Evidence of Substituent-Induced Electronic Interplay. Effect of the Remote Aromatic Ring Substituent of Phenyl Benzoates on the Sensitivity of the Carbonyl Unit to Electronic Effects of Phenyl or Benzoyl Ring Substituents
Author:
Affiliation:
1. Department of Chemistry, University of Turku, FIN-20014 Turku, Finland
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo035521u
Reference27 articles.
1. Conformational dependence of substituent effects in the solvolyses of the 1,1-diphenyl-2,2,2-trifluoroethyl system
2. Correlation analysis of carbonyl carbon 13C NMR chemical shifts, IR absorption frequencies and rate coefficients of nucleophilic acyl substitutions. A novel explanation for the substituent dependence of reactivity
3. Electron-Withdrawing Substituents Decrease the Electrophilicity of the Carbonyl Carbon. An Investigation with the Aid of 13C NMR Chemical Shifts, ν(CO) Frequency Values, Charge Densities, and Isodesmic Reactions To Interprete Substituent Effects on Reactivity
4. Comparison of the Electronic Structures of Imine and Hydrazone Side-Chain Functionalities with the Aid of 13C and 15N NMR Chemical Shifts and PM3 Calculations. The Influence of CN-Substitution on the Sensitivity to Aromatic Substitution
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