Zobrazeno 1 - 10
of 18
pro vyhledávání: '"T. S. Seitembetov"'
Autor:
M. M. Ismagulova, Zh. S. Nurmaganbetov, A. Zh. Turmukhambetov, T. S. Seitembetov, S. M. Adekenov
Publikováno v:
Eurasian Chemico-Technological Journal, Vol 11, Iss 3, Pp 199-205 (2009)
The indole alkaloid harmine was extracted from underground part of Peganum harmala L. With the purpose of obtaining the new biological active derivatives on base of alkaloid harmine the chemical modification was carried out. The p-toluolsulfochlorid,
Externí odkaz:
https://doaj.org/article/99a85332a4a046a18524907eb1bfc5a6
Autor:
T. S. Seitembetov, A. T. Kulyyasov, Yu. V. Gatilov, V. A. Raldugin, I. Yu. Bagryanskaya, Makhmut M. Shakirov, S. M. Adekenov
Publikováno v:
Russian Chemical Bulletin. 47:1390-1394
A new sesquiterpenoid lactone was isolated from terrestrial parts ofArtemisia subchrysolepis Filat. and studied by X-ray diffraction analysis and CD spectroscopy. This compound was called subchrysine and identified as (1R,3S,4E,6R,7S)-3-acetoxy-1-hyd
Publikováno v:
Chemistry of Natural Compounds. 32:869-872
Alantolactone and isoalantolactone have been epoxidized with peracetic, m-chloroperbenzoic, and trifluoroperacetic acids. The structure of 4(15)-α-epoxyisoalactone has been established by an x-ray structural investigation.
Publikováno v:
Chemistry of Natural Compounds. 31:192-195
Results are given on the antitumoral activity of grosshemin derivatives. A new grosshemin derivative has been obtained by the interaction of its acetate with hydroxylamine.
Autor:
S. M. Adekenov, M. M. Shakirov, I. Yu. Bagryanskaya, Yu. V. Gatilov, V. A. Raldugin, A. T. Kulyjasov, T. S. Seitembetov
Publikováno v:
ChemInform. 29
Publikováno v:
Chemistry of Natural Compounds. 33:185-186
Phenolic derivatives ofα-santonin have been synthesized and their antioxidant effect has been studied.
Autor:
N. S. Prostakov, T. S. Seitembetov, P. I. Zakharov, V. K. Shevtsov, V. G. Pleshakov, V. P. Zvolinskii
Publikováno v:
Chemistry of Heterocyclic Compounds. 15:328-332
The M+ and [M-H]+ ion peaks are the peaks of maximum intensity in the mass spectra of Schiff bases belonging to the 4-aza-9-fluorenylidenearylamine series. The dependence of the relative intensity of the [M-H]+ fragment on the structures of the I–X
Publikováno v:
Chemistry of Heterocyclic Compounds. 15:535-540
The mass spectra of 15 compounds of the 4-azaphenanthrene series and their deutero analogs with bulky R substituents (R=-C≡CPh, -CH=CHPh, CHBr-CHBrPh,-CH=CHC6H4OCH3-p, -COOH, -COOC2H5, and -CONHNH2) in the ortho position relative to the nitrogen at
Autor:
V. F. Zakharov, N. S. Prostakov, V. P. Zvolinskii, V. G. Pleshakov, T. S. Seitembetov, A. A. Savina
Publikováno v:
Chemistry of Heterocyclic Compounds. 12:99-106
In an investigation of the conditions for the formation of Schiff bases from 3-methyl-2-azafluorenone and arylamines it was shown that the use of boron trifluoride etherate as the catalyst insures the highest yields. The fundamental possibility of th
Autor:
G. A. Vasil'ev, T. S. Seitembetov, N. S. Prostakov, V. K. Shevtsov, V. P. Zvolinskii, Alexey V. Varlamov, P. I. Zakharov, V. G. Pleshakov
Publikováno v:
Chemistry of Heterocyclic Compounds. 15:78-85
A mass-spectrometric study of 2- and 4-azafluorenones and their mono- and polymethyl derivatives showed that the presence of a methyl group in the benzene ring leads to a sharp increase in the relative intensity of the [M — H]+ ion peak. In contras