Kinetic solvent isotope effect studies on the methanolysis of 1-phenylethyl chlorides
Author:
Publisher
Wiley
Subject
Organic Chemistry,Physical and Theoretical Chemistry
Reference36 articles.
1. Solvolysis of 1-arylethyl tosylates. Kinetic and stereochemical tests for solvent participation
2. Doubly destabilized carbocations. Strong aryl delocalization and the attenuation of rate decelerating effects of trifluoromethyl and cyano groups
3. Formation and stability of ring-substituted 1-phenylethyl carbocations
4. Reactions of substituted 1-phenylethyl carbocations with alcohols and other nucleophilic reagents
5. General base catalysis of the addition of hydroxylic reagents to unstable carbocations and its disappearance
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2. Correlation of Rates of Solvolysis of Diphenylacetyl Chloride Using Extended Grunwald-Winstein Equation;Bulletin of the Korean Chemical Society;2015-08-28
3. Solvolysis of 1-alkyl-1-chloro-1-(4-methyl)phenylmethanes. Nucleophilic solvent intervention and extendedYBnCl scale;Journal of Physical Organic Chemistry;1997-12
4. Isokinetic behaviors in the addition reactions of aniline nucleophiles with benzylic carbocations;Journal of Physical Organic Chemistry;1996-10
5. Kinetics and Mechanism of Reactions of Benzhydryl Chlorides with Anilines;The Journal of Organic Chemistry;1995-12
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