Zobrazeno 1 - 10 of 18 pro vyhledávání: '"V. D. Bezuglyi"'
1
Polarographic examination of 5-aryl-2-(2-thienyl)-oxazoles and -1,3,4-oxadiazoles
Autor: V. F. Lavrushin, L. D. Patsenker, V. K. Polyakov, V. D. Bezuglyi, A. P. Shkumat
Publikováno v: Chemistry of Heterocyclic Compounds. 22:1255-1258
The polarographic behavior of 5-aryl-2-(2-thienyl)oxazoles and -1,3,4-oxadiazoles has been studied.
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::756f90845e2e20229c9c2414ad4ba16a
https://doi.org/10.1007/bf00471812
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2
Polarographic study of acridine and 9-chloroacridine and its derivatives in dimethylformamide
Autor: V. A. Shapovalov, A. N. Gaidukevich, Madikha B. Sidom, V. D. Bezuglyi
Publikováno v: Chemistry of Heterocyclic Compounds. 14:1350-1354
Polarographic data on the reduction of acridine (I) and its 9-chloro (II), 2-methoxy-9-chloro (III), 4-methoxy-9-chloro (IV), 2-methyl-9-chloro (V), 4-methyl-9-chloro (VI), 2,9-dichloro (VII), and 4,9-dichloro (VIII) derivatives and a mechanism for t
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::cc5109db2164d627a94d9333925fa31a
https://doi.org/10.1007/bf00487405
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3
Structure and half-wave potential in anils of araldehydes
Autor: V. D. Bezuglyi, V. N. Dmitrieva, L. V. Kononenko
Publikováno v: Theoretical and Experimental Chemistry. 1:297-300
Substituent effects are considered, and it is shown that a given substituent has effects on the activity of the-CH=N- group dependent on the benzene ring to which it is attached. An electron-donor substituent shifts El/2 towards the negative side if
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::75b947baf89946e3cfbef0b3411a71f7
https://doi.org/10.1007/bf00526347
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5
Investigation of the chemistry of phenoxazines
Autor: N. P. Shimanskaya, V. G. Vykhristyuk, I. Ya. Postovskii, G. B. Afanas'eva, V. D. Bezuglyi, K. I. Pashkevich
Publikováno v: Chemistry of Heterocyclic Compounds. 8:1216-1220
Depending on the position of the annelated benzene ring, benzophenoxazinones add thiophenols in the benzenoid, quinonoid, or both parts of the molecule to give mono- or diarylmercapto derivatives. A substituent in the benzenoid portion of the molecul
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::743c5af27f673e1d677d83ac7f4e693d
https://doi.org/10.1007/bf00475533
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8
Polarographic study of halogen and mercury substituted 1,3-oxazoles
Autor: V. D. Bezuglyi, G. P. Klimisha, O. P. Shvaika, N. P. Shimanskaya
Publikováno v: Chemistry of Heterocyclic Compounds. 3:481-483
A study is made of the polarographic behavior of some halogen and mercury derivatives of phenyloxazoles. By considering the mechanism of electroreduction, it is ascertained, that, the first polarographic wave corresponds to reduction of the halogen o
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::4e7627fd90d983108793b1d1c3e70d47
https://doi.org/10.1007/bf00481576
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9
A polarographic study of dihydronaphthoxazoles
Autor: N. P. Shimanskaya, V. D. Bezuglyi, I. F. Mikhailova
Publikováno v: Chemistry of Heterocyclic Compounds. 4:21-23
The polarographic behavior of four dihydronaphthoxazoles that have not been studied previously has been investigated. It has been shown that the dihydronaphthoxazoles are reduced at higher positive potenials than the corresponding diaryloxazoles beca
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::ad17d96ceeb4da832efb3740ca51af2a
https://doi.org/10.1007/bf00478068
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