Reactions of 4-nitro-1,2,3-triazole with alkylating agents and compounds with activated multiple bonds (in Russian)
Journal Article
·
· Chem. Heterocycl. Compd. (Engl. Transl.); (United States)
OSTI ID:6164804
When 4-nitro-1,2,3-triazole is alkylated, a mixture of N1- and N2-isomers is formed, with the latter usually predominating. The same behavior is also observed in addition reactions of 4-nitrotriazole to activated multiple bonds.
- Research Organization:
- A. A. Zhdanov Irkutsk State Univ., Angarsk, USSR
- OSTI ID:
- 6164804
- Journal Information:
- Chem. Heterocycl. Compd. (Engl. Transl.); (United States), Journal Name: Chem. Heterocycl. Compd. (Engl. Transl.); (United States) Vol. 22:7; ISSN CHCCA
- Country of Publication:
- United States
- Language:
- Russian
Similar Records
Structural basis of the impact sensitivities of 1-picryl-1,2,3-triazole, 2-picryl-1,2,3-triazole, 4-nitro-1-picryl-1,2,3-triazole, and 4-nitro-2-picryl-1,2,3-triazole
Nucleosides of 4-methylthio-1,2,3-triazol-5-yl-carboxylic acid derivatives
Synthesis of 5-aryl-4-(2-acetylaminobenzoyl)-1,2,3-triazoles with the /sup 15/N isotope at the terminal positions of the triazole rings and the tautomeric composition
Journal Article
·
Wed Jan 25 23:00:00 EST 1989
· Journal of Physical Chemistry; (USA)
·
OSTI ID:5305148
Nucleosides of 4-methylthio-1,2,3-triazol-5-yl-carboxylic acid derivatives
Journal Article
·
Sat Aug 01 00:00:00 EDT 1987
· Chem. Heterocycl. Compd. (Engl. Transl.); (United States)
·
OSTI ID:5099453
Synthesis of 5-aryl-4-(2-acetylaminobenzoyl)-1,2,3-triazoles with the /sup 15/N isotope at the terminal positions of the triazole rings and the tautomeric composition
Journal Article
·
Mon Dec 19 23:00:00 EST 1988
· J. Org. Chem. USSR (Engl. Transl.); (United States)
·
OSTI ID:5970547
Related Subjects
37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CHEMISTRY
400201* -- Chemical & Physicochemical Properties
ACRYLONITRILE
ACTIVATION ENERGY
ALCOHOLS
ALKYLATING AGENTS
ALKYLATION
AZOLES
BINDING ENERGY
CATALYTIC EFFECTS
CHEMICAL BONDS
CHEMICAL REACTIONS
CHEMICAL SHIFT
CHROMATOGRAPHY
DECOMPOSITION
DMSO
ENERGY
ETHANOL
HALOGENATED ALIPHATIC HYDROCARBONS
HETEROCYCLIC COMPOUNDS
HYDROGEN COMPOUNDS
HYDROXY COMPOUNDS
INFRARED SPECTRA
INORGANIC ACIDS
IODINATED ALIPHATIC HYDROCARBONS
ISOMERIZATION
ISOMERS
METHANOL
METHYL IODIDE
NITRILES
NITRO COMPOUNDS
NMR SPECTRA
ORGANIC COMPOUNDS
ORGANIC HALOGEN COMPOUNDS
ORGANIC IODINE COMPOUNDS
ORGANIC NITROGEN COMPOUNDS
ORGANIC SULFUR COMPOUNDS
PHOSPHORIC ACID
PYROLYSIS
SEPARATION PROCESSES
SPECTRA
SULFOXIDES
THERMOCHEMICAL PROCESSES
TRIAZOLES
400201* -- Chemical & Physicochemical Properties
ACRYLONITRILE
ACTIVATION ENERGY
ALCOHOLS
ALKYLATING AGENTS
ALKYLATION
AZOLES
BINDING ENERGY
CATALYTIC EFFECTS
CHEMICAL BONDS
CHEMICAL REACTIONS
CHEMICAL SHIFT
CHROMATOGRAPHY
DECOMPOSITION
DMSO
ENERGY
ETHANOL
HALOGENATED ALIPHATIC HYDROCARBONS
HETEROCYCLIC COMPOUNDS
HYDROGEN COMPOUNDS
HYDROXY COMPOUNDS
INFRARED SPECTRA
INORGANIC ACIDS
IODINATED ALIPHATIC HYDROCARBONS
ISOMERIZATION
ISOMERS
METHANOL
METHYL IODIDE
NITRILES
NITRO COMPOUNDS
NMR SPECTRA
ORGANIC COMPOUNDS
ORGANIC HALOGEN COMPOUNDS
ORGANIC IODINE COMPOUNDS
ORGANIC NITROGEN COMPOUNDS
ORGANIC SULFUR COMPOUNDS
PHOSPHORIC ACID
PYROLYSIS
SEPARATION PROCESSES
SPECTRA
SULFOXIDES
THERMOCHEMICAL PROCESSES
TRIAZOLES