Azoxy- and Azoferrocenes, andN-(Ferrocenylarylmethylene)anilines Formed via Aryliminodimagnesium(IDMg) Procedure. Effect of Ferrocenyl Group on IDMg Reaction and Molecular Structures of Products-Reference-Cited by-同舟云学术

Azoxy- and Azoferrocenes, andN-(Ferrocenylarylmethylene)anilines Formed via Aryliminodimagnesium(IDMg) Procedure. Effect of Ferrocenyl Group on IDMg Reaction and Molecular Structures of Products

Published:1988-01 Issue:1 Volume:61 Page:237-245
ISSN:0009-2673
Container-title:Bulletin of the Chemical Society of Japan
language:en
Short-container-title:BCSJ

Author:

Tsutsumi Toshiki,Okubo Masao,Yasuoka Noritake,Katsube Yukiteru

Publisher

The Chemical Society of Japan

Subject

General Chemistry

Link

https://www.jstage.jst.go.jp/article/bcsj1926/61/1/61_1_237/_pdf

Reference18 articles.

1. Aryliminodimagnesium Reagents. XII. The Distribution of Products in the Condensation with Nitrobenzothiazoles. Reduction of Electron-Donating Ability of Reagent by the Interaction with Thiazolyl Group

2. Correlation of Oxidation and Reduction Potentials of Reactants with Product Distribution in the Reactions of Various Organomagnesium Reagents with Aromatic Carbonyl and Nitro Compounds

3. Preparation of Methoxy-substituted Diaryl Ketone AnilsviaPhenyliminodimagnesium Intermediate

4. Iminodimagnesium Reagents. Condensation Reaction with Ketones. Direct Preparation of Anils and a Hydrazone of Xanthone

5. Aryliminodimagnesium Reagents. IV. The Independent Preparation of Unsymmetrically Substituted Azoxyarene Isomers and Their Deoxygenation

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