Zobrazeno 1 - 10
of 98
pro vyhledávání: '"Arkady A. Dudinov"'
Autor:
Valeriya G. Melekhina, Andrey N. Komogortsev, Boris V. Lichitsky, Vitaly S. Mityanov, Artem N. Fakhrutdinov, Arkady A. Dudinov, Vasily A. Migulin, Yulia V. Nelyubina, Elizaveta K. Melnikova, Michail M. Krayushkin
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 15, Iss 1, Pp 2840-2846 (2019)
The condensation of primary amines with N-(1-(4-hydroxy-6-methyl-2-oxo-2H-pyran-3-yl)-2-oxo-2-arylethyl)acetamides was explored. Thus, a previously unknown recyclization of the starting material was observed in acidic ethanol in the presence of an am
Externí odkaz:
https://doaj.org/article/02ae62c4cca2438885c73ce66370e5b8
Autor:
Michael M. Krayushkin, Boris V. Lichitsky, Denis V. Kozhinov, Sergey N. Ivanov, Arkady A. Dudinov
Publikováno v:
ARKIVOC, Vol 2003, Iss 13, Pp 147-156 (2003)
Externí odkaz:
https://doaj.org/article/c5801ee9c05b4c6b819f3482dc3b087a
Autor:
Valeriya G. Melekhina, Boris V. Lichitsky, Artem N. Fakhrutdinov, Arkady A. Dudinov, Andrey N. Komogortsev, M. M. Krayushkin
Publikováno v:
Russian Chemical Bulletin. 69:758-762
A convenient method for the synthesis previously unknown hydroxy-containing aryl(hetaryl)-ethenes (terarylenes) with a pyrazole bridge was elaborated, which is based on the reaction of hydrazines with the products of condensation of allomaltol with a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d8746e5967bd088b6739043cde3a4844
https://doi.org/10.1007/s11172-020-2829-0
https://doi.org/10.1007/s11172-020-2829-0
Autor:
Leonid D. Konyushkin, Delphine Gorses, Alexander V. Samet, Victor V. Semenov, Marina N. Semenova, Arkady A. Dudinov, Evgenii N Khodot, Mikhail M. Krayushkin, Eugenia A. Silyanova, Alexei S. Karpov, Boris V. Lichitsky, Thomas Radimerski, Alex S. Kiselyov, Andrey N. Komogortsev
Publikováno v:
ACS Combinatorial Science. 21:805-816
1,3-Substituted pyrazolo[3,4-b]pyridinones 11-18 were synthesized by a three-component condensation of Meldrum's acid with aryl aldehydes and 1,3-substituted 5-aminopyrazoles. Their biological activity was evaluated using the in vivo phenotypic sea u
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::aa5709419948b56c9ec086d82231691b
https://doi.org/10.1021/acscombsci.9b00135
https://doi.org/10.1021/acscombsci.9b00135
Autor:
Boris V. Lichitsky, Elizaveta K. Melnikova, M. M. Krayushkin, Arkady A. Dudinov, Vasily A. Migulin, Vitaly S. Mityanov, Yulia V. Nelyubina, Artem N. Fakhrutdinov, Andrey N. Komogortsev, Valeriya G. Melekhina
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 15, Iss 1, Pp 2840-2846 (2019)
Beilstein Journal of Organic Chemistry
Beilstein Journal of Organic Chemistry
The condensation of primary amines with N-(1-(4-hydroxy-6-methyl-2-oxo-2H-pyran-3-yl)-2-oxo-2-arylethyl)acetamides was explored. Thus, a previously unknown recyclization of the starting material was observed in acidic ethanol in the presence of an am
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::38f5bde8c0247e2f18121b142336ae0a
https://doaj.org/article/02ae62c4cca2438885c73ce66370e5b8
https://doaj.org/article/02ae62c4cca2438885c73ce66370e5b8
Autor:
Artem N. Fakhrutdinov, Boris V. Lichitsky, M. M. Krayushkin, Arkady A. Dudinov, Andrey N. Komogortsev, Alexander D. Tretyakov
Publikováno v:
Journal of Heterocyclic Chemistry. 56:3081-3087
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e98f01002e855321532ea227ebfa9a2b
https://doi.org/10.1002/jhet.3706
https://doi.org/10.1002/jhet.3706
Autor:
Alexander D. Tretyakov, Andrey N. Komogortsev, M. M. Krayushkin, Boris V. Lichitsky, Arkady A. Dudinov
Publikováno v:
Chemistry of Heterocyclic Compounds. 55:818-822
Herein, we report the studies of the multicomponent reaction of 5-hydroxy-2-methyl-4H-pyran-4-one with carbonyl compounds and Meldrum's acid. General methods for the synthesis of 6-methyl-3,4-dihydropyrano[3,2-b]pyran-2,8-diones, 3-(3-hydroxy-6-methy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0d886c0a2503a4b93247b51203ee768b
https://doi.org/10.1007/s10593-019-02542-1
https://doi.org/10.1007/s10593-019-02542-1
Autor:
Artem N. Fakhrutdinov, Arkady А. Dudinov, Boris V. Lichitsky, Constantine S. Krylov, Mikhail M. Krayushkin, Andrey N. Komogortsev
Publikováno v:
Chemistry of Heterocyclic Compounds. 55:851-855
A convenient method for the synthesis of previously unknown imidazo[4,5-b]pyridine-2,5(4H,6H)-diones has been developed, based on a three-component condensation of 4-imino-1-phenylimidazolidin-2-one with aldehydes and Meldrum's acid. The possibility
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bb1c3b7ef28930aca4fb86b4fed3c3fc
https://doi.org/10.1007/s10593-019-02548-9
https://doi.org/10.1007/s10593-019-02548-9
Autor:
B. V. Lichitski, Arkady A. Dudinov, Andrey N. Komogortsev, M. M. Krayushkin, Vitaly S. Mityanov, Valeriya G. Melekhina, Valerii Z. Shirinian
Publikováno v:
Russian Chemical Bulletin. 67:1873-1877
A convenient method was developed for the synthesis of previously unknown 1,2-diketones, based on the condensation of 5-hydroxy-2-methyl-4H-pyran-4-one with arylglyoxals. The study demonstrated the possibility of using these compounds to synthesize n
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b054dca25f93a84736da533488a67151
https://doi.org/10.1007/s11172-018-2301-6
https://doi.org/10.1007/s11172-018-2301-6
Autor:
Arkady A. Dudinov, М. М. Krayushkin, K. A. Lyssenko, B. V. Lichitskii, Vitaly S. Mityanov, А. N. Komogortsev, Yu. О. Gorbunov
Publikováno v:
Russian Chemical Bulletin. 67:504-509
A convenient method for the synthesis of previously unknown substituted 3-hydroxy-5,5- dimethyl-2-(2-arylbenzofuran-3-yl)cyclohex-2-enones, 4-hydroxy-6-methyl-3-(2-arylbenzofuran- 3-yl)-2H-pyran-2-ones, and 2-hydroxy-3-(2-arylbenzofuran-3-yl) naphtho
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6546ee147a430345972d82863b5ff0cd
https://doi.org/10.1007/s11172-018-2101-z
https://doi.org/10.1007/s11172-018-2101-z