The reactions of O -(4-nitrophenyl) S -aryl dithiocarbonates with anilines: Effects on the relative nucleofugality
Author:
Affiliation:
1. Facultad de Química; Pontificia Universidad Católica de Chile; Casilla 306 Santiago 6094411 Chile
2. Centro de Química Médica, Facultad de Medicina; Clínica Alemana Universidad del Desarrollo; Santiago 7710162 Chile
Publisher
Wiley
Subject
Organic Chemistry,Physical and Theoretical Chemistry
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/poc.3818/fullpdf
Reference28 articles.
1. Kinetics and Mechanisms of Reactions of Thiol, Thiono, and Dithio Analogues of Carboxylic Esters with Nucleophiles
2. Mechanistic study on the substitution reactions ofO-ethylS-aryl dithiocarbonates with quinuclidines
3. Kinetics and mechanism of the aminolysis of thioesters and thiocarbonates in solution
4. Kinetics and mechanism of the aminolysis of O-ethyl S-aryl dithiocarbonates in acetonitrile
5. Kinetics and Mechanism of the Aminolysis of S-Aryl O-Ethyl Dithiocarbonates in Acetonitrile
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1. Kinetic study on pyridinolysis of aryl benzenesulfonates: factors governing regioselectivity and reaction mechanism;Canadian Journal of Chemistry;2022-05
2. Nucleofugality hierarchy, in the aminolysis reaction of 4-cyanophenyl 4-nitrophenyl carbonate and thionocarbonate. Experimental and theoretical study;New Journal of Chemistry;2021
3. The effect of the electrophilic group on the hierarchy of nucleofuges in the aminolysis reactions of thiol- and dithiocarbonates with secondary alicyclic amines: A kinetic and theoretical study;New Journal of Chemistry;2019
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