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
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Reference14 articles.
1. The Walden Inversion: Configurational Effects in the Solvolytic Reactions of α-Phenylethyl Chloride1
2. Kinetic Studies on Solvolysis. VIII. Phenolysis of Optically Active α-Phenethyl Chloride in Phenol-Benzene Solven—Three-stage Mechanism in the SN1-Type Solvolysis
3. The Kinetics and Stereochemistry of the Decomposition of Secondary Alkyl Chlorosulfites1
4. The Decomposition of Secondary Alkyl Chlorosulfites. II. Solvent Effects and Mechanisms
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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. Stereochemistry of the cross-coupling reaction of chiral alkylsilanes with aryl triflates: a novel approach to optically active compounds;Journal of the American Chemical Society;1990-10
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