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- W2018707498 abstract "Tonghaosu, 2-[(Z)-hexa-2,4-diynylidene]-1,6-dioxaspiro[4,4]non-3-ene (1a), and its spiroketal enol ether analogues (1b–d and 2) were efficiently converted into interesting cyclopentenone derived oxabicyclic compounds. By applying this reaction protocol the natural product chrycorin was easily synthesized in its racemic form. A reaction mechanism for this is proposed." @default.
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- W2018707498 date "2002-07-05" @default.
- W2018707498 modified "2023-09-26" @default.
- W2018707498 title "Acid catalysed rearrangement of a spiroketal enol ether. An easy synthesis of chrycorin" @default.
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- W2018707498 doi "https://doi.org/10.1039/b205229f" @default.
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