Zobrazeno 1 - 10
of 35
pro vyhledávání: '"V. I. Vinogradova"'
Publikováno v:
Chemistry of Natural Compounds. 59:331-335
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::36e8ae82a8bc4f89b5ac969c32f4552d
https://doi.org/10.1007/s10600-023-03987-9
https://doi.org/10.1007/s10600-023-03987-9
Autor:
A. U. Ubaidullaev, V. I. Vinogradova, Sh. N. Zhurakulov, N. I. Mukarramov, Kh. M. Bobakulov, K. A. Turgunov, B. Tashkhodzhaev
Publikováno v:
Chemistry of natural compounds. 58(6)
Bromination of the furanoquinoline alkaloid haplophyllidine by molecular bromine and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6b8892a6743b5b817bf376a4a378f036
https://pubmed.ncbi.nlm.nih.gov/36406158
https://pubmed.ncbi.nlm.nih.gov/36406158
Publikováno v:
Chemistry of Natural Compounds. 52:463-467
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a97b3ab06efb124f3c0366714c055a3c
https://doi.org/10.1007/s10600-016-1673-9
https://doi.org/10.1007/s10600-016-1673-9
Autor:
Z. A. Khushbaktova, S. O. Osipova, Sh. B. Rakhimov, V. I. Vinogradova, Vladimir Nikolaevich Syrov, Zh. I. Islamova
Publikováno v:
Pharmaceutical Chemistry Journal. 47:209-212
The antiparasitic (antihymenolepiatic and antileishmaniatic) activity of several N-benzyl derivatives of the alkaloid cytisine and 3-bromocytisine was studied. The structure–activity relationship in the series of synthesized compounds was analyzed.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::09d979cf1a9348ece00d09631a9fe5e1
https://doi.org/10.1007/s11094-013-0929-y
https://doi.org/10.1007/s11094-013-0929-y
Autor:
V I Vinogradova
Publikováno v:
Izvestiya MGTU MAMI. 2:304-307
Construction of theoretical sports biomechanics by one-man efforts causes complications. It requires sportsmanship knowledge, anthropomorphous mechanism (AM) modeling skills, AM motion modeling by differential equations, a computer numerical analyze
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fed3d557e36f8c7482f2eb0700e7c1ea
https://doi.org/10.17816/2074-0530-69822
https://doi.org/10.17816/2074-0530-69822
Autor:
B. T. Salimov, I. A. Bessonova, V. A. Tel'nov, M. N. Sultankhodzhaev, S. F. Aripova, R. Shakirov, M. V. Telezhenetskaya, I. A. Israilov, T. S. Tulyaganov, V. I. Vinogradova, V. I. Akhmedzhanova
Publikováno v:
Chemistry of Natural Compounds. 32:737-858
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::46dd2b1b1545d278fb93f051e7990a2e
https://doi.org/10.1007/bf01375127
https://doi.org/10.1007/bf01375127
Autor:
R. Shakirov, M. V. Telezhenetskaya, I. A. Bessonova, S. F. Aripova, I. A. Israilov, M. N. Sultankhodzhaev, V. I. Vinogradova, V. I. Akhmedzhanova, T. S. Tulyaganov, B. T. Salimov, V. A. Tel'nov
Publikováno v:
Chemistry of Natural Compounds. 32:216-334
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a79e67753240b74d6c8d14abc40a3d60
https://doi.org/10.1007/bf01373865
https://doi.org/10.1007/bf01373865
Publikováno v:
Chemistry of Natural Compounds. 38:344-346
Acylation of cytisine with benzocrown-ethercarboxylic acid chlorides produced a series of new cytisine derivatives containing B12C4, B15C5, DB18C6, and DB24C8 fragments.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c6cc0be518cf678fa2f99a4879a028ea
https://doi.org/10.1023/a:1021626008424
https://doi.org/10.1023/a:1021626008424
Publikováno v:
Chemistry of Natural Compounds. 29:760-766
The Pictet—Spengler condensation of bis-β-phenylethylbenzylamines with a central diphenyl ether group has given a new series of substituted bis-2-benzyltetrahydroisoquinolines the fragmentation of which under electron impact is determined by the p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::586778d57b48c020ebd43960687cd0b3
https://doi.org/10.1007/bf00629646
https://doi.org/10.1007/bf00629646
Publikováno v:
Chemistry of Natural Compounds. 29:341-345
A number of N-benzyltetrahydroisoquinolines forming analogues of sendaverine have been synthesized. Results on the pharmacological activity of the compounds synthesized are presented.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::13f2d4fde8c97e2b9ac4a8fd7947024b
https://doi.org/10.1007/bf00630535
https://doi.org/10.1007/bf00630535