Journal: Russian Journal of General Chemistry

Short name
Russ. J. Gen. Chem.
IF
0.87
SJR
0.23
Показатели журнала
IF
0.779
SJR
0.191
Год
2021
Квартиль
Q4
IF
0.868
SJR
0.226
Год
2020
Квартиль
Q4
IF
0.716
SJR
0.221
Год
2019
Квартиль
Q4
IF
0.643
SJR
0.217
Год
2018
Квартиль
Q4
IF
0.658
SJR
0.225
Год
2017
Квартиль
Q4
IF
0.553
SJR
0.200
Год
2016
Квартиль
Q4
IF
0.481
SJR
0.213
Год
2015
Квартиль
Q4
IF
0.477
SJR
0.229
Год
2014
Квартиль
Q4
IF
0.418
SJR
0.220
Год
2013
Квартиль
Q4
IF
0.432
SJR
0.203
Год
2012
Квартиль
Q4
IF
0.467
SJR
0.199
Год
2011
Квартиль
Q4
IF
0.394
SJR
0.178
Год
2010
Квартиль
Q4

Papers

Impact Factor

Scientific Journal Ranking

2020

15.
Synthesis and Bioactivity of 5-Aryl-4-acyl-3-hydroxy-1-[2-(imidazolyl-3-yl)ethyl]3-pyrroline-2-ones
V. L. Gein
N. N. Kasimova
S. V. Chaschina
A. V. Starkova
Andrei Yankin
Russian Journal of General Chemistry
 , vol.
90
 , pp.
202-207
 , 2020
[DOI:
10.1134/s1070363220020061
 ] [ IF:
0.868
 , SJR:
0.226
 ]

2019

14.
Synthesis and Structure of 5-Aryl-4-[hydroxy(phenyl)methylene]-1-[2-(1H-indol-3-yl)ethyl]pyrrolidine-2,3-diones
V. L. Gein
L. I. Varkentin
M. I. Kazantseva
M. V. Dmitriev
Andrei Yankin
Russian Journal of General Chemistry
 , vol.
89
 , pp.
2196-2200
 , 2019
[DOI:
10.1134/s1070363219110057
 ] [ IF:
0.716
 , SJR:
0.221
 ]
13.
Reactions of 2-Acetyl-5-hydroxy-5-methyl-3-phenylcyclohexanone and Alkyl 4-Hydroxy-4-methyl-2-oxo-6-phenylcyclohexanecarboxylates with Nucleophilic Reagents
V. L. Gein
N. V. Nosova
A. V. Vagapova
N. V. Dozmorova
Andrei Yankin
Russian Journal of General Chemistry
 , vol.
89
 , pp.
1353-1359
 , 2019
[DOI:
10.1134/s1070363219070016
 ] [ IF:
0.716
 , SJR:
0.221
 ]
12.
Synthesis and Biological Activity of 4,5,6,7-Tetrahydro-2H-indazole Derivatives
V. L. Gein
Andrei Yankin
N. V. Nosova
E. B. Levandovskaya
V. V. Novikova
I. P. Rudakova
Russian Journal of General Chemistry
 , vol.
89
 , pp.
1169-1176
 , 2019
[DOI:
10.1134/s1070363219060112
 ] [ IF:
0.716
 , SJR:
0.221
 ]
11.
Synthesis and Biological Activity of 5-Aryl-N-{4-[(1,3-thiazol-2-yl)sulfamoyl]phenyl}-1-phenyl-1H-pyrazole-3-carboxamides and Their Salts
V. L. Gein
O. V. Bobrovskaya
A. A. Russkikh
V. V. Novikova
O. N. Gein
Yu. N. Karpenko
S. V. Chashchina
M. V. Dmitriev
Andrei Yankin
Russian Journal of General Chemistry
 , vol.
89
 , pp.
680-688
 , 2019
[DOI:
10.1134/s1070363219040078
 ] [ IF:
0.716
 , SJR:
0.221
 ]

2017

10.
Formation of variable-composition iron(III) hydrosilicates with the сhrysotile structure
Andrey Krasilin
V. V. Panchuk
V. G. Semenov
V. V. Gusarov
Russian Journal of General Chemistry
 , vol.
86
 , pp.
2581-2588
 , 2017
[DOI:
10.1134/s1070363216120021
 ] [ IF:
0.658
 , SJR:
0.225
 ]

2016

9.
Reactions of N-arylamides of acetoacetic acid with ninhydrin in the presence of piperidine
Andrei Yankin
N. V. Nosova
M. V. Dmitriev
V. L. Gein
Russian Journal of General Chemistry
 , vol.
86
 , pp.
1199-1201
 , 2016
[DOI:
10.1134/s1070363216050376
 ] [ IF:
0.553
 , SJR:
0.200
 ]
8.
Formation of 6-aryl-2-methyl-4-oxo-N,N’-diphenyl-2-cyclohexene-1,3-dicarboxamides from acetoacetanilide and aromatic aldehydes catalyzed by a mixture of aryl amines and iodine
V. L. Gein
Andrei Yankin
N. V. Nosova
M. V. Dmitriev
O. E. Nasakin
Russian Journal of General Chemistry
 , vol.
86
 , pp.
58-61
 , 2016
[DOI:
10.1134/s1070363216010114
 ] [ IF:
0.553
 , SJR:
0.200
 ]

2015

7.
Energy model of bilayer nanoplate scrolling: Formation of chrysotile nanoscroll
Andrey Krasilin
V. V. Gusarov
Russian Journal of General Chemistry
 , vol.
85
 , pp.
2238-2241
 , 2015
[DOI:
10.1134/s1070363215100047
 ] [ IF:
0.481
 , SJR:
0.213
 ]
6.
Multicomponent synthesis and antimicrobial activity of alkyl 4-arylamino-1,2,6-triaryl-1,2,5,6-tetrahydropyridine-3-carboxylates
Andrei Yankin
N. V. Nosova
V. L. Gein
M. V. Tomilov
Russian Journal of General Chemistry
 , vol.
85
 , pp.
844-850
 , 2015
[DOI:
10.1134/s1070363215040131
 ] [ IF:
0.481
 , SJR:
0.213
 ]
5.
Synthesis of N,N′,2-triaryl-6-hydroxy-6-methyl-4-oxocyclohexane-1,3-dicarboxamides and their reactions with p-toluidine and hydrazine hydrate
V. L. Gein
T. F. Odegova
Andrei Yankin
N. V. Nosova
Russian Journal of General Chemistry
 , vol.
85
 , pp.
46-52
 , 2015
[DOI:
10.1134/s1070363215010089
 ] [ IF:
0.481
 , SJR:
0.213
 ]
4.
Energy of formation of chrysotile nanotubes
Andrey Krasilin
V. V. Gusarov
Russian Journal of General Chemistry
 , vol.
84
 , pp.
2359-2363
 , 2015
[DOI:
10.1134/s1070363214120019
 ] [ IF:
0.481
 , SJR:
0.213
 ]

2011

3.
Phenyl(acyloxy)fluorosilanes C6H5Si(OCOR) n F3−n (n = 1, 2) and phenyl(acyloxy)fluorochlorosilanes C6H5Si(OCOR)FCl
S. V. Basenko
Lev Zelenkov
M. G. Voronkov
A. I. Albanov
D. A. Shabalin
Russian Journal of General Chemistry
 , vol.
81
 , pp.
2487-2489
 , 2011
[DOI:
10.1134/s1070363211120103
 ] [ IF:
0.467
 , SJR:
0.199
 ]
2.
Phenylhalosilazanes
S. V. Basenko
Lev Zelenkov
M. G. Voronkov
A. I. Albanov
Russian Journal of General Chemistry
 , vol.
81
 , pp.
2493-2497
 , 2011
[DOI:
10.1134/s1070363211120127
 ] [ IF:
0.467
 , SJR:
0.199
 ]

2010

1.
Phenyl(fluoro)chlorodisiloxanes
S. V. Basenko
Lev Zelenkov
M. G. Voronkov
A. I. Albanov
Russian Journal of General Chemistry
 , vol.
80
 , pp.
242-244
 , 2010
[DOI:
10.1134/s107036321002009x
 ] [ IF:
0.394
 , SJR:
0.178
 ]