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- W2023991666 abstract "DEOXYANISOIN is prepared by reducing anisoin on heating with alcoholic stannous chloride hydrochloric acid solution1, or tin in alcoholic hydrochloric acid solution2, or distillation with zinc in an atmosphere of carbon dioxide3. It has also been prepared by heating hydroanisoin with dilute sulphuric acid4 (the product reported by this method had a melting point of 95°, which would be 15° lower than that of pure deoxyanisoin), or with a mixture of hydrochloric and acetic acids2. Hydroanisoin itself is obtained by electrolytic reduction of anisaldehyde in alkaline solution using nickel, platinum5,6 or copper7 as cathodes, or by the action of sodium amalgam on an ethereal solution of anisoin3, or catalytic reduction of anisil or anisoin using platinum oxide2." @default.
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- W2023991666 date "1950-09-01" @default.
- W2023991666 modified "2023-09-25" @default.
- W2023991666 title "Preparation of Deoxyanisoin and some Stilbenes: Reducing Action of Sodium Glycollate in Glycols" @default.
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- W2023991666 doi "https://doi.org/10.1038/166525a0" @default.
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