A Retentive SN1 Hydrolysis in Aqueous Acrylonitrile and the Polymerization of Acrylonitrile Initiated by the SN1 Hydrolysis Intermediate
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Reference5 articles.
1. Kinetic Studies of Solvolysis. XI. The Steric Course of the Phenolyses of Optically Active α-Phenylethyl Chloride in Mixtures of Various Phenols and Organic Solvents—A Mechanism for the SN1 Reaction with a Net Retention of Configuration
2. The SN1 Hydrolysis of α-Phenylethyl Chloride Proceeding with the Retention of the Configuration in Binary Mixtures of Phenol and Water
3. The Stereochemical Course of Amine Replacement Reactions. Some Reactions of d-(+)-N,N,N-Trimethyl-α-phenylethylammonium Iodide
4. Additions and Corrections-The Stereochemical Course of Amine Replacement Reactions
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1. Number and Structure of Solvolysis Intermediates. IV. The Phenolysis of 1-(p-Tolyl)ethylp-Nitrobenzoate: The Mechanism via a Single Stable Ion-Pair Intermediate with High Selectivity for Nucleophiles;Bulletin of the Chemical Society of Japan;1994-03
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. Phenolysis and competing methanolysis of optically active 1-phenylethyl chloride in sterically hindered 2,6-dialkylphenol solvents;Journal of the Chemical Society, Perkin Transactions 2;1975
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