Structure−Reactivity Correlations in the Aminolysis of Ethyl S-Aryl Thiolcarbonates
Author:
Affiliation:
1. Facultad de Química, Pontificia Universidad Católica de Chile, Casilla 306, Santiago 22, Chile
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo990531%2B
Reference31 articles.
1. Stepwise Mechanism of the Aminolysis of O-Ethyl S-(4-Nitrophenyl) Thiocarbonate
2. Kinetics and Mechanism of the Pyridinolysis of O-Ethyl S-Aryl Thiocarbonates in Aqueous Solution
3. Concerted mechanism of the aminolysis of O-ethyl S-(2,4-dinitrophenyl) thiocarbonate
4. Concerted mechanism of the reactions of secondary alicyclic amines with O-ethyl S-(2,4,6-trinitrophenyl) thiocarbonate
5. Kinetics and Mechanism of the Reactions of Anilines with Ethyl S-Aryl Thiocarbonates
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1. Predicting the reaction mechanism of nucleophilic substitutions at carbonyl and thiocarbonyl centres of esters and thioesters;Journal of Physical Organic Chemistry;2012-12
2. Kinetics and mechanism of the reactions of methyl 2,4,6-trinitrophenyl carbonate with anilines;Arkivoc;2010-12-26
3. Kinetics and Mechanism of Pyridinolysis of Aryl Dithiocyclopentanecarboxylates in Acetonitrile;Bulletin of the Korean Chemical Society;2010-08-20
4. ChemInform Abstract: Structure-Reactivity Correlations in the Aminolysis of Ethyl S-Aryl Thiolcarbonates.;ChemInform;2010-06-12
5. Kinetics and mechanism of the pyridinolysis of diaryl carbonates;Journal of Physical Organic Chemistry;2008-09
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