Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Pavel А. Slepukhin"'
The features of the Michael reaction in ([1,2,4]triazolo[4,3-a][1,3,5]triazin-5-yl)dinitromethanides
Autor:
Olga V. Golovina, Victor E. Parfenov, Pavel А. Slepukhin, Dmitry V. Khakimov, Aleksei B. Sheremetev, Vladimir V. Bakharev
Publikováno v:
Chemistry of Heterocyclic Compounds. 58:506-513
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5cea4d69bd6faf9fc1529fa3b4b0eb13
https://doi.org/10.1007/s10593-022-03120-8
https://doi.org/10.1007/s10593-022-03120-8
Autor:
Marina V. Goryaeva, Olesya А. Fefelova, Yanina V. Burgart, Marina А. Ezhikova, Mikhail I. Kodess, Pavel А. Slepukhin, Galina А. Triandafilova, Sergey Yu. Solodnikov, Olga P. Krasnykh, Victor I. Saloutin
Publikováno v:
Chemistry of Heterocyclic Compounds. 58:421-431
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4568295be778f694721fe361364fc9fe
https://doi.org/10.1007/s10593-022-03108-4
https://doi.org/10.1007/s10593-022-03108-4
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:
Pavel А. Slepukhin, Yana L Esaulkova, G. G. Danagulyan, Olga S Zarubina, R. E. Trifonov, Olga M. Nesterova, Vladimir V. Zarubaev, Vladimir V Tolstyakov, Yulia N. Pavlyukova, Anna А Muryleva, Vladimir А Ostrovskii
Publikováno v:
Chemistry of Heterocyclic Compounds. 57:448-454
Nonannulated tetrazolylpyrimidines in the structure of which the heterocyclic fragments are separated by hydrazinocarbonylmethyl, methylpyrazolyl groups or a sulfur atom were synthesized. Some of these compounds showed moderate in vitro activity agai
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a30f2fb62fb3979276a1caabde19ad9f
https://doi.org/10.1007/s10593-021-02922-6
https://doi.org/10.1007/s10593-021-02922-6
Autor:
Valeriy O. Filimonov, Tetyana Beryozkina, Vasiliy А. Bakulev, Zhijin Fan, Pavel А. Slepukhin, Lidiya N. Dianova
Publikováno v:
Chemistry of Heterocyclic Compounds. 56:1341-1347
The reaction of 5-amino-1-aryl-1,2,3-triazole-4-carbothioamides with sulfonyl chlorides and acetyl and benzoyl chlorides is accompanied by the Dimroth rearrangement and proceeds regiospecifically with the formation of 5-arylamino-2-sulfonyl(acyl)-1,2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b42368ac8f7811c8107ede697173d3ba
https://doi.org/10.1007/s10593-020-02820-3
https://doi.org/10.1007/s10593-020-02820-3
Autor:
Pavel А. Slepukhin, Oleg N. Chupakhin, Alexey P. Krinochkin, Sravya Gundala, Grigory V. Zyryanov, Dmitry S. Kopchuk, Padmavathi Venkatapuram, Albert F. Khasanov, Valery N. Charushin, Igor L. Nikonov
Publikováno v:
Chemistry of Heterocyclic Compounds. 55:978-984
The reaction of 3,6-bis(het)aryl-1,2,4-triazines (hetaryl ≠ 2-pyridyl) with aryne intermediates generated in situ was studied. As a result, novel 1,4-bis(het)arylisoquinolines were synthesized with yields of up to 45%. The main rules of the reactio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4bba26a20d3ae587395d6b9147a7ad9d
https://doi.org/10.1007/s10593-019-02565-8
https://doi.org/10.1007/s10593-019-02565-8
Autor:
Grigory V. Zyryanov, Vladimir L. Rusinov, Oleg N. Chupakhin, Dmitry S. Kopchuk, Victor V. Fedotov, Pavel А. Slepukhin, Egor K. Voinkov, Valery N. Charushin, Konstantin V. Savateev, Eugeny N. Ulomskiy
Publikováno v:
Chemistry of Heterocyclic Compounds. 55:989-992
The previously described L-argininium 5-methyl-6-nitro-7-oxo-4,7-dihydro-1,2,4-triazolo[1,5-a]pyrimidinide monohydrate and piperidinium 5-methyl-6-nitro-7-oxo-4,7-dihydro-1,2,4-triazolo[1,5-a]pyrimidinide, which has not been described previously, wer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::93fe16e017e20eacb87bae35e7cd4e76
https://doi.org/10.1007/s10593-019-02567-6
https://doi.org/10.1007/s10593-019-02567-6
Autor:
Tatiana А. Pospelova, Dmitriy M. Mazur, Lidiya N. Dianova, Vasiliy А. Bakulev, Valeriy O. Filimonov, Tetyana Beryozkina, Pavel А. Slepukhin
Publikováno v:
Chemistry of Heterocyclic Compounds. 55:547-553
Sulfonylation of 1,2,3-thiadiazolecarboxylic acid amidines in the presence of a base was found to be accompanied by the Cornforth rearrangement of the 1,2,3-thiadiazole ring into 1,2,3-triazole leading to the formation of 2-substituted 1,2,3-triazole
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1370f6d5c0b402fb08b07babced91ad3
https://doi.org/10.1007/s10593-019-02494-6
https://doi.org/10.1007/s10593-019-02494-6
Autor:
Irina G. Ovchinnikova, Elena V. Kalita, Marina А. Ezhikova, Dmitry G. Kim, Pavel А. Slepukhin, Vladimir V. Sharutin, Mikhail I. Kodess, Anna V. Vasilenko
Publikováno v:
Chemistry of Heterocyclic Compounds. 55:566-572
The sequence of condensation, alkylation, and halocyclization reactions during the synthesis of the target 2,3-dihydro[1,3]oxazolo[3,2-a]-pyridinium salts was investigated. The effect of basic catalysis on the chemoselectivity of the reaction of malo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::35bc4288dc5a2a514f5f4052a4ca6b64
https://doi.org/10.1007/s10593-019-02497-3
https://doi.org/10.1007/s10593-019-02497-3
Publikováno v:
Chemistry of Heterocyclic Compounds. 54:1153-1160
A three-step method was designed and developed on the basis of retrosynthetic analysis for the synthesis of hybrid molecules containing a thiazole ring and an N-sulfonyl amidine fragment, connected by a methylene linker. The mechanism of the last ste
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::755600ab3718456ae8d409af96efcf78
https://doi.org/10.1007/s10593-019-02407-7
https://doi.org/10.1007/s10593-019-02407-7