Abstract
The total synthesis of d,l-hapalindoles J and U has been accomplished. Hapalindole J was prepared in 11% overall yield over 11 synthetic steps and hapalindole U was prepared in 25% overall yield over 13 synthetic steps from commercially available materials. The route employs a novel silyl ether-based strategy for accessing the 6:5:6:6 ring system of the hapalindoles rapidly and in good yields. © 2011 American Chemical Society.
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CITATION STYLE
APA
Rafferty, R. J., & Williams, R. M. (2012). Total synthesis of hapalindoles J and U. Journal of Organic Chemistry, 77(1), 519–524. https://doi.org/10.1021/jo202139k
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