The Retentive Solvolysis. VII. Structural Effect of the Leaving Group on the Steric Course of the SN1 Phenolysis of 1-Phenylethyl Systems
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/bcsj1926/43/5/43_5_1545/_pdf
Reference21 articles.
1. Kinetic Studies on Solvolysis. VIII. Phenolysis of Optically Active α-Phenethyl Chloride in Phenol-Benzene Solven—Three-stage Mechanism in the SN1-Type Solvolysis
2. 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
3. The SN1 Hydrolysis of α-Phenylethyl Chloride Proceeding with the Retention of the Configuration in Binary Mixtures of Phenol and Water
4. Reductive Cleavage of Toluenesulfonates with Sodium Naphthalene1
5. Some aspects of the solvolysis of 1-phenylethyl chloride
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2. Number and structure of solvolysis intermediates. Part 3.SN1 solvolysis of 2,2-Dimethyl-1-(p-Methoxyphenyl)Propylp-Nitrobenzoate: Mechanism of the common ion salt effects arising at the stage of the second ion-pair intermediate;Journal of Physical Organic Chemistry;1994-05
3. 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
4. Number and Structure of Solvolysis Intermediates. Part 2. A Novel Example of the Common Ion Rate Depression Arising at the Stage of the Second Ion Pair Intermediate in the SN1 Solvolysis;Bulletin of the Chemical Society of Japan;1993-06
5. Retentive Solvolysis. 16. Reinvestigation of the Retentive Phenolysis of 1-Phenylethyl Chloride. The Mechanism and the Structure of Ion Pair Intermediate;Bulletin of the Chemical Society of Japan;1988-09
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