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Keto-Enol Tautomerism in the Series of 3-Substituted Chromen-2-Ones
Ist Teil von
材料科学与工程:中英文B版, 2012, Vol.2 (10), p.505-512
Erscheinungsjahr
2012
Quelle
EZB Free E-Journals
Beschreibungen/Notizen
The aim of the present work was to study the keto-enolic tautomeria of 3-substituted chromen-2-ones. The enolic and ketonic form of the substrate was found to be the predominant one in a nonpolar (CCI4) and polar solvent, respectively. Some behavior peculiarities of 3-(1-(4-dimethylaminophenyl)-3-phenylpropyl)-3H-chromen-2 were revealed, namely, enolization by an aliphatic fragment, which is untypical for substituted chromen-2-ones. The solvent effect on tautomeric equilibrium shifting is shown by means of spectral techniques (ЯМР и УФ cneKxpocronnn). A chemometric MILCA-based technique was used to estimate the contents of the ketonic and enolic forms.