Abstract
(graph presented) A strategy for synthesis of the hexahydroxanthene moiety of the natural products schweinfurthin A, B, and D is described. The relative stereochemistry in the key cationic cyclization step is established through the preference of the phenylselenide substituent for an equatorial orientation.
Cite
CITATION STYLE
APA
Treadwell, E. M., Neighbors, J. D., & Wiemer, D. F. (2002). A cascade cyclization approach to schweinfurthin B. Organic Letters, 4(21), 3639–3642. https://doi.org/10.1021/ol0266368
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.
Already have an account? Sign in
Sign up for free