Zobrazeno 1 - 10
of 18
pro vyhledávání: '"A. G. Mayants"'
Autor:
A. G. Mayants, S. S. Gordeichuk, L. M. Tishchenko, V. N. Vladimirov, S. V. Mikhailova, V. A. Shlyapochnikov
Publikováno v:
Chemistry of Heterocyclic Compounds. 29:395-401
For the example of a salt of azotetrazole, for the first time we have investigated the azotetrazole-1,2,3,4,5-pentazine tautomerism. Upon treatment of an excess of the disodium salt of azotetrazole with dilute sulfuric acid, we isolated 5-substituted
Publikováno v:
ChemInform. 24
Autor:
S. S. Gordeichuk, V. S. Klimenko, V. V. Erina, V. S. Kus'min, Yu. N. Burtsev, K. G. Pyreseva, A. G. Mayants, V. N. Leibzon
Publikováno v:
ChemInform. 24
Autor:
S. S. Gordeichuk, A. G. Mayants, S. V. Mikhailova, V. A. Shlyapochnikov, L. M. Tishchenko, V. N. Vladimirov
Publikováno v:
ChemInform. 25
Publikováno v:
ChemInform. 25
Autor:
A. G. Mayants, V. V. Erina
Publikováno v:
ChemInform. 25
Autor:
K. G. Pyreseva, Yu. N. Burtsev, V. S. Klimenko, V. V. Erina, V. N. Leibzon, V. S. Kuz'min, S. S. Gordeichuk, A. G. Mayants
Publikováno v:
Chemistry of Heterocyclic Compounds. 27:854-858
1(2)-Methyl-5-aminotetrazoles and 2-(Β-cyanoethyl)-5-aminotetrazole are nitrated by tetranitromethane in the presence of bases with the formation of salts of the corresponding 5-nitroaminotetrazole derivatives. In contrast to this, decyanoethylation
Publikováno v:
Chemistry of Heterocyclic Compounds. 29:906-908
The reaction of 5-hydrazinotetrazole with formaldehyde in acid media was studied. Copolymers of these compounds are formed at pH ∼ 6.0. In contrast, opening of the tetrazole ring and formation of a previously unknown copolymer of 1,3,4-aza-2-azido-
Publikováno v:
Chemistry of Heterocyclic Compounds. 28:1149-1151
The heating of the hydrate of 5-diazomethylazotetrazole in an aqueous medium led to the isolation, for the first time, of 5-hydroxymethylazotetrazole — the proposed intermediate product in the isolation of 5-hydrazinotetrazole from 5-diazomethylazo
Publikováno v:
Chemistry of Heterocyclic Compounds. 28:785-787
The electrochemical reduction of 5-nitroamino- and 2-methyl-5-nitroaminotetrazoles at the first wave potential consumes six electrons, while the reduction at the second wave potential consumes eight or nine electrons. The preparative reduction of 2-m