Zobrazeno 1 - 10 of 24 pro vyhledávání: '"B D, Sviridov"'
1
[Untitled]
Autor: T. P. Klimova, B. D. Sviridov, A. V. Antonyuk, T. A. Babushkina
Publikováno v: Russian Journal of Coordination Chemistry. 28:71-74
d,l-Hexamethylpropyleneamino oxime (HMPAO) was synthesized and isolated from a mixture of d,l - and meso-isomers. The structure of the conformers was studied using 1H NMR spectroscopy over a broad range of pH. A method for estimating the amount of me
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::03a2e6f4c026ade3c5781faf7029616e
https://doi.org/10.1023/a:1013724123029
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2
Preparation of a ready-for-injection radiopharmaceutical based on MIBI using99mTc from a centralized extraction generator
Autor: T. N. Dorontchenkova, V. N. Romanovsky, A. V. Antonjuk, A. O. Malysheva, M. P. Zykov, B. D. Sviridov, D. W. Wester, S. A. Bartenev, N. T. Usatcheva, G. E. Kodina
Publikováno v: Journal of Radioanalytical and Nuclear Chemistry. 221:227-229
A modified method for synthesizing MIBI is described. A ready-for-injection using the synthesized MIBI is prepared. The99mTc source is a centralized extraction generator.
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::440517e542a707bc9e0a6f8b2b72a12e
https://doi.org/10.1007/bf02035274
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3
[Obtaining liposomal preparations of various biologically active substances by the method of detergent flow analysis]
Autor: N S, Griaznova, R M, Petiushenko, I V, Beliavskaia, L N, Berezovskaia, V G, Zhukov, B D, Sviridov, Iu O, Sazykin, S M, Navashin
Publikováno v: Antibiotiki i khimioterapiia = Antibiotics and chemoterapy [sic]. 37(7)
It was shown that detergent dialysis could be successfully used for liposomal encapsulation of substances belonging to different chemical groups with diverse therapeutic activity such as rifampicin, aclarubicin, amphotericin B, pefloxacin and insulin
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::8a9ee38a5a55f396409bb870843ee1d5
https://pubmed.ncbi.nlm.nih.gov/1456805
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4
Effect of nature of substituents on photochemical behavior of 2,6-disubstituted 1,4-benzoquinones
Autor: L. P. Gryzunova, B. D. Sviridov, V. M. Kuznets, K. De Jonge, V. V. Ershov, G. A. Nikiforov, H. J. Hageman
Publikováno v: Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 27:1908-1911
1. We studied the photochemical transformations of some 2,6-disubstituted 1,4-benzoquinones in aliphatic alcohols, acetic acid, and aromatic hydrocarbons. 2. In aliphatic alcohols the photolysis of the quinones leads to the formation of only reductio
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::c27a99844105b27ad7f452794a73827b
https://doi.org/10.1007/bf00929256
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6
Mechanism of the reaction between 2,6-diphenyl-1,4-benzoquinone and alphatic diamines
Autor: M. V. Serdobov, B. D. Sviridov, R. V. Poponova, V. I. Porkhun
Publikováno v: Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 32:88-94
1. The existence of rigid and labile donor-acceptor complexes in the 2,6-diphenyl-1,4-benzoquinone-ethylenediamine system, the stability of which is determined by the rate of consumption of the 2,6-diphenyl-1,4-benzoquinone, has been demonstrated by
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::582f252301a480bbad5f6516e6dec44c
https://doi.org/10.1007/bf01167766
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7
A study, using CNP methods, of the mechanism of the photochemical reduction of 2,6-disubstituted 1,4-benzoquinones by alcohols
Autor: B. D. Sviridov, V. V. Ershov, Kh. I. Khageman, G. A. Nikiforov, C. R. H. I. De Jonge, A. Z. Yankelevich, V. M. Kuznets
Publikováno v: Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 28:1167-1173
1. CNP methods have been used to study the photoreduction of 2,6-dimethyl- and 2,6-diphenyl-1,4-benzoquinones in aliphatic alcohols; a mechanism covering the photolysis has been advanced, and its validity confirmed. 2. The character of the primary ra
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::794ff6f0d938e9543569efff49e428cd
https://doi.org/10.1007/bf00947377
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8
Reaction of carbene of cyclohexadienone type with multiple bonds of conjugated dienes
Autor: V. V. Ershov, B. D. Sviridov, G. A. Nikiforov
Publikováno v: Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 23:339-342
1. The 1,2-addition products are formed initially when the cyclohexadienone carbene is reacted with the multiple bonds of conjugated dienes, which are isomerized under the conditions for the thermolysis of the quinone diazide, but are stable under ph
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::9613cede5da00e882b301f18d5d7c9bc
https://doi.org/10.1007/bf00924683
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10
Chemical polarization of nuclei in reactions of cyclohexadienone carbenes with halogen-containing organic compounds
Autor: Eh.T. Lippmaa, Sh. A. Markaryan, B. D. Sviridov, G. A. Nikiforov, T. I. Pekhk, L. G. Plekhanova, V. V. Ershov, Anatolii L Buchachenko, S. V. Rykov
Publikováno v: Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 23:86-91
The thermolysis of 2,6-di-tert-butyl-p-benzoquinone diazide in a medium of halogenated hydrocarbons was investigated by the method of chemically induced polarization of nuclei. The cyclohexadienone carbene formed during thermolysis reacts with the me
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::52334d1da0ab60e3d38ee58b791911db
https://doi.org/10.1007/bf00922319
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