Abstract
(Chemical Equation Presented) Apoptolidins A-D are microbial secondary metabolites shown to be selectively cytotoxic against several cancer cell lines and noncytotoxic against normal cells. Total syntheses of apoptolidinones A and D are reported. The efficient synthetic strategy leading to the apoptolidinones features construction of the common 20-membered macrolactone by an intramolecular Suzuki reaction and stereocontrolled aldol reactions establishing the C19/C20 and C22/C23 stereocenters. In contrast to apoptolidin A, the aglycones apoptolidinone A and D were shown to be noncytotoxic when evaluated against human lung cancer cells (H292). © 2008 American Chemical Society.
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CITATION STYLE
Ghidu, V. P., Wang, J., Wu, B., Liu, Q., Jacobs, A., Marnett, L. J., & Sulikowski, G. A. (2008). Synthesis and evaluation of the cytotoxicity of apoptolidinones A and D. Journal of Organic Chemistry, 73(13), 4949–4955. https://doi.org/10.1021/jo800545r
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