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• W2950490023 startingPage "673" @default.
• W2950490023 abstract "Systematic synthesis of mono- and bis-THF ring cores, synthetic intermediates of antitumor annonaceous acetogenins, has been achieved by asymmetric alkynylation and subsequent stereodivergent THF ring formation as key steps. The asymmetric alkynylation of α-oxyaldehyde and α-tetrahydrofuranic aldehyde with (S)-3-butyne-1,2-diol derivatives gave good yield with very high diastereoselectivity. These adducts were converted into mono- and bis-THF cores via two kinds of one-pot THF ring formation, respectively. In addition, the total synthesis of murisolin, which shows cytotoxic activity against human tumor cell lines with potency from 105 to 106 times that of adriamycin, was also achieved." @default.
• W2950490023 created "2019-06-27" @default.
• W2950490023 creator A5005153343 @default.
• W2950490023 date "2004-10-01" @default.
• W2950490023 modified "2023-09-23" @default.
• W2950490023 title "Systematic Synthesis of Antitumor <i>Annonaceous</i> Acetogenins" @default.
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• W2950490023 doi "https://doi.org/10.1248/yakushi.124.673" @default.
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