Zobrazeno 1 - 10
of 14
pro vyhledávání: '"O. N. Verkhozina"'
Autor:
F. A. Pokatilov, V. N. Kizhnyaev, T. V. Golobokova, L. I. Vereshchagin, A. G. Proidakov, O. N. Verkhozina, A. I. Smirnov
Publikováno v:
Chemistry of Heterocyclic Compounds. 47:456-463
Polynuclear noncondensed systems in which the azole rings are bound by urethane or carbamide fragments have been synthesized by the reaction of azole carboxylic acid azides with heterocyclic alcohols.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::799c1e8f92edd8d7d9e69e3c1fd5cf4d
https://doi.org/10.1007/s10593-011-0781-5
https://doi.org/10.1007/s10593-011-0781-5
Autor:
E. A. Krakhotkina, F. A. Pokatilov, R. G. Zhitov, T. V. Golobokova, O. N. Verkhozina, V. N. Kizhnyaev, L. I. Vereshchagin
Publikováno v:
Polymer Science Series B. 53:317-323
Linear, star-shaped, and hyperbranched oligomeric compounds containing tetrazole cycles in the main chains are synthesized via the polycondensation (polyalkylation) of N-H unsubstituted bis(tetrazoles), tris(tetrazoles), and tetrakis(tetrazoles) with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3969c35c15fc9cee192d5349901e5906
https://doi.org/10.1134/s156009041106008x
https://doi.org/10.1134/s156009041106008x
Autor:
O. N. Verkhozina, T. L. Petrova, F. A. Pokatilov, M. V. Kazantseva, E. A. Krakhotkina, V. N. Kizhnyaev
Publikováno v:
Polymer Science Series B. 53:144-150
High-molecular-mass compounds (ionenes) containing charged imidazole and 1,2,4-triazole rings in the main chain are synthesized via the reaction of dihaloalkanes with bis(azoles) of various structures. It is shown that azole-containing ionenes can be
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cb5ce3be821bbc4df412a4ffbb62a986
https://doi.org/10.1134/s1560090411030043
https://doi.org/10.1134/s1560090411030043
Publikováno v:
Chemistry of Heterocyclic Compounds. 46:206-211
Polynuclear structures containing several heterocycles of various types were synthesized by the reaction of cyanuric chloride and its mono- and dichloro derivatives with triazoles and tetrazoles in the presence of bases.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0fdba7b98e2f59fe6795f5659ef815f4
https://doi.org/10.1007/s10593-010-0493-2
https://doi.org/10.1007/s10593-010-0493-2
Autor:
G. V. Ratovskii, T. L. Petrova, F. A. Pokatilov, V. N. Kizhnyaev, O. V. Tyukalova, O. N. Verkhozina, L. I. Vereshchagin, A. G. Prodaikov
Publikováno v:
Russian Journal of Applied Chemistry. 82:1769-1775
Interaction of cyanuric chloride and its mono and dichloro derivatives with ammonium or sodium 4-nitro-1,2,3-triazolates and polymer-analogous transformations of tetrazole-containing polymers were used to synthesize polynuclear systems and macromolec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::97b95bb6a253fdfbab5c47fecef293f6
https://doi.org/10.1134/s1070427209100048
https://doi.org/10.1134/s1070427209100048
Publikováno v:
Chemistry of Heterocyclic Compounds. 44:1158-1163
The reaction of 5-substituted mono-and polytetrazoles with heterocyclic acid chlorides and trifluoroacetic acid anhydride gave branched polynuclear 1,3,4-oxadiazole systems.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cefd03bf97f65327ca0fcc7a03b0d7b5
https://doi.org/10.1007/s10593-008-0163-9
https://doi.org/10.1007/s10593-008-0163-9
Autor:
F. A. Pokatilov, A. G. Proidakov, S. K. Strunevich, V. N. Kizhnyaev, O. N. Verkhozina, L. I. Vereshchagin
Publikováno v:
Russian Journal of Organic Chemistry. 43:1710-1714
5-Substituted tetrazoles readily react with trifluoroacetic anhydride at 20–25°C to give the corresponding 2-substituted 5-trifluoromethyl-1,3,4-oxadiazoles, in contrast to published data according to which the title compounds are converted into 1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bffd4b58db422113e35859202a13b4af
https://doi.org/10.1134/s1070428007110218
https://doi.org/10.1134/s1070428007110218
Autor:
Lyudmila I. Larina, Tamara I. Vakul'skaya, O. N. Verkhozina, V. A. Lopyrev, Gennadii V. Dolgushin, I. A. Titova
Publikováno v:
Chemistry of Heterocyclic Compounds. 42:1427-1434
The vicarious nucleophilic substitution of hydrogen in symmetrical and vicinal nitrotriazoles by 1,1,1-trimethylhydrazinium iodide in t-BuOK/DMSO was studied by ESR. In the ESR monitoring of the reactions the primary radical-anions of 4-nitro-2-pheny
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5143820eb256277713d294b8d69df0f4
https://doi.org/10.1007/s10593-006-0259-z
https://doi.org/10.1007/s10593-006-0259-z
Publikováno v:
Russian Journal of Organic Chemistry. 40:1156-1161
Cycloaddition of organic mono- and diazides to the triple bond of propargyl esters of mono- and dicarboxylic acids gave rise to polycyclic 1,2,3-triazole-substituted carboxylates. Dipropargyl dicarboxylates with diazides afforded oligomeric products
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c7738dae2d38a96ce4816d6d76388581
https://doi.org/10.1023/b:rujo.0000045898.10072.7f
https://doi.org/10.1023/b:rujo.0000045898.10072.7f
Autor:
F. A. Pokatilov, V. N. Kizhnyaev, S. K. Strunevich, O. N. Verkhozina, A. G. Proidakov, L. I. Vereshchagin
Publikováno v:
ChemInform. 39
5-Substituted tetrazoles readily react with trifluoroacetic anhydride at 20–25°C to give the corresponding 2-substituted 5-trifluoromethyl-1,3,4-oxadiazoles, in contrast to published data according to which the title compounds are converted into 1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6d23238d99bbd7cedcbb8801cdb6dece
https://doi.org/10.1002/chin.200816142
https://doi.org/10.1002/chin.200816142