Zobrazeno 1 - 10
of 23
pro vyhledávání: '"M. Yu. Krysin"'
Publikováno v:
Russian Journal of Applied Chemistry. 95:264-269
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e52ffd20dffa11627a81340241919b20
https://doi.org/10.1134/s1070427222020057
https://doi.org/10.1134/s1070427222020057
Autor:
Vladimir B. Sulimov, I. S. Ilin, Danil C. Kutov, E A Volosnikova, Kh. S. Shikhaliev, O V Pyankov, A. V. Sulimov, Nadezhda V. Stolpovskaya, V Yu Chirkova, S V Belenkaya, Anna Tashchilova, D. V. Krylskiy, M. Yu. Krysin, D N Shcherbakov
Publikováno v:
Biomeditsinskaia khimiia. 67(3)
Docking and quantum-chemical methods have been used for screening of drug-like compounds from the own database of the Voronezh State University to find inhibitors the SARS-CoV-2 main protease, an important enzyme of the coronavirus responsible for th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d4b5b74cba376e35b5c304494b22f9ca
https://pubmed.ncbi.nlm.nih.gov/34142533
https://pubmed.ncbi.nlm.nih.gov/34142533
Publikováno v:
Chemistry of Heterocyclic Compounds. 50:1280-1290
The Stolle type reaction of 3,4-dihydro-1H-spiro[quinoline-2,1'-cycloalkane] hydrochlorides with oxalyl chloride gave 6-methyl-5,6-dihydrospiro[pyrrolo[3,2,1-ij]quinoline-4,1'-cycloalkane]-1,2-diones, which were used in cyclocondensation with various
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9b0f26e1a524e4c0ca5f1da20a619606
https://doi.org/10.1007/s10593-014-1590-4
https://doi.org/10.1007/s10593-014-1590-4
Publikováno v:
Chemistry of Heterocyclic Compounds. 50:1316-1321
The reaction of 1,2-diamino-4-phenylimidazole with 5,5-R,R1-cyclohexane-1,3-diones and with the dimethyl formamide dimethyl acetal or triethyl orthoformate gives 7,7-R,R1-3-amino-1-phenyl-7,8-di-hydroimidazo[1,5-b]cinnolin-9(6H)-ones in good yield. T
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d0656394e7459bdf04479a2bbf7f4f1b
https://doi.org/10.1007/s10593-014-1594-0
https://doi.org/10.1007/s10593-014-1594-0
Autor:
Sergey I. Firgang, E. S. Malikova, G. A. Stashina, S. M. Medvedeva, M. Yu. Krysin, Kh. S. Shikhaliev
Publikováno v:
Chemistry of Heterocyclic Compounds. 50:537-543
A 1,3-dipolar cycloaddition reaction of N-aryl maleimides with azomethine ylides obtained from aromatic aldehydes and alkyl(3-oxopiperazin-2-yl)acetates gave a new heterocyclic system – decahydro-3bH-pyrrolo[3',4':3,4]pyrrolo[1,2-a]pyrazine.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::91412c1197984874ea01f8e5455f39bf
https://doi.org/10.1007/s10593-014-1504-5
https://doi.org/10.1007/s10593-014-1504-5
Publikováno v:
Chemistry of Heterocyclic Compounds. 50:587-589
Imidazotriazines are used as dyes, luminophores, and corrosion inhibitors [1, 2]. Earlier these compounds were obtained on the basis of diaminopyridinium salts, and this was not economically feasible. We decided to study an alternative method for the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::68da483a6a112246be8b852e2da31671
https://doi.org/10.1007/s10593-014-1512-5
https://doi.org/10.1007/s10593-014-1512-5
Publikováno v:
ChemInform. 46
The reaction of 1,2-diamino-4-phenylimidazole with 5,5-R,R1-cyclohexane-1,3-diones and with the dimethyl formamide dimethyl acetal or triethyl orthoformate gives 7,7-R,R1-3-amino-1-phenyl-7,8-di-hydroimidazo[1,5-b]cinnolin-9(6H)-ones in good yield. T
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6e37dfb0c23e124c7d137c610805f547
https://doi.org/10.1002/chin.201526219
https://doi.org/10.1002/chin.201526219
Publikováno v:
Chemistry of Heterocyclic Compounds. 42:935-942
The previously unknown three component condensation of hetarylguanidines, orthoesters, and active methylene carbonyl compounds has been studied. Depending on the nature of the latter products of both linear combination and subsequent cyclizationl lea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::889f496a00a238d060c761852814ca87
https://doi.org/10.1007/s10593-006-0183-2
https://doi.org/10.1007/s10593-006-0183-2
Publikováno v:
ChemInform. 45
using the three-component reaction of 1,2-diaminoimidazoles (I) with primary amines and formaldehyde
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b8c99e3ec3f52585d26c8055ba27d487
https://doi.org/10.1002/chin.201451187
https://doi.org/10.1002/chin.201451187
Autor:
S. M. Medvedeva, E. S. Malikova, Kh. S. Shikhaliev, M. Yu. Krysin, G. A. Stashina, Sergey I. Firgang
Publikováno v:
ChemInform. 45
The title cycloaddition reaction furnishes representatives of a new heterocyclic system, decahydropyrrolopyrrolopyrazine, as a mixture of exo- and endo-diastereomers.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2064db3d0aeb3e658ce98d06c5f16ab3
https://doi.org/10.1002/chin.201451181
https://doi.org/10.1002/chin.201451181