Stereochemical Studies on the Nuclear Alkylation of Phenols with 1-Phenylethyl Chloride and the Acidic Rearrangement of the 1-Phenylethyl Ethers of Phenols in the Phenolic Solvents-Reference-Cited by-同舟云学术

Stereochemical Studies on the Nuclear Alkylation of Phenols with 1-Phenylethyl Chloride and the Acidic Rearrangement of the 1-Phenylethyl Ethers of Phenols in the Phenolic Solvents

Published:1974-07 Issue:7 Volume:47 Page:1770-1776
ISSN:0009-2673
Container-title:Bulletin of the Chemical Society of Japan
language:en
Short-container-title:BCSJ

Author:

Okamoto Kunio,Kinoshita Tomomi,Makino Osamu

Publisher

The Chemical Society of Japan

Subject

General Chemistry

Link

https://www.jstage.jst.go.jp/article/bcsj1926/47/7/47_7_1770/_pdf

Reference14 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 Retentive Solvolysis. VII. Structural Effect of the Leaving Group on the Steric Course of the SN1 Phenolysis of 1-Phenylethyl Systems

4. Stereochemical Evidence for a Concerted Displacement Mechanism in Acidic Aromatic Alkylations. The Nuclear Alkylation of Phenols with α-Phenethyl Chloride1

5. Phenolyses of 1-Adamantyl Chloride, Bromide, andp-Toluenesulfonate in Binary Mixtures of Phenol with Benzene. The Rates and the Product Distribution

Cited by 7 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. Number and structure of solvolysis intermediates. Part 1. A comparison of nucleophilic reactions on in situ generated carbocations with solvolysis reactions for 2,2-dimethyl-1-(p-methoxyphenyl)propyl cation;Journal of the Chemical Society, Perkin Transactions 2;1992

2. 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

3. Retentive Solvolysis. 15. Salt Effect on the Retentive Phenolyses of 1-(p-Substituted phenyl)ethylp-Nitrobenzoates. The Pattern of Salt Effect and the Number of Ion-Pair Intermediates in the SN1 Solvolysis;Bulletin of the Chemical Society of Japan;1988-08

4. 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

5. Retentive Solvolysis. 13. The Number and the Stability of Carbocation Intermediate in theSN1 Phenolysis. Salt Effect on Retentive Phenolyses of Optically Active 2,2-Dimethyl-1-(p-substituted phenyl)propylp-Nitrobenzoates;Bulletin of the Chemical Society of Japan;1986-09