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- W2140424719 abstract "The reaction of acyclic enaminones with methoxymethylene Meldrum's acid afforded N-adduct and/or C-adduct of enaminones in moderate to good yields. The regiochemistry of this reaction depends on the N-amino substituent of the enaminone. The C-adduct is a precursor to 2-pyridones. X-ray analysis of two N-adducts were investigated and the Z-s-Z configuration assigned." @default.
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- W2140424719 date "2003-01-01" @default.
- W2140424719 modified "2023-09-24" @default.
- W2140424719 title "Reaction of acyclic enaminones with methoxymethylene meldrum's acid: synthetic and structural implications" @default.
- W2140424719 doi "https://doi.org/10.1590/s0103-50532003000100017" @default.
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