Zobrazeno 1 - 5
of 5
pro vyhledávání: '"I. V. Shahkeldyan"'
Publikováno v:
Russian Journal of Organic Chemistry. 56:2039-2042
The reaction of 5,7-dinitroquinolin-8-ol with NaBH4 produces a reactive hydride σ-complex, the treatment of which with a solution of acetic acid gives 5,7-dinitro-5,6-dihydroquinolin-8-ol. The protonation of the acetone σ-complex of 5,7-dinitroquin
Autor:
I. I. Surova, I. V. Blokhin, Yu. M. Atroshchenko, E. V. Ivanova, I. V. Shahkeldyan, Ivan V. Fedyanin
Publikováno v:
Chemistry of Heterocyclic Compounds. 49:1000-1008
A series of 1,5-dinitro-3,3-diazabicyclo[3.3.1]nonan-2-one derivatives has been synthesized by Mannich condensation of the hydride adduct of 2-hydroxy-3,5-dinitropyridine with formaldehyde and primary amines. The structure of the obtained compounds w
Autor:
N. A. Troitskii, M. B. Nikishina, V. A. Subbotin, Yu. A. Efremov, M. V. Kopyshev, E. N. Alifanova, Yu. M. Atroshchenko, I. V. Shahkeldyan, E. K. Melekhina
Publikováno v:
Russian Journal of Organic Chemistry. 39:589-595
A series of 7-carboxy-3-R-1,5-dinitro-3-azabicyclo[3.3.1]non-6-enes was synthesized by reduction of 3,5-dinitrobenzoic acid with sodium borohydride followed by Mannich reaction with formaldehyde and primary amines. The mechanism of decomposition unde
Autor:
Ivan V. Fedyanin, I. V. Shahkeldyan, I. I. Surova, E. V. Ivanova, I. V. Blokhin, Yu. M. Atroshchenko
Publikováno v:
ChemInform. 45
The Mannich condensation of the hydride adduct of 2-hydroxy-3,5-dinitropyridine with formaldehyde and primary amines leads to 1,5-dinitro-3,3-diazabicyclo[3.3.1]nonan-one derivatives (IV) or (V), depending on the reaction temperature.
Autor:
E. N. Alifanova, M. V. Kopyshev, E. K. Melekhina, M. B. Nikishina, I. V. Shahkeldyan, V. A. Subbotin, Yu. M. Atroshchenko, Yu. A. Efremov, N. A. Troitskii
Publikováno v:
ChemInform. 35