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-Reference-Cited by-同舟云学术

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

Published:1986-09 Issue:9 Volume:59 Page:2843-2849
ISSN:0009-2673
Container-title:Bulletin of the Chemical Society of Japan
language:en
Short-container-title:BCSJ

Author:

Kinoshita Tomomi,Ikai Keizo,Kashimura Tugunori,Fujiwara Masataka,Okamoto Kunio

Publisher

The Chemical Society of Japan

Subject

General Chemistry

Link

https://www.jstage.jst.go.jp/article/bcsj1926/59/9/59_9_2843/_pdf

Reference32 articles.

1. Use of added sodium azide as a mechanistic probe for solovolysis reactions

2. .alpha.-Deuterium effects on the rates of solvolysis of a 2-adamantyl sulfonate ester

3. Stereochemistry of ion-pair return associated with solvolysis of para-substituted benzyhydryl p-nitrobenzoates

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1. Nature of Salt Effects and Mechanism of Covalent Bond Heterolysis;Progress in Reaction Kinetics and Mechanism;2007-08

2. Special salt effect in monomolecular heterolysis reactions;Russian Journal of General Chemistry;2006-09

3. 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

4. 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

5. 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