Zobrazeno 1 - 10
of 33
pro vyhledávání: '"B. S. Kikot"'
Autor:
Z. S. Shprakh, N. A. Oborotova, M. A. Krasnova, A. P. Polozkova, O. L. Orlova, V. L. Bagirova, A. Yu. Baryshnikov, N. E. Ryshkova, P. V. Lopatin, E. V. Ignat’eva, B. S. Kikot
Publikováno v:
Pharmaceutical Chemistry Journal. 35:274-278
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::af6c7fe571a241cd99025d838581c96e
https://doi.org/10.1023/a:1011973524048
https://doi.org/10.1023/a:1011973524048
Autor:
L. G. Gatinskaya, S. A. Polonskii, E. V. Ignat’eva, N. A. Oborotova, B. S. Kikot, A. P. Polozkova, P. V. Lopatin, A. Yu. Baryshnikov, P. A. Chel'tsov, O. L. Orlova
Publikováno v:
Pharmaceutical Chemistry Journal. 35:442-449
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1e765124578255862360d80910f0eb7f
https://doi.org/10.1023/a:1013792524750
https://doi.org/10.1023/a:1013792524750
Autor:
A. P. Polozkova, Z. S. Shprakh, A. Yu. Baryshnikov, N. A. Oborotova, N. I. Zimakova, O. L. Orlova, B. S. Kikot, L. I. Smirnova
Publikováno v:
Pharmaceutical Chemistry Journal. 35:690-694
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3b926951b158aea409f4e1ced0144084
https://doi.org/10.1023/a:1015356916790
https://doi.org/10.1023/a:1015356916790
Autor:
A. P. Arzamastsev, L. G. Gatinskaya, N. A. Oborotova, N. I. Zimakova, E. V. Ignat’eva, A. P. Polozkova, B. S. Kikot, E. Yu. Kolesnikova, T. I. Klochkova, A. P. Bud'ko
Publikováno v:
Pharmaceutical Chemistry Journal. 33:624-627
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f6f140eb2bf93eef254bd1d4622d7fcc
https://doi.org/10.1007/bf02508292
https://doi.org/10.1007/bf02508292
Autor:
B. S. Kikot, T. I. Klochkova, T. V. Matveeva, I. V. Yartseva, Victor P. Krasnov, N. F. Kunenkova, E. V. Ignat’eva, Galina L. Levit, O. N. Chupakhin, V. I. Romanenko
Publikováno v:
Pharmaceutical Chemistry Journal. 38:274-276
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f3adbfab0d1839a917eeb8eb5f8a554d
https://doi.org/10.1023/b:phac.0000042095.44485.58
https://doi.org/10.1023/b:phac.0000042095.44485.58
Publikováno v:
Chemistry of Heterocyclic Compounds. 15:1142-1146
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6e374c2096cbfe1d3994b92cc7fa677b
https://doi.org/10.1007/bf00471920
https://doi.org/10.1007/bf00471920
Publikováno v:
Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 38:1383-1387
1. The strong bathochromic shift of the absorption bands of aminoazo compounds in acid medium is due to the formation of a cation of quinoid structure. 2. Aminoazo compounds are weak NH acids in aprotic polar solvents, and they form the corresponding
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d4d2f62292fd4db46f33174d2f1d987d
https://doi.org/10.1007/bf00978423
https://doi.org/10.1007/bf00978423
Publikováno v:
Chemistry of Heterocyclic Compounds. 15:150-153
In a study of the IR absorption spectra of diastereomeric (with respect to phosphorus) 2′,3′-O-alkylphosphonates of nucleosides it was shown that the IR spectra of the diastereomers differ at 820–860 (ΝO-P-O), 1040–1060 (ΝP-O-C), and 1250
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::40c81bc33dab06f54deebb3e50cdd5a4
https://doi.org/10.1007/bf00480356
https://doi.org/10.1007/bf00480356
Autor:
Yu. D. Timoshenkova, I. A. Korbukh, Yu. A. Pentin, M. N. Preobrazhenskaya, F. F. Blanko, L. V. Sennitskaya, B. S. Kikot
Publikováno v:
Chemistry of Heterocyclic Compounds. 13:537-542
It is shown on the basis of a study of the IR spectra of indazoles, pyrazolopyridines, and pyrazolopyrazine in the solid state and of their N-deutero-substituted derivatives and hydrochlorides at room temperature and at the temperature of liquid nitr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3e288a7dbe2a1c63817e5d0a5091eb2a
https://doi.org/10.1007/bf00473203
https://doi.org/10.1007/bf00473203
Publikováno v:
Bulletin of the Academy of Sciences, USSR Division of Chemical Science. 13:894-897
1. The behavior of diazonium salts in solutions was studied by means of the IR absorption spectra in the region of 2200–2300 cm−1. Diazonium salts are dissociated into ions in dimethylformamide, methanol, acetone, and ethyl acetate. 2. In dilute
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::63efd977b7129ec1b57280a8e36b6340
https://doi.org/10.1007/bf01141637
https://doi.org/10.1007/bf01141637