Inductive and field effects in aromatic substitution. Part III. Comparison of the substituents X and CH2X in nitration
Author:
Publisher
Royal Society of Chemistry (RSC)
Subject
Organic Chemistry,Physical and Theoretical Chemistry
Link
http://pubs.rsc.org/en/content/articlepdf/1971/J2/J29710000719
Cited by 9 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. The MCactivity coefficient function for acid–base equilibria. Part 4. Limitations of empirical relationships involving observed nitration rates and acidity functions;J. Chem. Soc., Perkin Trans. 2;1977
2. Electrophilic aromatic reactivities via pyrolysis of 1-arylethyl esters. Part 13. Carbon–carbon hyperconjugation and the origin of the Baker–Nathan effect;J. Chem. Soc., Perkin Trans. 2;1977
3. .alpha.-Substituted toluenes and 3-substituted propenes. Evaluation of substituent effects via carbon-13 nuclear magnetic resonance spectroscopy;The Journal of Organic Chemistry;1976-09
4. Substituent effect of the bromomethyl group. Carbon-13 magnetic resonance study;The Journal of Organic Chemistry;1976-03
5. Inductive and field effects in aromatic substitution. Part IX. Assessment of results;Journal of the Chemical Society, Perkin Transactions 2;1976
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