Azulene-Substituted Aromatic Amines. Synthesis and Amphoteric Redox Behavior of N,N-Di(6-azulenyl)-p-toluidine and N,N,N‘,N‘-Tetra(6-azulenyl)-p-phenylenediamine and Their Derivatives-Reference-Cited by-同舟云学术

Azulene-Substituted Aromatic Amines. Synthesis and Amphoteric Redox Behavior of N,N-Di(6-azulenyl)-p-toluidine and N,N,N‘,N‘-Tetra(6-azulenyl)-p-phenylenediamine and Their Derivatives

Published:2005-02-16 Issue:6 Volume:70 Page:2285-2293
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Ito Shunji¹,Kubo Takahiro¹,Morita Noboru¹,Ikoma Tadaaki¹,Tero-Kubota Shozo¹,Kawakami Jun¹,Tajiri Akio¹

Affiliation:

1. Department of Materials Science and Technology, Faculty of Science and Technology, Hirosaki University, Hirosaki 036-8561, Department of Chemistry, Graduate School of Science, Tohoku University, Sendai 980-8578, and Institute of Multidisciplinary Research for Advanced Materials, Tohoku University, Sendai 980-8577, Japan

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo048489s

Reference21 articles.

1. Synthesis and Properties of Novel Derivatives of 1,3,5-Tris(diarylamino)benzenes for Electroluminescent Devices

2. Multistage Organic Redox Systems—A General Structural Principle

3. The electrochemical reduction of fluorenone imine, 9-aminofluorene, and several N-substituted derivatives in dimethylformamide

4. Reductive metallation

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