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- W1970985989 abstract "Condensation of Betti base analogue amino naphthols with substituted benzaldehydes led to 1,3-diaryl-2,3-dihydro-1H-naphth[1,2-e][1,3]oxazines (3–9) which proved to be three-component (r1–o–r2) tautomeric mixtures in CDCl3 at 300 K. The electronic effects of the 3-aryl groups on the ratios of the ring-chain tautomeric forms at equilibrium could be described by the equation log KX=ρσ++log KX=H. The value of the intercept was found to be strongly influenced by the steric arrangement of the 1,3-diaryl substituents." @default.
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- W1970985989 date "2003-04-01" @default.
- W1970985989 modified "2023-09-23" @default.
- W1970985989 title "Substituent effects in the ring-chain tautomerism of 1,3-diaryl-2,3-dihydro-1H-naphth[1,2-e][1,3]oxazines" @default.
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- W1970985989 doi "https://doi.org/10.1016/s0040-4020(03)00331-4" @default.
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