Aryliminodimagnesium Reagents. XIV. Reactions with Nitrobenzenes Having Electronegativeortho-Substituents. Effects of Reaction Conditions on Condensation, Replacement, and Substitution
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/bcsj1926/61/10/61_10_3581/_pdf
Reference14 articles.
1. Azoxy- and Azoferrocenes, andN-(Ferrocenylarylmethylene)anilines Formed via Aryliminodimagnesium(IDMg) Procedure. Effect of Ferrocenyl Group on IDMg Reaction and Molecular Structures of Products
2. Aryliminodimagnesium Reagents. III. The Deoxygenative Condensation with Nitroso- and Nitroarenes: Electronic Effect of Substituents on Product Distribution
3. Aryliminodimagnesium Reagents. XI. Two-Electron Oxidation of the Reagent Molecules in the Reaction with Some Oxidizing Agents and with Strongly Push-Pull Substituted α-Benzylideneacetophenones
4. Aryliminodimagnesium Reagents. VII. The Moderate Electron-donating Ability Estimated by Oxidation Peak Potentials
5. Correlation of Oxidation and Reduction Potentials of Reactants with Product Distribution in the Reactions of Various Organomagnesium Reagents with Aromatic Carbonyl and Nitro Compounds
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2. A two-step oxidative aromatic substitution of hydrogen as a convenient way to 2-nitrodiarylamines;Tetrahedron;2016-12
3. Phenazines and TheirN-Oxides as Products of Cyclization ofN-Aryl-2-nitrosoanilines - Disproof of the Reported Homolytic Cross-Coupling Process Leading to Benzo[c]cinnoline Oxides;European Journal of Organic Chemistry;2014-10-28
4. N-Aryl-2-nitrosoanilines as intermediates in the synthesis of substituted phenazines from nitroarenes;Tetrahedron Letters;2011-11
5. Simple Synthesis of N-Aryl-2-nitrosoanilines in the Reaction of Nitroarenes with Aniline Anion Derivatives;Synthesis;2010-08-25
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