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Electron-topological, energetic and π-electron delocalization analysis of ketoenamine-enolimine tautomeric equilibrium
The ketoenamine-enolimine tautometic equilibrium has been studied by the analysis of aromaticity and electron-topological parameters. The influence of substituents on the energy of the transition state and of the tautomeric forms has been investigated for different positions of chelate chain. The qu...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer-Verlag
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3249559/ https://www.ncbi.nlm.nih.gov/pubmed/21523531 http://dx.doi.org/10.1007/s00894-011-1075-7 |