Zobrazeno 1 - 10
of 22
pro vyhledávání: '"G. Ruchkina"'
Publikováno v:
Theoretical Foundations of Chemical Engineering. 54:1052-1056
New research results, as well as those published earlier by the authors, on the synthesis of azo compounds based on nitroanilines obtained by the chemical transformation of 2,4,6-trinitrotoluene and 1,3,5-trinitrobenzene are generalized. It is shown
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::802437a8bdce2d8d05aed418ec172e10
https://doi.org/10.1134/s0040579520050139
https://doi.org/10.1134/s0040579520050139
Publikováno v:
Russian Chemical Bulletin. 68:74-78
2,4,6-Trihydroxy-3-methylbenzoic acid was obtained by NaHCO3 carboxylation of 2,4,6-trihydroxytoluene. The heterocyclization and esterification of the above acid were studied.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1607e2fd01dcbdb6d39e072ad1f1f1e0
https://doi.org/10.1007/s11172-019-2418-2
https://doi.org/10.1007/s11172-019-2418-2
Publikováno v:
Chemical Engineering. 20:440-444
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::575769b5bb83682b0d7000bf7458e1ef
https://doi.org/10.31044/1684-5811-2019-20-10-440-444
https://doi.org/10.31044/1684-5811-2019-20-10-440-444
Autor:
A. Popova, G. Ruchkina
Publikováno v:
Государство и право. :33-41
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::766641e2d036e6d8ec7f4708926f0f52
https://doi.org/10.31857/s013207690002071-0
https://doi.org/10.31857/s013207690002071-0
Publikováno v:
Russian Chemical Bulletin. 67:878-883
New 1,3-dihydroxyacridine-9-carboxylic acids were obtained by Pfitzinger reaction from 2,4,6-trihydroxytoluene (methylphloroglucinol). Their bromination and azo-coupling reactions were studied. Computer simulation was used to determine potential phar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8356723ff7aa2b2c83d17b874b411bb3
https://doi.org/10.1007/s11172-018-2152-1
https://doi.org/10.1007/s11172-018-2152-1
Publikováno v:
Russian Journal of Organic Chemistry. 51:1572-1577
Proceeding from 2,4,6-trihydroxytoluene (methylphloroglucinol) dihydroxy-2H-1-benzopyran-2-ones were prepared, and also their bromo and acyl derivatives. The structure of compounds synthesized was established, and their potential pharmacokinetic prop
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d7bd0afa2f69510e24f40472b60895ce
https://doi.org/10.1134/s1070428015110093
https://doi.org/10.1134/s1070428015110093
Autor:
S. S. Bobylev, S. A. Shevelev, A. G. Ruchkina, Dmitry N. Kuznetsov, K. I. Kobrakov, Artem N. Fakhrutdinov, A. Kh. Shakhnes
Publikováno v:
Russian Chemical Bulletin. 64:154-160
5,7-Dihydroxy-4,8-dimethylchromen-2-one was synthesized based on methyl phloroglucinol and its spectral and physicochemical characteristics were obtained. Reactions of the newly synthesized coumarin with different diazonium salts were studied, condit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::702633da25828cf4197f577f699be017
https://doi.org/10.1007/s11172-015-0836-3
https://doi.org/10.1007/s11172-015-0836-3
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Publikováno v:
Chemistry of Heterocyclic Compounds. 47:441-447
Treatment of 3,5-dichloropyrid-2-ylhydrazine, and of mono- and dinitrophenylhydrazines with acetoacetic ester gave hydrazones and the products of their cyclization, namely pyrazolols. It was shown that acetoacetic ester 2,4-dinitrophenylhydrazone cyc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d6ca1d73f0013933748e863548cd9acb
https://doi.org/10.1007/s10593-011-0778-0
https://doi.org/10.1007/s10593-011-0778-0
Publikováno v:
Chemistry of Heterocyclic Compounds. 39:283-307
Data on the synthesis of hydrazinopyridines, their properties, and their application in various fields over the last 30 years are reviewed.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::108c7211bfe548bc860a34178d20773d
https://doi.org/10.1023/a:1023954524573
https://doi.org/10.1023/a:1023954524573