Application of Grunwald–Winstein correlation analyses with Y BnBr scales to the solvolysis of benzoyl bromides
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference33 articles.
1. Solvent and substituent effects in solvolyses of benzoyl chlorides. Variation of mechanisms from Grunwald–Winstein correlation analyses with YBnCl scales †
2. Microemulsion-promoted changes of reaction mechanisms: solvolysis of substituted benzoyl chlorides
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1. Reaction Mechanism Studies Involving the Correlation of the Rates of Solvolysis of Benzoyl and P-Nitrobenzoyl P-Toluenesulfonates;Journal of Chemical Research;2014-07
2. Effect of nucleophilic solvent on the kinetic parameters of the reactions of unimolecular heterolysis. Mechanism of the covalent bond heterolysis;Russian Journal of General Chemistry;2010-08
3. Kinetics and mechanism of unimolecular heterolysis of cage-like compounds: XXI. Solvent effect on the realtive rate of heterolysis of 2-methyland 2-phenyl-2-haloadamantanes. Role of activation parameters;Russian Journal of Organic Chemistry;2009-09
4. Mechanisms of Solvolyses of Acid Chlorides and Chloroformates. Chloroacetyl and Phenylacetyl Chloride as Similarity Models;The Journal of Organic Chemistry;2005-09-27
5. Solvent Polarity and Organic Reactivity in Mixed Solvents: Evidence Using a Reactive Molecular Probe To Assess the Role of Preferential Solvation in Aqueous Alcohols;The Journal of Organic Chemistry;2005-01-28
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