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- W2004977103 abstract "The first synthesis of squamostanal-A (1), separated as a degradation product of tetrahydrofuranic acetogenins, is described. Iodide 7, which corresponds to the latent aldehyde moiety of 1, was prepared through a 2-step sequence from 13-[tetrahydropyran-2'- yloxy]-2-tridecyn-l-ol (5). The NaHMDS-based coupling reaction of 7 with γ-lactone 8 gave compound 9, which by a 3-step sequence, was coverted to 1." @default.
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- W2004977103 date "1996-01-01" @default.
- W2004977103 modified "2023-10-17" @default.
- W2004977103 title "Synthesis of Squamostanal-A" @default.
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- W2004977103 doi "https://doi.org/10.1271/bbb.60.526" @default.
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