The Reversible Consecutive Mechanism for the Reaction of Trinitroanisole with Methoxide Ion
Author:
Affiliation:
1. Department of Chemistry and Biochemistry, Utah State University, Logan, Utah 84322, United States
2. Department of Chemistry, The State Key Laboratory of Elemento-Organic Chemistry, Nankai University, Tianjin 300071, China
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo101859n
Reference34 articles.
1. The ortho: para Ratio in Activation of Aromatic Nucleophilic Substitution by the Nitro Group1
2. 488. The kinetics and mechanisms of some colour reactions of aromatic nitro-compounds at low temperatures. Part II. 2 : 4 : 6-Trinitroanisole
3. A Calorimetric Procedure for Determining Free Energies, Enthalpies, and Entropies for the Formation of Acid-Base Adducts
4. Reactions of aromatic nitro-compounds in alkaline media. Part XI. Structural investigations by proton magnetic resonance spectroscopy
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