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• W2059762993 abstract "Density functional (B3LYP) calculations, using the 6-31G basis set, have been employed to study the title reactions. For the model reaction (H(2)C=C-NH(+)=CH(2) + H(2)C=CH(2)), a complex has been formed with 6.2 kcal/mol of stabilization energy and the transition state is 4.0 kcal/mol above this complex, but 2.1 kcal/mol below the reactants. However, the substituent effects are quite remarkable. When ethene is substituted by electron-withdrawing group CN, the reaction could also yield six-membered-ring products, but the energy barriers are all more than 7 kcal/mol, which shows that CN group unfavors the reaction. The other substituents, such as CH(3)O and CH(3) groups, have also been considered in the present work, and the results show that they are favorable for the formation of six-membered-ring adducts. The calculated results have been rationalized with frontier orbital interaction and topological analysis." @default.
• W2059762993 created "2016-06-24" @default.
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• W2059762993 date "2003-04-29" @default.
• W2059762993 modified "2023-09-25" @default.
• W2059762993 title "Theoretical Studies on Cycloaddition Reactions between the 2-Aza-1,3-butadiene Cation and Olefins" @default.
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• W2059762993 doi "https://doi.org/10.1021/jo0340713" @default.
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