Abstract
The proton affinities of a series of aminofurans and their aza derivatives were calculated by a nonempirical method in the STO-3G basis set. A correlation was established between the proton affinities and the position of the heteroatoms in the ring.
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For Communication 1, see [1].
Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 2, pp. 175–178, February, 1987.
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Shokhen, M.A., Andrianov, V.G., Eremeev, A.V. et al. Dependence of the reactivity of five-membered aromatic heterocycles on their structure. 2. Effect of aza substitution on the proton affinity of aminofurans. Chem Heterocycl Compd 23, 143–146 (1987). https://doi.org/10.1007/BF00663849
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DOI: https://doi.org/10.1007/BF00663849