Gilleron, M., Fournié, J. J., Pougny, J. R. & Puzo, G. Synthesis and serological properties of methyl 2,6-dideoxy-4-O-Me-α-D and L-arabino-hexopyranoside present in the glycolipid phenolic antigen of Mycobactkrium kansasii. J. Carbohyd. Chem. 7, 733–748 (1988).
5. Kubo, H., Kozawa, I., Takao, K. & Tadano, K. Stereoselective synthesis of highly enantioenriched 3-methyl-2-cyclohexen-1-ones possessing an asymmetric quaternary carbon as C-4 or C-6: a sugar template approach. Tetrahedron Lett. 49, 1203–1207 (2008).
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