Zobrazeno 1 - 10
of 53
pro vyhledávání: '"S I Filimonov"'
Publikováno v:
Russian Journal of Organic Chemistry. 59:324-327
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::df303b6b82e50719a85bfbbe29951b68
https://doi.org/10.1134/s1070428023020148
https://doi.org/10.1134/s1070428023020148
Autor:
E. S. Makarova, M. V. Kabanova, S. I. Filimonov, Zh. V. Chirkova, A. A. Shetnev, K. Yu. Suponitsky
Publikováno v:
Russian Chemical Bulletin. 71:2255-2262
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::afe0f75881a980772482df7078267763
https://doi.org/10.1007/s11172-022-3653-5
https://doi.org/10.1007/s11172-022-3653-5
Publikováno v:
Russian Chemical Bulletin. 71:1034-1042
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::54d4261891631056bbbcb88d2dc1d52e
https://doi.org/10.1007/s11172-022-3505-3
https://doi.org/10.1007/s11172-022-3505-3
Publikováno v:
Pharmaceutical Chemistry Journal. 56:22-28
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d9f91a3ba2690f09532e4636afa14b0b
https://doi.org/10.1007/s11094-022-02596-0
https://doi.org/10.1007/s11094-022-02596-0
Publikováno v:
From Chemistry Towards Technology Step-By-Step. 3:79-85
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7cb1a5d13096b0b9c4aa156afecf3831
https://doi.org/10.52957/27821900_2022_02_79
https://doi.org/10.52957/27821900_2022_02_79
Autor:
S. I. Filimonov, A. S. Danilova, Mariya V. Kabanova, Anton Shetnev, E. S. Makarova, E. A. Smirnova
Publikováno v:
Russian Chemical Bulletin. 70:1377-1382
A regioselective method for the synthesis of substituted (4R*,5S*,6R*)-2-thioxohexahydro-pyrimidine-5-carbohydrazides from the corresponding diastereomers of hexahydro-2H-chromeno[4,3-d]pyrimidines was developed. In acidic medium, the obtained hydraz
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d092a24a3c42919fa15c44bed2124e05
https://doi.org/10.1007/s11172-021-3226-z
https://doi.org/10.1007/s11172-021-3226-z
Autor:
Valeria A. Panova, Anton Shetnev, Sergey V. Baykov, M. V. Zhmykhova, Marina Tarasenko, S. I. Filimonov, P. M. Kutuzova
Publikováno v:
Russian Journal of General Chemistry. 91:985-990
Abstract A two-stage method for the preparation of 2-(3-carboxymethylindazol-1-yl)anilines using the N-arylation reaction of 3-carboxymethylindazoles with o-nitrohaloarenes and subsequent reduction of nitro-containing intermediates with tin(II) chlor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b093bdd47a436b0a20e7182333a123b7
https://doi.org/10.1134/s1070363221060049
https://doi.org/10.1134/s1070363221060049
Autor:
Zh. V. Chirkova, S. I. Filimonov, Valeria A. Panova, Anton Shetnev, S. A. Ivanovskii, T. N. Sudzilovskaya
Publikováno v:
Russian Chemical Bulletin. 69:1965-1970
New pyrazolo[1,5-a]quinoxalin-4-ones were obtained by reductive cyclization from the corresponding 1-(2-nitroaryl)pyrazole-5-carboxylates. Alternatively, pyrazolo[1,5-a]quinoxalines were prepared from N-hydroxypyrazolo[1,5-a]quinoxalines.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5449ceb099bed0501e0ee81232e729ca
https://doi.org/10.1007/s11172-020-2986-1
https://doi.org/10.1007/s11172-020-2986-1
Publikováno v:
Russian Journal of Organic Chemistry. 56:1383-1391
A facile synthesis of para-quinones derived from fused benzimidazoles with a bridgehead nitrogen atom was developed. The heterocyclic quinone core formed as a result of reductive cyclization of ortho-nitroarenes containing alicyclic and aromatic azah
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c5707afb4df851f95fb7e4820557ce99
https://doi.org/10.1134/s1070428020080084
https://doi.org/10.1134/s1070428020080084
Publikováno v:
Russian Chemical Bulletin. 68:1196-1199
A general and efficient method has been developed for the synthesis of NH-indoles bearing electron-accepting substituents via the modification of corresponding N-hydroxyindoles.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0fb57722b8e748519a7c24cc8b38dd6b
https://doi.org/10.1007/s11172-019-2539-7
https://doi.org/10.1007/s11172-019-2539-7