Computation and structural elucidation of compounds formed via epoxide alcoholysis

• Autor(a) principal: Alvarenga, Elson S.
• Data de Publicação: 2019
• Outros Autores: Teixeira, Milena G., Lopes, Dayane T., Demuner, Antonio J.
• Tipo de documento: Artigo
• Idioma: eng
• Título da fonte: LOCUS Repositório Institucional da UFV
• Texto Completo: http://dx.doi.org/10.1002/mrc.4818; http://www.locus.ufv.br/handle/123456789/24259
• topic: 13C NMR; 1H NMR; DP4; Epoxide; Isobenzofuranone; MAE; Phthalides; γ‐lactones

Isobenzofuranones are known for their wide range of biological activities such as fungicide, insecticide, and anticancer. The search for novel bioactive compounds was performed by reaction of epoxide 2 with methanol, ethanol, propan‐1‐ol, propan‐2‐ol, and butan‐1‐ol. The mechanism for the stereoselective and stereospecific epoxide opening with methanol was reasoned by calculating the transition states for the two putative structures (rac)‐3a and (rac)‐3b. The compound (rac)‐3a is the kinetic product as inferred from the lower energies of its transition state (TS1). The 1H and 13C nuclear magnetic resonance (NMR) chemical shifts for these two candidate structures were calculated and compared with the experimental data using mean absolute error (MAE) and DP4 analyses. Therefore, the relative stereochemistry of (rac)‐3a was established by the mechanism, MAE, and DP4 approaches. The hydroxyl group was acetylated to surpass the problem of signal overlapping of H5 and H6 in the 1H NMR. The relative stereochemistry of the corresponding ester determined by NMR interpretation was in agreement with the structure of (rac)‐3a.