Zobrazeno 1 - 10
of 67
pro vyhledávání: '"S. L. Bogza"'
Publikováno v:
Журнал органічної та фармацевтичної хімії, Vol 18, Iss 4(72), Pp 23-27 (2020)
Aim. To synthesize 4-cyanoindolo[2,3-c]pyrilium salts and examine their reactivity towards N-nucleophiles. Results and discussion. The acylation reaction of 2-(indolyl-3)-2-aroylacetonitriles under acid catalysis conditions was studied. 4-Cyanoindolo
Externí odkaz:
https://doaj.org/article/be519b83de6d4d6eb57dcbc8b5e369f1
Publikováno v:
Journal of Education, Health and Sport, Vol 7, Iss 1, Pp 525-533 (2017)
Objective of the research. Provide the analysis of the neurologic deficit in dynamics under the experimental traumatic brain injury and methods of its correction by Carbacetam. Materials and the methods of research. The research was held by means of
Externí odkaz:
https://doaj.org/article/cd35648ce444439981f7103b5f1d2a9c
Autor:
L. Ya. Shtanova, P. I. Yanchuk, S. P. Vesеlsky, O. V. Tsymbalyuk, T. V. Vovkun, V. S. Moskvina, O. V. Shablykina, S. L. Bogza, V. N. Baban, A. A. Kravchenko, V. P. Khilya
Publikováno v:
The Ukrainian Biochemical Journal, Vol 92, Iss 6, Pp 85-94 (2003)
Parkinson’s disease (PD) is a chronic and progressive age-related neurodegenerative disorder. Accumulation of α-synuclein aggregates, oxidative stress, mitochondrial dysfunction and lipid metabolism disturbance are thought to be the key violations
Externí odkaz:
https://doaj.org/article/d5c4715a35d7471ab95a743a5e762df4
Autor:
N. M. Bogdan, Kyiv Ukrorgsyntes Ltd, D.S. Stepanova, S. L. Bogza, V.V. Pendiukh, S.Yu. Sujkov
Publikováno v:
Reports of the National Academy of Sciences of Ukraine. :62-71
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::00649c3050b3bf1a8af62cb0e27d43b6
https://doi.org/10.15407/dopovidi2020.07.062
https://doi.org/10.15407/dopovidi2020.07.062
Autor:
S.P. Veselsky, O. V. Tsymbalyuk, I. P. Yanchuk, V. P. Khilya, T. V. Vovkun, S. L. Bogza, O. V. Shablykina, L. Ya. Shtanova, Viktoria S. Moskvina
Publikováno v:
Biopolymers and Cell. 35:356-370
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b89c76891ea43621a87d0400cada0e13
https://doi.org/10.7124/bc.000a13
https://doi.org/10.7124/bc.000a13
Publikováno v:
Reports of the National Academy of Sciences of Ukraine. :81-87
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::76d688b179126fe20fb0cee4bf33b5fd
https://doi.org/10.15407/dopovidi2018.04.081
https://doi.org/10.15407/dopovidi2018.04.081
Autor:
L. S. Skorokhod, S. Yu. Suikov, V. I. Pavlovskii, A. V. Pulya, S. L. Bogza, V. Kh. Kravtsov, I. I. Seifullina
Publikováno v:
Journal of Structural Chemistry. 59:497-501
Hydrazone [HydrHSal]∙Н2О is synthesized for the first time by the interaction of 2-(7-bromo-2-oxo-5- phenyl-3H-1,4-benzdiazepin-1-yl)acetohydrazide (gidazepam) with salicylic aldehyde and characterized by the elemental analysis, thermogravimetry,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3ee40042ed4c9135a3c7220d96d7e773
https://doi.org/10.1134/s002247661802035x
https://doi.org/10.1134/s002247661802035x
Autor:
S. L. Bogza
Publikováno v:
Nauka ta Innovacii, Vol 11, Iss 6, Pp 85-93 (2015)
Review of the investigations in the field of heterocyclic chemistry and medicinal chemistry in the Department of Biologically Active Compounds of L.M. Litvinenko Institute of Physical Organic and Coal Chemistry of NAS of Ukraine is presented. The res
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fb2a6de31bd8288dbe8a14e9b8ba60cc
https://doi.org/10.15407/scin11.06.085
https://doi.org/10.15407/scin11.06.085
Publikováno v:
Chemistry of Heterocyclic Compounds. 49:1352-1357
A method for the synthesis of 2-R-2-(1-aryl-7,8-dimethoxy-5H-2,3-benzodiazepin-4-yl)acetic acid esters from 2-R-2-(1-aryl-7,8-dimethoxy-5H-2,3-benzodiazepin-4-ylsulfanyl)acetic acid esters through Eschenmoser reaction has been developed.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::aabc782d475f8f004fc658d2d1f2969f
https://doi.org/10.1007/s10593-013-1384-0
https://doi.org/10.1007/s10593-013-1384-0
Publikováno v:
Chemistry of Heterocyclic Compounds. 49:317-324
A method has been developed for the cyclization of 4-aryl-1-hydrazino-5H-2,3-benzodiazepine and 1-aryl-4-hydrazino-5H-2,3-benzodiazepine into 3-R-6-aryl-7H-[1,2,4]triazolo[3,4-a]- and 3-R-6-aryl-7H-[1,2,4]triazolo[4,3-c]benzodiazepine derivatives wit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4c6de3613fd344e8cd5db7209f155d7c
https://doi.org/10.1007/s10593-013-1249-6
https://doi.org/10.1007/s10593-013-1249-6