Prediction of the kinetic stability of N ‐alkyl‐X‐pyridinium ions in dichloromethane
Author:
Affiliation:
1. Faculty of Pharmacy and Biochemistry University of Zagreb Zagreb Croatia
Publisher
Wiley
Subject
Organic Chemistry,Physical and Theoretical Chemistry
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/poc.4248
Reference32 articles.
1. Pyridinium salts: from synthesis to reactivity and applications
2. New insights into aliphatic nucleophilic substitution reactions from the use of pyridines as leaving groups
3. Kinetics and mechanism of nucleophilic displacements with heterocyclics as leaving groups. Part 24. Rates and mechanism for the solvolysis of N-tert-alkylpyridinium cations in a variety of solvents
4. Solvolytic reactivity of pyridinium ions
5. Nucleofugalities of Neutral Leaving Groups in 80 % Aqueous Acetonitrile
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1. A DFT Model Reaction and a Procedure for Predicting the Nucleofugality of Tertiary Heterocyclic Amines;Croatica Chemica Acta;2023
2. Nucleofugality of diphenylphosphinate and kinetic stabilities of secondary and tertiary benzylic diphenylphosphinates in aqueous solvents;International Journal of Chemical Kinetics;2022-07
3. Mechanism of solvolysis of substituted benzyl chlorides in aqueous ethanol;Tetrahedron;2022-01
4. Mechanism of Solvolyses of Substituted Benzyl Bromides in 80 % Ethanol;Croatica Chemica Acta;2022
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