Zobrazeno 1 - 10
of 25
pro vyhledávání: '"T. M. Gabbasov"'
Publikováno v:
Chemistry of Natural Compounds. 58:1108-1113
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::870683eeaaf2eacd11bdc78455909a27
https://doi.org/10.1007/s10600-022-03878-5
https://doi.org/10.1007/s10600-022-03878-5
Publikováno v:
Chemistry of Natural Compounds. 58:784-787
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e69ad45a750b676e6a08ce5586b9ac08
https://doi.org/10.1007/s10600-022-03796-6
https://doi.org/10.1007/s10600-022-03796-6
Publikováno v:
Chemistry of Natural Compounds. 57:1066-1073
New lappaconitine, N-deacetyllappaconitine, and lappaconine derivatives with C-19 C–C-bonded substituents were prepared from lappaconitine–isoxazolidine hybrids by reductive and oxidative opening of isoxazolidine rings annelated to the lappaconit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4c4190e85161dc0b899fee2085873b59
https://doi.org/10.1007/s10600-021-03551-3
https://doi.org/10.1007/s10600-021-03551-3
Publikováno v:
Chemistry of Natural Compounds. 57:727-730
Oxidative halogenation of lappaconitine and N-deacetyllappaconitine HBr or HCl in the presence of H2O2 in MeOH was associated upon bromination by N-20-deethylation and produced the 3′,5′-dibromo derivative of N-20-nordeacetyllappaconitine; upon c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dc11eb25f36b2128675e22bd7f0954ff
https://doi.org/10.1007/s10600-021-03459-y
https://doi.org/10.1007/s10600-021-03459-y
Publikováno v:
Chemistry of Natural Compounds. 57:512-515
A series of new lappaconitine structural analogs were prepared via esterification of the lappaconine C-4 hydroxyl by aromatic acids.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::de8b1a972541e21d79590c4fa981b009
https://doi.org/10.1007/s10600-021-03399-7
https://doi.org/10.1007/s10600-021-03399-7
Publikováno v:
Russian Chemical Bulletin. 70:515-519
Bromination of lappaconitine with a KBr—H2O2 mixture in 20% H2SO4, as well as with molecular Br2 in either Py, CH2Cl2, CH3COOH, or DMSO did not occur, while the initial lappaconitine was isolated from the reaction mixture. Such a bromination with m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ed96f30466f13ba50dd2465141c39afb
https://doi.org/10.1007/s11172-021-3117-3
https://doi.org/10.1007/s11172-021-3117-3
Autor:
S. F. Petrova, A. Z. Sadikov, Sergey P. Ivanov, T. M. Gabbasov, M. S. Yunusov, E. M. Tsyrlina, Sh. Sh. Sagdullaev, E. I. Andrianova
Publikováno v:
Chemistry of Natural Compounds. 56:767-770
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3a8b7a2cec46039a23a48fdf15556871
https://doi.org/10.1007/s10600-020-03145-5
https://doi.org/10.1007/s10600-020-03145-5
Autor:
E. M. Tsyrlina, Sergey P. Ivanov, Leonid V. Spirikhin, N. V. Valiev, A. Z. Sadikov, M. S. Yunusov, Sh. Sh. Sagdullaev, A. A. Akhiyarov, Alexander N. Lobov, T. M. Gabbasov
Publikováno v:
Russian Chemical Bulletin. 69:567-571
The data on antiarrhythmic drugs based on diterpene alkaloid lappaconitine are summarized. N-Deacetyllappaconitine is the main metabolite of allapinin and a potential antiarrhythmics for intravenous use. The basicity of two nitrogen atoms of this com
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8dfd712c6be0ae9b131bb3878c4fbdc5
https://doi.org/10.1007/s11172-020-2800-0
https://doi.org/10.1007/s11172-020-2800-0
Publikováno v:
Chemistry of Natural Compounds. 57:594-596
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c6f18589bcda343ef140ee5c1c6ab2a1
https://doi.org/10.1007/s10600-021-03428-5
https://doi.org/10.1007/s10600-021-03428-5
Publikováno v:
Doklady Chemistry. 495:175-177
The reaction of [3 + 2] cycloaddition of a lappaconitine-based nitrone with N,N-diethylallylamine is accompanied by the formation of two minor products, unusual for the reaction of this type, containing the pyrrole cycle. The structures of the produc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d0f5d4c60980365b7d2a8a11247dd427
https://doi.org/10.1134/s0012500820110038
https://doi.org/10.1134/s0012500820110038