Zobrazeno 1 - 10
of 62
pro vyhledávání: '"M. K. Polievktov"'
Publikováno v:
Chemistry of Heterocyclic Compounds. 27:511-516
The polarographic behavior of derivatives of 2-aminomethyleneindoxyl and 3-aminomethyleneoxindole in anhydrous DMF has been studied and the results compared with data on the polarographic reduction of substituted aminomethyleneacetophenones and of re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ee5cf40a0cf463b9b1b5f23d1363bfae
https://doi.org/10.1007/bf00473996
https://doi.org/10.1007/bf00473996
Publikováno v:
Chemistry of Heterocyclic Compounds. 13:391-394
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3f7dabb26ef7693b39ac7b1468df21ab
https://doi.org/10.1007/bf00482781
https://doi.org/10.1007/bf00482781
Publikováno v:
Chemistry of Heterocyclic Compounds. 11:909-914
The polarographic reduction of the sydnoneimmonium cation (I) was investigated in the case of 3-β-phenylisopropylsydnoneimine hydrochloride (sydnophen). The effect of the pH, alcohol concentration, ionic strength, and surface-active substances was s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3d18fbd23e5cde1e1d89b95904d2b556
https://doi.org/10.1007/bf00470488
https://doi.org/10.1007/bf00470488
Publikováno v:
Chemistry of Heterocyclic Compounds. 15:1352-1356
The dependence of the hydrolysis of 1-methyl-2-benzoylmethylenehexahydroazepine on the pH of the solution was studied. It is shown that the dependence of the observed rate constant (kobs) on the pH is represented by a bell-shaped curve. At pH 3–6,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::67e982d1054e2ca526567581510af43d
https://doi.org/10.1007/bf00514742
https://doi.org/10.1007/bf00514742
Publikováno v:
Chemistry of Heterocyclic Compounds. 17:261-267
The mechanism of the polarographic reduction of cyclic enamino ketones of the pyrrolidine, piperidine, and hexahydroazepine series of two types, viz., compounds in which the α-carbon atom of the enamine is included in the azoheteroring, and enamino
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::779ed8ea65b4026d1c2292d32ac3d665
https://doi.org/10.1007/bf00505990
https://doi.org/10.1007/bf00505990
Publikováno v:
Pharmaceutical Chemistry Journal. 9:413-417
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::99788bb478f91f280894827406521efa
https://doi.org/10.1007/bf00758784
https://doi.org/10.1007/bf00758784
Autor:
I. G. Markova, M. K. Polievktov
Publikováno v:
Pharmaceutical Chemistry Journal. 8:644-647
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e7f74de7e56ed3ff928b022cfca488e1
https://doi.org/10.1007/bf00761198
https://doi.org/10.1007/bf00761198
Autor:
Vladimir G. Granik, A. B. Grigor'ev, M. K. Polievktov, V. E. Serokhvostova, O. Ya. Belyaeva, R. G. Glushkov, T. F. Vlasova
Publikováno v:
Chemistry of Heterocyclic Compounds. 12:1348-1352
3-Oxo-4-N,N-dime thylaminomethyle necapro- and valerolactams were synthesized by reaction of dimethylformamid e acetal with c~-oxocapro- and valerolactams, and the kinetics of the hydrolysis of the former in acid and alkaline media were investigated
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c92c8857e6a2bbeb08763e232ac19c80
https://doi.org/10.1007/bf00476724
https://doi.org/10.1007/bf00476724
Publikováno v:
Chemistry of Heterocyclic Compounds. 13:1217-1220
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::099d492c1207e63d67eb2f71886bc7ff
https://doi.org/10.1007/bf00475950
https://doi.org/10.1007/bf00475950
Autor:
M. K. Polievktov, E. E. Mikhlina, A. D. Yanina, L. N. Yakhontov, K. F. Turchin, Z. M. Klimanova, I. G. Markova, O. N. Volzhina, V. A. Bondarenko, V. Ya. Vorob'eva, N. A. Komarova
Publikováno v:
Pharmaceutical Chemistry Journal. 13:751-754
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fdd49b6d59b47a610246bc312fde1c26
https://doi.org/10.1007/bf00789534
https://doi.org/10.1007/bf00789534