Abstract
Transformations of diepoxy derivatives of terpinolene under conditions of homogeneous and heterogeneous acid catalysis were studied. Qualitative and quantitative compositions of the reaction mixtures were found to depend on the acidity of the medium and mutual orientation of the epoxide rings in the p-menthane skeleton. The experimental data were compared with the results of computer simulation of the most probable transformation pathways in terms of molecular mechanics and quantum-chemical methods.
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