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- W1995704042 endingPage "2786" @default.
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- W1995704042 abstract "Synthetic approaches to the furanocembrane family of natural products, e.g. lophotoxins, pukalides, bipinnatins, based on: i) an intramolecular cyclisation of an α,β-unsaturated acyl radical intermediate into a conjugated enone, viz.18 → 17, and ii) an intramolecular Stille coupling reaction involving a 2-stannylfuran and a vinyl iodide, i.e.67 → 68, are described. A total synthesis of bis-deoxylophotoxin 71a, the probable biological precursor to the neurotoxin lophotoxin 1, isolated from species of the Pacific sea whip Lophogorgia, is then presented." @default.
- W1995704042 created "2016-06-24" @default.
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- W1995704042 date "2005-01-01" @default.
- W1995704042 modified "2023-10-10" @default.
- W1995704042 title "Synthetic studies towards furanocembrane diterpenes. A total synthesis of bis-deoxylophotoxin" @default.
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- W1995704042 doi "https://doi.org/10.1039/b504545b" @default.
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