Zobrazeno 1 - 10
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pro vyhledávání: '"N N, SUVOROV"'
Autor:
N. N. Suvorov
Publikováno v:
Vestnik of Saint Petersburg State University of Culture. 1:82-89
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::93ee4b731ee09916988591247c38e8e8
https://doi.org/10.30725/2619-0303-2020-1-82-89
https://doi.org/10.30725/2619-0303-2020-1-82-89
Autor:
N. N. Suvorov
Publikováno v:
Vestnik of Saint Petersburg State University of Culture. :49-56
Culture is considered as a set of practices whose purpose is the establishment of entity, product and percipient activities. In the artistic practices used versatile technology. They include Museum, gallery, curator, art collecting. Characteristics o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2375714b2826c86e90b2975bfe02c6d4
https://doi.org/10.30725/2619-0303-2017-2-49-56
https://doi.org/10.30725/2619-0303-2017-2-49-56
Autor:
N. N. Suvorov, Andrey E. Shchekotikhin, D. A. Silaev, I. G. Makarov, V. N. Buyanov, E. P. Baberkina
Publikováno v:
Chemistry of Heterocyclic Compounds. 38:543-546
The previously unknown 4,11-dimethoxynaphtho[2,3-f]indazole-5,10-dione has been obtained by the thermal cyclization of N-nitroso derivative of 2-acetamido-3-methyl-1,4-dimethoxyanthraquinone.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e958d24e10160a0bcf3df4ef89577a12
https://doi.org/10.1023/a:1019552927885
https://doi.org/10.1023/a:1019552927885
Autor:
E. P. Baberkina, Andrey E. Shchekotikhin, V. E. Zhigachev, M. E. Zhukova, V. N. Buyanov, N. N. Suvorov
Publikováno v:
Chemistry of Heterocyclic Compounds. 37:1234-1237
The corresponding Mannich bases have been synthesized by the aminomethylation of 6-methyl-1H-pyrrolo[2,3-a]- and 4-methyl-3H-pyrrolo[3,2-c]phenanthridinium iodides. The interaction of 6-chloro-phenanthridine with indoline and with 5-amino-N-acetylind
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bf2aa0e1a450798e29ec59a4294fa130
https://doi.org/10.1023/a:1013897410464
https://doi.org/10.1023/a:1013897410464
Publikováno v:
Chemistry of Heterocyclic Compounds. 37:827-833
2-(Diphenylmethan-4-yl)- and 2-(dibenzyl-4-yl)indoles have been synthesized by the Fischer reaction. Reactions carried out included azo coupling, formylation, and nitrosation. The corresponding 3-substituted derivatives were obtained.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a3009c6039186b92ed2769ec3f4647f3
https://doi.org/10.1023/a:1012439205723
https://doi.org/10.1023/a:1012439205723
Publikováno v:
Chemistry of Heterocyclic Compounds. 37:944-948
4,11-Dihydroxynaphtho[2,3-f]indole-5,10-dione (pyrroloquinizarin), its 11-dehydroxy derivative, and Mannich base were synthesized by demethylation of previously obtained methoxynaphtho[2,3-f]indole-5,10-diones.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7e1c7308542854d971bc02ff75560ec1
https://doi.org/10.1023/a:1012727331823
https://doi.org/10.1023/a:1012727331823
Autor:
L. N. Kurkovskaya, M. I. Sikharulidze, N. N. Suvorov, G. A. Palavandishvili, T. E. Khoshtariya, N. T. Mirziashvili
Publikováno v:
Chemistry of Heterocyclic Compounds. 37:1168-1172
A method has been developed for N-alkylating 3H-pyrrolo[2,3-c]phenothiazine 11,11-dioxide with alkyl chlorides in absolute dimethylformamide in the presence of sodium hydroxide.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e415042acc1bcdcf12c2b5e36e38e122
https://doi.org/10.1023/a:1013200321134
https://doi.org/10.1023/a:1013200321134
Publikováno v:
Chemistry of Heterocyclic Compounds. 36:1284-1288
N-Acetylation and several N-alkylation reactions have been carried out for the previously synthesized 4,11-dimethoxynaphtho[2,3-f]indole-5,10-dione.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::44937b67adce41ff7414f32ccb72ce12
https://doi.org/10.1023/a:1017567317083
https://doi.org/10.1023/a:1017567317083
Publikováno v:
Chemistry of Heterocyclic Compounds. 34:816-821
1H, 10H-benzo[e]pyrrolo[3,2-g]indole-2,9-dicarboxylic acid dichloride has been synthesized and condensed with amines and phenols to give the corresponding diamides and activated diesters. The mass spectra of the dichloride and several diamides have b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ba06350b3fe1e111f6e658b86c07be3d
https://doi.org/10.1007/bf02251689
https://doi.org/10.1007/bf02251689
Autor:
N. N. Suvorov, I. Sh. Chikvaidze, T. P. Radkevich, N. Sh. Megrelishvili, T. A. Gus'kova, Sh. A. Samsoniya, O. V. Baklanova
Publikováno v:
Pharmaceutical Chemistry Journal. 32:29-32
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8b44a22261f8cb46c1ba9f97a548ce3d
https://doi.org/10.1007/bf02464223
https://doi.org/10.1007/bf02464223