Kinetic Studies of Solvolysis. XIII. The Solvolyses of Optically-active α-Phenylethyl Chloride in Binary Mixtures of Phenol and Water—The SN1 Hydrolysis with the Retention of the Configuration-Reference-Cited by-同舟云学术

Kinetic Studies of Solvolysis. XIII. The Solvolyses of Optically-active α-Phenylethyl Chloride in Binary Mixtures of Phenol and Water—The SN1 Hydrolysis with the Retention of the Configuration

Published:1967-03 Issue:3 Volume:40 Page:624-628
ISSN:0009-2673
Container-title:Bulletin of the Chemical Society of Japan
language:en
Short-container-title:BCSJ

Author:

Okamoto Kunio,Hayashi Masayuki,Komatsu Koichi,Shingu Haruo

Publisher

The Chemical Society of Japan

Subject

General Chemistry

Reference22 articles.

1. Substitution at a Saturated Carbon Atom. IV. A Clarification of the Mechanism of Solvolyses of 2-Octyl Sulfonates. Stereochemical Considerations1

2. Substitution at a Saturated Carbon Atom. V. A Clarification of the Mechanism of Solvolyses of 2-Octyl Sulfonates. Kinetic Considerations1

3. Stereochemistry of Acetolysis of Alkyl Sulfonates1

4. Salt Effects in the Stereochemistry of Acetolysis of 2-Octyl p-Toluenesulfonate1

Cited by 12 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Some aspects of the solvolysis of 1-phenylethyl chloride;Recueil des Travaux Chimiques des Pays-Bas;2010-09-02

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