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

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.",

author = "Shokhen, \{M. A.\} and Andrianov, \{V. G.\} and Eremeev, \{A. V.\} and Barmina, \{S. V.\}",

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AU - Barmina, S. V.

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AB - 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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