A theoretical DFT investigation of the reaction of 3,4-dihydro-2H-pyrrole-1-oxide (nitrone) with two alkenes cis- and trans-2-butene has been thoroughly probed at B3LYP/6-31G(d) level of theory. The regioselectivity as well as the detailed mechanism of reaction has been studied and analyzed. The reaction is characterized by a concerted asynchronous mechanism and the products P2 and P4 are the most favorable products kinetically and thermodynamically. A good agreement with the experimental data has been found.
Primary Language | English |
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Subjects | Physical Chemistry (Other) |
Journal Section | Research Article |
Authors | |
Early Pub Date | January 16, 2025 |
Publication Date | |
Submission Date | September 2, 2024 |
Acceptance Date | December 29, 2024 |
Published in Issue | Year 2025 Volume: 9 Issue: 4 |
Journal Full Title: Turkish Computational and Theoretical Chemistry
Journal Abbreviated Title: Turkish Comp Theo Chem (TC&TC)