Zobrazeno 1 - 10
of 57
pro vyhledávání: '"V. S. Matiichuk"'
Publikováno v:
Aktualʹnì Pitannâ Farmacevtičnoï ì Medičnoï Nauki ta Praktiki, Vol 14, Iss 3, Pp 320-327 (2021)
The problem of finding effective low-toxic anticancer agents is one of the most important in modern medicine and pharmacy. Despite a large selection of anticancer drugs and a variety of mechanisms of their action, the effectiveness of existing drugs
Externí odkaz:
https://doaj.org/article/2546cc6c90554ff1aca329df70fe4731
Publikováno v:
Aktualʹnì Pitannâ Farmacevtičnoï ì Medičnoï Nauki ta Praktiki, Vol 12, Iss 2, Pp 129-134 (2019)
Condensed bicyclic systems with thiazolidine core being annulated to pyridine one occupy prominent place in medicinal chemistry because of their broad spectrum of pharmacological activities. So, the synthesis of new N3 substitutes thiazolo[4,5-b]pyri
Externí odkaz:
https://doaj.org/article/38c595cee4e84b48abcfbeb18b70aa47
Autor:
V. Ya. Horishny, V. S. Matiichuk
Publikováno v:
Russian Journal of Organic Chemistry. 56:1557-1561
The reactions of 2-cyano-3-oxobutanethioamide with ethyl 3-aryl-2-bromopropanoates and dialkyl acetylenedicarboxylates afforded a combinatorial library of new 2-[5-(R-benzyl)-4-oxo-1,3-thtiazolidin-2-ylidene]-3-oxobutanenitrile and [2-(1-cyano-2-oxop
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fc9737b78b8f4c9fd36f4db61a4d39b8
https://doi.org/10.1134/s1070428020090092
https://doi.org/10.1134/s1070428020090092
Publikováno v:
Russian Journal of Organic Chemistry. 53:62-65
Ethyl 1-aryl-4-acetyl-5-methyl-1H-pyrazole-3-carboxylates reacted with phenylhydrazine to give the corresponding hydrazones, ethyl 1-aryl-5-methyl-4-[1-(phenylhydrazinylidene)ethyl]-1H-pyrazole-3-carboxylates, which were converted to ethyl 1′-aryl-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ff07500f9550ebe47a04eeaf2bdb2887
https://doi.org/10.1134/s1070428017010110
https://doi.org/10.1134/s1070428017010110
Publikováno v:
Russian Journal of Organic Chemistry. 54:799-801
Reaction of 3-aryl-2-chloropropanal with 1-arylsulfonylpropan-2-ones in aqueous ammonia and alcohol under the conditions of Hantzsch pyrrole synthesis led to the selective formation of the products of interrupted Feist-Benary reaction, 2-(R-benzyl)-4
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9593424417692f8ffbf25f60cf651449
https://doi.org/10.1134/s1070428018050238
https://doi.org/10.1134/s1070428018050238
Publikováno v:
Aktualʹnì Pitannâ Farmacevtičnoï ì Medičnoï Nauki ta Praktiki, Vol 12, Iss 2, Pp 129-134 (2019)
Condensed bicyclic systems with thiazolidine core being annulated to pyridine one occupy prominent place in medicinal chemistry because of their broad spectrum of pharmacological activities. So, the synthesis of new N3 substitutes thiazolo[4,5-b]pyri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7138055023c4162dfa884bf553ba1852
https://doi.org/10.14739/2409-2932.2019.2.170974
https://doi.org/10.14739/2409-2932.2019.2.170974
Publikováno v:
Russian Journal of Organic Chemistry. 53:481-483
A convenient procedure was developed for the synthesis of 2-azidobicyclo[2.2.1]heptane whose click reaction with phenylacetylene afforded 1-(bicyclo[2.2.1]heptan-2-yl)-4-phenyl-1H-1,2,3-triazol, and its reactions with ethyl α-bromoacrylate and ethyl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::956952d0762071f4a3c5503dcecfe2a2
https://doi.org/10.1134/s1070428017030332
https://doi.org/10.1134/s1070428017030332
Publikováno v:
Russian Journal of Organic Chemistry. 50:275-279
Reaction of 5-methyl-1-aryl-1H-1,2,3-triazole-4-carbocylic acid chlorides with tryptamine derivatives afforded substituted 1-aryl-N-[2-(1H-indol-3-yl)ethyl]-5-methyl-1H-1,2,3-triazole-4-carboxamides. At heating these compounds in toluene in the prese
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3a0712875075693df20dd9fd0a6668ca
https://doi.org/10.1134/s1070428014020225
https://doi.org/10.1134/s1070428014020225
Publikováno v:
Russian Journal of Organic Chemistry. 48:519-522
A simple and convenient procedure was proposed for the synthesis of 4-aryl-3-bromobutan-2-ones from methyl vinyl ketone and arenediazonium bromides under Meerwein reaction conditions.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::305dcdeae0b5d647010291cafc6d5d40
https://doi.org/10.1134/s1070428012040094
https://doi.org/10.1134/s1070428012040094
Publikováno v:
Russian Journal of Organic Chemistry. 53:479-480
(4-Amino-1,3-thiazol-2-ylsulfanyl)acetic acids were synthesized by reaction of α-thiocyanatonitriles with sulfanylacetic acid in boiling acetonitrile.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::59a751be2b97a1af5839e44dc681f948
https://doi.org/10.1134/s1070428017030320
https://doi.org/10.1134/s1070428017030320