The reductive aromatization of naphthalene diimide: a versatile platform for 2,7-diazapyrenes

Author:

Nakazato Takumi12345,Kamatsuka Takuto12345,Inoue Junichi67895,Sakurai Tsuneaki67895ORCID,Seki Shu67895ORCID,Shinokubo Hiroshi12345ORCID,Miyake Yoshihiro12345ORCID

Affiliation:

1. Department of Molecular and Macromolecular Chemistry

2. Graduate School of Engineering

3. Nagoya University

4. Nagoya 464-8603

5. Japan

6. Department of Molecular Engineering, Graduate School of Engineering

7. Kyoto University

8. Nishikyo-ku

9. Kyoto 615-8510

Abstract

The reductive aromatization of naphthalene diimide provides tetrapivaloxy-2,7-diazapyrene, which serves as a versatile platform toward peripherally substituted 2,7-diazapyrenes.

Funder

Japan Society for the Promotion of Science

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,Metals and Alloys,Surfaces, Coatings and Films,General Chemistry,Ceramics and Composites,Electronic, Optical and Magnetic Materials,Catalysis

Reference46 articles.

1. R. G. Harvey , Polycyclic Aromatic Hydrocarbons , Wiley-VCH , Weinheim , 1997

2. K. Müllen and G.Wegner , Electronic Materials: The Oligomer Approach , Wiley-VCH , Weinheim , 1998

3. Carbon-Rich Compounds , ed. M. M. Haley and R. R. Tykwinski , Wiley-VCH , Weinheim , 2006

4. Functional Organic Materials , ed. T. J. J. Müller and U. H. F. Bunz , Wiley-VCH , Weinheim , 2007

5. C−H Activation for the Construction of C−B Bonds

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