Tetrahydroxanthones by Sequential Pd-Catalyzed C鈭扥 and C鈭扖 Bond Construction and Use in the Identification of the 鈥淎ntiausterity鈥?Pharmacophore of the Kigamicins
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文摘
Readily available C-acylated cycloalkanones undergo efficient Pd catalyzed ring closure/cross-coupling providing 7-substituted tetrahydroxanthones in a single operation. One of the synthesized derivatives (depicted) is shown to selectively kill pancreatic cancer (PANC-1) cells under conditions of nutrient deprivation indicating that the tetrahydroxanthone is responsible, in part, for the 鈥渁ntiausterity鈥?effects of the naturally occurring kigamicins.

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