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- W3201112309 abstract "The first total synthesis of the antimalarial natural product chaetoxanthone B is described. The synthesis was completed in five steps from commercially available materials in 21% overall yield. A Heck coupling reaction provided the key aryl alkene intermediate that yielded chaetoxanthone B upon acid catalyzed intramolecular ketalization to form the dioxane/tetrahydropyran ring system." @default.
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- W3201112309 date "2021-10-01" @default.
- W3201112309 modified "2023-10-14" @default.
- W3201112309 title "Total synthesis of (±)-chaetoxanthone B" @default.
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- W3201112309 doi "https://doi.org/10.1016/j.tetlet.2021.153390" @default.
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