A5088706427- Energetic Materials and Combustion
- Synthesis and Biological Evaluation
- Structural and Chemical Analysis of Organic and Inorganic Compounds
- Chemical Thermodynamics and Molecular Structure
- Synthesis and Characterization of Heterocyclic Compounds
- Thermal and Kinetic Analysis
- Chemical Reaction Mechanisms
- Chemical Reactions and Mechanisms
- Crystallization and Solubility Studies
- X-ray Diffraction in Crystallography
- Synthesis of Tetrazole Derivatives
- Inorganic and Organometallic Chemistry
- Coordination Chemistry and Organometallics
- Synthesis and biological activity
- Crystallography and molecular interactions
- Mass Spectrometry Techniques and Applications
- Logic, programming, and type systems
- Synthesis of Organic Compounds
- Phenothiazines and Benzothiazines Synthesis and Activities
- Analytical chemistry methods development
- Pluripotent Stem Cells Research
- Synthesis and Reactions of Organic Compounds
- Computability, Logic, AI Algorithms
- Synthesis and pharmacology of benzodiazepine derivatives
- Algorithms and Data Compression
Skolkovo Institute of Science and Technology
2023
Institute of Bioorganic Chemistry
2023
Saint-Petersburg State University of Technology and Design
2016-2019
Institute of Problems of Chemical Physics
2018
Electronics Design (Estonia)
2012-2015
NS Kurnakova Institute of General and Inorganic Chemistry
2000-2005
Russian Academy of Sciences
2002
St. Petersburg State Technological Institute
2001
Abstract The nucleophilic displacement of two nitro groups in 3,4-bis(3-nitrofurazan-4-yl)furoxan with ammonia, primary aliphatic amines and hydrazine leads to formation a novel heterocyclic system, 7H-tris[1,2,5]oxadiazolo[3,4-b:3′,4′-d:3″,4″-f]azepine. reaction compound 1 secondary proceeds typical way for nitrofurazans when the nitro-group starting is substituted by RR’N-group.