DFT study on the mechanism of the Diels–Alder reactions leading to bicyclo[4.2.0]octenones

The regioselectivity and mechanism of the Diels–Alder reaction (DA) between 2-substituted cyclobut-2-enones and some electron-rich 1,3-butadiene derivatives, were studied using density functional theory (DFT). Four possible reaction pathways, which are related to the formation of bicyclo[4.2.0]oct-3...

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Bibliographic Details
Published in:Progress in reaction kinetics and mechanism 2016-01, Vol.41 (1), p.67-75
Main Authors: Haghdadi, Mina, Moradi, Ali, Bosra, Hassan Ghasemnejad
Format: Article
Language:English
Subjects:
Bonding
Cycloaddition
Density functional theory
Derivatives
Diels-Alder reactions
Energy use
Formations
Pathways
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Summary:The regioselectivity and mechanism of the Diels–Alder reaction (DA) between 2-substituted cyclobut-2-enones and some electron-rich 1,3-butadiene derivatives, were studied using density functional theory (DFT). Four possible reaction pathways, which are related to the formation of bicyclo[4.2.0]oct-3-en-7-ones, were investigated using natural bond orbital analysis, geometrical parameter and energy analysis and also DFT-based reactivity indices. The energy and bond order analyses show that the larger activation energy prevents the formation of meta products. Therefore ortho products are preferred and the process follows an asynchronous concerted mechanism with a polar nature via DA cycloaddition. Moreover, high regio- and stereoselectivity have been seen in the DA reaction of 2-cyanocyclobut-2-enone.
ISSN:1468-6783
1471-406X
DOI:10.3184/146867816X14506899861213