Zobrazeno 1 - 10
of 23
pro vyhledávání: '"T. G. Koksharova"'
Publikováno v:
ChemInform. 24
Autor:
A. R. Tumanova, A. L. Lapidus, Vasiliy A. Bakulev, S. D. Pirozhkov, T. G. Koksharova, V. S. Mokrushin, N. V. Volkova
Publikováno v:
ChemInform. 25
Autor:
V. I. Il'chenko, N. V. Volkova, V. G. Platonov, I. R. Shcherbakova, L. N. Dianova, T. G. Koksharova
Publikováno v:
Pharmaceutical Chemistry Journal. 26:255-258
Autor:
V. I. Il'enko, G. M. Anoshina, N. V. Volkova, G. G. Vatulina, T. G. Koksharova, L. N. Dianova
Publikováno v:
Pharmaceutical Chemistry Journal. 26:134-137
Publikováno v:
Chemistry of Heterocyclic Compounds. 28:321-323
Nucleophilic substitution of 5-methylthio- and 5-cyanomethylthio-7-amino-s-triazolo[1,5-c]pyrimidines has been carried out using sodium hydroxide, ammonia, hydrazine hydrate, and four amines. The cyanomethyl group is particularly reactive under these
Autor:
A. R. Tumanova, N. V. Volkova, A. L. Lapidus, S. D. Pirozhkov, V. S. Mokrushin, Vasiliy A. Bakulev, T. G. Koksharova
Publikováno v:
Bulletin of the Russian Academy of Sciences Division of Chemical Science. 41:178-180
A new method has been developed for the synthesis of the ethyl ester of the mononitrile of malonic acid by the carbonylation of benzenesulfonyloxyacetonitrile in absolute ethanol in the presence of cobalt carbonyl. The yield of the desired product wa
Publikováno v:
Chemistry of Heterocyclic Compounds. 13:330-333
Autor:
N. V. Volkova, T. G. Koksharova, V. N. Konyukhov, L. N. Dianova, Vasiliy A. Bakulev, O. S. Anisimova
Publikováno v:
Chemistry of Heterocyclic Compounds. 21:355-358
Aminonitrile cleavage of the cyclic system was observed in the reaction of s-triazolo[1,5-c]pyrimidine derivatives with aryl (alkyl) halides in an alkaline medium or in dimethylfonnamide. It is shown that this transformation proceeds through the form
Publikováno v:
Chemistry of Heterocyclic Compounds. 13:326-329
The dissociation constants of 1-oxo-4-hydroxypyridazino[4,5-b]quinoxaline were measured by potentiometric titration. It is shown that this compound is a dibasic acid. Its reaction with organic bases, acids, alkalis, and oxidizing agents was studied.
Autor:
T. G. Lobova, A. S. Barybin, T. E. Zubova, Z. V. Pushkareva, V. N. Sokolova, T. G. Koksharova, Z. P. Sof'ina, Yu. A. Rozin
Publikováno v:
Pharmaceutical Chemistry Journal. 16:184-187