Dynamics of reaction of ion pairs in aqueous solution: racemization of the chiral ion pair intermediate of solvolysis of (S)-1-(4-methylphenyl)ethylpentafluorobenzoate
Author:
Publisher
Wiley
Subject
Organic Chemistry,Physical and Theoretical Chemistry
Reference20 articles.
1. On the importance of reactions of carbocation ion pairs in water: common ion inhibition of solvolysis of 1-(4-methoxyphenyl)-2,2,2-trifluoroethyl bromide and trapping of an ion-pair intermediate by solvent
2. On the importance of carbocation intermediates in bimolecular nucleophilic substitution reactions in aqueous solution
3. Dynamics for Reaction of an Ion Pair in Aqueous Solution: The Rate Constant for Ion Pair Reorganization
4. Dynamics for Reaction of an Ion Pair in Aqueous Solution: Reactivity of Carboxylate Anions in Bimolecular Carbocation−Nucleophile Addition and Unimolecular Ion Pair Collapse
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1. Racemisation in Chemistry and Biology;Chemistry – A European Journal;2020-03-23
2. Formation and mechanism for reactions of ring-substituted phenonium ions in aqueous solution;Journal of Physical Organic Chemistry;2015-11-30
3. Swain–Scott relationships for nucleophile addition to ring-substituted phenonium ions;Canadian Journal of Chemistry;2015-04
4. Effect of nucleophilic solvent on the kinetic parameters of the reactions of unimolecular heterolysis. Mechanism of the covalent bond heterolysis;Russian Journal of General Chemistry;2010-08
5. Dynamics for reactions of ion pairs in aqueous solution: reactivity of tosylate anion ion paired with the highly destabilized 1-(4-methylphenyl)-2,2,2-trifluoroethyl carbocation;Journal of Physical Organic Chemistry;2010-01-13
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