Zobrazeno 1 - 10
of 36
pro vyhledávání: '"Alexander A. Gidaspov"'
Autor:
Kyrill Yu. Suponitsky, Ivan V. Fedyanin, Valentina A. Karnoukhova, Vladimir A. Zalomlenkov, Alexander A. Gidaspov, Vladimir V. Bakharev, Aleksei B. Sheremetev
Publikováno v:
Molecules, Vol 26, Iss 24, p 7452 (2021)
Co-crystallization is an elegant technique to tune the physical properties of crystalline solids. In the field of energetic materials, co-crystallization is currently playing an important role in the engineering of crystals with improved performance.
Externí odkaz:
https://doaj.org/article/b59eb20d9dab40a19c99727162c47901
Autor:
Vladimir V. Bakharev, Alexander А. Gidaspov, Vladimir А. Zalomlenkov, Victor E. Parfenov, Olga V. Golovina, Pavel А. Slepukhin
Publikováno v:
Chemistry of Heterocyclic Compounds. 58:153-158
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::788b011d8d7a7ded2e5b8bef1fd91a61
https://doi.org/10.1007/s10593-022-03068-9
https://doi.org/10.1007/s10593-022-03068-9
Autor:
Alexander A. Lashakov, Vladimir A. Zalomlenkov, Kyrill Yu. Suponitsky, Svetlana V. Osintseva, Aleksei A. Anisimov, Ivan V. Ananyev, Alexander A. Gidaspov
Publikováno v:
Chemistry of Heterocyclic Compounds. 57:266-273
It is well known that the densest molecular crystals formed by molecules consisting of C, H, N, O, and F atoms are those of polynitro compounds that do not and cannot participate in strong intermolecular interactions. At the same time, many “typica
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4d5d75acfa7eb2f9fa16ff613da711ce
https://doi.org/10.1007/s10593-021-02903-9
https://doi.org/10.1007/s10593-021-02903-9
Autor:
Alexander F. Smol'yakov, Kyrill Yu. Suponitsky, Artem V. Khakhalev, Alexander A. Gidaspov, Ivan V. Ananyev, Aleksei B. Sheremetev
Publikováno v:
ChemistrySelect. 5:14543-14548
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c691e01e17e4b96bcd3a169d487bd765
https://doi.org/10.1002/slct.202004020
https://doi.org/10.1002/slct.202004020
Publikováno v:
Chemistry of Heterocyclic Compounds. 53:659-669
This review covers the methods applicable for the synthesis of (dinitromethyl)azines: nitration of azine derivatives, azine ring formation,nucleophilic su bstitution in azine rings by the action of dinitrocarbanions, and denitration of trinitromethyl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e84dc14646d05616fd3bee3aa986e49b
https://doi.org/10.1007/s10593-017-2107-8
https://doi.org/10.1007/s10593-017-2107-8
Autor:
Eugenia V. Selezneva, Alexander A. Gidaspov, Irina V. Ul′yankina, Victor E. Parfenov, Anna V. Zavodskaya, Vladimir V. Bakharev, A. K. Shiryaev
Publikováno v:
Chemistry of Heterocyclic Compounds. 52:1054-1060
The results of pioneering research on the alkylation of fused [1,2,4]triazolo[1,5-a][1,3,5]triazine system are presented, including computational studies of the reaction between 5-dimethylamino[1,2,4]triazolo[1,5-a][1,3,5]triazin-7(3H)-one and bromoe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::19990f496f45596667c6af32cdb9cd2a
https://doi.org/10.1007/s10593-017-2006-z
https://doi.org/10.1007/s10593-017-2006-z
Autor:
Victor E. Parfenov, A. K. Shiryaev, Alexander A. Gidaspov, Pavel A. Slepukhin, Vladimir V. Bakharev
Publikováno v:
Chemistry of Heterocyclic Compounds. 52:1061-1069
The alkylation reactions of fused tetrazolo[1,5-a][1,3,5]triazine system were studied. The results of quantum-chemical calculations for the reaction of 5-(dimethylamino)tetrazolo[1,5-a][1,3,5]triazin-7(3H)-one with ethyl bromide are presented. The re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8e39128599e9463bf247cc6a12056e22
https://doi.org/10.1007/s10593-017-2007-y
https://doi.org/10.1007/s10593-017-2007-y
Autor:
Boris B. Averkiev, Eugenia V. Selezneva, Marat R. Baymuratov, Victor E. Parfenov, Alexander A. Gidaspov, Vladimir V. Bakharev, Aleksei B. Sheremetev
Publikováno v:
Heterocyclic Communications. 22:7-10
A simple and convenient method for the preparation of 2,4-disubstituted 1,3,5-triazine-nitrolic acids has been developed. The first example of nitrolic acid with Z-configuration was revealed by X-ray crystallographic analysis.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::063286e922ea3b33e8bf6c86f81cc2c3
https://doi.org/10.1515/hc-2015-0218
https://doi.org/10.1515/hc-2015-0218
Autor:
Kyrill Yu. Suponitsky, Alexander A. Gidaspov, Vladimir V. Bakharev, Valery G. Nikitin, Aleksei B. Sheremetev
Publikováno v:
RSC Advances. 6:104325-104329
An efficient and reliable synthesis of 2,4,6-tris(2-fluoro-2,2-dinitroethoxy)-1,3,5-triazine (1) has been developed. The ether 1 was fully characterized by IR and multinuclear NMR spectroscopy, and X-ray crystal structure determinations. The compound
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3514daa6fde80d2ee712370f0e4360bd
https://doi.org/10.1039/c6ra24629j
https://doi.org/10.1039/c6ra24629j
Autor:
Vladimir A. Zalomlenkov, Marina I. Struchkova, Victor E. Parfenov, Aleksei B. Sheremetev, Vladimir V. Bakharev, David B. Lempert, Nadezhda V. Palysaeva, Evgeniy V. Yurtaev, Kyrill Yu. Suponitsky, Alexander A. Gidaspov
Publikováno v:
RSC Advances. 6:34921-34934
The multicomponent reaction of 2,4,6-trichloro-1,3,5-triazine with potassium trinitromethane and trinitroethanol was exploited for the first synthesis of the hetaryl trinitroethyl ether, 2,4-bis(2,2,2-trinitroethoxy)-6-trinitrometyl-1,3,5-triazine 13
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a835af4634391ddd7c5b7a3dd4432016
https://doi.org/10.1039/c6ra05826d
https://doi.org/10.1039/c6ra05826d