Solvolysis of 1-Aryl-1-tert-butylmethyl Bromides. Hammett-Type Correlation Analysis and RevisedYBnBrScale
Author:
Publisher
Wiley
Subject
General Chemistry
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/jccs.199900107/fullpdf
Reference23 articles.
1. Neighboring Carbon and Hydrogen. VIII. Solvolysis of Optically Active α-Phenylneopentyl Derivatives1,2
2. Substituent Effects. 22. The Solvolysis of α-t-Butylbenzyl Tosylates
3. Kinetic effects of thiourea addition on benzylic solvolyses
4. Solvolysis of 1-alkyl-1-chloro-1-(4-methyl)phenylmethanes. Nucleophilic solvent intervention and extendedYBnCl scale
5. Solvolysis of 1-Aryl-1-tert-butylmethyl Chlorides. Solvent Effects on the Hammett-type Correlation Analysis
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1. Sixty Years of the Grunwald–Winstein Equation: Development and Recent Applications;Journal of Chemical Research;2008-02
2. Solvent Effects on the Solvolysis of Some Secondary Tosylates. Applications ofYBnOTsandYxBnOTsScales to Mechanistic Studies;Journal of the Chinese Chemical Society;2003-02
3. Kinetics and mechanism of monomolecular heterolysis of commercial organohalogen compounds: XXXIII. Correlation analysis of solvation effects in monomolecular heterolysis of 1-bromo-1-methylcyclopentane, 1-bromo-1-methylcyclohexane, and 2-bromo-2-methyladamantane;Russian Journal of General Chemistry;2003
4. Solvolysis of 1-tert-Butyl-1-(4-phenoxyphenyl) Methyl Bromide and Chloride. Further Example for Possible Contribution of Non-canonical Resonance Structure in the Transition State;Journal of the Chinese Chemical Society;2001-12
5. Application of Grunwald–Winstein correlation analyses with Y BnBr scales to the solvolysis of benzoyl bromides;Tetrahedron;2001-04
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