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- W2950267074 abstract "α-Lithiated alkylphosphonic esters react with substituted cyclohex-2-enones either at the carbonyl group (addition yielding 2-hydroxyalkylphosphonic products) or at the β-carbon (addition–elimination yielding δ-keto phosphonates). Both types of products undergo smooth aromatization when treated with I2 in MeOH or with pyridinium perbromide in AcOH leading to a variety of benzylphosphonic esters substituted in the aromatic ring with the methoxy or hydroxy groups. Mechanisms of the aromatization reactions are discussed." @default.
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- W2950267074 date "2010-08-04" @default.
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- W2950267074 title "ChemInform Abstract: Reaction of Phosphorus-Stabilized Carbanions with Cyclic Enones. Aromatization of the Substitution and Addition Products." @default.
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- W2950267074 doi "https://doi.org/10.1002/chin.199640166" @default.
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