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- W2943478612 endingPage "3308" @default.
- W2943478612 startingPage "3299" @default.
- W2943478612 abstract "An account of our previously disclosed total synthesis of the aryltetralin lignan natural product podophyllotoxin, a building block used in the synthesis of the FDA-approved anticancer drug etoposide, is disclosed. A C–H activation disconnection was viewed as being amenable to the preparation of E-ring modified analogs but proved challenging to execute. Various insights into palladium-catalyzed C–H arylation reactions on complex scaffolds are reported ultimately leading to the implementation of this strategy and the synthesis of compounds inaccessible by semisynthetic means." @default.
- W2943478612 created "2019-05-09" @default.
- W2943478612 creator A5028532942 @default.
- W2943478612 creator A5057467468 @default.
- W2943478612 creator A5068241154 @default.
- W2943478612 creator A5064485578 @default.
- W2943478612 date "2019-06-01" @default.
- W2943478612 modified "2023-10-14" @default.
- W2943478612 title "Total synthesis of podophyllotoxin and select analog designs via C–H activation" @default.
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