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- W2936607568 abstract "To shed more insight into the regioselectivities observed in the reactions between 3,5-diaminopyrazoles and N-acyl imidates or N-ethoxy imidate yielding the corresponding substituted pyrazolo[1,5-a]-[1,3,5] triazines or pyrazolo[1,5-a][1,3,5] triazinones, DFT calculations are carried out using B3LYP/6-31++G (d, p) method. The favored mechanism and the experimental regioselectivity of this reaction are rationalized by calculations of activation energy, natural atomic charge, and Fukui indexes derived from density functional theory. The present study shows that the experimental trends of the relative reactivities and regioselectivities of these reactions are correctly predicted using these computational levels." @default.
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- W2936607568 date "2019-07-01" @default.
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- W2936607568 title "Theoretical study of the mechanism and regioselectivity in the formation of pyrazolo[1,5-a]-[1,3,5]-triazines and pyrazolo[1,5-a]-[1,3,5]triazinones: A DFT study" @default.
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- W2936607568 doi "https://doi.org/10.1016/j.cplett.2019.04.054" @default.
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