Synfacts 2006(5): 0420-0420  
DOI: 10.1055/s-2006-934393
Synthesis of Natural Products and Potential Drugs
© Georg Thieme Verlag Stuttgart · New York

Synthesis of Fostriecin and 8-epi-Fostriecin

Contributor(s): Philip Kocienski, Fiona Black
K. Maki, R. Motoki, K. Fujii, M. Kanai, T. Kobayashi, S. Tamura, M. Shibasaki*
The University of Tokyo, Japan
Further Information

Publication History

Publication Date:
21 April 2006 (online)

Significance

Fostriecin is a cytotoxic antibiotic isolated from Streptomyces pulveraceus. A synthetic route to fostriecin and 8-epi-fostriecin is reported in which all four stereocenters are installed using catalytic asymmetric methods. An enantio­selective cyanosilylation protocol developed within the group was employed to form the C-8 stereo­center in C. Both enantiomers were synthesized with high enantioselectivity by changing the metal of the catalyst from titanium to gadolinium thus allowing the synthesis of both Fostriecin and 8-epi-Fostriecin.