Zobrazeno 1 - 10
of 28
pro vyhledávání: '"A. B. Eresko"'
Publikováno v:
Russian Journal of Organic Chemistry. 57:180-185
Heterocyclization of ethyl 2-acetyl(aroyl)-5-methylthieno[2,3-b]thiophene-3-acetates with hydrazine hydrate has been studied. A dependence of the reaction direaction on the nature of the substituent in the acyl fragment was established. The heterocyc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e8c541553e8cd8afb8faeb30b99311d7
https://doi.org/10.1134/s107042802102007x
https://doi.org/10.1134/s107042802102007x
Autor:
E. V. Raksha, V. S. Tolkunov, A. A. Voitash, S. V. Tolkunov, A. V. Muratov, Yu. V. Berestneva, A. B. Eresko
Publikováno v:
Russian Journal of Organic Chemistry. 56:1929-1936
A new synthetic approach to fused azepines was demonstrated on an example of the synthesis of 2-methyl-2,3,4,5-tetrahydro-1H-[1]benzothieno[2,3-c]azepine. The key stage of the synthesis is the formation of the azepine ring under the Eschweiler–Clar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::eba7563cc936c07a48347d239c2a36a4
https://doi.org/10.1134/s1070428020110068
https://doi.org/10.1134/s1070428020110068
Publikováno v:
Russian Journal of Organic Chemistry. 55:345-350
A number of new 1-substituted 5,10-dihydro[1,2]diazepino[4,5-b]indole-4(3H)-ones were synthesized, and their structural modification was performed to obtain previously unknown amino and fused triazolo derivatives.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::58f000612ab063503c887af8c71fc6b3
https://doi.org/10.1134/s1070428019030126
https://doi.org/10.1134/s1070428019030126
Autor:
Yu. V. Berestneva, A. A. Voitash, V Yu Popov, A. B. Eresko, D I Matveyeva, E. V. Raksha, S Yu Zinchenko, A. V. Muratov
Publikováno v:
International Journal of Chemistry and Research. 1:9-12
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6b846c1e7702502af29e3597326d37e5
https://doi.org/10.18689/ijcr-1000102
https://doi.org/10.18689/ijcr-1000102
Autor:
A. A. Voitash, Yu. I. Yurasov, E. V. Raksha, V. A. Glazunova, A. V. Muratov, I. A. Verbenko, A. B. Eresko, O. N. Oskolkova, M. V. Savoskin, Yuliya Berestneva, A. A. Davydova
Publikováno v:
Springer Proceedings in Materials ISBN: 9783030764807
This paper presents the results of complex investigations of structural and physicochemical properties of thermally expanded graphite (TEG) based on graphite nitrate, cointercalated with formic and acetic acids. Consideration was given to possibility
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bf65bf33ab034a6014683306dcf0bbf4
https://doi.org/10.1007/978-3-030-76481-4_5
https://doi.org/10.1007/978-3-030-76481-4_5
Publikováno v:
Russian Journal of Organic Chemistry. 54:861-866
A new strategy has been proposed for the synthesis of 5H-[1]benzofuro[2,3-d][1,2]diazepines containing two aryl substituents in the diazepine fragment. The key stage of the synthesis is intramolecular cyclization of the corresponding hydrazides under
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a2a570fd5c725e6447dc21a1ea49862c
https://doi.org/10.1134/s1070428018060064
https://doi.org/10.1134/s1070428018060064
Autor:
S. V. Tolkunov, T. M. Chervyakova, V. S. Tolkunova, A. B. Eresko, D. V. Galaktionova, Alexey V. Varlamov, Tatiana N. Borisova, Leonid G. Voskressensky, Maria D. Matveeva
Publikováno v:
Chemistry of Heterocyclic Compounds. 50:1338-1345
1-Aryl-substituted tetrahydrothieno[3,2-с]pyridines easily undergo domino reactions with activated alkynes, giving good yields of the corresponding tetrahydrothieno[2,3-d]azocines. The reactions of 1-methyl-substituted tetrahydrothieno[3,2-с]pyridi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::447664ece58e5a8ce52b5197b12186a0
https://doi.org/10.1007/s10593-014-1597-x
https://doi.org/10.1007/s10593-014-1597-x
Publikováno v:
Chemistry of Heterocyclic Compounds. 49:941-948
Acylation of 5-(benzothiophen-3-yl)pyrimidine-2,4,6(1H,3H,5H)-trione using acetic and propionic anhydride in the presence of 70% perchloric acid gave the 6-methyl(ethyl)-1,3-dioxo-1,2,3,4-tetra-hydro[1]benzothieno[3',2':4,5]pyrano[2,3-d]pyrimidin-5-i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5aed5b295f7bece27fec3229069d9a5f
https://doi.org/10.1007/s10593-013-1329-7
https://doi.org/10.1007/s10593-013-1329-7
Autor:
Tatiana N. Borisova, Cosimo Altomare, Leonid G. Voskressensky, Anna V. Listratova, S. A. Kovaleva, S. V. Tolkunov, V. S. Tolkunov, M. De Candia, Alexey V. Varlamov, A. B. Eresko
Publikováno v:
Chemistry of Heterocyclic Compounds. 49:930-940
A study was carried out on the domino transformations of tetrahydrobenzofuro[2,3-c]pyridines and tetrahydrobenzofuro[3,2-c]pyridines by the action of activated alkynes in methanol and acetonitrile. This reaction is a new method for the synthesis of s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f7ee1eae6593855ec3379d2d414c4840
https://doi.org/10.1007/s10593-013-1328-8
https://doi.org/10.1007/s10593-013-1328-8
Autor:
I. V. Klimenko, Elena R. Andreeva, A. V. Lobanov, A. B. Eresko, N. A. Turovskij, O. O. Udartseva, G. E. Zaikov, V. N. Gorshenev, G. A. Gromova, M. Ya. Mel’nikov, E. V. Raksha, G. S. Larionova, Yu. G. Gorbunova, Ludmila Buravkova, Yu. V. Berestneva
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a6ecec21570a734da6b6bad275f71f1e
https://doi.org/10.1201/9781315366333-13
https://doi.org/10.1201/9781315366333-13