Zobrazeno 1 - 10
of 51
pro vyhledávání: '"G. A. Suboch"'
Publikováno v:
Russian Journal of Organic Chemistry. 58:1628-1636
Publikováno v:
Russian Journal of Organic Chemistry. 58:1637-1640
Publikováno v:
Russian Journal of Organic Chemistry. 56:1412-1420
Dialkyl 5-amino-2-hydroxy-4,6-dimethylisophthalates were synthesized for the first time by the reduction of the corresponding nitroso derivatives with sodium dithionite. The pKa and pKBH+ values of the synthesized compounds were determined and taken
Autor:
Ilya G. Povarov, Alexey V. Lubyashkin, Ekaterina V. Neupokoeva, G. A. Suboch, Nikita A. Shilenkov, Ivan V. Peterson, Mikhail S. Tovbis
Publikováno v:
Journal of Siberian Federal University. Chemistry. :405-412
For the previously obtained 1-isopropyl-3-α-naphthyl-5-methoxymethyl-4-nitrosopyrazole, a reduction reaction with hydrazine hydrate was performed. It was first synthesized by 1-isopropyl-3-α-naphthyl- 5-methoxymethyl-4-aminopyrazole which was then
Autor:
Ivan V. Peterson, G. A. Suboch, A. V. Lyubyashkin, V. V. Efimov, E. V. Neupokoeva, Mikhail S. Tovbis
Publikováno v:
Russian Journal of Organic Chemistry. 55:1081-1084
A previously unknown isonitroso diketone containing a naphthalen-1-yl substituent was synthesized. Its condensation with hydrazine hydrate resulted in the isolation for the first time of 3-(memoxymemyl)-5-(naphthalen-1-yl)-4-nitroso-1H-pyrazole. The
Autor:
M. V. Kulagina, E. S. Semichenko, A. A. Abramov, Alexander A. Kondrasenko, G. A. Suboch, N. A. Gavrilova
Publikováno v:
Russian Journal of Organic Chemistry. 55:1234-1237
N-(Adamantan-1-yl)alkyl-substituted 5-nitrosoquinolin-6-amines were synthesized for the first time by the amination of 5-nitrosoquinolin-6-ol with primary N-[(adamantan-1-yl)alkyl]amines. The resulting nitrosoquinolinamines were reduced with hydrazin
Publikováno v:
Russian Journal of Organic Chemistry. 55:991-994
Completely substituted p-nitrosophenols were synthesized by cyclocondensation of dimethyl 3-oxopentanedioate with 2-(hydroxyimino)-1-pyridylbutane-1,3-diones. The yield of the final product depended on the position of the nitrogen atom in the pyridyl
Autor:
Alexey V. Lyubyashkin, Ilya G. Povarov, Mikhail S. Tovbis, Viktor V. Efimov, G. A. Suboch, Anna S. Kositsyna
Publikováno v:
Journal of Siberian Federal University. Chemistry. :240-247
For the newly synthesized 3-aryl-5-methoxymethyl-4-amino-1H-pyrazoles the sulfonylation reaction of the amino group by p-acetamidobenzenesulfonyl chloride was carried out. As a result, sulfanilamide derivatives of substituted aminopyrazoles identifie
Publikováno v:
Russian Journal of Organic Chemistry. 55:730-733
Dimethyl 5-amino-2-hydroxy-4,6-dimethylisophthalate and dimethyl 5-amino-2-hydroxy-4,6-dimethylisophthalate were obtained in the free form for the first time. The products were sulfonylated with p-toluenesulfonyl to obtain previously unknown dialkyl
Autor:
M. S. Novikov, K. I. Kobrakov, Alexander S. Semeikin, Yu. N. Klimochkin, Fedor I. Zubkov, S. M. Medvedeva, Elena L. Gavrilova, L. G. Voskresenskii, Valery N. Charushin, Albert T. Lebedev, Alexander V. Aksenov, Ludmila L. Rodina, S. V. Kurbatov, Sergey M. Ivanov, Alexander P. Molchanov, Irina P. Beletskaya, Oleg N. Chupakhin, Elena A. Krasnokutskaya, Nicolai A. Aksenov, L. M. Mironovich, D. N. Kuznetsov, L. Ya. Zakharova, Mikhail P. Koroteev, Vad. V. Negrebetskii, O. A. Golubchikov, A. S. Fisyuk, A. V. Kolobov, Sergey Z. Vatsadze, Sergey P. Gromov, Vitaly A. Osyanin, Igor S. Antipin, Ivan I. Stoikov, A. I. Konovalov, Almira Kurbangalieva, Mikhail A. Kuznetsov, E. R. Kofanov, Victor D. Filimonov, Pavel A. Stuzhin, Valerij A. Nikolaev, A. Yu. Egorova, Nikolai V. Zyk, Alexander F. Khlebnikov, M. K. Grachev, Vladimir Burilov, Kh. S. Shikhaliev, Igor G. Zenkevich, Timur I. Madzhidov, Alexander N. Reznikov, D. B. Berezin, Svetlana E. Solovieva, Dmitrii A. Lemenovskii, Yu. I. Baukov, Valerii F. Traven, Andrey E. Shchekotikhin, A. Yu. Fedorov, R. S. Begunov, A. I. Rusakov, Valery S. Petrosyan, Alexander S. Tikhomirov, O. N. Burov, Mikhail S. Tovbis, T. A. Shmigol, O. V. Fedotova, V. Yu. Orlov, G. A. Suboch, A. K. Brel, V. I. Maslennikova, G. P. Sagitullina, M. Yu. Krasavin, Vakhid A. Mamedov, A. V. Nemtarev, S. V. Lisina, Aleksander V. Vasilyev, Alexander A. Korlyukov, V. G. Nenaidenko, M. E. Kletskii, Irina A. Balova, Oleg G. Sinyashin, Alexander V. Nyuchev
Publikováno v:
Russian Journal of Organic Chemistry. 54:157-371
This review is devoted to the scientific achievements of the departments of organic chemistry in higher schools of Russia within the past decade.