Zobrazeno 1 - 10
of 32
pro vyhledávání: '"V. A. Osyanin"'
Autor:
D. V. Osipov, A. A. Artyomenko, K. S. Korzhenko, D. A. Rashchepkina, O. P. Demidov, V. A. Osyanin
Publikováno v:
Russian Journal of Organic Chemistry. 59:422-437
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::70fb5c6f5cea3bc94832011c0f608574
https://doi.org/10.1134/s1070428023030107
https://doi.org/10.1134/s1070428023030107
Publikováno v:
Russian Chemical Bulletin. 71:2451-2459
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0818ef51c132c7af309afffc3c3045ce
https://doi.org/10.1007/s11172-022-3673-1
https://doi.org/10.1007/s11172-022-3673-1
Autor:
Anastasia E. Sibiryakova, Eugene V. Radchenko, Dmitry V. Osipov, Anton V. Lukashenko, M. V. Leonova, Larisa N. Shishkina, Yulia A. Gruzd, Vera A. Shadrikova, M. R. Baimuratov, Vadim A. Shiryaev, Ilya M. Tkachenko, O. A. Serova, E. A. Ivleva, Vladimir A. Palyulin, Alexander N. Reznikov, V. A. Osyanin, Kseniya M. Bormasheva, N. I. Bormotov, Yuri N. Klimochkin, Nikolay S. Zefirov
Publikováno v:
European Journal of Medicinal Chemistry. 158:214-235
The hepatitis C caused by the hepatitis C virus (HCV) is an acute and/or chronic liver disease ranging in severity from a mild brief ailment to a serious lifelong illness that affects up to 3% of the world population and imposes significant and incre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::58e2c1e7176c5d4725dc30b63d7481a7
https://doi.org/10.1016/j.ejmech.2018.08.009
https://doi.org/10.1016/j.ejmech.2018.08.009
Publikováno v:
Chemistry of Heterocyclic Compounds. 50:1528-1533
The reaction of Mannich bases derived from 2-naphthol with 4-(2-nitrovinyl)morpholine or N,N-di-methyl(2-nitrovinyl)amine in acetic anhydride gives 2-nitro-1H-benzo[f]chromenes. This reaction may be regarded formally as the addition of a push-pull ol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c42c782e84e638ebeb44971d732cdd7f
https://doi.org/10.1007/s10593-014-1620-2
https://doi.org/10.1007/s10593-014-1620-2
Publikováno v:
Chemistry of Heterocyclic Compounds. 50:1199-1202
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b2b3e60cec5a211118c3ab240060d107
https://doi.org/10.1007/s10593-014-1582-4
https://doi.org/10.1007/s10593-014-1582-4
Publikováno v:
Chemistry of Heterocyclic Compounds. 49:683-688
5a-Amino-5aH,11H-chromeno[2,3-b]chromene-11a(12H)-carbonitriles were synthesized from malono-nitrile and o-quinone methides, generated in situ by the thermolysis of phenolic Mannich bases in the presence of 1,8-diazabicyclo[5.4.0]undec-7-ene. It was
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::78beec6c40e851b131a6480983091311
https://doi.org/10.1007/s10593-013-1298-x
https://doi.org/10.1007/s10593-013-1298-x
Publikováno v:
Russian Journal of Organic Chemistry. 49:398-402
3-Amino-1H-benzo[f]chromene-2-carbonitriles were synthesized by non-catalytic reaction from Mannich bases of the naphthalene series and malononitrile. Reactive 1-benzylidene(or methylidene)naphthalen-2(1H)-ones were presumed as intermediate products.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d1174d9088f13d1588773a6105893f11
https://doi.org/10.1134/s1070428013030147
https://doi.org/10.1134/s1070428013030147
Publikováno v:
Synthetic Communications. 42:2639-2647
A simple, efficient, and environmentally benign method has been developed for the exclusive formation of synthetically significant 1H-benzotriazol-1-ylalkylphenols from hydroxybenzyl alcohols and benzotriazole.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::536062804b65fa0bd57a9a22acc74771
https://doi.org/10.1080/00397911.2011.563452
https://doi.org/10.1080/00397911.2011.563452
Publikováno v:
Chemistry of Heterocyclic Compounds. 47:845-850
Products of heterocyclization, 9,10-dimethoxy-12,13-dihydro-7aH,15H-naphtho[1',2':5,6][1,3]oxazino-[2,3-a]isoquinolines, were isolated on condensing 6,7-dimethoxy-3,4-dihydroisoquinoline with 1-dimethylaminomethyl-2-naphthols. In the case of o-hydrox
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1b690bb175b6c982eb90d0fd73b906e3
https://doi.org/10.1007/s10593-011-0845-6
https://doi.org/10.1007/s10593-011-0845-6
Publikováno v:
Pharmaceutical Chemistry Journal. 44:303-306
The biological activities of 4-(1H-azol-1-ylmethyl)benzoic acid hydrazides were assessed by studying leukocyte responses to these compounds. The study compounds were found to have stimulatory actions on the body’s general resistance mechanisms.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b108e3d5d0be2da9bed90bd28322917d
https://doi.org/10.1007/s11094-010-0455-0
https://doi.org/10.1007/s11094-010-0455-0