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- W2009371572 abstract "Amphidinolide X, a 16-membered cytotoxic macrodiolide, and its 12Z-isomer have been synthesized via ring-closing metathesis (RCM) for assembling the C12-C13 trisubstituted double bond. A 29:71 E/Z mixture was obtained from the seco substrate appended with a bulky C8-ODPS group in 50-65% combined yields by using 20 mol% of the second-generation Grubbs initiator and the corresponding indenylidene ruthenium complex. Amphidinolide X and 12Z-isomer exhibit similar cytotoxicity (IC50: 7.6-13.9 µg/mL) against A549, KB, and HL60 cell lines." @default.
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- W2009371572 date "2008-06-11" @default.
- W2009371572 modified "2023-09-30" @default.
- W2009371572 title "Total Synthesis of Amphidinolide X and Its 12<i>Z</i>-Isomer by Formation of the C12-C13 Trisubstituted Double Bond via Ring-Closing Metathesis" @default.
- W2009371572 doi "https://doi.org/10.1055/s-2008-1077885" @default.
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