Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Konstantin K, Bosov"'
Autor:
Konstantin K. Bosov, Ekaterina V. Pivovarova, Irina A. Krupnova, Gennady T. Sukhanov, Anna G. Sukhanova, Yulia V. Filippova
Publikováno v:
Materials, Vol 16, Iss 22, p 7068 (2023)
Using 1H NMR spectroscopy, we studied the relative mobility of the NO2 group in 1-alkyl-5-nitro-1,2,4-triazoles in the reaction of nucleophilic heterocyclic substitution by aliphatic oligoethers. The main pathways of the SNipso substitution process a
Externí odkaz:
https://doaj.org/article/af12cf75ef9e4e26aca762a36e06f4fd
Autor:
Gennady T. Sukhanov, Konstantin K. Bosov, Yulia V. Filippova, Anna G. Sukhanova, Irina A. Krupnova, Ekaterina V. Pivovarova
Publikováno v:
Materials, Vol 15, Iss 19, p 6936 (2022)
An N-glycidyl-5-aminotetrazole homopolymer was synthesized herein by nucleophilic substitution of 5-aminotetrazole heterocycles for chlorine atoms in poly-(epichlorohydrin)-butanediol. Copolymers of N-glycidyl-5-aminotetrazole and glycidyl azide with
Externí odkaz:
https://doaj.org/article/b952cdc78e1149ddb4d57258806a98b4
Autor:
Gennady T. Sukhanov, Yulia V. Filippova, Yuri V. Gatilov, Anna G. Sukhanova, Irina A. Krupnova, Konstantin K. Bosov, Ekaterina V. Pivovarova, Vyacheslav I. Krasnov
Publikováno v:
Materials, Vol 15, Iss 3, p 1119 (2022)
The regularities and synthetic potentialities of the alkylation of 4(5)-nitro-1,2,3-triazole in basic media were explored, and new energetic ionic and nitrotriazole-based coordination compounds were synthesized in this study. The reaction had a gener
Externí odkaz:
https://doaj.org/article/c3799a12c20543109efe1b9fd50ad473
Autor:
Konstantin K. Bosov, Yulia V. Filippova, Ekaterina V. Pivovarova, G. T. Sukhanov, A. G. Sukhanova, Irina A. Krupnova
Publikováno v:
Propellants, Explosives, Pyrotechnics. 46:1526-1536
Autor:
Gennady T. Sukhanov, Yulia V. Filippova, Yuri V. Gatilov, Anna G. Sukhanova, Konstantin K. Bosov, Irina A. Krupnova, Ekaterina V. Pivovarova
Publikováno v:
Mendeleev Communications. 32:215-217
Autor:
Konstantin K. Bosov, Ekaterina V. Pivovarova, A. G. Sukhanova, Yurii V. Gatilov, Yuliya V. Filippova, G. T. Sukhanov, Irina А. Krupnova
Publikováno v:
Chemistry of Heterocyclic Compounds. 56:1440-1448
The directions of thermodynamically controlled rearrangements and transformations of alkyl substituents under the conditions of acidcatalyzed alkylation of unsubstituted and 5(3)-substituted 3(5)-nitro-1H-1,2,4-triazoles with butyl alcohols (n-, i-,
Autor:
Irina Yu. Bagryanskaya, Konstantin K. Bosov, Yuliya V. Filippova, A. G. Sukhanova, G. T. Sukhanov
Publikováno v:
Chemistry of Heterocyclic Compounds. 55:1197-1203
1-(Adamantan-1-yl)-1H-1,2,3-triazoles and a series of 1-(adamantan-1-yl)-3-alkyl-1,2,3-triazolium salts were synthesized by regioselective adamantylation of 1,2,3-triazole derivatives. The direction of the attack by the adamantyl cation at the N-1 ni
Autor:
Gennady T, Sukhanov, Yulia V, Filippova, Yuri V, Gatilov, Anna G, Sukhanova, Irina A, Krupnova, Konstantin K, Bosov, Ekaterina V, Pivovarova, Vyacheslav I, Krasnov
Publikováno v:
Materials (Basel, Switzerland). 15(3)
The regularities and synthetic potentialities of the alkylation of 4(5)-nitro-1,2,3-triazole in basic media were explored, and new energetic ionic and nitrotriazole-based coordination compounds were synthesized in this study. The reaction had a gener
Publikováno v:
Russian Chemical Bulletin. 62:111-116
Alkylation of 4(5)-nitro-1,2,3-triazole with alcohols in concentrated H2SO4 occurs at all three endocyclic N atoms, giving a mixture of isomeric N(1)-, N(2)-, and N(3)-alkyl-4-nitro-1,2,3-triazoles (alkyl is isopropyl, sec-butyl, and cyclohexyl). The
Publikováno v:
ChemInform. 45
The alkylation of the title compounds occurs at all three endocyclic N-atoms leading to a mixture of N(1)-, N(2)-, and N(3)-alkyl-4-nitro-1,2,3-triazoles.