The SN1 Hydrolysis of α-Phenylethyl Chloride Proceeding with the Retention of the Configuration in Binary Mixtures of Phenol and Water
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Reference12 articles.
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1. Nucleophilic Substitution Catalyzed by a Supramolecular Cavity Proceeds with Retention of Absolute Stereochemistry;Journal of the American Chemical Society;2014-10-07
2. Retentive solvolysis. Part 14. The methanol-perturbed phenolysis of optically active 2,2-dimethyl-1-(p-methoxyphenyl)propyl p-nitrobenzoate. The mechanism and the structure of the second ion-pair intermediate;Journal of the Chemical Society, Perkin Transactions 2;1988
3. Solvent molecules and carbocation intermediates in solvolyses;Pure and Applied Chemistry;1984-01-01
4. Retentive solvolysis. Part 12. Mechanism of the reaction of optically active 1-(p-methoxyphenyl)ethyl trifluoroacetate with phenol and methanol in benzene and cyclohexane;Journal of the Chemical Society, Perkin Transactions 2;1980
5. Retentive solvolysis. Part XI. Retentive phenolyses of optically active secondary and tertiary systems without a group imposing configurational restriction;Journal of the Chemical Society, Perkin Transactions 2;1976
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