The quest for a better system for evaluating pi-electron substituent constant: a comparison of benzoic, acrylic and tria-, penta-, heptafulvene-based carboxylic acids. A computational study
Author:
Affiliation:
1. National Medicines Institute; 30/34 Chełmska Street 00-725 Warszawa Poland
Publisher
Wiley
Subject
Organic Chemistry,Physical and Theoretical Chemistry
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/poc.3187/fullpdf
Reference22 articles.
1. Sigma- and Pi-Electron Delocalization: Focus on Substituent Effects
2. The Effect of Structure upon the Reactions of Organic Compounds. Benzene Derivatives
3. Linear Free Energy Relationships from Rates of Esterification and Hydrolysis of Aliphatic and Ortho-substituted Benzoate Esters
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1. Recent Advances in the Chemistry of Pentafulvenes;Chemical Reviews;2017-02-02
2. Substituent effects on the ring-opening mechanism ofgem-dibromospiropentanes to related allenes: a theoretical study;Journal of Physical Organic Chemistry;2015-09-15
3. A study on the influence of intramolecular OH⋯X (X=O and S) hydrogen bond formation on the aromaticity of heptafulvene derivatives, in which the methylene is replaced by AlH2-, BH2-, NH and O groups;Computational and Theoretical Chemistry;2014-07
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