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-Reference-Cited by-同舟云学术

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

Published:1994-03 Issue:3 Volume:67 Page:816-823
ISSN:0009-2673
Container-title:Bulletin of the Chemical Society of Japan
language:en
Short-container-title:BCSJ

Author:

Kinoshita Tomomi,Shibayama Koichi,Takemoto Masaki,Takeuchi Ken’ichi

Publisher

The Chemical Society of Japan

Subject

General Chemistry

Link

https://www.jstage.jst.go.jp/article/bcsj/67/3/67_3_816/_pdf

Reference50 articles.

1. Retentive Solvolysis. 16. Reinvestigation of the Retentive Phenolysis of 1-Phenylethyl Chloride. The Mechanism and the Structure of Ion Pair Intermediate

2. 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

3. 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

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