Dependence of the reactivity of five-membered aromatic heterocycles on their structure. 2. Effect of aza substitution on the proton affinity of aminofurans

M. A. Shokhen; V. G. Andrianov; A. V. Eremeev; S. V. Barmina

doi:10.1007/bf00663849

Dependence of the reactivity of five-membered aromatic heterocycles on their structure. 2. Effect of aza substitution on the proton affinity of aminofurans

M. A. Shokhen, V. G. Andrianov, A. V. Eremeev, S. V. Barmina

Latvian Academy of Sciences

Research output: Contribution to journal › Article › peer-review

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.

Original language	English
Pages (from-to)	143-146
Number of pages	4
Journal	Chemistry of Heterocyclic Compounds
Volume	23
Issue number	2
DOIs	https://doi.org/10.1007/bf00663849
State	Published - Feb 1987
Externally published	Yes

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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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Dependence of the reactivity of five-membered aromatic heterocycles on their structure. 2. Effect of aza substitution on the proton affinity of aminofurans

Abstract

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