Zobrazeno 1 - 10
of 19
pro vyhledávání: '"S B, Goncharenko"'
Publikováno v:
Pharmaceutical Chemistry Journal. 26:769-772
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a2fe4091d9ef118599457bb75edca6aa
https://doi.org/10.1007/bf00770632
https://doi.org/10.1007/bf00770632
Publikováno v:
Biulleten' eksperimental'noi biologii i meditsiny. 127(2)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d50210b639054b2bf23299af9be8cb0c
https://pubmed.ncbi.nlm.nih.gov/10095956
https://pubmed.ncbi.nlm.nih.gov/10095956
Publikováno v:
Chemistry of Heterocyclic Compounds. 19:792-795
Methods for the synthesis of 6-arylamino-5,5-diethyl-3H,5H-pyrimidine-2,4-diones from the corresponding 6-thioxo and 6-amino derivatives were developed. The isomeric 2-arylamino-5,5-diethyl-1H,5H-pyrimidine-4,6-diones were obtained by the reaction of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::010fee528450b0fe35947d13daaa69a4
https://doi.org/10.1007/bf00506111
https://doi.org/10.1007/bf00506111
Autor:
E. A. Usachev, V. G. Voronin, L. E. Pchelintseva, A. S. Zaks, Yu. N. Portnov, S. B. Goncharenko, Yu. M. Rabotnikov
Publikováno v:
Pharmaceutical Chemistry Journal. 20:259-264
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1a3da97a416b96d21f880ccf1f713f59
https://doi.org/10.1007/bf00758814
https://doi.org/10.1007/bf00758814
Publikováno v:
Chemistry of Heterocyclic Compounds. 14:675-678
A mixture of isomers that differ with respect to the position of the methyl group is formed in the methylation of 5,5-diethyl-6-imino-5,6-dihydro[1H, 3H]pyrimidine-2,4-dione with excess methyl iodide in the presence of ethoxide. Isomerization of the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f82ffef5a1b5d5bc087b291b3d09e488
https://doi.org/10.1007/bf00481146
https://doi.org/10.1007/bf00481146
Publikováno v:
Chemistry of Heterocyclic Compounds. 12:443-448
The mass spectra of 2- and 4-thiobarbituric acids and some of their close analogs at ionizing voltages of 70 and 14 eV are compared. Qualitative and quantitative differences in the behavior of these compounds under the influence of electron impact we
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::71a35946914540fef4a4c197158de692
https://doi.org/10.1007/bf00480436
https://doi.org/10.1007/bf00480436
Autor:
Yu. M. Rabotnikov, Yu. V. Portnov, S. B. Goncharenko, L. E. Pchelintseva, V. G. Voronin, E. A. Usachev, A. S. Zaks
Publikováno v:
Pharmaceutical Chemistry Journal. 20:332-335
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2793cd5686fcfd5f09e738e3b90165b6
https://doi.org/10.1007/bf00758614
https://doi.org/10.1007/bf00758614
Publikováno v:
Chemistry of Heterocyclic Compounds. 14:667-671
The mass spectra of 2- and 4-iminobarbituric acid derivatives were studied in relation to the mass spectra of their oxygen analogs. It is shown that the pathways of fragmentation of the investigated compounds depend on the type of substituent attache
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bfcc0af717afe329bcf5ce5fc93297cf
https://doi.org/10.1007/bf00481144
https://doi.org/10.1007/bf00481144
Publikováno v:
Chemistry of Heterocyclic Compounds. 10:1102-1104
Under the influence of phosphorus oxychloride, 1-acylpyrazolines condense to give 3-pyrazolinylpyrazoles; cleavage of the pyrazoline molecule occurs at the C3-N2 bond.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c918a68826ba646bdd943ded7558e309
https://doi.org/10.1007/bf00472135
https://doi.org/10.1007/bf00472135
Publikováno v:
Chemistry of Heterocyclic Compounds. 13:1137-1139
On the basis of data from the IR spectra of 4-thiobarbituric acid derivatives, and their deutero analogs, and similarly constructed model compounds, it was established that the investigated substances exist in the thione lactam form and form two type
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2132586dfdc2207019aefeb75484aa04
https://doi.org/10.1007/bf00480155
https://doi.org/10.1007/bf00480155