The evaluation of chemoselectivity in multicomponent domino Knoevenagel/Diels-Alder reaction: A DFT study

Herein, the chemoselectivity of the multicomponent domino Knoevenagel/Diels-Alder reaction is investigated in terms of theoretical calculations. The structures of reagents, transition states, intermediates and products are optimized at the M062X/6-31+G(d,p) level of theory. The reaction mechanism involves processes of bond rotation, isomerization, asymmetric cycloaddition, acid-base and nucleophile-electrophile competitions, which are studied for the purpose of delivering a clear information of the mechanism in terms of chemoselectivity considerations. Accordingly, the chemoselectivity of the reaction is controlled by the releasing acetone during the decomposition of Meldrum acid in the presence of methanol and L-proline (Delta G(#) = 61.45 kcal** mol(-1)). Comparing calculated results (gas and solvent phase) with the experimental ones showed that using these reagents are the kinetical favourite path for the chemoselective multicomponent cascade Knoevenagel/Diels-Alder reaction to produce the predominant product (>95 %). The results suggest that the creation of cis-spiro cyclohexanone is the predominant chemoselective product under kinetic control of the desired enone.

Automated summary

The chemoselectivity of the multicomponent domino Knoevenagel/Diels-Alder reaction was investigated using theoretical calculations. The reaction mechanism was found to be controlled by the release of acetone during the decomposition of Meldrum acid, leading to the predominant product formation.