Aryliminodimagnesium Reagents. VII. The Moderate Electron-donating Ability Estimated by Oxidation Peak Potentials
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/bcsj1926/57/9/57_9_2679/_pdf
Reference11 articles.
1. Aryliminodimagnesium Reagents. VI. The Reactions with Conjugated Carbonyl Compounds. The Initial Coordination and the Electron-transfer in the Reactions of Organomagnesium Reagents
2. Aryliminodimagnesium Reagents. III. The Deoxygenative Condensation with Nitroso- and Nitroarenes: Electronic Effect of Substituents on Product Distribution
3. Substituent effect on the electrochemical oxidation of arylmethyl anions. 3. Effect of methyl substitution on diarylmethyl anions
4. Anodic NN Linkage by Oxidation of Anions of Primary and Secondary Amines
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1. Electrochemistry of Organomagnesium Compounds;PATAI'S Chemistry of Functional Groups;2009-12-15
2. Reaction of Magnesium Reagent Having C-Mg, N-Mg and O-Mg Bonds—Entire Features of Reactions and Exact Use of Reagents—;NIPPON KAGAKU KAISHI;2000
3. REACTION OF ARYLIMODIMAGNESIUM WITH AROMATIC BIFUNCTIONAL NITRILES: COMPETITION AND/OR COOPERATION OF FUNCTIONAL GROUPS AFFECTED BY ELECTRON-ACCEPTING ABILITY AND LOCATION;Journal of Physical Organic Chemistry;1997-04
4. Benzamidines, alkamidines and formamidines formed by use of aryl- and alkyliminodimagnesium: Molar ratio and structure of reagent governing the reaction;Journal of Physical Organic Chemistry;1996-04
5. Reactions of iminodimagnesium reagents with 1,4-quinones: Their structural factors governing the modes of reactions;Journal of Physical Organic Chemistry;1994-10
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