2-AZAANTHRACENE

Authors

  • Olga S. Taniya 1 Department of Organic and Biomolecular Chemistry, Chemical Engineering Institute, Ural Federal University, 19 Mira Str., K-2, Yekaterinburg, 620002, Russian Federation 2 I. Ya. Postovskiy Institute of Organic Synthesis, Ural Division of the Russian Academy of Sciences, 22 S. Kovalevskoy Str., Yekaterinburg, 620219, Russian Federation
  • Dmitry S. Kopchuk 1 Department of Organic and Biomolecular Chemistry, Chemical Engineering Institute, Ural Federal University, 19 Mira Str., K-2, Yekaterinburg, 620002, Russian Federation 2 I. Ya. Postovskiy Institute of Organic Synthesis, Ural Division of the Russian Academy of Sciences, 22 S. Kovalevskoy Str., Yekaterinburg, 620219, Russian Federation
  • Albert F. Khasanov 1 Department of Organic and Biomolecular Chemistry, Chemical Engineering Institute, Ural Federal University, 19 Mira Str., K-2, Yekaterinburg, 620002, Russian Federation 2 I. Ya. Postovskiy Institute of Organic Synthesis, Ural Division of the Russian Academy of Sciences, 22 S. Kovalevskoy Str., Yekaterinburg, 620219, Russian Federation
  • Igor S. Kovalev Department of Organic and Biomolecular Chemistry, Chemical Engineering Institute, Ural Federal University, 19 Mira Str., K-2, Yekaterinburg, 620002, Russian Federation
  • Grigory V. Zyryanov 1 Department of Organic and Biomolecular Chemistry, Chemical Engineering Institute, Ural Federal University, 19 Mira Str., K-2, Yekaterinburg, 620002, Russian Federation 2 I. Ya. Postovskiy Institute of Organic Synthesis, Ural Division of the Russian Academy of Sciences, 22 S. Kovalevskoy Str., Yekaterinburg, 620219, Russian Federation
  • Valery N. Charushin 1 Department of Organic and Biomolecular Chemistry, Chemical Engineering Institute, Ural Federal University, 19 Mira Str., K-2, Yekaterinburg, 620002, Russian Federation 2 I. Ya. Postovskiy Institute of Organic Synthesis, Ural Division of the Russian Academy of Sciences, 22 S. Kovalevskoy Str., Yekaterinburg, 620219, Russian Federation
  • Oleg N. Chupakhin 1 Department of Organic and Biomolecular Chemistry, Chemical Engineering Institute, Ural Federal University, 19 Mira Str., K-2, Yekaterinburg, 620002, Russian Federation 2 I. Ya. Postovskiy Institute of Organic Synthesis, Ural Division of the Russian Academy of Sciences, 22 S. Kovalevskoy Str., Yekaterinburg, 620219, Russian Federation

DOI:

https://doi.org/10.1007/5099

Keywords:

2-azaantracene, arynes, cycloaddirion, PASE-methods

Abstract

Microreview focuses on the main modern synthetic approaches toward 2-azaanthracene and its derivatives. These approaches are: inverse electron-demand aza-Diels–Alder reactions, cross coupling, cyclization reactions. These modern  methods are more environmentally friendly and cost- and/or atomefficient compared to the earlier reported approaches.

Author Biographies

Olga S. Taniya, 1 Department of Organic and Biomolecular Chemistry, Chemical Engineering Institute, Ural Federal University, 19 Mira Str., K-2, Yekaterinburg, 620002, Russian Federation 2 I. Ya. Postovskiy Institute of Organic Synthesis, Ural Division of the Russian Academy of Sciences, 22 S. Kovalevskoy Str., Yekaterinburg, 620219, Russian Federation

Department of Organic and Biomolecular Chemistry

Junior Scientist

Dmitry S. Kopchuk, 1 Department of Organic and Biomolecular Chemistry, Chemical Engineering Institute, Ural Federal University, 19 Mira Str., K-2, Yekaterinburg, 620002, Russian Federation 2 I. Ya. Postovskiy Institute of Organic Synthesis, Ural Division of the Russian Academy of Sciences, 22 S. Kovalevskoy Str., Yekaterinburg, 620219, Russian Federation

I. Ya. Postovskiy Institute of Organic Synthesis, Ural Division of the Russian Academy of Sciences

Scientist

Albert F. Khasanov, 1 Department of Organic and Biomolecular Chemistry, Chemical Engineering Institute, Ural Federal University, 19 Mira Str., K-2, Yekaterinburg, 620002, Russian Federation 2 I. Ya. Postovskiy Institute of Organic Synthesis, Ural Division of the Russian Academy of Sciences, 22 S. Kovalevskoy Str., Yekaterinburg, 620219, Russian Federation

Department of Organic and Biomolecular Chemistry, Chemical Engineering Institute, Ural Federal University

Junior Scientist

Igor S. Kovalev, Department of Organic and Biomolecular Chemistry, Chemical Engineering Institute, Ural Federal University, 19 Mira Str., K-2, Yekaterinburg, 620002, Russian Federation

Department of Organic and Biomolecular Chemistry, Chemical Engineering Institute, Ural Federal University

Junior Scientist

Grigory V. Zyryanov, 1 Department of Organic and Biomolecular Chemistry, Chemical Engineering Institute, Ural Federal University, 19 Mira Str., K-2, Yekaterinburg, 620002, Russian Federation 2 I. Ya. Postovskiy Institute of Organic Synthesis, Ural Division of the Russian Academy of Sciences, 22 S. Kovalevskoy Str., Yekaterinburg, 620219, Russian Federation

Department of Organic and Biomolecular Chemistry

Professor

 

Valery N. Charushin, 1 Department of Organic and Biomolecular Chemistry, Chemical Engineering Institute, Ural Federal University, 19 Mira Str., K-2, Yekaterinburg, 620002, Russian Federation 2 I. Ya. Postovskiy Institute of Organic Synthesis, Ural Division of the Russian Academy of Sciences, 22 S. Kovalevskoy Str., Yekaterinburg, 620219, Russian Federation

I. Ya. Postovskiy Institute of Organic Synthesis, Ural Division of the Russian Academy of Sciences

Director

Oleg N. Chupakhin, 1 Department of Organic and Biomolecular Chemistry, Chemical Engineering Institute, Ural Federal University, 19 Mira Str., K-2, Yekaterinburg, 620002, Russian Federation 2 I. Ya. Postovskiy Institute of Organic Synthesis, Ural Division of the Russian Academy of Sciences, 22 S. Kovalevskoy Str., Yekaterinburg, 620219, Russian Federation

I. Ya. Postovskiy Institute of Organic Synthesis, Ural Division of the Russian Academy of Sciences

Scientific Adviser

Downloads

Published

2019-07-23

Issue

Vol. 55 No. 6 (2019): Celebrating the 85th birthday of Professor, Academician Oleg Nikolaevich Chupakhin.

Section

Heterocycles in Focus