The stabilities of Meisenheimer complexes. Part 41. Kinetic studies of adduct formation and nucleophilic substitution in the reactions of hydroxide ions with 1-X-3,5-dinitrobenzenes and with 1-X-4-chloro-3,5-dinitrobenzenes (X = H, CF3, CO2–) in water–dimethyl sulphoxide mixtures. The effect of a chloro-substituent on the rate of nucleophilic attack-Reference-Cited by-同舟云学术

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The stabilities of Meisenheimer complexes. Part 41. Kinetic studies of adduct formation and nucleophilic substitution in the reactions of hydroxide ions with 1-X-3,5-dinitrobenzenes and with 1-X-4-chloro-3,5-dinitrobenzenes (X = H, CF3, CO2–) in water–dimethyl sulphoxide mixtures. The effect of a chloro-substituent on the rate of nucleophilic attack

Published:1986 Issue:1 Volume: Page:187-192
ISSN:0300-9580
Container-title:J. Chem. Soc., Perkin Trans. 2
language:en
Short-container-title:J. Chem. Soc., Perkin Trans. 2

Author:

Crampton Michael R.,Greenhalgh Colin

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/1986/P2/P29860000187

Cited by 10 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

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3. Fluoride ion as a nucleophile and a leaving group in aromatic nucleophilic substitution reactions;Journal of Fluorine Chemistry;1993-04

4. Solvent effects in aromatic nucleophilic substitution reactions in non-polar aprotic solvents. Inhibition by electron-donor-acceptor (EDA) complexation of the substrate by aromatic solvents;Journal of Physical Organic Chemistry;1992-09

5. Kinetic and thermodynamic preferences in the reactions of thiolate ions with 1-substituted-2,4,6-trinitrobenzenes;Journal of the Chemical Society, Perkin Transactions 2;1990

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