Zobrazeno 1 - 10
of 10
pro vyhledávání: '"S. L. Kuznetsova"'
Autor:
Yu. E. Sapozhnikov, G. V. Kiseleva, R. D. Davletov, E. V. Klimakova, T. P. Vorob’eva, S. L. Kuznetsova, V. S. Pilyugin, Z. B. Galeeva, N. A. Sapozhnikova, G. E. Chikisheva
Publikováno v:
Russian Journal of General Chemistry. 78:446-450
A procedure has been developed for the synthesis of bis(2-arylcarbonylamino-1H-benzimidazol-5-yl) sulfones by reaction of the corresponding substituted benzoyl chloride with sodium cyanamide and subsequent treatment of the N-cyanobenzamide thus forme
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::eebbcf0357145133813f9cd31764efb3
https://doi.org/10.1134/s1070363208030195
https://doi.org/10.1134/s1070363208030195
Autor:
G. V. Kiseleva, L. V. Yakovleva, Yu. E. Sapozhnikov, E. V. Klimakova, T. P. Vorob’eva, V. S. Pilyugin, G. E. Chikisheva, S. L. Kuznetsova
Publikováno v:
Russian Journal of Applied Chemistry. 81:459-464
A procedure was developed for preparing 2-nitro-4-thiocyanoaniline by thiocyanation of 2-nitroaniline with ammonium thiocyanate in acetic acid in the presence of bromine as oxidant.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e9c0ebe4e469b63482aa9adebaa7a3ea
https://doi.org/10.1134/s1070427208030233
https://doi.org/10.1134/s1070427208030233
Autor:
E. V. Klimakova, Yu. E. Sapozhnikov, G. E. Chikisheva, G. V. Kiseleva, S. L. Kuznetsova, A. M. Davydov, R. D. Davletov, N. A. Sapozhnikova, T. P. Vorob’eva, V. S. Pilyugin, R. Kh. Yumadilov
Publikováno v:
Russian Journal of General Chemistry. 76:1653-1659
Derivatives of 1H-benzimidazol-2-amine and halo-, nitro-, methoxy-, and hydroxy-substituted benzoic acids were synthesized, and their fungicide activity against pure Fusarium culmorum and Helminthosporium sativum cultures and pathogenic microflora of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a152b5846eadaabfbe2b9731364bdc42
https://doi.org/10.1134/s1070363206100264
https://doi.org/10.1134/s1070363206100264
Autor:
V. S. Pilyugin, Yu. E. Sapozhnikov, S. L. Kuznetsova, N. A. Sapozhnikova, G. E. Chikisheva, G. V. Kiseleva, E. V. Klimakova, T. P. Vorob’eva
Publikováno v:
Russian Journal of General Chemistry. 76:1327-1330
A procedure has been developed for the synthesis of bis(arylcarbonylamino-1H-benzimidazol-5-yl) ethers by reaction of the corresponding substituted benzoyl chloride with sodium cyanamide, followed by treatment of the resulting N-cyanobenzamide with 4
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c24c2aae68b094a789275d323a048f5a
https://doi.org/10.1134/s1070363206080305
https://doi.org/10.1134/s1070363206080305
Autor:
A. N. Mikhailyuk, G. E. Chikireva, G. V. Kiseleva, V. S. Pilyugin, V. M. Kosareva, S. L. Kuznetsova
Publikováno v:
Russian Journal of General Chemistry. 74:393-398
Products of the reactions methyl N-[5(6)-(4-aminophenylsulfanyl)benzimidazol-2-yl]carbamate with phthalic anhydrides, involving the aniline nitrogen atoms, were obtained. Biological properties (embryotoxicity and toxicity) of the products and their m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bb56fe2d450650a268d2fcdbaf473546
https://doi.org/10.1023/b:rugc.0000030396.95958.31
https://doi.org/10.1023/b:rugc.0000030396.95958.31
Autor:
V. S. Pilyugin, V. M. Kosareva, S. L. Kuznetsova, A. N. Mikhailyuk, G. V. Kiseleva, R. B. Valitov
Publikováno v:
Russian Journal of General Chemistry. 73:1293-1296
Methyl 5(6)-(4-aminophenylthio)-2-benzimidazolylcarbamate reacts with aliphatic and aromatic isocyanates to give mono- and disubstitution products. The former are formed by the reaction involving the aniline nitrogen and the latter, by the reaction i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::aa01312a850ea8458eb6208b73c5bdb0
https://doi.org/10.1023/b:rugc.0000007660.04499.c1
https://doi.org/10.1023/b:rugc.0000007660.04499.c1
Autor:
V. M. Kosareva, S. L. Kuznetsova, A. N. Mikhailyuk, G. V. Kiseleva, G. E. Chikisheva, V. S. Pilyugin
Publikováno v:
Russian Journal of General Chemistry. 73:1105-1109
Procedures were developed for preparing 3,4,4'- and 2',3,4-triaminodiphenyl ethers by the reaction of 4-acetylaminophenol with, respectively, 4-nitro- or 2-nitrochlorobenzene, followed by nitration of the resulting 4-acetylamino-4'- or -2'-nitrodiphe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::358502a771dc5dd22db3dda459662e91
https://doi.org/10.1023/b:rugc.0000007620.98209.c6
https://doi.org/10.1023/b:rugc.0000007620.98209.c6
Publikováno v:
Russian Journal of General Chemistry. 73:244-248
Procedures have been developed for the acylation of 4-amino-4'-nitrodiphenyl sulfide with an almost quantitative yield by the action of acetic anhydride in aprotic organic solvents and subsequent nitration of 4-acetylamino-4'-nitrodiphenyl sulfide wi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::41b717eca56807d1a5a37ff18e81f8c6
https://doi.org/10.1023/a:1024744122254
https://doi.org/10.1023/a:1024744122254
Publikováno v:
Fibre Chemistry. 27:427-430
Cellulose diacetate and triacetate films 6–55 µm thick with a total porosity of 0.8–2% were prepared by pouring a solution on an immobile surface and by calendering. Sorption of H2S and CO2 gases and acetone vapors on these films was investigate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3ebd82addd206ea43d9968787364be38
https://doi.org/10.1007/bf00556175
https://doi.org/10.1007/bf00556175
Autor:
T. P. Vorobyeva, V. M. Kosareva, G. E. Chikisheva, E. V. Klimakova, G. V. Kiseleva, V. S. Pilyugin, A. N. Mikhailyuk, S. L. Kuznetsova
Publikováno v:
ChemInform. 36
A procedure was developed for preparation of methyl 5(6)-(4-aminophenoxy)- and 5(6)-(2-aminophenoxy)-2-benzimidazolyl carbamates by reaction of 3,4,4`-triaminodiphenyl or 3,4,2`-triaminodiphenyl ethers respectively with methyl cyanocarbamate in water
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::32e66fda8214168bd3fd2c157147dffa
https://doi.org/10.1002/chin.200514133
https://doi.org/10.1002/chin.200514133