Zobrazeno 1 - 10
of 18
pro vyhledávání: '"E. A. Lisitsa"'
Autor:
Y. G. Shipilov, E. S. Lisitsa
Publikováno v:
Евразийская интеграция: экономика, право, политика, Vol 0, Iss 2, Pp 67-71 (2019)
Spitsbergen (Svalbard) - polar archipelago located in the Arctic Ocean. The Svalbard Treaty was signed in 1920, granting full sovereignty to Norway. But despite the fact that the question of the legal status of Spitsbergen resolved, there still contr
Externí odkaz:
https://doaj.org/article/1688d88f988e42b285d6b8e0a4350be2
Autor:
Tatiyana V. Apanasovich, E. V. Lisitsa, M. M. Shytsik, Vladimir V. Apanasovich, Mikalai M. Yatskou
Publikováno v:
Journal of Applied Spectroscopy. 81:996-1003
We have developed a simulation model for three-channel luminescent images of cancer cells. We do a comparative analysis of two methods for segmentation of objects within three-channel luminescent images, employed in the CellProfiler and CellDataMiner
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ad06c878b62682a1a27a3aa4e589db4d
https://doi.org/10.1007/s10812-015-0041-z
https://doi.org/10.1007/s10812-015-0041-z
Publikováno v:
Russian Chemical Bulletin. 56:1595-1602
The reactions of 3-[N-chloracetylamino-N-(4-nitrophenyl)]-2-formylindole (1a) with 2-(N, N-dialkylamino)ethylamines afford complex condensation products 7b,c consisting of two similar but not identical diazepinoindole fragments. For the reaction of c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b8f3d502bcc6142f91b883ff906ee3de
https://doi.org/10.1007/s11172-007-0249-z
https://doi.org/10.1007/s11172-007-0249-z
Autor:
Vladimir G Granik, D. M. Papakhin, V. A. Parshin, S. Yu. Ryabova, L. M. Alekseeva, E. A. Lisitsa, N. A. Rastorgueva
Publikováno v:
Russian Chemical Bulletin. 55:2278-2284
Reactions of 3-[(N-aryl-N-chloroacetyl)amino]-2-formylindoles with substituted anilines gave 1,4-diaryl-2-oxo-1,2,3,6-tetrahydro[1,4]diazepino[6,5-b]indol-4-ium chlorides and those with 4-aminopyridine yielded 4-amino-1-(1-aryl-2-oxo-2,5-dihydro-1H-p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dda4a456ab3a4363612930dc9b8931df
https://doi.org/10.1007/s11172-006-0583-6
https://doi.org/10.1007/s11172-006-0583-6
Publikováno v:
Pharmaceutical Chemistry Journal. 38:109-112
The class of isomeric pyrimidoindoles and their derivatives contain many compounds possessing biological activity of various types, including analgesic [1, 2], vasodilating [3], antihypoxant [4], antiinflammatory [5], inotropic [6], etc. Recently, it
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bb991eb609ece42ae525b1fe780a0c1e
https://doi.org/10.1023/b:phac.0000032491.18510.b3
https://doi.org/10.1023/b:phac.0000032491.18510.b3
Publikováno v:
Russian Chemical Bulletin. 52:1386-1398
A number of 1-aryl-2-oxo-1,2,3,6-tetrahydro[1,4]diazepino[6,5-b]indole 4-oxides were synthesized based on 3-[N-aryl-N-(chloroacetyl)amino]-2-formylindoles. The nature of the substituent in the 1-aryl fragment has a pronounced influence on the course
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0250e65ede063c09f93dda3008290f99
https://doi.org/10.1023/a:1024887429776
https://doi.org/10.1023/a:1024887429776
Publikováno v:
Chemistry of Heterocyclic Compounds. 28:1289-1292
3-Ethoxycarbonylquinuclidine obtained by the Grob method is a mixture of 3-ethoxycarbonyl-1-azabicylo-[2.2.2]- and, according to 13C NMR data, 5-ethoxycarbonyl-5-azatricyclo[3.2.1.02,7]octanes (∼16∶2∶1). 3-Ethoxy-carbonylquinuclidine was purifi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::87e4ffaf7e5600a6e1c5db05ef4c0a39
https://doi.org/10.1007/bf00532080
https://doi.org/10.1007/bf00532080
Autor:
S. S. Kiselev, M. I. Evstratova, Vladimir G Granik, S. Yu. Ryabova, N. S. Masterova, L. M. Alekseeva, E. A. Lisitsa
Publikováno v:
ChemInform. 38
Reactions of 2-(3,3-diamino-2-cyanoprop-2-enylidene)indolin-3-ones with amide acetals afforded derivatives of 3-aminomethyleneamino-2-cyano-9-oxo-9H-pyrrolo[1,2-a]indole and 3-amino-2-cyano-9-oxo-9H-pyrrolo[1,2-a]indole. The rate and pathway of the r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::72bb4c3e08e5fc7e30a656c70cb3a9af
https://doi.org/10.1002/chin.200745118
https://doi.org/10.1002/chin.200745118
Publikováno v:
ChemInform. 38
3-Arylamino-2-formylindoles were converted into oximes and then acetylated to give the corresponding O-acetyl derivatives. Chloroacetylation of the latter was accompanied by elimination of acetic acid, yielding 3-(N-aryl-N-chloroacetyl)amino-2-cyanoi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c2681f20b9e61371badef6413495632b
https://doi.org/10.1002/chin.200716142
https://doi.org/10.1002/chin.200716142
Publikováno v:
ChemInform. 35
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8697c580cdf8e0bef671891a54908476
https://doi.org/10.1002/chin.200430149
https://doi.org/10.1002/chin.200430149