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- W2024202362 abstract "Electrochemical reduction of 2-acetylnaphthalene gives the isomeric 2,3-di-(2-naphthyl)butane-2,3-diols in good yield. The (±)-isomer is formed in greater amount, with degree of stereoselectivity 0·27 in alkaline and 0·09 in acid solution. Synthesis of these diols from a diketone and 2-naphthylmagnesium bromide or methyl-lithium obeys Cram's rule with high stereoselectivity. Stereochemical assignments to the diols are made by an n.m.r. method." @default.
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- W2024202362 date "1971-01-01" @default.
- W2024202362 modified "2023-10-14" @default.
- W2024202362 title "Electrochemical reactions. Part IX. Reduction of 2-acetylnaphthalene. Stereochemistry of the isomeric 2,3-di-(2-naphthyl)butane-2,3-diols" @default.
- W2024202362 doi "https://doi.org/10.1039/j39710000683" @default.
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