Kinetic Studies on SN Ar Reactions of Substituted Benzofurazan Derivatives: Quantification of the Electrophilic Reactivities and Effect of Amine Nature on Reaction Mechanism-Reference-Cited by-同舟云学术

Kinetic Studies on SN Ar Reactions of Substituted Benzofurazan Derivatives: Quantification of the Electrophilic Reactivities and Effect of Amine Nature on Reaction Mechanism

Published:2017-10-26 Issue:12 Volume:49 Page:835-846
ISSN:0538-8066
Container-title:International Journal of Chemical Kinetics
language:en
Short-container-title:Int. J. Chem. Kinet.

Author:

Raissi H.¹,Jamaoui I.¹,Goumont R.²,Boubaker T.¹

Affiliation:

1. Laboratoire C.H.P.N.R; Faculté des Sciences de Monastir; Université de Monastir; 5019 Monastir Tunisie

2. Institut Lavoisier de Versailles; UMR 8180; Université de Versailles; 78035 Versailles Cedex France

Publisher

Wiley

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Reference47 articles.

1. Ranking the Reactivity of Superelectrophilic Heteroaromatics on the Electrophilicity Scale

2. Kinetics and mechanism of phenoxide anions addition to 4-nitrobenzofurazan in aqueous solution

3. Single-Electron Transfer in σ-Complexation Reactions of 2,6-Dimethoxy-3,5-dinitropyridine with Para-X-phenoxide Anions in Aqueous Solution

4. Nucleophilicities of Para-Substituted Phenoxide Ions in Water and Correlation Analysis

5. Water and hydroxide ion pathways in the σ-complexation of superelectrophilic 2-aryl-4,6-dinitrobenzotriazole 1-oxides in aqueous solution. A kinetic and thermodynamic study

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